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Kidney International
|
March 29, 2026
Absence of glomerular IgA1 deposition despite overexpression of galactose-deficient IgA1 in the B cell c1galt1 knockout mouse
Jingyi Wu, Tong Xie, Zhao Zhang, et al.
Kidney International Reports
|
October 26, 2020
IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank
Kittiya Sukcharoen, Seth A Sharp, Nicholas J Thomas, et al.
Kidney International Reports
|
March 19, 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome
Thomas M Oates, Moumita Barua, Susie Gear, et al.
Clinical Kidney Journal
|
February 26, 2015
A novel LMX1B mutation in a family with end-stage renal disease of 'unknown cause'
Noel Edwards, Sarah J Rice, Shreya Raman, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
May 14, 2011
Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees
Yiannis Athanasiou, Konstantinos Voskarides, Daniel P Gale, et al.
Plos One
|
March 22, 2013
Epistatic role of the MYH9/APOL1 region on familial hematuria genes
Konstantinos Voskarides, Panayiota Demosthenous, Louiza Papazachariou, et al.
Journal of the American Society of Nephrology : JASN
|
February 18, 2017
Galactosylation of IgA1 Is Associated with Common Variation in <i>C1GALT1</i>
Daniel P Gale, Karen Molyneux, David Wimbury, et al.
Genes
|
September 28, 2023
Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice
Constantinos Deltas, Gregory Papagregoriou, Stavroula F Louka, et al.
The Journal of Clinical Investigation
|
August 27, 2024
Quantifying variant contributions in cystic kidney disease using national-scale whole-genome sequencing
Omid Sadeghi-Alavijeh, Melanie My Chan, Gabriel T Doctor, et al.
Haematologica
|
October 17, 2009
Erythropoietin administration in humans causes a marked and prolonged reduction in circulating hepcidin
Damien R Ashby, Daniel P Gale, Mark Busbridge, et al.
Page
of 12
Search research articles
Search
Showing results (51-60 of 115) with videos related to
Sort By:
Page
of 12
Kidney International
|
March 29, 2026
Absence of glomerular IgA1 deposition despite overexpression of galactose-deficient IgA1 in the B cell c1galt1 knockout mouse
Jingyi Wu, Tong Xie, Zhao Zhang, et al.
Kidney International Reports
|
October 26, 2020
IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank
Kittiya Sukcharoen, Seth A Sharp, Nicholas J Thomas, et al.
Kidney International Reports
|
March 19, 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome
Thomas M Oates, Moumita Barua, Susie Gear, et al.
Clinical Kidney Journal
|
February 26, 2015
A novel LMX1B mutation in a family with end-stage renal disease of 'unknown cause'
Noel Edwards, Sarah J Rice, Shreya Raman, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
May 14, 2011
Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees
Yiannis Athanasiou, Konstantinos Voskarides, Daniel P Gale, et al.
Plos One
|
March 22, 2013
Epistatic role of the MYH9/APOL1 region on familial hematuria genes
Konstantinos Voskarides, Panayiota Demosthenous, Louiza Papazachariou, et al.
Journal of the American Society of Nephrology : JASN
|
February 18, 2017
Galactosylation of IgA1 Is Associated with Common Variation in <i>C1GALT1</i>
Daniel P Gale, Karen Molyneux, David Wimbury, et al.
Genes
|
September 28, 2023
Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice
Constantinos Deltas, Gregory Papagregoriou, Stavroula F Louka, et al.
The Journal of Clinical Investigation
|
August 27, 2024
Quantifying variant contributions in cystic kidney disease using national-scale whole-genome sequencing
Omid Sadeghi-Alavijeh, Melanie My Chan, Gabriel T Doctor, et al.
Haematologica
|
October 17, 2009
Erythropoietin administration in humans causes a marked and prolonged reduction in circulating hepcidin
Damien R Ashby, Daniel P Gale, Mark Busbridge, et al.
Page
of 12