Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Donna M. Michel"'
Autor:
Michele H. Mokrzycki, Paul L. Kimmel, David Vlahov, Jeffrey S. Berns, Cheryl A. Winkler, Taras K. Oleksyk, Donald W. Bowden, William A. Briggs, Jeffrey B. Kopp, Stephen M. Korbet, Michael W. Smith, Barry I. Freedman, Eric E. Simon, Tejinder S. Ahuja, Louise M. McKenzie, Jeffrey R. Schelling, Richard A. Dart, George W. Nelson, Hiroshi Kajiyama, Randall C. Johnson, Monique E. Cho, Howard Trachtman, Donna M. Michel
Publikováno v:
Nature Genetics. 40:1175-1184
The increased burden of chronic kidney and end-stage kidney diseases (ESKD) in populations of African ancestry has been largely unexplained. To identify genetic variants predisposing to idiopathic and HIV-1–associated focal segmental glomeruloscler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7d403944ff06931bddb21984143b544
https://doi.org/10.1038/ng.226
https://doi.org/10.1038/ng.226
Autor:
Michelle H. Mokrzycki, Jeffrey B. Kopp, Michael C. Smith, Stephen M. Korbet, Jeffrey S. Berns, Sher L. Hendrickson, Howard Trachtman, Donna M. Michel, Jeffrey R. Schelling, Yu C. Zhou, Monique E. Cho, Elizabeth Binns-Roemer, Eric E. Simon, Richard A. Dart, Paul L. Kimmel, Cheryl A. Winkler, Gregory D. Kirk, William A. Briggs, Louise M. McKenzie, Tejinder S. Ahuja
Publikováno v:
Journal of the American Society of Nephrology. 18:2987-2995
Mutations in NPHS2, the gene that encodes podocin, are well-established causes of both familial and sporadic steroid-resistant focal segmental glomerulosclerosis (FSGS) in the pediatric population, but have not been well-characterized in late-onset d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7c63b9ea007eba8239be2a26e30d607
https://doi.org/10.1681/asn.2007030319
https://doi.org/10.1681/asn.2007030319
Autor:
Alvin H. Moss, Donna M. Michel
Publikováno v:
Advances in Chronic Kidney Disease. 12:196-201
Recent guidelines recommend shared decision making between patients and nephrologists as the model for dialysis decision making. A key component of this shared decision making is obtaining informed consent. As part of this process, nephrologists have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebefd3827061d3f9032f8c68e0b859ad
https://doi.org/10.1053/j.ackd.2005.01.003
https://doi.org/10.1053/j.ackd.2005.01.003
Publikováno v:
American Journal of Nephrology. 20:324-328
Calciphylaxis is a rare but frequently fatal complication in patients with end-stage renal disease. Original concepts regarding groups at risk for the disease, predisposing factors, and associated morbidity have changed significantly in the past few
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb8ddd99f48d218a7be057832428eb86
https://doi.org/10.1159/000013608
https://doi.org/10.1159/000013608
Autor:
Howard Trachtman, Jeffrey R. Schelling, Donna M. Michel, Tejinder S. Ahuja, Jeffrey B. Kopp, Sophie Limou, David J. Friedman, Richard A. Dart, Michele H. Mokrzycki, Stephen M. Korbet, Randall C. Johnson, Justyna Fryc, William A. Briggs, Karmini Sampath, George W. Nelson, Paul L. Kimmel, Ping An, Cheryl A. Winkler, Eric E. Simon, David Vlahov, Jeffrey S. Berns, Giulio Genovese, Martin R. Pollak, Michael C. Smith
Trypanolytic variants in APOL1, which encodes apolipoprotein L1, associate with kidney disease in African Americans, but whether APOL1-associated glomerular disease has a distinct clinical phenotype is unknown. Here we determined APOL1 genotypes for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846031f28964816a1f63ffb1519ea493
https://europepmc.org/articles/PMC3231787/
https://europepmc.org/articles/PMC3231787/
Autor:
Paul L. Kimmel, Eric E. Simon, John R. Sedor, Jeffrey B. Kopp, Tejinder S. Ahuja, David Vlahov, Jeffrey S. Berns, Richard A. Dart, Howard Trachtman, Michael C. Smith, Mohammed S. Orloff, Stephen M. Korbet, Donna M. Michel, William A. Briggs, Michele H. Mokrzycki, Sudha K. Iyengar, Katrina A.B. Goddard, Cheryl A. Winkler, Jeffrey R. Schelling
Publikováno v:
Physiological genomics. 21(2)
Wilms’ tumor gene ( WT1) is important for nephrogenesis and gonadal growth. WT1 mutations cause Denys-Drash and Frasier syndromes, which are characterized by glomerular scarring. To test whether genetic variations in WT1 and WIT1 (gene immediately
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aadab23c7030316b1ccfeb535bd86a2f
https://pubmed.ncbi.nlm.nih.gov/15687485
https://pubmed.ncbi.nlm.nih.gov/15687485
Autor:
Carolyn J. Kelly, Donna M. Michel
Publikováno v:
Journal of the American Society of Nephrology : JASN. 9(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a83edfbf96e18ce4e6581896c84f1279
https://pubmed.ncbi.nlm.nih.gov/9513915
https://pubmed.ncbi.nlm.nih.gov/9513915