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Cytoplasmic Streaming in the Drosophila Oocyte: Video 5
A video from the 2016 review by Margot E. Quinlan "Cytoplasmic Streaming in the Drosophila Oocyte" from the Annual Review of Cell and Developmental Biology.
Shown: The actin mesh in a stage 9 Drosophila oocyte is labeled by UtrnCH-GFP (the actin binding calponin homology domain of utrophin which labels filamentous actin). Images were acquired every 10 seconds.
Crafting a Manuscript: It's Easier to Take Your Voice Out Than to Get It Back In
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Are We Getting Further Away from Organizations?
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Research Ideas: Where to Look for Inspiration
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Having a Broader Influence on the Field: Why Being an Editor Matters
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
For Love of Basketball: How to Stay Engaged and Motivated
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Do You Need a Program of Research?
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Successful Scholars Also Publish: Developing a Portfolio of Research
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Where Do We Discover New Constructs?
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Go to Where the Action Is: Why We Need More Experience In and With Organizations
The Inspiration Behind Escalation of Commitment Research
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Beyond Hammers and Nails: Toward a Social Psychology of Organizations
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
The Dominance of Publishing in Top-Tier Journals: A Tale of Caution
Barry M. Staw Professor Emeritus at the Haas School of Business talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad College of Business at Michigan State University.
Moving On Out: Transport and Packaging of Influenza Viral RNA into Virions: Video 1
A video from the 2016 review by Seema S. Lakdawala Ervin Fodor and Kanta Subbarao "Moving On Out: Transport and Packaging of Influenza Viral RNA into Virions" from the Annual Review of Virology.
Shown: Inverted selective plane illumination microscopy video of Madin-Darby canine kidney (MDCK) cells infected with influenza A/WSN/33 PA-green fluorescent protein (GFP). MDCK cells were infected for 16 h and imaged for 30 min with an entire cell volume captured every 2 s. Scale bar = 10 µm. Video reproduced with permission from Reference 10.
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 1
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: Cell lysis following λ infection as seen under phase-contrast illumination (see also Figure 2e). The cell is infected at t = 0 and lyses at t ≈ 80 min. Video courtesy of Louis McLane and Samuel Skinner; Golding lab (unpublished).
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 2
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: Tracking the postinfection decision (see also Figure 2d ). Phage capsids were labeled using gpD-YFP. At t = 0 two cells are each infected by a single phage (green) and one cell is infected by three phages. The two cells infected by single phages go into the lytic pathway as indicated by the intracellular production of new phage capsids (green). The cell infected by three phages goes into the lysogenic pathway as indicated by the activity of a PRE-mCherry reporter (red). Eventually the lytic pathway results in cell lysis whereas the lysogenic cell continues to grow and divide. Video reproduced from Zeng et al. 2010 Cell 141:682–91 with permission from Elsevier.
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 3
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: PR activity during lysogen induction (see also Figure 2g ). In the reporter strain mRNA from the PR promoter is labeled using MS2-GFP (green) whereas the genome locus where the reporter resides is labeled using TetR-mCherry (red). The cells are λ lysogens. At t = 20 min mitomycin C is added leading to transient derepression of PR and induction of the dormant prophage. The prophage used is lysis deficient; hence the cells do not lyse at the end of the induction process. Video courtesy of Jing Zhang Louis McLane and Samuel Skinner; Golding lab (unpublished).
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 4
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: Single-molecule imaging of CI production (yellow) during stable lysogeny. Video reproduced from Hensel et al. 2012 Nat. Struct. Mol. Biol. 19:797–802 with permission from Macmillan Publishers Ltd.; see that reference for more information.
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 5
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: A single gpD-YFP-labeled λ phage (green) diffusing near and on the Escherichia coli cell (red). Two examples are shown sequentially. For more information see Rothenberg et al. 2011 Biophys. J. 100:2875–82. Video courtesy of Eli Rothenberg Samuel Skinner and Ido Golding (unpublished).
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 6
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: DNA injection into the cell. The λ genome initially inside the capsid was labeled using a SYTOX Orange DNA dye. Video reproduced from Van Valen et al. 2010 Curr. Biol. 22:1339–43 with permission from Elsevier; see that reference for more information.
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 7
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: Spatiotemporal dynamics of phage (red) and bacterial (green) genome loci inside the infected Escherichia coli cell during the lysogenic pathway (see Figure 2b ). The phage genome is labeled using mCherry-ParB. In the same cell the bacterial attB site is detected using an orthogonal ParB system and a GFP. For more information see Tal et al. 2014 PNAS 111:7308–12. Video courtesy of Louis McLane and Samuel Skinner; Golding lab (unpublished).
Single-Cell Studies of Phage λ: Hidden Treasures Under Occam's Rug: Video 8
A video from the 2016 review by Ido Golding "Single-Cell Studies of Phage λ: Hidden Treasures Under Occam’s Rug" from the Annual Review of Virology.
Shown: Spatiotemporal dynamics of the phage genome inside the cell during the lytic pathway. At t = 0 min the cell is infected by a gpD-YFP-labeled phage (green). At t = 5 min a SeqA-ECFP focus corresponding to the injected phage DNA appears. Later this focus is converted to two foci corresponding to two hemimethylated phage DNAs. The cell eventually lyses (not shown). Video reproduced from Shao et al. 2015 Biophys. J. 108:2048–60 with permission from Elsevier.
More than Meets the Eye: Hidden Structures in the Proteome: Video 1
A video from the 2016 review by Hal Wasserman and Erica Ollmann Saphire "More than Meets the Eye: Hidden Structures in the Proteome" from the Annual Review of Virology.
