Markers of kidney cell lineage (Homo sapiens)
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Description
This pathway contains a timely and spatially differentiated map of cell markers for kidney development. These are relevant to study the congenital anomalies of kidney and urinary tract (CAKUT) disorders.
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Ontology Terms
Bibliography
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- Bohnenpoll T, Bettenhausen E, Weiss AC, Foik AB, Trowe MO, Blank P, Airik R, Kispert A; ''Tbx18 expression demarcates multipotent precursor populations in the developing urogenital system but is exclusively required within the ureteric mesenchymal lineage to suppress a renal stromal fate.''; Dev Biol, 2013 PubMed Europe PMC Scholia
- Munro DAD, Wineberg Y, Tarnick J, Vink CS, Li Z, Pridans C, Dzierzak E, Kalisky T, Hohenstein P, Davies JA; ''Macrophages restrict the nephrogenic field and promote endothelial connections during kidney development.''; Elife, 2019 PubMed Europe PMC Scholia
- Boyle S, Shioda T, Perantoni AO, de Caestecker M; ''Cited1 and Cited2 are differentially expressed in the developing kidney but are not required for nephrogenesis.''; Dev Dyn, 2007 PubMed Europe PMC Scholia
- Kobayashi H, Liu Q, Binns TC, Urrutia AA, Davidoff O, Kapitsinou PP, Pfaff AS, Olauson H, Wernerson A, Fogo AB, Fong GH, Gross KW, Haase VH; ''Distinct subpopulations of FOXD1 stroma-derived cells regulate renal erythropoietin.''; J Clin Invest, 2016 PubMed Europe PMC Scholia
- Guillaume R, Bressan M, Herzlinger D; ''Paraxial mesoderm contributes stromal cells to the developing kidney.''; Dev Biol, 2009 PubMed Europe PMC Scholia
- Kobayashi A, Valerius MT, Mugford JW, Carroll TJ, Self M, Oliver G, McMahon AP; ''Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development.''; Cell Stem Cell, 2008 PubMed Europe PMC Scholia
- Yoshino K, Rubin JS, Higinbotham KG, Uren A, Anest V, Plisov SY, Perantoni AO; ''Secreted Frizzled-related proteins can regulate metanephric development.''; Mech Dev, 2001 PubMed Europe PMC Scholia
- Hatini V, Huh SO, Herzlinger D, Soares VC, Lai E; ''Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2.''; Genes Dev, 1996 PubMed Europe PMC Scholia
- Mugford JW, Sipilä P, McMahon JA, McMahon AP; ''Osr1 expression demarcates a multi-potent population of intermediate mesoderm that undergoes progressive restriction to an Osr1-dependent nephron progenitor compartment within the mammalian kidney.''; Dev Biol, 2008 PubMed Europe PMC Scholia
- Yallowitz AR, Hrycaj SM, Short KM, Smyth IM, Wellik DM; ''Hox10 genes function in kidney development in the differentiation and integration of the cortical stroma.''; PLoS One, 2011 PubMed Europe PMC Scholia
- Schnabel CA, Godin RE, Cleary ML; ''Pbx1 regulates nephrogenesis and ureteric branching in the developing kidney.''; Dev Biol, 2003 PubMed Europe PMC Scholia
- Wilson SB, Little MH; ''The origin and role of the renal stroma.''; Development, 2021 PubMed Europe PMC Scholia
- Boyle S, Misfeldt A, Chandler KJ, Deal KK, Southard-Smith EM, Mortlock DP, Baldwin HS, de Caestecker M; ''Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epithelia.''; Dev Biol, 2008 PubMed Europe PMC Scholia
- Brunskill EW, Sequeira-Lopez ML, Pentz ES, Lin E, Yu J, Aronow BJ, Potter SS, Gomez RA; ''Genes that confer the identity of the renin cell.''; J Am Soc Nephrol, 2011 PubMed Europe PMC Scholia
- Munro DAD, Hohenstein P, Davies JA; ''Cycles of vascular plexus formation within the nephrogenic zone of the developing mouse kidney.''; Sci Rep, 2017 PubMed Europe PMC Scholia
- Schmidt-Ott KM, Chen X, Paragas N, Levinson RS, Mendelsohn CL, Barasch J; ''c-kit delineates a distinct domain of progenitors in the developing kidney.''; Dev Biol, 2006 PubMed Europe PMC Scholia
- Christians A, Kesdiren E, Hennies I, Hofmann A, Trowe MO, Brand F, Martens H, Gjerstad AC, Gucev Z, Zirngibl M, Geffers R, Seeman T, Billing H, Bjerre A, Tasic V, Kispert A, Ure B, Haffner D, Dingemann J, Weber RG; ''Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2.''; Hum Genet, 2023 PubMed Europe PMC Scholia
- Kesdiren E, Martens H, Brand F, Werfel L, Wedekind L, Trowe MO, Schmitz J, Hennies I, Geffers R, Gucev Z, Seeman T, Schmidt S, Tasic V, Fasano L, Bräsen JH, Kispert A, Christians A, Haffner D, Weber RG; ''Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.''; Eur J Hum Genet, 2024 PubMed Europe PMC Scholia
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