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Gursimran Chandhok

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 5, 2016
Presynaptic Deficits at Neuromuscular Junctions: A Specific Cause and Potential Target of Axonal Neuropathy in Type 2 Charcot-Marie-Tooth DiseaseGursimran Chandhok, Ming Shiuan Soh
Micropublication Biology|December 19, 2022
Novel putative interactors of FZO-1/mitofusin 2 identified using large-scale yeast two-hybrid screening in <i>C. elegans</i>Samiksha Dhananjay, Brent Neumann, Gursimran Chandhok
Molecules (Basel, Switzerland)|October 6, 2015
Therapeutic Oligonucleotides Targeting Liver Disease: TTR AmyloidosisChristoph Niemietz, Gursimran Chandhok, Hartmut Schmidt
Biological Reviews of the Cambridge Philosophical Society|October 26, 2017
Structure, function, and regulation of mitofusin-2 in health and diseaseGursimran Chandhok, Michael Lazarou, Brent Neumann
World Journal of Gastroenterology|April 29, 2016
Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell linesGursimran Chandhok, Judit Horvath, Annu Aggarwal, et al.
Plos One|June 4, 2014
The effect of zinc and D-penicillamine in a stable human hepatoma ATP7B knockout cell lineGursimran Chandhok, Nadine Schmitt, Vanessa Sauer, et al.
Canadian Journal of Gastroenterology & Hepatology|August 30, 2018
Portal Hypertensive Polyposis in Advanced Liver Cirrhosis: The Unknown Entity?David Kara, Anna Hüsing-Kabar, Hartmut Schmidt, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 25, 2017
FAP plasma-induced cellular toxicityChristoph Niemietz, Gursimran Chandhok, Lutz Fleischhauer, et al.
Scientific Reports|August 17, 2022
Synaptic branch stability is mediated by non-enzymatic functions of MEC-17/αTAT1 and ATAT-2Jean-Sébastien Teoh, Amruta Vasudevan, Wenyue Wang, et al.
Annals of Human Genetics|April 5, 2013
Wilson disease mutation pattern with genotype-phenotype correlations from Western India: confirmation of p.C271* as a common Indian mutation and identification of 14 novel mutationsAnnu Aggarwal, Gursimran Chandhok, Theodor Todorov, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 5, 2016
Presynaptic Deficits at Neuromuscular Junctions: A Specific Cause and Potential Target of Axonal Neuropathy in Type 2 Charcot-Marie-Tooth DiseaseGursimran Chandhok, Ming Shiuan Soh
Micropublication Biology|December 19, 2022
Novel putative interactors of FZO-1/mitofusin 2 identified using large-scale yeast two-hybrid screening in <i>C. elegans</i>Samiksha Dhananjay, Brent Neumann, Gursimran Chandhok
Molecules (Basel, Switzerland)|October 6, 2015
Therapeutic Oligonucleotides Targeting Liver Disease: TTR AmyloidosisChristoph Niemietz, Gursimran Chandhok, Hartmut Schmidt
Biological Reviews of the Cambridge Philosophical Society|October 26, 2017
Structure, function, and regulation of mitofusin-2 in health and diseaseGursimran Chandhok, Michael Lazarou, Brent Neumann
World Journal of Gastroenterology|April 29, 2016
Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell linesGursimran Chandhok, Judit Horvath, Annu Aggarwal, et al.
Plos One|June 4, 2014
The effect of zinc and D-penicillamine in a stable human hepatoma ATP7B knockout cell lineGursimran Chandhok, Nadine Schmitt, Vanessa Sauer, et al.
Canadian Journal of Gastroenterology & Hepatology|August 30, 2018
Portal Hypertensive Polyposis in Advanced Liver Cirrhosis: The Unknown Entity?David Kara, Anna Hüsing-Kabar, Hartmut Schmidt, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 25, 2017
FAP plasma-induced cellular toxicityChristoph Niemietz, Gursimran Chandhok, Lutz Fleischhauer, et al.
Scientific Reports|August 17, 2022
Synaptic branch stability is mediated by non-enzymatic functions of MEC-17/αTAT1 and ATAT-2Jean-Sébastien Teoh, Amruta Vasudevan, Wenyue Wang, et al.
Annals of Human Genetics|April 5, 2013
Wilson disease mutation pattern with genotype-phenotype correlations from Western India: confirmation of p.C271* as a common Indian mutation and identification of 14 novel mutationsAnnu Aggarwal, Gursimran Chandhok, Theodor Todorov, et al.
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