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Weizhen Tan

Showing results (11-20 of 30) with videos related to

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American Journal of Human Genetics|May 24, 2016
Mutations in SLC26A1 Cause NephrolithiasisHeon Yung Gee, Ikhyun Jun, Daniela A Braun, et al.
Kidney International Reports|February 22, 2021
Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent ApproachesVerena Klämbt, Youying Mao, Ronen Schneider, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 9, 2018
Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in childrenDavid Schapiro, Ankana Daga, Jennifer A Lawson, et al.
JAMA Network Open|May 8, 2023
Perspectives of Rare Disease Experts on Newborn Genome SequencingNina B Gold, Sophia M Adelson, Nidhi Shah, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2014
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndromeCarolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, et al.
American Journal of Medical Genetics. Part A|August 7, 2018
Mutations in WDR4 as a new cause of Galloway-Mowat syndromeDaniela A Braun, Shirlee Shril, Aditi Sinha, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 14, 2018
Genetic variants in the LAMA5 gene in pediatric nephrotic syndromeDaniela A Braun, Jillian K Warejko, Shazia Ashraf, et al.
Nature Genetics|February 16, 2016
Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndromeDaniela A Braun, Carolin E Sadowski, Stefan Kohl, et al.
Hypertension (Dallas, Tex. : 1979)|February 28, 2018
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeJillian K Warejko, Markus Schueler, Asaf Vivante, et al.
The Journal of Clinical Investigation|October 24, 2017
Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndromeJia Rao, Shazia Ashraf, Weizhen Tan, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|May 24, 2016
Mutations in SLC26A1 Cause NephrolithiasisHeon Yung Gee, Ikhyun Jun, Daniela A Braun, et al.
Kidney International Reports|February 22, 2021
Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent ApproachesVerena Klämbt, Youying Mao, Ronen Schneider, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 9, 2018
Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in childrenDavid Schapiro, Ankana Daga, Jennifer A Lawson, et al.
JAMA Network Open|May 8, 2023
Perspectives of Rare Disease Experts on Newborn Genome SequencingNina B Gold, Sophia M Adelson, Nidhi Shah, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2014
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndromeCarolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, et al.
American Journal of Medical Genetics. Part A|August 7, 2018
Mutations in WDR4 as a new cause of Galloway-Mowat syndromeDaniela A Braun, Shirlee Shril, Aditi Sinha, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 14, 2018
Genetic variants in the LAMA5 gene in pediatric nephrotic syndromeDaniela A Braun, Jillian K Warejko, Shazia Ashraf, et al.
Nature Genetics|February 16, 2016
Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndromeDaniela A Braun, Carolin E Sadowski, Stefan Kohl, et al.
Hypertension (Dallas, Tex. : 1979)|February 28, 2018
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic SyndromeJillian K Warejko, Markus Schueler, Asaf Vivante, et al.
The Journal of Clinical Investigation|October 24, 2017
Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndromeJia Rao, Shazia Ashraf, Weizhen Tan, et al.
Pageof 3