63 related articles for article (PubMed ID: 23838094)
1. Foxc1 gene null mutation causes ectopic budding and kidney hypoplasia but not dysplasia.
Komaki F; Miyazaki Y; Niimura F; Matsusaka T; Ichikawa I; Motojima M
Cells Tissues Organs; 2013; 198(1):22-7. PubMed ID: 23838094
[TBL] [Abstract][Full Text] [Related]
2. Disruption of Gen1 causes ectopic budding and kidney hypoplasia in mice.
Li Y; Yu M; Tan L; Xue S; Du X; Wang C; Wu X; Xu H; Shen Q
Biochem Biophys Res Commun; 2022 Jan; 589():173-179. PubMed ID: 34922199
[TBL] [Abstract][Full Text] [Related]
3. Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract.
Kume T; Deng K; Hogan BL
Development; 2000 Apr; 127(7):1387-95. PubMed ID: 10704385
[TBL] [Abstract][Full Text] [Related]
4. The mouse forkhead gene Foxc1 is required for primordial germ cell migration and antral follicle development.
Mattiske D; Kume T; Hogan BL
Dev Biol; 2006 Feb; 290(2):447-58. PubMed ID: 16412416
[TBL] [Abstract][Full Text] [Related]
5. Characterization of Kidney and Skeleton Phenotypes of Mice Double Heterozygous for Foxc1 and Foxc2.
Motojima M; Tanimoto S; Ohtsuka M; Matsusaka T; Kume T; Abe K
Cells Tissues Organs; 2016; 201(5):380-9. PubMed ID: 27193493
[TBL] [Abstract][Full Text] [Related]
6. Angiotensin type II receptor expression and ureteral budding.
Oshima K; Miyazaki Y; Brock JW; Adams MC; Ichikawa I; Pope JC
J Urol; 2001 Nov; 166(5):1848-52. PubMed ID: 11586245
[TBL] [Abstract][Full Text] [Related]
7. Identification of Tgf beta1i4 as a downstream target of Foxc1.
Sommer P; Napier HR; Hogan BL; Kidson SH
Dev Growth Differ; 2006 Jun; 48(5):297-308. PubMed ID: 16759280
[TBL] [Abstract][Full Text] [Related]
8. Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.
Machida A; Okuhara S; Harada K; Iseki S
Congenit Anom (Kyoto); 2014 Aug; 54(3):172-7. PubMed ID: 24417671
[TBL] [Abstract][Full Text] [Related]
9. Transcription factor Foxc1 is involved in anterior part of cranial base formation.
Mya N; Furutera T; Okuhara S; Kume T; Takechi M; Iseki S
Congenit Anom (Kyoto); 2018 Sep; 58(5):158-166. PubMed ID: 29322554
[TBL] [Abstract][Full Text] [Related]
10. Congenital anomalies of the kidney and urinary tract--role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene.
Pope JC; Brock JW; Adams MC; Miyazaki Y; Stephens FD; Ichikawa I
J Urol; 2001 Jan; 165(1):196-202. PubMed ID: 11125405
[TBL] [Abstract][Full Text] [Related]
11. Hnf1b and Pax2 cooperate to control different pathways in kidney and ureter morphogenesis.
Paces-Fessy M; Fabre M; Lesaulnier C; Cereghini S
Hum Mol Genet; 2012 Jul; 21(14):3143-55. PubMed ID: 22511595
[TBL] [Abstract][Full Text] [Related]
12. Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.
Cella W; de Vasconcellos JP; de Melo MB; Kneipp B; Costa FF; Longui CA; Costa VP
Invest Ophthalmol Vis Sci; 2006 May; 47(5):1803-9. PubMed ID: 16638984
[TBL] [Abstract][Full Text] [Related]
13. The forkhead genes, Foxc1 and Foxc2, regulate paraxial versus intermediate mesoderm cell fate.
Wilm B; James RG; Schultheiss TM; Hogan BL
Dev Biol; 2004 Jul; 271(1):176-89. PubMed ID: 15196959
[TBL] [Abstract][Full Text] [Related]
14. Canonical Wnt signaling regulates Foxc1/2 expression in P19 cells.
Savage J; Voronova A; Mehta V; Sendi-Mukasa F; Skerjanc IS
Differentiation; 2010 Jan; 79(1):31-40. PubMed ID: 19782461
[TBL] [Abstract][Full Text] [Related]
15. Foxc1 and Foxc2 are indispensable for the maintenance of nephron and stromal progenitors in the developing kidney.
Motojima M; Tanaka M; Kume T
J Cell Sci; 2022 Oct; 135(19):. PubMed ID: 36073617
[TBL] [Abstract][Full Text] [Related]
16. Screening for mutations in BMP4 and FOXC1 genes in congenital anomalies of the kidney and urinary tract in humans.
Nakano T; Niimura F; Hohenfellner K; Miyakita E; Ichikawa I
Tokai J Exp Clin Med; 2003 Oct; 28(3):121-6. PubMed ID: 15055404
[TBL] [Abstract][Full Text] [Related]
17. Cerebrovascular defects in Foxc1 mutants correlate with aberrant WNT and VEGF-A pathways downstream of retinoic acid from the meninges.
Mishra S; Choe Y; Pleasure SJ; Siegenthaler JA
Dev Biol; 2016 Dec; 420(1):148-165. PubMed ID: 27671872
[TBL] [Abstract][Full Text] [Related]
18. The role of FoxC1 in early Xenopus development.
Cha JY; Birsoy B; Kofron M; Mahoney E; Lang S; Wylie C; Heasman J
Dev Dyn; 2007 Oct; 236(10):2731-41. PubMed ID: 17705306
[TBL] [Abstract][Full Text] [Related]
19. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.
Strungaru MH; Dinu I; Walter MA
Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):228-37. PubMed ID: 17197537
[TBL] [Abstract][Full Text] [Related]
20. Forkhead transcription factors, Foxc1 and Foxc2, are required for the morphogenesis of the cardiac outflow tract.
Seo S; Kume T
Dev Biol; 2006 Aug; 296(2):421-36. PubMed ID: 16839542
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
