Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Carlton M Bates"'
Autor:
Kenneth A Walker, Sunder Sims-Lucas, Valeria E Di Giovanni, Caitlin Schaefer, Whitney M Sunseri, Tatiana Novitskaya, Mark P de Caestecker, Feng Chen, Carlton M Bates
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0167191 (2016)
[This corrects the article DOI: 10.1371/journal.pone.0056062.].
Externí odkaz:
https://doaj.org/article/b7b42fdc09684e79b42ef4a55c0330fe
Autor:
Sunder Sims-Lucas, Caitlin Schaefer, Daniel Bushnell, Jacqueline Ho, Alison Logar, Edward Prochownik, George Gittes, Carlton M Bates
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65993 (2013)
The renal endothelium has been debated as arising from resident hemangioblast precursors that transdifferentiate from the nephrogenic mesenchyme (vasculogenesis) and/or from invading vessels (angiogenesis). While the Foxd1-positive renal cortical str
Externí odkaz:
https://doaj.org/article/af53d293bc5d4def9c407868aea1ca7e
Autor:
Kenneth A Walker, Sunder Sims-Lucas, Valeria E Di Giovanni, Caitlin Schaefer, Whitney M Sunseri, Tatiana Novitskaya, Mark P de Caestecker, Feng Chen, Carlton M Bates
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56062 (2013)
Pax3cre-mediated deletion of fibroblast growth factor receptor 2 (Fgfr2) broadly in renal and urinary tract mesenchyme led to ureteric bud (UB) induction defects and vesicoureteral reflux (VUR), although the mechanisms were unclear. Here, we investig
Externí odkaz:
https://doaj.org/article/27336f0a723a4a379b51629d31793d8e
Publikováno v:
Pediatric Nephrology. 37:1721-1731
Urothelium is a specialized multilayer epithelium that lines the urinary tract from the proximal urethra to the kidney. In addition to proliferation and differentiation during development, urothelial injury postnatally triggers a robust regenerative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdb76ded99d42ee319d672e2a5495e37
https://doi.org/10.1007/s00467-021-05239-w
https://doi.org/10.1007/s00467-021-05239-w
Autor:
Carlton M. Bates, Jacqueline Ho, Sunder Sims-Lucas, Débora M. Cerqueira, Brynn E Shrom, Melissa J Anslow, Daniel Bushnell, Andrew J. Bodnar
Publikováno v:
Pediatric research
BACKGROUND: Vesicoureteral reflux (VUR), backflow of urine into the kidney, is associated with urinary tract infections and chronic kidney disease. Integrity of the vesicoureteral junction (VUJ), where reflux occurs, is determined largely by proper i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d28d59c36bfc29d9b0ef9b73ec83ed65
https://doi.org/10.1038/s41390-020-0788-7
https://doi.org/10.1038/s41390-020-0788-7
Publikováno v:
Pediatric Research. 87:834-838
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b86dcb38c78ac2dd06087a6b0fb3fa56
https://doi.org/10.1038/s41390-019-0745-5
https://doi.org/10.1038/s41390-019-0745-5
Publikováno v:
Am J Pathol
Keratinocyte growth factor (KGF) improves cyclophosphamide-induced bladder injury. To understand the mechanisms, we subcutaneously administered KGF to mice 24 hours before i.p. cyclophosphamide administration, followed by histologic assays and immuno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7d898be34b757c510c40935a9ce457e
https://doi.org/10.1016/j.ajpath.2019.09.015
https://doi.org/10.1016/j.ajpath.2019.09.015
Publikováno v:
Pediatric Nephrology ISBN: 9783642278433
Pediatric Nephrology
Pediatric Nephrology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f99c6c331449ba1ebb7ba23e41ea6585
https://doi.org/10.1007/978-3-030-52719-8_1
https://doi.org/10.1007/978-3-030-52719-8_1
Publikováno v:
Am J Pathol
Keratinocyte growth factor (KGF) drives phosphorylated (activated) AKT (pAKT) in bladder urothelium, which correlates with cytoprotection from cyclophosphamide. The current study determined whether: i) KGF modifies AKT targets [B-cell lymphoma protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d3a54bd53c69645adce61b84a0514fe
https://pubmed.ncbi.nlm.nih.gov/35063403
https://pubmed.ncbi.nlm.nih.gov/35063403
Publikováno v:
Kidney Int
Nephronophthisis is an autosomal recessive kidney disease with high genetic heterogeneity. Understanding the functions of the individual genes contributing to this disease is critical for delineating the pathomechanisms of this disorder. Here, we inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6188d9d612764bcfb0127e06330e09f3
https://doi.org/10.1016/j.kint.2019.04.014
https://doi.org/10.1016/j.kint.2019.04.014