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Nephron
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August 14, 2019
Autosomal Recessive Alport Syndrome Unveiled by Pregnancy
Erika 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 transcription
Johannes 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 influence
Martin 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 glomerulosclerosis
Sung 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 activity
Robert Carrasquillo, Dequan Tian, Sneha Krishna, et al.
Scientific Reports
|
October 31, 2019
Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutations
Hanshuang 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 Podocytopathy
Hua 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 glomerulosclerosis
Moumita 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 excretion
Hakan R Toka, Giulio Genovese, David B Mount, et al.
Page
of 17
Search research articles
Search
Showing results (51-60 of 167) with videos related to
Sort By:
Page
of 17
Nephron
|
August 14, 2019
Autosomal Recessive Alport Syndrome Unveiled by Pregnancy
Erika 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 transcription
Johannes 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 influence
Martin 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 glomerulosclerosis
Sung 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 activity
Robert Carrasquillo, Dequan Tian, Sneha Krishna, et al.
Scientific Reports
|
October 31, 2019
Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutations
Hanshuang 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 Podocytopathy
Hua 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 glomerulosclerosis
Moumita 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 excretion
Hakan R Toka, Giulio Genovese, David B Mount, et al.
Page
of 17