Shown: Morphs modeling how the VP40 dimer might transition to the matrix-assembling linear hexamer (this video) and the RNA-binding octameric ring (Video 2). In each of these videos N-terminal domains are blue and C-terminal domains are orange. In this video construction of the hexamer form the dimer it is modeled that three VP40 dimers gather at the membrane surface. It is hypothesized that an electrostatic interaction with lipid head groups triggers conformational rearrangement and assembly of the hexamer. Note that in the crystal structure of this hexamer (PDB: 4LDD) the central VP40 is upside down. In Video 2 the crystal structure of the octameric ring (PDB: 1H2D; Gomis-Ruth et al. 2003 Structure 11:423–33) reveals a 3-nt RNA bound to each N-terminal domain. RNA is illustrated here as the trigger that begins the conformational rearrangement. However it is not yet known what the trigger of this rearrangement is. We thank Dr. Zachary Bornholdt for the use of these models and videos originally published as supplemental figures in Bornholdt et al. 2013 Cell 154:763–74.
More than Meets the Eye: Hidden Structures in the Proteome: Video 2
A video from the 2016 review by Hal Wasserman and Erica Ollmann Saphire "More than Meets the Eye: Hidden Structures in the Proteome" from the Annual Review of Virology.
Shown: Morphs modeling how the VP40 dimer might transition to the matrix-assembling linear hexamer (Video 1) and the RNA-binding octameric ring (this video). In each of these videos N-terminal domains are blue and C-terminal domains are orange. In Video 1 construction of the hexamer form the dimer it is modeled that three VP40 dimers gather at the membrane surface. It is hypothesized that an electrostatic interaction with lipid head groups triggers conformational rearrangement and assembly of the hexamer. Note that in the crystal structure of this hexamer (PDB: 4LDD) the central VP40 is upside down. In this video the crystal structure of the octameric ring (PDB: 1H2D; Gomis-Ruth et al. 2003 Structure 11:423–33) reveals a 3-nt RNA bound to each N-terminal domain. RNA is illustrated here as the trigger that begins the conformational rearrangement. However it is not yet known what the trigger of this rearrangement is. We thank Dr. Zachary Bornholdt for the use of these models and videos originally published as supplemental figures in Bornholdt et al. 2013 Cell 154:763–74.
More than Meets the Eye: Hidden Structures in the Proteome: Video 3
A video from the 2016 review by Hal Wasserman and Erica Ollmann Saphire "More than Meets the Eye: Hidden Structures in the Proteome" from the Annual Review of Virology.
Shown: A modeled morph between the two folds of lymphotactin. Residues 61–70 have been modeled into the final structure to facilitate the final morph and allow the complete α-helix to be included. The beginning structure is the originally disordered Ltn10 monomeric form that functions as a chemokine (PDB: 1J8I). The final structure is one protomer of the biologically active dimer Ltn40 which functions in chemotaxis (PDB: 1J8I).
The Magellanic Stream: Circumnavigating the Galaxy: Figure 4
A video from the 2016 review by Elena D'Onghia and Andrew J. Fox "The Magellanic Stream: Circumnavigating the Galaxy" from the Annual Review of Astronomy and Astrophysics.
Shown: Gas projection in the simulated Magellanic System (red scale). This model reproduces the length of the Magellanic Stream and Leading Arm as well as the Magellanic Bridge connecting the Small and Large Magellanic Clouds (SMC and LMC). In this animation the SMC has completed three passages around the LMC. Adapted from Besla et al. (2012) with permission.
Visual Adaptation: Supplemental Video 1
A supplemental video from the 2015 review by Michael A. Webster "Visual Adaptation" from the Annual Review of Vision Science.
Shown: Demonstrations of adaptation aftereffects described in the review. For each the same image is presented before or after 10 s of adaptation to an adapting image. The aftereffects refer to changes in the appearance of the image following the adaptation. Images illustrating color and blur aftereffects are courtesy of Menka Webster. Images illustrating face aftereffects are from Matsumoto D Ekman P. 1988. Japanese and Caucasian facial expressions of emotion (JACFEE) and neutral faces (JACneuf). Dep. Psychol. San Francisco State Univ.
Livestock's Lure and Liabilities
Herrero et al. "Livestock and the Environment: What Have We Learned in the Past Decade?" Annual Review of Environment and Resources (2015)
Patterns of Gun Violence in the United States
Wintemute. "The Epidemiology of Firearm Violence in the Twenty-First Century United States" Annual Review of Public Health (2015).
Data Visualization and Statistical Graphics in Big Data Analysis: Video 1
A video from the 2016 review by Dianne Cook Eun-Kyung Lee and Mahbubul Majumder "Data Visualization and Statistical Graphics in Big Data Analysis" from the Annual Review of Statistics and Its Application.
Shown: Still image of video showing plane movements across the United States on a normal day of operations January 19 2006. The video includes red-eye planes leaving the West Coast for the East Coast the East Coast waking up and sporadic delayed flights. The code (including links to the data) is available at https://github.com/heike/usflights. An accompanying video at https://vimeo.com/119233996 shows operations during a northeastern snow day March 13 1993. Used with the permission of Heike Hofmann.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 1
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 1 Unwinding of a single molecule of λ DNA by RecBCD.
This video shows unwinding of a single molecule of λ DNA – stained with YOYO-1 attached to a 1-μm polystyrene bead (stained nonspecifically by YOYO-1) and captured by an optical trap by a single RecBCD enzyme at 37°C in the presence of 1 mM ATP; DNA is extend by solution flow from the bottom to the top. This molecule unwound at ∼440 bp/sec and dissociated after ∼26800 bp. Published with permissions from Reference 30.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 2
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 2 Unwinding of a single molecule of DNA by RecBCD.
