Kume T - Search Results

1

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerbäck S, Morissette J, Bhattacharya S, Hogan B, Raymond V, Walter MA. Mears AJ, et al. Among authors: kume t. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

2

The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus.

Kume T, Deng KY, Winfrey V, Gould DB, Walter MA, Hogan BL. Kume T, et al. Cell. 1998 Jun 12;93(6):985-96. doi: 10.1016/s0092-8674(00)81204-0. Cell. 1998. PMID: 9635428 Free article.

3

The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye.

Kidson SH, Kume T, Deng K, Winfrey V, Hogan BL. Kidson SH, et al. Among authors: kume t. Dev Biol. 1999 Jul 15;211(2):306-22. doi: 10.1006/dbio.1999.9314. Dev Biol. 1999. PMID: 10395790 Free article.

4

Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles.

Winnier GE, Kume T, Deng K, Rogers R, Bundy J, Raines C, Walter MA, Hogan BL, Conway SJ. Winnier GE, et al. Among authors: kume t. Dev Biol. 1999 Sep 15;213(2):418-31. doi: 10.1006/dbio.1999.9382. Dev Biol. 1999. PMID: 10479458 Free article.

5

Minimal phenotype of mice homozygous for a null mutation in the forkhead/winged helix gene, Mf2.

Kume T, Deng K, Hogan BL. Kume T, et al. Mol Cell Biol. 2000 Feb;20(4):1419-25. doi: 10.1128/MCB.20.4.1419-1425.2000. Mol Cell Biol. 2000. PMID: 10648626 Free PMC article.

6

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. Kume T, et al. Development. 2000 Apr;127(7):1387-95. doi: 10.1242/dev.127.7.1387. Development. 2000. PMID: 10704385

7

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development.

Smith RS, Zabaleta A, Kume T, Savinova OV, Kidson SH, Martin JE, Nishimura DY, Alward WL, Hogan BL, John SW. Smith RS, et al. Among authors: kume t. Hum Mol Genet. 2000 Apr 12;9(7):1021-32. doi: 10.1093/hmg/9.7.1021. Hum Mol Genet. 2000. PMID: 10767326

8

The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis.

Kume T, Jiang H, Topczewska JM, Hogan BL. Kume T, et al. Genes Dev. 2001 Sep 15;15(18):2470-82. doi: 10.1101/gad.907301. Genes Dev. 2001. PMID: 11562355 Free PMC article.

9

The winged helix transcription factor Foxc1a is essential for somitogenesis in zebrafish.

Topczewska JM, Topczewski J, Shostak A, Kume T, Solnica-Krezel L, Hogan BL. Topczewska JM, et al. Among authors: kume t. Genes Dev. 2001 Sep 15;15(18):2483-93. doi: 10.1101/gad.907401. Genes Dev. 2001. PMID: 11562356 Free PMC article.

10

The mouse forkhead gene Foxc1 is required for primordial germ cell migration and antral follicle development.

Mattiske D, Kume T, Hogan BL. Mattiske D, et al. Among authors: kume t. Dev Biol. 2006 Feb 15;290(2):447-58. doi: 10.1016/j.ydbio.2005.12.007. Epub 2006 Jan 17. Dev Biol. 2006. PMID: 16412416 Free article.

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