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Kidney International
|
January 4, 2026
The authors reply
Katie Wong, Sherry Masoud, David Pitcher, et al.
Kidney International
|
June 29, 2025
Quantifying association of early proteinuria and estimated glomerular filtration rate changes with long-term kidney failure in C3 glomerulopathy and immune-complex membranoproliferative glomerulonephritis using the United Kingdom RaDaR Registry
Sherry Masoud, Katie Wong, David Pitcher, et al.
Clinical Science (London, England : 1979)
|
December 8, 2018
First identification of <i>PODXL</i> nonsense mutations in autosomal dominant focal segmental glomerulosclerosis
Fu-Jun Lin, Lei Yao, Xue-Qing Hu, et al.
BMC Genomics
|
April 19, 2015
Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies
Adam P Levine, Thomas M F Connor, D Deren Oygar, et al.
Plos One
|
November 20, 2009
Evidence for a lack of a direct transcriptional suppression of the iron regulatory peptide hepcidin by hypoxia-inducible factors
Melanie Volke, Daniel P Gale, Ulrike Maegdefrau, et al.
Annals of Human Genetics
|
October 10, 2022
Segregation analysis identifies specific alpha-defensin (DEFA1A3) SNP-CNV haplotypes in predisposition to IgA nephropathy
Nzar A A Shwan, Eric C Moise, Paula E Necsoiu, et al.
Journal of the American Society of Nephrology : JASN
|
August 4, 2025
Authors' Reply: Questions Regarding the Analysis of Long-Term Outcomes in Nephrotic Syndrome
David Pitcher, Bruce Hendry, Alex Mercer, et al.
Blood
|
April 2, 2011
Dysregulation of the HIF pathway due to VHL mutation causing severe erythrocytosis and pulmonary arterial hypertension
Jonathan Bond, Daniel P Gale, Thomas Connor, et al.
Kidney International Reports
|
July 1, 2026
Unanswered Questions About Microscopic Hematuria With Tubulopathy
Guy H Neild, D Deren Oygar, Ahmet Behlul, et al.
Kidney International
|
February 17, 2024
A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathy
Cătălin D Voinescu, Monika Mozere, Giulio Genovese, et al.
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Search research articles
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Showing results (31-40 of 115) with videos related to
Sort By:
Page
of 12
Kidney International
|
January 4, 2026
The authors reply
Katie Wong, Sherry Masoud, David Pitcher, et al.
Kidney International
|
June 29, 2025
Quantifying association of early proteinuria and estimated glomerular filtration rate changes with long-term kidney failure in C3 glomerulopathy and immune-complex membranoproliferative glomerulonephritis using the United Kingdom RaDaR Registry
Sherry Masoud, Katie Wong, David Pitcher, et al.
Clinical Science (London, England : 1979)
|
December 8, 2018
First identification of <i>PODXL</i> nonsense mutations in autosomal dominant focal segmental glomerulosclerosis
Fu-Jun Lin, Lei Yao, Xue-Qing Hu, et al.
BMC Genomics
|
April 19, 2015
Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies
Adam P Levine, Thomas M F Connor, D Deren Oygar, et al.
Plos One
|
November 20, 2009
Evidence for a lack of a direct transcriptional suppression of the iron regulatory peptide hepcidin by hypoxia-inducible factors
Melanie Volke, Daniel P Gale, Ulrike Maegdefrau, et al.
Annals of Human Genetics
|
October 10, 2022
Segregation analysis identifies specific alpha-defensin (DEFA1A3) SNP-CNV haplotypes in predisposition to IgA nephropathy
Nzar A A Shwan, Eric C Moise, Paula E Necsoiu, et al.
Journal of the American Society of Nephrology : JASN
|
August 4, 2025
Authors' Reply: Questions Regarding the Analysis of Long-Term Outcomes in Nephrotic Syndrome
David Pitcher, Bruce Hendry, Alex Mercer, et al.
Blood
|
April 2, 2011
Dysregulation of the HIF pathway due to VHL mutation causing severe erythrocytosis and pulmonary arterial hypertension
Jonathan Bond, Daniel P Gale, Thomas Connor, et al.
Kidney International Reports
|
July 1, 2026
Unanswered Questions About Microscopic Hematuria With Tubulopathy
Guy H Neild, D Deren Oygar, Ahmet Behlul, et al.
Kidney International
|
February 17, 2024
A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathy
Cătălin D Voinescu, Monika Mozere, Giulio Genovese, et al.
Page
of 12