This video shows translocation of an individual RecBCD molecule along χ-containing λ DNA visualized by virtue of a fluorescent 40-nm particle attached to a biotinylated RecD subunit. Solution flow is left to right. The very bright spot to the left is the 1-μm polystyrene bead to which nanoparticles are bound nonspecifically in the optical trap. Note that the nanoparticle--RecBCD complex can be seen to pause for about 6.6 s and then it continues to translocate but at a much reduced speed (∼145 bp/sec versus ∼1120 bp/sec prior to χ-recognition). Published with permission from Reference 54.
Data Visualization and Statistical Graphics in Big Data Analysis: Video 2
A video from the 2016 review by Dianne Cook Eun-Kyung Lee and Mahbubul Majumder "Data Visualization and Statistical Graphics in Big Data Analysis" from the Annual Review of Statistics and Its Application.
Shown: Use of interactive graphics to explore rankings of statistics departments in the United States. The plots show rating variables as side-by-side dotplots (left) a cluster analysis (center top) and a scatterplot of 5th-percentile rank computed using the S (vertical) and R (horizontal) methods (center bottom) and institution name lookup (right). Selecting an institution highlights (yellow) its values in each of the other plots. Cornell University is highlighted: We can see that its rank by the two methods differs substantially with a good R rank (around 5) but not such a good S rank (around 30). On the ranking criteria the department is around the middle of the pack: It is average in terms of number of publications and citations has few women faculty and students and accepts students with lower GRE scores than most statistics departments.
Data Visualization and Statistical Graphics in Big Data Analysis: Figure 9
A video from the 2016 review by Dianne Cook Eun-Kyung Lee and Mahbubul Majumder "Data Visualization and Statistical Graphics in Big Data Analysis" from the Annual Review of Statistics and Its Application.
Shown: Eulerian parallel coordinate plots (PCPs) of nutritional measurements of chocolates. The Eulerian PCP more strongly indicates a difference between the two types of chocolate milk (orange) and dark (red) and from the scagnostic describing separation displayed by the histogram (blue) we learn that higher values occur when fiber is one of the two variables indicating its importance as a variable. A simple interaction added to this plot using gridSVG highlights the line closest to the mouse cursor so that we can follow it throughout the plot.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 3
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 3 Interrupting and restarting single molecules of RecBCD during DNA unwinding.
This video compares unwinding of three individual molecules of λ DNA by three different single molecules of RecBCD whose initial velocities are comparable. Solution flow is left to right. For each the bright spot to the left is the 1-μm polystyrene bead to which YOYO-1 is bound nonspecifically in the optical trap. Unwinding is transiently paused by moving the molecules into a solution of EDTA (denoted by “Paused” during the video) and then resumed by returning the molecules to a solution of Mg2+:ATP. The change in relative unwinding rate is visually evident. Videos are representative of data collected and reported in Reference 31 although the video itself is previously unpublished.
Ocean Basin Evolution and Global-Scale Plate Reorganization Events Since Pangea Breakup: Supplemental Video 1
A supplemental video from the 2016 review by R. Dietmar Müller Maria Seton Sabin Zahirovic Simon E. Williams Kara J. Matthews Nicky M. Wright Grace E. Shephard Kayla T. Maloney Nicholas Barnett-Moore Maral Hosseinpour Dan J. Bower and John Cannon "Ocean Basin Evolution and Global-Scale Plate Reorganization Events Since Pangea Breakup" from the Annual Review of Earth and Planetary Sciences.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 4
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 4 Unwinding of a single molecule of λ DNA by RecQ detected using fluorescent SSB and imaged using TIRF microscopy.
Initially the dsDNA tethered at each end to the surface of a flow cell is fluorescent due to intercalation of the YO-PRO-1 dye molecules. As a solution containing 200 mM NaCl is introduced into the flow cell the dye dissociates and fluorescence disappears. Subsequently a solution containing 80 nM RecQ and SSBAF488 is introduced into the flow cell to initiate unwinding. The solution fills the channel 24 s into the video. The flow when on goes from left to right in the video. The elapsed time is indicated in hours:minutes:seconds and scale bar is 5 μm. Published with permission from Reference 73.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 5
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 5 Salt-induced intramolecular condensation of SSB-ssDNA imaged using TIRF microscopy.
Video of a single molecule of SSBAF488-coated λ ssDNA tethered at one end and imaged using TIRF microscopy contracting in length upon increasing [NaOAc] from 0 to 100 mM. Solution flow is left to right. The video frames were rendered into a topological intensity map. Time zero corresponds to the time at which the pump was turned on. The dead time of the experiment was approximately 25 s due to the volume in the lines between the syringe valve and the microfluidic chamber. Published with permission from Reference 102.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 6
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 6 Condensation of SSB in the absence of free protein during a transient increase from 0 to 100 mM NaOAc.
Video of a single molecule of SSBAF488-coated λ ssDNA contracting in length as the salt concentration is increased from 0 to 100 mM NaOAc and then subsequently reduced back to zero mM conducted in the absence of free SSBAF488. Solution flow is left to right. The flow cell was extensively washed with buffer to remove free SSB protein before beginning the experiment. Video recording began when the pump was turned on requiring ∼40-50 s for the dead volume to be flushed from the lines to the flow chamber. SSBAF488 was omitted from both of the high-salt washes and from the 0 mM wash. Published with permission from Reference 102.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 7
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 7 Direct imaging of nucleation and growth of RecA on SSB-coated ssDNA using TIRF microscopy.
