Aita VM - Search Results

1

A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus.

Aita VM, Liu J, Knowles JA, Terwilliger JD, Baltazar R, Grunn A, Loth JE, Kanyas K, Lerer B, Endicott J, Wang Z, Penchaszadeh G, Gilliam TC, Baron M. Aita VM, et al. Am J Hum Genet. 1999 Jan;64(1):210-7. doi: 10.1086/302185. Am J Hum Genet. 1999. PMID: 9915960 Free PMC article.

2

Mapping complex traits in diseases of the hair and skin.

Aita VM, Christiano AM, Gilliam TC. Aita VM, et al. Exp Dermatol. 1999 Dec;8(6):439-52. doi: 10.1111/j.1600-0625.1999.tb00302.x. Exp Dermatol. 1999. PMID: 10597133 Review.

3

Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21.

Aita VM, Liang XH, Murty VV, Pincus DL, Yu W, Cayanis E, Kalachikov S, Gilliam TC, Levine B. Aita VM, et al. Genomics. 1999 Jul 1;59(1):59-65. doi: 10.1006/geno.1999.5851. Genomics. 1999. PMID: 10395800 Free article.

4

A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions.

Aita VM, Ahmad W, Panteleyev AA, Kozlowska U, Kozlowska A, Gilliam TC, Jablonska S, Christiano AM. Aita VM, et al. Exp Dermatol. 2000 Apr;9(2):157-62. doi: 10.1034/j.1600-0625.2000.009002157.x. Exp Dermatol. 2000. PMID: 10772391

5

Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.

Kljuic A, Bazzi H, Sundberg JP, Martinez-Mir A, O'Shaughnessy R, Mahoney MG, Levy M, Montagutelli X, Ahmad W, Aita VM, Gordon D, Uitto J, Whiting D, Ott J, Fischer S, Gilliam TC, Jahoda CA, Morris RJ, Panteleyev AA, Nguyen VT, Christiano AM. Kljuic A, et al. Among authors: aita vm. Cell. 2003 Apr 18;113(2):249-60. doi: 10.1016/s0092-8674(03)00273-3. Cell. 2003. PMID: 12705872 Free article.

6

C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria.

Frank J, Wang X, Lam HM, Aita VM, Jugert FK, Goerz G, Merk HF, Poh-Fitzpatrick MB, Christiano AM. Frank J, et al. Among authors: aita vm. Ann Hum Genet. 1998 May;62(Pt 3):225-30. doi: 10.1046/j.1469-1809.1998.6230225.x. Ann Hum Genet. 1998. PMID: 9803266

7

A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Fujita R, Bingham E, Forsythe P, McHenry C, Aita V, Navia BA, Dry K, Segal M, Devoto M, Bruns G, Wright AF, Ott J, Sieving PA, Swaroop A. Fujita R, et al. Am J Hum Genet. 1996 Jul;59(1):152-8. Am J Hum Genet. 1996. PMID: 8659520 Free PMC article.

8

A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

Ahmad W, Brancolini V, ul Faiyaz MF, Lam H, ul Haque S, Haider M, Maimon A, Aita VM, Owen J, Brown D, Zegarelli DJ, Ahmad M, Ott J, Christiano AM. Ahmad W, et al. Among authors: aita vm. Am J Hum Genet. 1998 Apr;62(4):987-91. doi: 10.1086/301799. Am J Hum Genet. 1998. PMID: 9529357 Free PMC article. No abstract available.

9

Alopecia universalis associated with a mutation in the human hairless gene.

Ahmad W, Faiyaz ul Haque M, Brancolini V, Tsou HC, ul Haque S, Lam H, Aita VM, Owen J, deBlaquiere M, Frank J, Cserhalmi-Friedman PB, Leask A, McGrath JA, Peacocke M, Ahmad M, Ott J, Christiano AM. Ahmad W, et al. Among authors: aita vm. Science. 1998 Jan 30;279(5351):720-4. doi: 10.1126/science.279.5351.720. Science. 1998. PMID: 9445480

10

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. Among authors: aita vm. Hum Hered. 2001;51(3):160-8. doi: 10.1159/000053337. Hum Hered. 2001. PMID: 11173967

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