Footz T - 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: footz t. 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

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: footz t. Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2531-8. doi: 10.1167/iovs.04-0167. Invest Ophthalmol Vis Sci. 2004. PMID: 15277473

3

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: footz t. 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

4

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: footz t. 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

5

Analyses of a novel L130F missense mutation in FOXC1.

Ito YA, Footz TK, Murphy TC, Courtens W, Walter MA. Ito YA, et al. Arch Ophthalmol. 2007 Jan;125(1):128-35. doi: 10.1001/archopht.125.1.128. Arch Ophthalmol. 2007. PMID: 17210863

6

Elliptical anterior iris stromal defects associated with PAX6 gene sequence changes.

Sharan S, Mirzayans F, Footz T, Walter M, Levin AV. Sharan S, et al. Among authors: footz t. J AAPOS. 2008 Aug;12(4):340-3. doi: 10.1016/j.jaapos.2007.11.021. Epub 2008 Apr 25. J AAPOS. 2008. PMID: 18440259

7

Human p32 is a novel FOXC1-interacting protein that regulates FOXC1 transcriptional activity in ocular cells.

Huang L, Chi J, Berry FB, Footz TK, Sharp MW, Walter MA. Huang L, et al. Invest Ophthalmol Vis Sci. 2008 Dec;49(12):5243-9. doi: 10.1167/iovs.07-1625. Epub 2008 Aug 1. Invest Ophthalmol Vis Sci. 2008. PMID: 18676636

8

Glaucoma-associated WDR36 variants encode functional defects in a yeast model system.

Footz TK, Johnson JL, Dubois S, Boivin N, Raymond V, Walter MA. Footz TK, et al. Hum Mol Genet. 2009 Apr 1;18(7):1276-87. doi: 10.1093/hmg/ddp027. Epub 2009 Jan 15. Hum Mol Genet. 2009. PMID: 19150991

9

Analysis of mutations of the PITX2 transcription factor found in patients with Axenfeld-Rieger syndrome.

Footz T, Idrees F, Acharya M, Kozlowski K, Walter MA. Footz T, et al. Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2599-606. doi: 10.1167/iovs.08-3251. Epub 2009 Feb 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19218601

10

Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia.

Ito YA, Footz TK, Berry FB, Mirzayans F, Yu M, Khan AO, Walter MA. Ito YA, et al. Invest Ophthalmol Vis Sci. 2009 Aug;50(8):3573-9. doi: 10.1167/iovs.08-3032. Epub 2009 Mar 11. Invest Ophthalmol Vis Sci. 2009. PMID: 19279310

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