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Martin R Pollak

Showing results (51-60 of 167) with videos related to

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Nephron|August 14, 2019
Autosomal Recessive Alport Syndrome Unveiled by PregnancyErika R Drury, Isaac E Stillman, Martin R Pollak, et al.
American Journal of Physiology. Cell Physiology|January 9, 2009
TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcriptionJohannes Schlöndorff, Donato Del Camino, Robert Carrasquillo, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 31, 2014
The glomerulus: the sphere of influenceMartin R Pollak, Susan E Quaggin, Melanie P Hoenig, et al.
Journal of Molecular Biology|January 1, 2008
Crystal structure of the actin-binding domain of alpha-actinin-4 Lys255Glu mutant implicated in focal segmental glomerulosclerosisSung Haeng Lee, Astrid Weins, David B Hayes, et al.
BMC Cell Biology|November 23, 2012
SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activityRobert Carrasquillo, Dequan Tian, Sneha Krishna, et al.
Scientific Reports|October 31, 2019
Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutationsHanshuang Shao, Bentley Wingert, Astrid Weins, et al.
Journal of the American Society of Nephrology : JASN|January 14, 2021
Dysregulated Dynein-Mediated Trafficking of Nephrin Causes INF2-related PodocytopathyHua Sun, Chandra Perez-Gill, Johannes S Schlöndorff, et al.
Kidney International|September 20, 2013
Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosisMoumita Barua, Eric Shieh, Johannes Schlondorff, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2011
Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2)Hua Sun, Johannes S Schlondorff, Elizabeth J Brown, et al.
Plos One|August 31, 2013
Frequency of rare allelic variation in candidate genes among individuals with low and high urinary calcium excretionHakan R Toka, Giulio Genovese, David B Mount, et al.
Pageof 17

Showing results (51-60 of 167) with videos related to

Sort By:
Pageof 17
Nephron|August 14, 2019
Autosomal Recessive Alport Syndrome Unveiled by PregnancyErika R Drury, Isaac E Stillman, Martin R Pollak, et al.
American Journal of Physiology. Cell Physiology|January 9, 2009
TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcriptionJohannes Schlöndorff, Donato Del Camino, Robert Carrasquillo, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 31, 2014
The glomerulus: the sphere of influenceMartin R Pollak, Susan E Quaggin, Melanie P Hoenig, et al.
Journal of Molecular Biology|January 1, 2008
Crystal structure of the actin-binding domain of alpha-actinin-4 Lys255Glu mutant implicated in focal segmental glomerulosclerosisSung Haeng Lee, Astrid Weins, David B Hayes, et al.
BMC Cell Biology|November 23, 2012
SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activityRobert Carrasquillo, Dequan Tian, Sneha Krishna, et al.
Scientific Reports|October 31, 2019
Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutationsHanshuang Shao, Bentley Wingert, Astrid Weins, et al.
Journal of the American Society of Nephrology : JASN|January 14, 2021
Dysregulated Dynein-Mediated Trafficking of Nephrin Causes INF2-related PodocytopathyHua Sun, Chandra Perez-Gill, Johannes S Schlöndorff, et al.
Kidney International|September 20, 2013
Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosisMoumita Barua, Eric Shieh, Johannes Schlondorff, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2011
Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2)Hua Sun, Johannes S Schlondorff, Elizabeth J Brown, et al.
Plos One|August 31, 2013
Frequency of rare allelic variation in candidate genes among individuals with low and high urinary calcium excretionHakan R Toka, Giulio Genovese, David B Mount, et al.
Pageof 17