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Roger C Wiggins

Showing results (51-60 of 61) with videos related to

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Journal of the American Society of Nephrology : JASN|June 10, 2015
Proximal Tubules Have the Capacity to Regulate Uptake of AlbuminMark C Wagner, Silvia B Campos-Bilderback, Mahboob Chowdhury, et al.
Journal of the American Society of Nephrology : JASN|September 21, 2013
Urine podocyte mRNAs, proteinuria, and progression in human glomerular diseasesLarysa Wickman, Farsad Afshinnia, Su Q Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 11, 2007
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)Rasheed Gbadegesin, Bernward G Hinkes, Bethan E Hoskins, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 5, 2014
Glomerular disease: looking beyond pathologyRoger C Wiggins, Charles E Alpers, Lawrence B Holzman, et al.
JCI Insight|May 6, 2025
The growth hormone/IGF-1 axis is a risk factor for long-term kidney allograft failureMatthew Cusick, Viji Nair, Damian Fermin, et al.
JCI Insight|January 11, 2019
Organoid single cell profiling identifies a transcriptional signature of glomerular diseaseJennifer L Harder, Rajasree Menon, Edgar A Otto, et al.
The Journal of Clinical Investigation|May 25, 2011
mTORC1 activation in podocytes is a critical step in the development of diabetic nephropathy in miceKen Inoki, Hiroyuki Mori, Junying Wang, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Nature Genetics|November 7, 2006
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversibleBernward Hinkes, Roger C Wiggins, Rasheed Gbadegesin, et al.
The Journal of Clinical Investigation|November 26, 2013
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruptionShazia Ashraf, Heon Yung Gee, Stephanie Woerner, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Journal of the American Society of Nephrology : JASN|June 10, 2015
Proximal Tubules Have the Capacity to Regulate Uptake of AlbuminMark C Wagner, Silvia B Campos-Bilderback, Mahboob Chowdhury, et al.
Journal of the American Society of Nephrology : JASN|September 21, 2013
Urine podocyte mRNAs, proteinuria, and progression in human glomerular diseasesLarysa Wickman, Farsad Afshinnia, Su Q Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 11, 2007
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)Rasheed Gbadegesin, Bernward G Hinkes, Bethan E Hoskins, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 5, 2014
Glomerular disease: looking beyond pathologyRoger C Wiggins, Charles E Alpers, Lawrence B Holzman, et al.
JCI Insight|May 6, 2025
The growth hormone/IGF-1 axis is a risk factor for long-term kidney allograft failureMatthew Cusick, Viji Nair, Damian Fermin, et al.
JCI Insight|January 11, 2019
Organoid single cell profiling identifies a transcriptional signature of glomerular diseaseJennifer L Harder, Rajasree Menon, Edgar A Otto, et al.
The Journal of Clinical Investigation|May 25, 2011
mTORC1 activation in podocytes is a critical step in the development of diabetic nephropathy in miceKen Inoki, Hiroyuki Mori, Junying Wang, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Nature Genetics|November 7, 2006
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversibleBernward Hinkes, Roger C Wiggins, Rasheed Gbadegesin, et al.
The Journal of Clinical Investigation|November 26, 2013
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruptionShazia Ashraf, Heon Yung Gee, Stephanie Woerner, et al.
Pageof 7