R01 AR044924/AR/NIAMS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2006	1
2007	2
2008	4
2009	10
2010	8
2011	4
2012	4
2013	3
2014	3
2024	0

1

Broken hearts, woolly hair, and tattered skin: when desmosomal adhesion goes awry.

Bazzi H, Christiano AM. Bazzi H, et al. Curr Opin Cell Biol. 2007 Oct;19(5):515-20. doi: 10.1016/j.ceb.2007.08.001. Epub 2007 Oct 24. Curr Opin Cell Biol. 2007. PMID: 17951043 Free PMC article. Review.

2

Mutations in the SLURP-1 gene underlie Mal de Meleda in three Pakistani families.

Wajid M, Kurban M, Shimomura Y, Christiano AM. Wajid M, et al. J Dermatol Sci. 2009 Oct;56(1):27-32. doi: 10.1016/j.jdermsci.2009.06.012. Epub 2009 Aug 18. J Dermatol Sci. 2009. PMID: 19692209

3

Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma.

Dua-Awereh MB, Shimomura Y, Kraemer L, Wajid M, Christiano AM. Dua-Awereh MB, et al. J Dermatol Sci. 2009 Mar;53(3):192-7. doi: 10.1016/j.jdermsci.2008.11.005. Epub 2009 Jan 20. J Dermatol Sci. 2009. PMID: 19157795 Free PMC article.

4

Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis.

DeStefano GM, Fantauzzo KA, Petukhova L, Kurban M, Tadin-Strapps M, Levy B, Warburton D, Cirulli ET, Han Y, Sun X, Shen Y, Shirazi M, Jobanputra V, Cepeda-Valdes R, Cesar Salas-Alanis J, Christiano AM. DeStefano GM, et al. Proc Natl Acad Sci U S A. 2013 May 7;110(19):7790-5. doi: 10.1073/pnas.1216412110. Epub 2013 Apr 19. Proc Natl Acad Sci U S A. 2013. PMID: 23603273 Free PMC article.

5

A novel mutation in the cathepsin C gene in a Pakistani family with Papillon-Lefevre syndrome.

Kurban M, Cheng T, Wajid M, Kiuru M, Shimomura Y, Christiano AM. Kurban M, et al. J Eur Acad Dermatol Venereol. 2010 Aug;24(8):967-9. doi: 10.1111/j.1468-3083.2010.03575.x. Epub 2010 Mar 4. J Eur Acad Dermatol Venereol. 2010. PMID: 20236208 Free PMC article.

6

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. 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.

7

Identification of distinct mutations in AAGAB in families with type 1 punctate palmoplantar keratoderma.

Furniss M, Higgins CA, Martinez-Mir A, Horev L, Petukhova L, Stanimirović A, Miljković J, Zlotogorski A, Christiano AM. Furniss M, et al. J Invest Dermatol. 2014 Jun;134(6):1749-1752. doi: 10.1038/jid.2014.4. Epub 2014 Jan 3. J Invest Dermatol. 2014. PMID: 24390136 Free PMC article. No abstract available.

8

Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene.

Cabral RM, Kurban M, Rothman L, Wajid M, Shimomura Y, Petukhova L, Christiano AM. Cabral RM, et al. J Hum Genet. 2013 Aug;58(8):566-7. doi: 10.1038/jhg.2013.44. Epub 2013 May 23. J Hum Genet. 2013. PMID: 23697977 No abstract available.

9

Copy number variations on chromosome 4q26-27 are associated with Cantu syndrome.

Kurban M, Kim CA, Kiuru M, Fantauzzo K, Cabral R, Abbas O, Levy B, Christiano AM. Kurban M, et al. Dermatology. 2011;223(4):316-20. doi: 10.1159/000333800. Epub 2012 Feb 3. Dermatology. 2011. PMID: 22310962 Free PMC article.

10

Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis.

Shimomura Y, Wajid M, Petukhova L, Shapiro L, Christiano AM. Shimomura Y, et al. J Invest Dermatol. 2009 Mar;129(3):622-8. doi: 10.1038/jid.2008.290. Epub 2008 Oct 2. J Invest Dermatol. 2009. PMID: 18830268 Free article.

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