This video first shows a flow-extended single molecule of 3′-biotinylated λ ssDNA coated with a fluorescent protein SSBAF488. The molecule was tethered to a streptavidin-coated glass surface within a microfluidic flow cell and visualized using total internal reflection fluorescence microscopy. Solution flow is left to right. SSBAF488 was exchanged with non-fluorescent SSB on the ssDNA in situ and filament assembly was initiated by injecting fluorescein labeled RecA (350 nM) with nucleotide cofactor (ATPγS). Filament assembly proceeded primarily in the absence of flow or laser excitation which were both used only during brief intermittent time-lapsed imaging. Images were processed and rendered into a topographical intensity map for clarity. Published with permission from Reference 110.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 8
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 8 Optical trapping and manipulation of single molecules of gapped λ DNA for direct imaging of RecA filament assembly.
This video first shows 1-μm streptavidin-coated polystyrene beads flowing through Channel 1 of a multichannel microfluidic flow chamber and the subsequent isolation of two beads by a split-beam dual optical trap (Step 1). Solution flow is left to right. The beads are then transferred to Channel 2 which contains gapped λ DNA molecules comprising 8155 nucleotides of SSB-coated ssDNA flanked by 21.08 and 24.59 kbp of YOYO-1 stained dsDNA; the gapped DNA is biotinylated at each of the molecule and is captured in situ by binding to the streptavidin-coated beads (Step 2). The molecule is then transferred to a DNA-free Channel 3 where the distal end of the flow-extended molecule is captured by the other bead which is micromanipulated using a steerable mirror in line with one of the infrared laser beams (Step 3). The molecule is then rotated perpendicular to flow and imaged in buffer optimized for visualizing YOYO-1 stained dsDNA in Channel 4 (Step 4). The molecule is then transferred to Channel 5 containing Mg2+:ATPγS which accelerates YOYO-1 dissociation (Step 6). The molecule was then successively incubated in reaction buffer containing fluorescein labeled RecA Mg2+:ATPγS and either RecOR or RecFOR and imaged in Channel 5 to measure the rates of nucleation and growth (Step 7). Published with permission from Reference 110.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 9
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 9 Composite video depicting the experimental procedure used to visualize DNA pairing on single λ DNA-dumbbell molecules by optical trapping.
A DNA pairing reaction (2 min) was performed with the 430 nt substrate at a 2 μm bead distance. Text and illustrations were inserted at appropriate places to facilitate description. A four-channel flow cell with a flow-free reservoir was used. Solution flow is top to bottom. First two 1-μm streptavidin-coated polystyrene beads are captured in dual optical traps. Next a single DNA molecule is captured on one bead. The DNA-dumbbell is made by sliding the DNA along the other bead until the biotinylated end attaches. The DNA end-to-end distance is set and the YOYO-1 dye is removed. The DNA-dumbbell is incubated with fluorescent RecA nucleoprotein filaments in the flow-free reservoir for 2 min. Afterward the DNA-dumbbell is moved to the observation channel and is extended to near contour length to image the pairing products. Published with permission from Reference 152.
Mechanics and Single-Molecule Interrogation of DNA Recombination: Supplemental Video 10
A supplemental video from the 2016 review by Jason C. Bell and Stephen C. Kowalczykowski "Mechanics and Single-Molecule Interrogation of DNA Recombination" from the Annual Review of Biochemistry.
Supplemental Video 10 Dissociation of heterologously paired RecA nucleoprotein filaments during a DNA pairing experiment.
Video performed as in Supplemental Video 9 showing RecA nucleoprotein filaments both heterologously bound and homologously bound (left and right red spots respectively) during the extension step of a pairing assay performed using the 1762 nt homologous ssDNA. As the beads are separated several loop-release events are observed involving the heterologously bound filament (left) before its dissociation from λ DNA whereas the homologously bound RecA nucleoprotein filament (right) remains stably bound. Published with permission from Reference 152.
Leading Leadership Research: A Framework for Research and Practice
David Day of The University of Western Australia Business School discusses his article "Leadership Development: An Outcome-Oriented Review Based on Time and Levels of Analyses." In this video he outlines a framework for leader development over time. Dr. Day explains that focusing research and intervention on proximal indicators like competencies and self-views helps determine longer-term outcomes such as hierarchical complexity and sophisticated sense-making matching these to the leaders’ environments.
Developing Your Leaders: Linking Short-Term Change to Long-Term Success
David Day of The University of Western Australia Business School discusses his article "Leadership Development: An Outcome-Oriented Review Based on Time and Levels of Analyses." In this video he outlines a framework for leader development over time. Dr. Day explains that focusing research and intervention on proximal indicators like competencies and self-views helps determine longer-term outcomes such as hierarchical complexity and sophisticated sense-making matching these to the leaders’ environments.
Lessons for Leadership Scholars: Where Can You Take Your Research?
What Can Leadership Development Do for Your Organization?
Lisa Dragoni of Wake Forest University discusses her article "Leadership Development: An Outcome-Oriented Review Based on Time and Levels of Analyses” which she co-wrote with David Day of the University of Western Australia Business School. In this video she reviews the research on leadership development. Dr. Dragoni outlines the conditions that support leadership development at an organizational level. These include interpersonal comfort among team members their expertise and shared mindset.
The Growing Impact of Citizen Astronomers
Marshall et al. "Ideas for Citizen Science in Astronomy"
Insect Flight: From Newton's Law to Neurons: Video 1
A video from the 2016 review by Z. Jane Wang "Insect Flight: From Newton's Law to Neurons" from the Annual Review of Condensed Matter Physics.
