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Showing results (101-110 of 138) with videos related to

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Proteins|October 25, 2023
Assessment of three-dimensional RNA structure prediction in CASP15Rhiju Das, Rachael C Kretsch, Adam J Simpkin, et al.
Journal of Virology|April 20, 2012
Structural analysis of coxsackievirus A7 reveals conformational changes associated with uncoatingJani J T Seitsonen, Shabih Shakeel, Petri Susi, et al.
Structure (London, England : 1993)|July 16, 2013
The structure of herpesvirus fusion glycoprotein B-bilayer complex reveals the protein-membrane and lateral protein-protein interactionUlrike E Maurer, Tzviya Zeev-Ben-Mordehai, Arun Prasad Pandurangan, et al.
Journal of the American Chemical Society|September 8, 2017
The Role of Disulfide Bond Replacements in Analogues of the Tarantula Toxin ProTx-II and Their Effects on Inhibition of the Voltage-Gated Sodium Ion Channel Na<sub>v</sub>1.7Zoë V F Wright, Stephen McCarthy, Rachael Dickman, et al.
Human Molecular Genetics|May 15, 2010
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulinsRavinesh A Kumar, Daniela T Pilz, Timothy D Babatz, et al.
Proteins|June 12, 2023
New prediction categories in CASP15Andriy Kryshtafovych, Maciej Antczak, Marta Szachniuk, et al.
Frontiers in Molecular Neuroscience|January 22, 2016
Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 FamilyVera M Kalscheuer, Victoria M James, Miranda L Himelright, et al.
Elife|June 5, 2019
Genetic diversity of CHC22 clathrin impacts its function in glucose metabolismMatteo Fumagalli, Stephane M Camus, Yoan Diekmann, et al.
Neurobiology of Disease|December 15, 2012
Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle diseaseVictoria M James, Anna Bode, Seo-Kyung Chung, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 21, 2017
Disruption of a Structurally Important Extracellular Element in the Glycine Receptor Leads to Decreased Synaptic Integration and Signaling Resulting in Severe Startle DiseaseNatascha Schaefer, Alexandra Berger, Johannes van Brederode, et al.
Pageof 14

Showing results (101-110 of 138) with videos related to

Sort By:
Pageof 14
Proteins|October 25, 2023
Assessment of three-dimensional RNA structure prediction in CASP15Rhiju Das, Rachael C Kretsch, Adam J Simpkin, et al.
Journal of Virology|April 20, 2012
Structural analysis of coxsackievirus A7 reveals conformational changes associated with uncoatingJani J T Seitsonen, Shabih Shakeel, Petri Susi, et al.
Structure (London, England : 1993)|July 16, 2013
The structure of herpesvirus fusion glycoprotein B-bilayer complex reveals the protein-membrane and lateral protein-protein interactionUlrike E Maurer, Tzviya Zeev-Ben-Mordehai, Arun Prasad Pandurangan, et al.
Journal of the American Chemical Society|September 8, 2017
The Role of Disulfide Bond Replacements in Analogues of the Tarantula Toxin ProTx-II and Their Effects on Inhibition of the Voltage-Gated Sodium Ion Channel Na<sub>v</sub>1.7Zoë V F Wright, Stephen McCarthy, Rachael Dickman, et al.
Human Molecular Genetics|May 15, 2010
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulinsRavinesh A Kumar, Daniela T Pilz, Timothy D Babatz, et al.
Proteins|June 12, 2023
New prediction categories in CASP15Andriy Kryshtafovych, Maciej Antczak, Marta Szachniuk, et al.
Frontiers in Molecular Neuroscience|January 22, 2016
Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 FamilyVera M Kalscheuer, Victoria M James, Miranda L Himelright, et al.
Elife|June 5, 2019
Genetic diversity of CHC22 clathrin impacts its function in glucose metabolismMatteo Fumagalli, Stephane M Camus, Yoan Diekmann, et al.
Neurobiology of Disease|December 15, 2012
Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle diseaseVictoria M James, Anna Bode, Seo-Kyung Chung, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 21, 2017
Disruption of a Structurally Important Extracellular Element in the Glycine Receptor Leads to Decreased Synaptic Integration and Signaling Resulting in Severe Startle DiseaseNatascha Schaefer, Alexandra Berger, Johannes van Brederode, et al.
Pageof 14