Wajid M - Search Results

1

FGF5 is a crucial regulator of hair length in humans.

Higgins CA, Petukhova L, Harel S, Ho YY, Drill E, Shapiro L, Wajid M, Christiano AM. Higgins CA, et al. Among authors: wajid m. Proc Natl Acad Sci U S A. 2014 Jul 22;111(29):10648-53. doi: 10.1073/pnas.1402862111. Epub 2014 Jul 2. Proc Natl Acad Sci U S A. 2014. PMID: 24989505 Free PMC article.

2

The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia.

Blaydon DC, Ishii Y, O'Toole EA, Unsworth HC, Teh MT, Rüschendorf F, Sinclair C, Hopsu-Havu VK, Tidman N, Moss C, Watson R, de Berker D, Wajid M, Christiano AM, Kelsell DP. Blaydon DC, et al. Among authors: wajid m. Nat Genet. 2006 Nov;38(11):1245-7. doi: 10.1038/ng1883. Epub 2006 Oct 15. Nat Genet. 2006. PMID: 17041604

3

Striate palmoplantar keratoderma resulting from a frameshift mutation in the desmoglein 1 gene.

Barber AG, Wajid M, Columbo M, Lubetkin J, Christiano AM. Barber AG, et al. Among authors: wajid m. J Dermatol Sci. 2007 Mar;45(3):161-6. doi: 10.1016/j.jdermsci.2006.11.013. Epub 2006 Dec 27. J Dermatol Sci. 2007. PMID: 17194569 Free PMC article.

4

A glycine substitution in the COL7A1 gene causes mild RDEB in a Pakistani family.

Kraemer L, Wajid M, Christiano AM. Kraemer L, et al. Among authors: wajid m. Eur J Dermatol. 2006 Nov-Dec;16(6):615-9. Eur J Dermatol. 2006. PMID: 17229600

5

Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family.

Wajid M, Bazzi H, Rockey J, Lubetkin J, Zlotogorski A, Christiano AM. Wajid M, et al. J Invest Dermatol. 2007 Jul;127(7):1779-82. doi: 10.1038/sj.jid.5700791. Epub 2007 Mar 29. J Invest Dermatol. 2007. PMID: 17392831 Free article. No abstract available.

6

Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia.

Ishii Y, Wajid M, Bazzi H, Fantauzzo KA, Barber AG, Blaydon DC, Nam JS, Yoon JK, Kelsell DP, Christiano AM. Ishii Y, et al. Among authors: wajid m. J Invest Dermatol. 2008 Apr;128(4):867-70. doi: 10.1038/sj.jid.5701078. Epub 2007 Sep 6. J Invest Dermatol. 2008. PMID: 17805348 Free article.

7

Nonsense mutations in the hairless gene underlie APL in five families of Pakistani origin.

Kim H, Wajid M, Kraemer L, Shimomura Y, Christiano AM. Kim H, et al. Among authors: wajid m. J Dermatol Sci. 2007 Dec;48(3):207-11. doi: 10.1016/j.jdermsci.2007.07.007. Epub 2007 Sep 14. J Dermatol Sci. 2007. PMID: 17869066 Free PMC article.

8

Mutations in the hairless gene underlie APL in three families of Pakistani origin.

Kraemer L, Wajid M, Shimomura Y, Christiano AM. Kraemer L, et al. Among authors: wajid m. J Dermatol Sci. 2008 Apr;50(1):25-30. doi: 10.1016/j.jdermsci.2007.10.012. J Dermatol Sci. 2008. PMID: 18164595 Free PMC article.

9

P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle.

Shimomura Y, Wajid M, Shapiro L, Christiano AM. Shimomura Y, et al. Among authors: wajid m. Development. 2008 Feb;135(4):743-53. doi: 10.1242/dev.006718. Epub 2008 Jan 16. Development. 2008. PMID: 18199584

10

Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair.

Shimomura Y, Wajid M, Ishii Y, Shapiro L, Petukhova L, Gordon D, Christiano AM. Shimomura Y, et al. Among authors: wajid m. Nat Genet. 2008 Mar;40(3):335-9. doi: 10.1038/ng.100. Epub 2008 Feb 24. Nat Genet. 2008. PMID: 18297072

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