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Kidney International
|
June 24, 2011
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome
Simone Sanna-Cherchi, Katelyn E Burgess, Shannon N Nees, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
July 7, 2025
Association of Collapsing Glomerulopathy with Donor Apolipoprotein L1 Risk Variants in Kidney Allografts from Black Donors
Ibrahim Batal, Alexei V Mikhailov, Syed A Husain, et al.
Kidney International Reports
|
August 7, 2023
Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease
Maddalena Marasa, Dina F Ahram, Atteeq U Rehman, et al.
Kidney International
|
May 26, 2020
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome
Nan Yang, Nan Wu, Shuangshuang Dong, et al.
Kidney International
|
December 26, 2025
Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis
Janewit Wongboonsin, Kristen M Gibson, Juntao Ke, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tract
Lisanne M Vendrig, Juntao Ke, Michael W T Tanck, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
April 18, 2020
Pilot Study of Return of Genetic Results to Patients in Adult Nephrology
Jordan G Nestor, Maddalena Marasa, Hila Milo-Rasouly, et al.
The Journal of Clinical Investigation
|
June 18, 2014
α-Intercalated cells defend the urinary system from bacterial infection
Neal Paragas, Ritwij Kulkarni, Max Werth, et al.
Nature Communications
|
January 23, 2026
Polar discontinuities, emergent conductivity, and critical twist-angle-dependent behaviour at wafer-bonded ferroelectric interfaces
Andrew Rogers, Kristina Holsgrove, Nils A Schäfer, et al.
Journal of the American Society of Nephrology : JASN
|
April 7, 2017
A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations <i>via</i> Dysregulation of Retinoic Acid Signaling
Asaf Vivante, Nina Mann, Hagith Yonath, et al.
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Search research articles
Search
Showing results (101-110 of 149) with videos related to
Sort By:
Page
of 15
Kidney International
|
June 24, 2011
Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome
Simone Sanna-Cherchi, Katelyn E Burgess, Shannon N Nees, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
July 7, 2025
Association of Collapsing Glomerulopathy with Donor Apolipoprotein L1 Risk Variants in Kidney Allografts from Black Donors
Ibrahim Batal, Alexei V Mikhailov, Syed A Husain, et al.
Kidney International Reports
|
August 7, 2023
Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease
Maddalena Marasa, Dina F Ahram, Atteeq U Rehman, et al.
Kidney International
|
May 26, 2020
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome
Nan Yang, Nan Wu, Shuangshuang Dong, et al.
Kidney International
|
December 26, 2025
Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis
Janewit Wongboonsin, Kristen M Gibson, Juntao Ke, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tract
Lisanne M Vendrig, Juntao Ke, Michael W T Tanck, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
April 18, 2020
Pilot Study of Return of Genetic Results to Patients in Adult Nephrology
Jordan G Nestor, Maddalena Marasa, Hila Milo-Rasouly, et al.
The Journal of Clinical Investigation
|
June 18, 2014
α-Intercalated cells defend the urinary system from bacterial infection
Neal Paragas, Ritwij Kulkarni, Max Werth, et al.
Nature Communications
|
January 23, 2026
Polar discontinuities, emergent conductivity, and critical twist-angle-dependent behaviour at wafer-bonded ferroelectric interfaces
Andrew Rogers, Kristina Holsgrove, Nils A Schäfer, et al.
Journal of the American Society of Nephrology : JASN
|
April 7, 2017
A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations <i>via</i> Dysregulation of Retinoic Acid Signaling
Asaf Vivante, Nina Mann, Hagith Yonath, et al.
Page
of 15