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Matthew G Sampson

Showing results (71-80 of 94) with videos related to

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Nature Communications|November 27, 2025
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatmentFlorian Buerger, Daanya Salmanullah, Lorrin Liang, et al.
JCI Insight|May 20, 2025
Loss of genome maintenance is linked to mTORC1 signaling and accelerates podocyte damageFabian Braun, Amrei M Mandel, Linda Blomberg, et al.
JAMA Network Open|August 25, 2022
Comparing Kidney Health Outcomes in Children, Adolescents, and Adults With Focal Segmental GlomerulosclerosisDebbie S Gipson, Jonathan P Troost, Cathie Spino, et al.
NPJ Genomic Medicine|December 2, 2024
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomesCourtney E French, Nancy C Andrews, Alan H Beggs, et al.
Kidney International|June 20, 2020
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndromeXiaoyuan Jia, Tomohiko Yamamura, Rasheed Gbadegesin, et al.
Nature Genetics|May 7, 2021
Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidneyJames M Eales, Xiao Jiang, Xiaoguang Xu, et al.
JAMA Network Open|March 11, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
The New England Journal of Medicine|May 16, 2019
Genomic Mismatch at <i>LIMS1</i> Locus and Kidney Allograft RejectionNicholas J Steers, Yifu Li, Zahida Drace, et al.
Kidney International|January 18, 2013
Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approachCrystal A Gadegbeku, Debbie S Gipson, Lawrence B Holzman, et al.
Pageof 10

Showing results (71-80 of 94) with videos related to

Sort By:
Pageof 10
Nature Communications|November 27, 2025
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatmentFlorian Buerger, Daanya Salmanullah, Lorrin Liang, et al.
JCI Insight|May 20, 2025
Loss of genome maintenance is linked to mTORC1 signaling and accelerates podocyte damageFabian Braun, Amrei M Mandel, Linda Blomberg, et al.
JAMA Network Open|August 25, 2022
Comparing Kidney Health Outcomes in Children, Adolescents, and Adults With Focal Segmental GlomerulosclerosisDebbie S Gipson, Jonathan P Troost, Cathie Spino, et al.
NPJ Genomic Medicine|December 2, 2024
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomesCourtney E French, Nancy C Andrews, Alan H Beggs, et al.
Kidney International|June 20, 2020
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndromeXiaoyuan Jia, Tomohiko Yamamura, Rasheed Gbadegesin, et al.
Nature Genetics|May 7, 2021
Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidneyJames M Eales, Xiao Jiang, Xiaoguang Xu, et al.
JAMA Network Open|March 11, 2026
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective VariantElena Martinelli, Juntao Ke, Atlas Khan, et al.
Journal of the American Society of Nephrology : JASN|October 1, 2024
Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathyBenjamin Wooden, Andrew Beenken, Elena Martinelli, et al.
The New England Journal of Medicine|May 16, 2019
Genomic Mismatch at <i>LIMS1</i> Locus and Kidney Allograft RejectionNicholas J Steers, Yifu Li, Zahida Drace, et al.
Kidney International|January 18, 2013
Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approachCrystal A Gadegbeku, Debbie S Gipson, Lawrence B Holzman, et al.
Pageof 10