P30 AR44535/AR/NIAMS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1998	5
1999	7
2000	4
2001	8
2002	3
2003	5
2004	1
2005	1
2006	1
2025	0

1

New approaches to therapy for mastocytosis. A case for treatment with kit kinase inhibitors.

Longley BJ, Ma Y, Carter E, McMahon G. Longley BJ, et al. Hematol Oncol Clin North Am. 2000 Jun;14(3):689-95. doi: 10.1016/s0889-8588(05)70302-6. Hematol Oncol Clin North Am. 2000. PMID: 10909046 Free article. Review.

2

Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members.

Cserhalmi-Friedman PB, Frank JA, Ahmad W, Panteleyev AA, Aita VM, Christiano AM. Cserhalmi-Friedman PB, et al. Exp Dermatol. 2001 Apr;10(2):95-9. doi: 10.1034/j.1600-0625.2001.010002095.x. Exp Dermatol. 2001. PMID: 11260247

3

Molecular basis for the rhino (hrrh-8J) phenotype: a nonsense mutation in the mouse hairless gene.

Ahmad W, Panteleyev AA, Sundberg JP, Christiano AM. Ahmad W, et al. Genomics. 1998 Nov 1;53(3):383-6. doi: 10.1006/geno.1998.5495. Genomics. 1998. PMID: 9799606 Free article.

4

Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix.

Djabali K, Aita VM, Christiano AM. Djabali K, et al. J Cell Sci. 2001 Jan;114(Pt 2):367-76. doi: 10.1242/jcs.114.2.367. J Cell Sci. 2001. PMID: 11148138

5

Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata.

Chuang GS, Martinez-Mir A, Geyer A, Engler DE, Glaser B, Cserhalmi-Friedman PB, Gordon D, Horev L, Lukash B, Herman E, Cid MP, Brenner S, Landau M, Sprecher E, Garcia Muret MP, Christiano AM, Zlotogorski A. Chuang GS, et al. J Am Acad Dermatol. 2005 Mar;52(3 Pt 1):410-6. doi: 10.1016/j.jaad.2004.08.051. J Am Acad Dermatol. 2005. PMID: 15761418 Free article.

6

Evidence for extensive locus heterogeneity in Naxos disease.

Djabali K, Martinez-Mir A, Horev L, Christiano AM, Zlotogorski A. Djabali K, et al. J Invest Dermatol. 2002 Mar;118(3):557-60. doi: 10.1046/j.0022-202x.2001.01627.x. J Invest Dermatol. 2002. PMID: 11874502 Free article. No abstract available.

7

Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from chile.

Frank J, Aita VM, Ahmad W, Lam H, Wolff C, Christiano AM. Frank J, et al. Hum Hered. 2001;51(3):160-8. doi: 10.1159/000053337. Hum Hered. 2001. PMID: 11173967

8

A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.

Ahmad W, Irvine AD, Lam H, Buckley C, Bingham EA, Panteleyev AA, Ahmad M, McGrath JA, Christiano AM. Ahmad W, et al. Am J Hum Genet. 1998 Oct;63(4):984-91. doi: 10.1086/302069. Am J Hum Genet. 1998. PMID: 9758627 Free PMC article.

9

PTCH mutations in squamous cell carcinoma of the skin.

Ping XL, Ratner D, Zhang H, Wu XL, Zhang MJ, Chen FF, Silvers DN, Peacocke M, Tsou HC. Ping XL, et al. J Invest Dermatol. 2001 Apr;116(4):614-6. doi: 10.1046/j.1523-1747.2001.01301.x. J Invest Dermatol. 2001. PMID: 11286632 Free article.

10

mda-7 (IL-24): signaling and functional roles.

Sarkar D, Su ZZ, Lebedeva IV, Sauane M, Gopalkrishnan RV, Dent P, Fisher PB. Sarkar D, et al. Biotechniques. 2002 Oct;Suppl:30-9. Biotechniques. 2002. PMID: 12395925

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