Shown: A model fly hovers briefly and succumbs to pitching instability. This is an example of flight instability with feedback control (1; also see Section 2).
Insect Flight: From Newton's Law to Neurons: Video 2
A video from the 2016 review by Z. Jane Wang "Insect Flight: From Newton's Law to Neurons" from the Annual Review of Condensed Matter Physics.
Shown: With a time-delayed discrete feedback control scheme the model fly can hover stably (1; also see Section 3.4).
The Role of Craving in Substance Use Disorders: Theoretical and Methodological Issues: Supplemental Video 1
A supplemental video from the 2016 review by Michael A. Sayette "The Role of Craving in Substance Use Disorders: Theoretical and Methodological Issues" from the Annual Review of Clinical Psychology.
Shear Banding of Complex Fluids: Supplemental Video 1
A video from the 2016 review by Thibaut Divoux Marc A. Fardin Sebastien Manneville and Sandra Lerouge "Shear Banding of Complex Fluids" from the Annual Review of Fluid Mechanics.
Shown: The temporal evolution of the global shear stress (left) during a shear startup experiments at a shear rate of 0.5 s−1 together with the velocity profiles (right) recorded simultaneously to the rheological data across the 1-mm gap a Taylor-Couette cell. The moving wall is located at r = 0 and the experiment is performed on a 1% w.t. Carbopol microgel.
Drop Impact on a Solid Surface: Supplemental Video 1
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: The impact of a mercury drop onto glass for similar impact conditions as Wortington’s sketch in Figure 1b. Courtesy of Erqiang Li.
Drop Impact on a Solid Surface: Supplemental Video 2
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Prompt splash during the impact of a mercury drop onto a superhydrophobized glass surface. Courtesy of Erqiang Li.
Drop Impact on a Solid Surface: Supplemental Video 3
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Corona splash of an ethanol drop impacting onto a dry glass plate. Courtesy of Erqiang Li.
Drop Impact on a Solid Surface: Supplemental Video 4
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Time-resolved interference imaging of the dimple formation and entrapment of an air disc under a water drop impacting a glass plate at low impact velocity. The view is through the bottom plate. The debt variation between a dark and bright fringe is 160 nm. Frame rate is 5 Mfps. From Li & Thoroddsen (2015).
Drop Impact on a Solid Surface: Supplemental Video 5
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Time-resolved interference imaging of the dimple formation and entrapment of an air disc under a water drop impacting a glass plate at high impact velocity. The compression of the air inside the disc is evident from the rapid expansion following the first contact. Frame rate is 5 Mfps. From Li & Thoroddsen (2015).
Drop Impact on a Solid Surface: Supplemental Video 6
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Entrapment of an air disc under a water drop impacting a glass plate. The view is through the bottom plate. The air disc contracts producing capillary waves on the free surface. These waves touch the glass at the center thereby entrapping a small microdrop inside the bubble inside the drop. Frame rate is 50 kfps. From Thoroddsen et al. (2003).
Drop Impact on a Solid Surface: Supplemental Video 7
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Prompt splash and entrapment of central air disc for impacting water drop at high velocity. Azimuthal instability is visible in the base of the ejecta. Frame rate is 500 kfps. From Thoroddsen et al. (2012).
Drop Impact on a Solid Surface: Supplemental Video 8
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Ejected microdroplets. The smallest and fastest droplets emerge first with progressively larger and slower droplets detaching from the front of the lamella. Frame rate is 1 Mfps. From Thoroddsen et al. (2012).
Drop Impact on a Solid Surface: Supplemental Video 9
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Ejected droplets and azimuthal undulations on the lamellar surface. Frame rate is 125 kfps. From Thoroddsen et al. (2012).
Drop Impact on a Solid Surface: Supplemental Video 10
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: Air entrapment under a levitated lamella resulting from local contacts ahead of the moving contact line. Frame rate is 62 kfps. From Thoroddsen et al. (2010).
Drop Impact on a Solid Surface: Supplemental Video 11
A supplemental video from the 2016 review by C. Josserand and S.T. Thoroddsen "Drop Impact on a Solid Surface" from the Annual Review of Fluid Mechanics.
Shown: The impact of a compound drop outer drop is a water/glycerin mixture of viscosity 2 cP. It contains 20 inner perfluorohexane droplets which are more dense and migrate toward the bottom free surface of the large drop. For impact velocity V ≃ 4 m/s drop D ≃ 4 mm. Frame rate is 12 kfps. Courtesy of Jiaming Zhang and Erqiang Li.
Bacterial Hydrodynamics: Supplemental Video 1
A supplemental video from the 2016 review by Eric Lauga "Bacterial Hydrodynamics" from the Annual Review of Fluid Dynamics.
Shown: Swimming Escherichia coli bacteria with fluorescently labeled flagellar filaments showing fluorescent bundles of flagellar filaments rotating and propelling individual cells forward. The details of the experimental procedure are given in Turner L Ryu WS Berg HC. 2000. Real-time imaging of fluorescent flagellar filaments. J. Bacteriol. 182:2793–801. The video is reproduced with permission from Howard Berg’s website at the Rowland Insitute Harvard University (http://www.rowland.harvard.edu/labs/bacteria/movies/ecoli.php).
Bacterial Hydrodynamics: Supplemental Video 2
A supplemental video from the 2016 review by Eric Lauga "Bacterial Hydrodynamics" from the Annual Review of Fluid Dynamics.
