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Asim A Beg

Showing results (11-20 of 20) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 1, 2006
The diacylglycerol-binding protein alpha1-chimaerin regulates dendritic morphologyPhilip Buttery, Asim A Beg, Ben Chih, et al.
Journal of Visualized Experiments : Jove|May 15, 2018
A Rapid and Facile Pipeline for Generating Genomic Point Mutants in C. elegans Using CRISPR/Cas9 RibonucleoproteinsHarriet Prior, Lauren MacConnachie, Jose L Martinez, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 13, 2015
α2-chimaerin is required for Eph receptor-class-specific spinal motor axon guidance and coordinate activation of antagonistic musclesTzu-Jen Kao, Georgina C B Nicholl, Jamie A Johansen, et al.
Cell Reports|April 25, 2019
An Intramolecular Salt Bridge Linking TDP43 RNA Binding, Protein Stability, and TDP43-Dependent NeurodegenerationBrittany N Flores, Xingli Li, Ahmed M Malik, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 13, 2015
Spillover transmission is mediated by the excitatory GABA receptor LGC-35 in C. elegansMeghan A Jobson, Chris M Valdez, Jann Gardner, et al.
Science Signaling|May 31, 2018
Dual phosphorylation of Ric-8A enhances its ability to mediate G protein α subunit folding and to stimulate guanine nucleotide exchangeMakaía M Papasergi-Scott, Hannah M Stoveken, Lauren MacConnachie, et al.
Human Mutation|August 30, 2012
A loss-of-function variant in the human histidyl-tRNA synthetase (HARS) gene is neurotoxic in vivoAimée Vester, Gisselle Velez-Ruiz, Heather M McLaughlin, et al.
HGG Advances|July 3, 2024
A model organism pipeline provides insight into the clinical heterogeneity of TARS1 loss-of-function variantsRebecca Meyer-Schuman, Allison R Cale, Jennifer A Pierluissi, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Predictive modeling provides insight into the clinical heterogeneity associated with <i>TARS1</i> loss-of-function mutationsRebecca Meyer-Schuman, Allison R Cale, Jennifer A Pierluissi, et al.
Brain : a Journal of Neurology|June 15, 2015
Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathiesDana Safka Brozkova, Tine Deconinck, Laurie Beth Griffin, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2006
The diacylglycerol-binding protein alpha1-chimaerin regulates dendritic morphologyPhilip Buttery, Asim A Beg, Ben Chih, et al.
Journal of Visualized Experiments : Jove|May 15, 2018
A Rapid and Facile Pipeline for Generating Genomic Point Mutants in C. elegans Using CRISPR/Cas9 RibonucleoproteinsHarriet Prior, Lauren MacConnachie, Jose L Martinez, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 13, 2015
α2-chimaerin is required for Eph receptor-class-specific spinal motor axon guidance and coordinate activation of antagonistic musclesTzu-Jen Kao, Georgina C B Nicholl, Jamie A Johansen, et al.
Cell Reports|April 25, 2019
An Intramolecular Salt Bridge Linking TDP43 RNA Binding, Protein Stability, and TDP43-Dependent NeurodegenerationBrittany N Flores, Xingli Li, Ahmed M Malik, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 13, 2015
Spillover transmission is mediated by the excitatory GABA receptor LGC-35 in C. elegansMeghan A Jobson, Chris M Valdez, Jann Gardner, et al.
Science Signaling|May 31, 2018
Dual phosphorylation of Ric-8A enhances its ability to mediate G protein α subunit folding and to stimulate guanine nucleotide exchangeMakaía M Papasergi-Scott, Hannah M Stoveken, Lauren MacConnachie, et al.
Human Mutation|August 30, 2012
A loss-of-function variant in the human histidyl-tRNA synthetase (HARS) gene is neurotoxic in vivoAimée Vester, Gisselle Velez-Ruiz, Heather M McLaughlin, et al.
HGG Advances|July 3, 2024
A model organism pipeline provides insight into the clinical heterogeneity of TARS1 loss-of-function variantsRebecca Meyer-Schuman, Allison R Cale, Jennifer A Pierluissi, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2024
Predictive modeling provides insight into the clinical heterogeneity associated with <i>TARS1</i> loss-of-function mutationsRebecca Meyer-Schuman, Allison R Cale, Jennifer A Pierluissi, et al.
Brain : a Journal of Neurology|June 15, 2015
Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathiesDana Safka Brozkova, Tine Deconinck, Laurie Beth Griffin, et al.
Pageof 2