Zobrazeno 1 - 10 of 20 pro vyhledávání: '"Katherine VanDenHeuvel"'
1
Akademický článek
Olfactomedin 4 as a novel loop of Henle‐specific acute kidney injury biomarker
Autor: Denise C. Hasson, Kelli Krallman, Katherine VanDenHeuvel, Shina Menon, Giovanna Piraino, Prasad Devarajan, Stuart L. Goldstein, Matthew N. Alder
Publikováno v: Physiological Reports, Vol 10, Iss 18, Pp n/a-n/a (2022)
Abstract Acute kidney injury (AKI) is associated with morbidity and mortality. Urinary biomarkers may disentangle its clinical heterogeneity. Olfactomedin 4 (OLFM4) is a secreted glycoprotein expressed in stressed neutrophils and epithelial cells. In
Externí odkaz: https://doaj.org/article/37361b0723e14d92b9cf84451a19f3f8
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2
Akademický článek
A mutant fibrinogen that is unable to form fibrin can improve renal phenotype in mice with sickle cell anemia
Autor: Marilou G. Narciso, Blair Hoeting, Jeanne M. James, Katherine VandenHeuvel, Md. Nasimuzzaman
Publikováno v: eJHaem, Vol 2, Iss 3, Pp 462-465 (2021)
Abstract Sickle cell anemia (SCA) causes nephropathy which may progress to kidney failure. To determine if soluble fibrinogen (FibAEK) can prevent kidney damage in mice with SCA, we performed bone marrow transplantation (BMT) of Berkeley sickle mice
Externí odkaz: https://doaj.org/article/93db2351794f4fe38a373f57f97d1c4a
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4
Akademický článek
Case Report: Atypical HUS Presenting With Acute Rhabdomyolysis Highlights the Need for Individualized Eculizumab Dosing
Autor: Stefanie W. Benoit, Tsuyoshi Fukuda, Katherine VandenHeuvel, David Witte, Christine Fuller, Jennifer Willis, Bradley P. Dixon, Keri A. Drake
Publikováno v: Frontiers in Pediatrics, Vol 10 (2022)
BackgroundAtypical hemolytic uremic syndrome (aHUS) is an ultra-rare orphan disease caused by dysregulated complement activation resulting in thrombotic microangiopathy. Although complement-mediated endothelial injury predominantly affects the renal
Externí odkaz: https://doaj.org/article/27c216cb11a0446faef5b77a8d198b03
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8
Primary hyperoxaluria diagnosed after kidney transplant: A review of the literature and case report of aggressive renal replacement therapy and lumasiran to prevent allograft loss
Autor: Charles D. Varnell, Alexander Bondoc, Francisco Flores, Katherine VandenHeuvel, Hillarey K. Stone, David K. Hooper
Publikováno v: Am J Transplant
Primary hyperoxaluria type 1 is a rare inherited disorder caused by abnormal liver glyoxalate metabolism leading to overproduction of oxalate, progressive kidney disease, and systemic oxalosis. While the disorder typically presents with nephrocalcino
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e05d843060f58b7238fa07a89659e57
https://doi.org/10.1111/ajt.16762
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10
MAP1LC3C regulates lysosomal exocytosis and induces zinc reprogramming in renal cancer cells
Autor: Rita Verma, Parul Aggarwal, James Reigle, Dina Secic, Collin Wetzel, Megan E. Bischoff, Katherine VandenHeuvel, Jacek Biesiada, Birgit Ehmer, Julio A. Landero Figueroa, David R. Plas, Mario Medvedovic, Jarek Meller, Maria F. Czyzyk-Krzeska
MAP1LC3C (LC3C) is a member of the microtubule associated family of proteins that are essential in the formation of autophagosomes and lysosomal degradation of cargo. LC3C has tumor suppressing activity and its expression is dependent on kidney cance
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bf0720b4e561045bb2fb77634b9f3b3d
https://doi.org/10.1101/2022.05.11.491473
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