Shown: Swimming Escherichia coli bacteria with fluorescently-labeled flagellar filaments showing individual run-and-tumble events with flagellar filaments unbundling cells turning and flagellar filaments rejoining the bundle. The details of the experimental procedure are given in Turner L Ryu WS Berg HC. 2000. Real-time imaging of fluorescent flagellar filaments. J. Bacteriol. 182:2793–801. The video is reproduced with permission from Howard Berg’s website at the Rowland Insitute Harvard University (http://www.rowland.harvard.edu/labs/bacteria/movies/ecoli.php).
Receptor Activity-Modifying Proteins (RAMPs): New Insights and Roles: Supplemental Video 1
A supplemental video from the 2016 review by Debbie L. Hay and Augen A. Pioszak "Receptor Activity-Modifying Proteins (RAMPs): New Insights and Roles" from the Annual Review of Pharmacology and Toxicology.
Mangrove Sedimentation and Response to Relative Sea-Level Rise: Visual Abstract
A visual abstract for the 2016 review by C.D. Woodroffe K. Rogers K.L. McKee C.E. Lovelock I.A. Mendelssohn and N. Saintilan "Mangrove Sedimentation and Response to Relative Sea-Level Rise" from the Annual Review of Marine Science.
A Conversation with Maarten Schmidt - Other Work and Future Directions
Sandra Faber talks with Maarten Schmidt about his life and career including the discovery of quasars. Video 4 of 4.
A Conversation with Maarten Schmidt - The Discovery of Quasars
Sandra Faber talks with Maarten Schmidt about his life and career including the discovery of quasars. Video 1 of 4.
A Conversation with Maarten Schmidt - Early Life, Education, and Other Work
Sandra Faber talks with Maarten Schmidt about his life and career including the discovery of quasars. Video 3 of 4.
A Conversation with Maarten Schmidt - Using Quasars to Establish that the Universe Evolves
Sandra Faber talks with Maarten Schmidt about his life and career including the discovery of quasars. Video 2 of 4.
Group Affect
In this video Sigal Barsade of the Wharton School at the University of Pennsylvania and Andrew Knight of Olin Business School at Washington University discuss their article “Group Affect” which they co-wrote for the 2015 Annual Review of Organizational Psychology and Organizational Behavior. They explain how emotional contagion helps maintain group cohesiveness in a professional environment and how leaders can cultivate positive affect for better results.
Retroviral Integrase: Then and Now: Video 1
A video from the 2015 review by Mark D. Andrake and Anna Marie Skalka "Retroviral Integrase: Then and Now" from the Annual Review of Virology.
Shown: Assembly of the prototype foamy virus (PFV) intasome (see Figure 3). This brief video portrays one possible scenario for how the PFV intasome may be assembled from PFV integrase (IN) monomers the predominant multimer found in solution. The complex is shown in ribbon representation with the inner subunits in red and blue. Viral DNA oligonucleotides are in orange ribbon ladder representation and the target DNA in yellow and black. The outer IN subunits only show the catalytic core domains and are colored gray. After the target DNA moves into place the view zooms in to one active site to show the location of active site metals (depicted as green spheres) and the DDE residues (shown in stick representation) that are required for metal binding. This video was generated using UCSF Chimera software [Pettersen et al. J. Comput. Chem. 25:1605–12 (2004)] with the coordinates of PDB 4E7K.
Flaviviridae Replication Organelles: Oh, What a Tangled Web We Weave: Video 1
A video from the 2015 review by David Paul and Ralf Bartenschlager "Flaviviridae Replication Organelles: Oh What a Tangled Web We Weave" from the Annual Review of Virology.
Shown: Morphology of dengue virus (DV) replication organelles. Electron tomography with 3D reconstruction reveals the continuity of endoplasmic reticulum membranes (yellow) and DV-induced vesicular invaginations. Budding of DV progeny virions (red) juxtaposed to vesicle openings is frequently observed. Golgi membranes are depicted in green. Adapted with permission from Welsch et al. Cell Host Microbe 5:365–75 (2009).
Flaviviridae Replication Organelles: Oh, What a Tangled Web We Weave: Video 2
A video from the 2015 review by David Paul and Ralf Bartenschlager "Flaviviridae Replication Organelles: Oh What a Tangled Web We Weave" from the Annual Review of Virology.
Shown: Morphology of hepatitis C virus (HCV) replication organelles consisting primarily of double-membrane vesicles (DMVs). Color-coded 3D surface model shows outer membranes of DMVs in light brown and inner membranes in orange. DMVs emerge as protrusions from the endoplasmic reticulum (dark brown) and are thus commonly found to be connected to this compartment. Small single-membrane vesicles are depicted in pink intermediate filaments in dark blue and Golgi membranes in green. Reproduced with permission from Romero-Brey et al. PLOS Pathog. 8:e1003056 (2012).
Continuous and Discontinuous RNA Synthesis in Coronaviruses: Video 1
A video from the 2015 review by Isabel Sola Fernando Almazán Sonia Zúñiga and Luis Enjuanes "Continuous and Discontinuous RNA Synthesis in Coronaviruses" from the Annual Review of Virology.
Shown: Model for the formation of genome high-order structures regulating N gene transcription. The upper linear scheme represents the coronavirus genome. The red line indicates the leader sequence in the 5′ end of the genome. The hairpin indicates the TRS-L. The gray line with arrowheads represents the nascent negative-sense RNA. The curved blue arrow indicates the template switch to the leader sequence during discontinuous transcription. The orange line represents the copy of the leader added to the nascent RNA after the template switch. The RNA-RNA interactions between the pE (nucleotides 26894 to 26903) and dE (nucleotides 26454 to 26463) and between the B-M in the active domain (nucleotides 26412 to 26421) and the cB-M in the 5′ end of the genome (nucleotides 477 to 486) are represented by solid lines. Dotted lines indicate the complementarity between positive-strand and negative-strand RNA sequences. Abbreviations: AD active domain secondary structure prediction; B-M B motif; cB-M complementary copy of the B-M; cCS-N complementary copy of the CS-N; CS-L conserved core sequence of the leader; CS-N conserved core sequence of the N gene; dE distal element; pE proximal element; TRS-L transcription-regulating sequence of the leader. Download a PowerPoint version of the animation.
