Walter MA - Search Results

1

FOXF2 is required for cochlear development in humans and mice.

Bademci G, Abad C, Incesulu A, Elian F, Reyahi A, Diaz-Horta O, Cengiz FB, Sineni CJ, Seyhan S, Atli EI, Basmak H, Demir S, Nik AM, Footz T, Guo S, Duman D, Fitoz S, Gurkan H, Blanton SH, Walter MA, Carlsson P, Walz K, Tekin M. Bademci G, et al. Among authors: walter ma. Hum Mol Genet. 2019 Apr 15;28(8):1286-1297. doi: 10.1093/hmg/ddy431. Hum Mol Genet. 2019. PMID: 30561639 Free PMC article.

2

Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning.

Mirzayans F, Mears AJ, Guo SW, Pearce WG, Walter MA. Mirzayans F, et al. Among authors: walter ma. Am J Hum Genet. 1997 Jul;61(1):111-9. doi: 10.1086/513894. Am J Hum Genet. 1997. PMID: 9245991 Free PMC article.

3

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: walter ma. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

4

Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders.

Kozlowski K, Walter MA. Kozlowski K, et al. Among authors: walter ma. Hum Mol Genet. 2000 Sep 1;9(14):2131-9. doi: 10.1093/hmg/9.14.2131. Hum Mol Genet. 2000. PMID: 10958652

5

Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1.

Saleem RA, Banerjee-Basu S, Berry FB, Baxevanis AD, Walter MA. Saleem RA, et al. Among authors: walter ma. Am J Hum Genet. 2001 Mar;68(3):627-41. doi: 10.1086/318792. Am J Hum Genet. 2001. PMID: 11179011 Free PMC article.

6

Molecular genetics of Axenfeld-Rieger malformations.

Lines MA, Kozlowski K, Walter MA. Lines MA, et al. Among authors: walter ma. Hum Mol Genet. 2002 May 15;11(10):1177-84. doi: 10.1093/hmg/11.10.1177. Hum Mol Genet. 2002. PMID: 12015277 Review.

7

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1.

Saleem RA, Banerjee-Basu S, Berry FB, Baxevanis AD, Walter MA. Saleem RA, et al. Among authors: walter ma. Hum Mol Genet. 2003 Nov 15;12(22):2993-3005. doi: 10.1093/hmg/ddg324. Epub 2003 Sep 23. Hum Mol Genet. 2003. PMID: 14506133

8

The wing 2 region of the FOXC1 forkhead domain is necessary for normal DNA-binding and transactivation functions.

Murphy TC, Saleem RA, Footz T, Ritch R, McGillivray B, Walter MA. Murphy TC, et al. Among authors: walter ma. Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2531-8. doi: 10.1167/iovs.04-0167. Invest Ophthalmol Vis Sci. 2004. PMID: 15277473

9

Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis.

Berry FB, Lines MA, Oas JM, Footz T, Underhill DA, Gage PJ, Walter MA. Berry FB, et al. Among authors: walter ma. Hum Mol Genet. 2006 Mar 15;15(6):905-19. doi: 10.1093/hmg/ddl008. Epub 2006 Jan 31. Hum Mol Genet. 2006. PMID: 16449236

10

FGF19 is a target for FOXC1 regulation in ciliary body-derived cells.

Tamimi Y, Skarie JM, Footz T, Berry FB, Link BA, Walter MA. Tamimi Y, et al. Among authors: walter ma. Hum Mol Genet. 2006 Nov 1;15(21):3229-40. doi: 10.1093/hmg/ddl400. Epub 2006 Sep 25. Hum Mol Genet. 2006. PMID: 17000708

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