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Showing results (291-300 of 320) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 8, 2020
Klotho regulation by albuminuria is dependent on ATF3 and endoplasmic reticulum stressVasiliki Delitsikou, George Jarad, Renuga Devi Rajaram, et al.
Kidney International|May 23, 2024
Tauroursodeoxycholic acid ameliorates renal injury induced by COL4A3 mutationShuwen Yu, Xiangchen Gu, Qimin Zheng, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Leveraging genomic biobanks to enhance genetic testing outcomes for kidney diseaseGretchen M Urban, Kulsoom Mohammad, Lakshna Sankar, et al.
The Journal of Clinical Endocrinology and Metabolism|November 27, 2019
Mutations in LAMB2 Are Associated With Albuminuria and Optic Nerve Hypoplasia With HypopituitarismMona Tahoun, Jennifer C Chandler, Emma Ashton, et al.
Journal of the American Society of Nephrology : JASN|June 7, 2014
Loss of the podocyte-expressed transcription factor Tcf21/Pod1 results in podocyte differentiation defects and FSGSYoshiro Maezawa, Tuncer Onay, Rizaldy P Scott, et al.
American Journal of Physiology. Cell Physiology|December 3, 2010
Biophysical properties of normal and diseased renal glomeruliHans M Wyss, Joel M Henderson, Fitzroy J Byfield, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Synaptopodin enables directional mechanoadaptation of integrin-based adhesionsChengqing Qu, Yuxuan Huang, Shumeng Jiang, et al.
Kidney360|April 14, 2022
Clear Evidence of <i>LAMA5</i> Gene Biallelic Truncating Variants Causing Infantile Nephrotic SyndromeYukimasa Taniguchi, China Nagano, Kiyotoshi Sekiguchi, et al.
Journal of the American Society of Nephrology : JASN|May 29, 2021
Identification of an Altered Matrix Signature in Kidney Aging and DiseaseMichael J Randles, Franziska Lausecker, Qingyang Kong, et al.
The Journal of Clinical Investigation|February 23, 2016
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosisHaiyang Yu, Mykyta Artomov, Sebastian Brähler, et al.
Pageof 32

Showing results (291-300 of 320) with videos related to

Sort By:
Pageof 32
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 8, 2020
Klotho regulation by albuminuria is dependent on ATF3 and endoplasmic reticulum stressVasiliki Delitsikou, George Jarad, Renuga Devi Rajaram, et al.
Kidney International|May 23, 2024
Tauroursodeoxycholic acid ameliorates renal injury induced by COL4A3 mutationShuwen Yu, Xiangchen Gu, Qimin Zheng, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Leveraging genomic biobanks to enhance genetic testing outcomes for kidney diseaseGretchen M Urban, Kulsoom Mohammad, Lakshna Sankar, et al.
The Journal of Clinical Endocrinology and Metabolism|November 27, 2019
Mutations in LAMB2 Are Associated With Albuminuria and Optic Nerve Hypoplasia With HypopituitarismMona Tahoun, Jennifer C Chandler, Emma Ashton, et al.
Journal of the American Society of Nephrology : JASN|June 7, 2014
Loss of the podocyte-expressed transcription factor Tcf21/Pod1 results in podocyte differentiation defects and FSGSYoshiro Maezawa, Tuncer Onay, Rizaldy P Scott, et al.
American Journal of Physiology. Cell Physiology|December 3, 2010
Biophysical properties of normal and diseased renal glomeruliHans M Wyss, Joel M Henderson, Fitzroy J Byfield, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Synaptopodin enables directional mechanoadaptation of integrin-based adhesionsChengqing Qu, Yuxuan Huang, Shumeng Jiang, et al.
Kidney360|April 14, 2022
Clear Evidence of <i>LAMA5</i> Gene Biallelic Truncating Variants Causing Infantile Nephrotic SyndromeYukimasa Taniguchi, China Nagano, Kiyotoshi Sekiguchi, et al.
Journal of the American Society of Nephrology : JASN|May 29, 2021
Identification of an Altered Matrix Signature in Kidney Aging and DiseaseMichael J Randles, Franziska Lausecker, Qingyang Kong, et al.
The Journal of Clinical Investigation|February 23, 2016
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosisHaiyang Yu, Mykyta Artomov, Sebastian Brähler, et al.
Pageof 32