Deep Recombination: RNA and ssDNA Virus Genes in DNA Virus and Host Genomes: Video 1
A video from the 2015 review by Kenneth M. Stedman "Deep Recombination: RNA and ssDNA Virus Genes in DNA Virus and Host Genomes" from the Annual Review of Virology.
Shown: Schematic of different virus classes [after Baltimore 1971 (10)] and the integration of some viruses into cellular genomes. Black arrows represent DNA. Red arrows represent RNA. Blue hexagons represent virus capsids. Blue arrows represent virus replication mechanisms to produce mRNA for protein translation. Gray arrows represent integration into the host genome with the thickness of the arrow representing the gross frequency of recombination. The recombination arrow from Class VI viruses the retroviruses proceeds through a dsDNA intermediate. Recombination between ssDNA viruses (Class II) and dsDNA genomes may proceed through dsDNA (lower arrow) or directly as ssDNA (upper arrow) (55). Recombination between Class V and Class III viruses is probably mediated by cellular retrotransposons (see Figure 2). Download a PowerPoint version of the animation.
Deep Recombination: RNA and ssDNA Virus Genes in DNA Virus and Host Genomes: Video 2
A video from the 2015 review by Kenneth M. Stedman "Deep Recombination: RNA and ssDNA Virus Genes in DNA Virus and Host Genomes" from the Annual Review of Virology.
Shown: Proposed LINE-1-mediated mechanism of integration of RNA virus genes into host genomes. LINE-1 elements in the host genome (blue rectangle) are transcribed into mRNA (red line). The resulting mRNAs are exported to the cytoplasm where they combine with ORF1 (light blue circles) and ORF2 (orange ovals) the products of the two LINE-1 open reading frames. These complexes can be either relocated to stress granules or reimported back into the nucleus (blue arrows) where they can recombine with the host genome (dark gray lines) by reverse transcription. RNA viruses (green hexagon) infect the cell and produce mRNA (orange lines) that can bind to the ORF products of LINE-1 and be imported to the nucleus for reverse transcription or possibly relocated to stress granules (green arrows). Download a PowerPoint version of the animation.
Motors, Anchors, and Connectors: Orchestrators of Organelle Inheritance: Supplemental Video 1
A video from the 2015 review by Barbara Knoblach and Richard A. Rachubinski "Motors Anchors and Connectors: Orchestrators of Organelle Inheritance" from the Annual Review of Cell and Developmental Biology.
Shown: Inp1p: an organelle connector that tethers peroxisomes to the cell cortex. Budding yeast cells contain static (anchored) and mobile peroxisomes. Live-cell video microscopy was performed on wild-type cells expressing the peroxisomal matrix protein mCherry-PTS1 and Inp1p-3×GFP. Merged images of the red and green channels are presented. Static peroxisomes contain Inp1p and thus appear yellow whereas mobile peroxisomes are devoid of Inp1p and appear red.
The Hepatitis B Virus Receptor: Supplemental Video 1
A video from the 2015 review by Wenhui Li "The Hepatitis B Virus Receptor" from the Annual Review of Cell and Developmental Biology.
Mechanism and Regulation of Cytoplasmic Dynein: Supplemental Video 1
A video from the 2015 review by Michael A. Cianfrocco Morgan E. DeSantis Andres E. Leschziner and Samara L. Reck-Peterson "Mechanism and Regulation of Cytoplasmic Dynein" from the Annual Review of Cell and Developmental Biology.
Shown: Dynein’s mechanochemical cycle. This video shows an animated version of dynein’s mechanochemical cycle as outlined in Figure 1d . The video illustrates a single step for a dynein head. In contrast to Figure 1d here we include a full dimer. The color coding is the same as that used in Figure 1. We use steps to describe dynein’s mechanochemical cycle in the main text and to illustrate it in Figure 1d . We indicate those steps in this Supplemental Video so the reader can refer to the main text for a full description of the changes that take place.
Adaptive Optics Ophthalmoscopy: Figure 8
A video from the 2015 review by Austin Roorda and Jacque L. Duncan "Adaptive Optics Ophthalmoscopy" from the Annual Review of Vision Science.
Shown: A video of a patient with type 1 diabetes taken using a 400 frame-per-second adaptive optics fundus camera.
Adaptive Optics Ophthalmoscopy: Figure 9
A video from the 2015 review by Austin Roorda and Jacque L. Duncan "Adaptive Optics Ophthalmoscopy" from the Annual Review of Vision Science.
Shown: A video of a patient with type 1 diabetes taken using a 400 frame-per-second adaptive optics fundus camera.
Koala Retroviruses: Evolution and Disease Dynamics
Maribeth V. Eiden of the Laboratory of Cellular and Molecular Regulation at the National Institute of Mental Health discusses her article “Koala Retroviruses: Evolution and Disease Dynamics” which she wrote with Wenqin Xu for the 2015 Annual Review of Virology.
Quantitative Resistance to Biotrophic Filamentous Plant Pathogens: Concepts, Misconceptions, and Mechanisms: Video 1
A video from the 2015 review by Rients E. Niks Xiaoquan Qi and Thierry C. Marcel "Quantitative Resistance to Biotrophic Filamentous Plant Pathogens: Concepts Misconceptions and Mechanisms" from the Annual Review of Phytopathology.
Shown: Seedling leaves of three barley genotypes infected by isolate 1.2.1 of Puccinia hordei the barley leaf rust fungus showing the difference in rate of pustule development in a monocyclic test. Times (in days and hours) after inoculation are indicated.
Genotypes are extremely susceptible (L94) partially resistant (Vada) and extremely high partially resistant (17-5-16). The pale flecks are immature infections and the orange pustules are mature sporulating reproduction organs of the fungus (uredinia).
Day 7 17:00: Almost all pustules on L94 are mature whereas only the first pustules on Vada are mature.
Day 9 2:00: Almost all pustules on Vada are mature and on 17-5-16 the first mature pustule has just appeared. Vada shows approximately 50% fewer mature pustules than L94.
Day 12 9:00: The final number ofmature pustules on 17-5-16 is 12 which is much less than on Vada and L94.
A Conversation with Adam Heller
Adam Heller Research Professor and Professor Emeritus of Chemical Engineering at the University of Texas at Austin and Chief Science Officer at SynAgile Corp. talks about his life and career with Elton J. Cairns Professor of the Graduate School Department of Chemical and Biomolecular Engineering at the University of California Berkeley and Faculty Senior Scientist at the Lawrence Berkeley National Laboratory. Dr. Heller discusses his and his family’s deportation from Hungary to Switzerland during the second World War and their move to British Mandate Palestine which eventually became Israel. He then recounts how his research allowed him to lead the development of one of the very first lithium batteries liquid lasers more efficient solar cells and a way to monitor the glucose concentration in the blood of diabetic patients.
Visual Guidance in Control of Grasping: Supplemental Video 1
A video from the 2015 review by Peter Janssen and Hansjörg Scherberger "Visual Guidance in Control of Grasping" from the Annual Review of Neuroscience.
Shown: A macaque monkey grasping a piece of apple after a bilateral injection of muscimol (B.E. Verhoef R. Vogels & P. Janssen unpublished observations).
Ed Schein – The Dangers of Abstraction
Edgar Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
There's More to Research than Just Doing Experiments: How Ed Schein Got His Start
Edgar H. Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
View all videos in this series:
- There's More to Research than Just Doing Experiments: How Ed Schein Got His Start
- Ed Schein – Realizing the Power of Experiential Learning
- Ed Schein – 50 Years of Organizational Psychology: Challenges in Application
- Ed Schein – Let's Focus on (National Organizational and Occupational) Culture
- Ed Schein – The Pitfalls of a Statistical Orientation
- Ed Schein – Advice for Young Scholars: Find Your Career Anchors
- Ed Schein – The Good Stuff Comes Out of Teams
- Ed Schein – Key Consulting Insights: The Power of Examples
- Ed Schein – The Dangers of Abstraction
Ed Schein – 50 Years of Organizational Psychology: Challenges in Application
Edgar H. Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
View all videos in this series:
- There's More to Research than Just Doing Experiments: How Ed Schein Got His Start
- Ed Schein – Realizing the Power of Experiential Learning
- Ed Schein – 50 Years of Organizational Psychology: Challenges in Application
- Ed Schein – Let's Focus on (National Organizational and Occupational) Culture
- Ed Schein – The Pitfalls of a Statistical Orientation
- Ed Schein – Advice for Young Scholars: Find Your Career Anchors
- Ed Schein – The Good Stuff Comes Out of Teams
- Ed Schein – Key Consulting Insights: The Power of Examples
- Ed Schein – The Dangers of Abstraction
Ed Schein – Advice for Young Scholars: Find Your Career Anchors
Edgar H. Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
Ed Schein – The Pitfalls of a Statistical Orientation
Edgar H. Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
Ed Schein – Let's Focus on (National, Organizational, and Occupational) Culture
Edgar H. Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
Ed Schein – Key Consulting Insights: The Power of Examples
Edgar Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
Ed Schein – Realizing the Power of Experiential Learning
Edgar H. Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick P. Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
Ed Schein – The Good Stuff Comes Out of Teams
Edgar Schein Professor Emeritus at the MIT Sloan School of Management talks about his life and career with Frederick Morgeson Eli Broad Professor of Management at the Eli Broad Graduate School of Management of Michigan State University.
Low-Temperature Kinetics and Dynamics with Coulomb Crystals: Supplemental Video 1
A supplemental video from the 2015 review by Brianna R. Heazlewood and Timothy P. Softley "Low-Temperature Kinetics and Dynamics with Coulomb Crystals" from the Annual Review of Physical Chemistry.
Shown: the rotating potential of a trapped ion in the applied RF field.
What We Learned from Our Justice Review: Takeaways from a Veteran and a Newcomer to the Justice Literature
Jason A. Colquitt and Kate P. Zipay of the Terry College of Business at the University of Georgia discuss their article “Justice Fairness and Employee Reactions” which they wrote for the 2015 Annual Review of Organizational Psychology and Organizational Behavior.
How Exactly Should You Measure Justice?
Jason A. Colquitt and Kate P. Zipay of the Terry College of Business at the University of Georgia discuss their article “Justice Fairness and Employee Reactions” which they wrote for the 2015 Annual Review of Organizational Psychology and Organizational Behavior.
Putting It all Together: Integrating Justice Theories
Jason A. Colquitt and Kate P. Zipay of the Terry College of Business at the University of Georgia discuss their article “Justice Fairness and Employee Reactions” which they wrote for the 2015 Annual Review of Organizational Psychology and Organizational Behavior.