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Vincent Aita

Research Profile

Disorders

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Chromosomes, Human, Pair 18

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Publications

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Ana Kljuic; Hisham Bazzi; John P Sundberg; Amalia Martinez-Mir; Ryan O'Shaughnessy; My G Mahoney; Moise Levy; Xavier Montagutelli; Wasim Ahmad; Vincent M Aita; Derek Gordon; Jouni Uitto; David Whiting; Jurg Ott; Stuart Fischer; T Conrad Gilliam; Colin A B Jahoda; Rebecca J Morris; Andrey Panteleyev; Vu Thuong Nguyen; Angela M Christiano
Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.
Abraham Zlotogorski; Andrey Panteleyev; Vincent M Aita; Angela M Christiano
Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions.
Wasim Ahmad; Marion S Ratterree; Andrey Panteleyev; Vincent M Aita; John P Sundberg; Angela M Christiano
Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene.

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All Publications

2003: Ana Kljuic; Hisham Bazzi; John P Sundberg; Amalia Martinez-Mir; Ryan O'Shaughnessy; My G Mahoney; Moise Levy; Xavier Montagutelli; Wasim Ahmad; Vincent M Aita; Derek Gordon; Jouni Uitto; David Whiting; Jurg Ott; Stuart Fischer; T Conrad Gilliam; Colin A B Jahoda; Rebecca J Morris; Andrey Panteleyev; Vu Thuong Nguyen; Angela M Christiano
Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.
Cell 2003;113(2):249-60.
2002: Abraham Zlotogorski; Andrey Panteleyev; Vincent M Aita; Angela M Christiano
Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions.
The Journal of investigative dermatology 2002;118(5):887-90.
2002: Wasim Ahmad; Marion S Ratterree; Andrey Panteleyev; Vincent M Aita; John P Sundberg; Angela M Christiano
Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene.
Laboratory animals 2002;36(1):61-7.
2001: Abraham Zlotogorski; Andrey Panteleyev; Vincent M Aita; Angela M Christiano
Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions.
The Journal of investigative dermatology 2001;117(6):1662-5.
2001: Peter B Cserhalmi-Friedman; J A Frank; Wasim Ahmad; Andrey Panteleyev; Vincent M Aita; Angela M Christiano
Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members.
Experimental dermatology 2001;10(2):95-9.
2001: J Frank; Peter B Cserhalmi-Friedman; Wasim Ahmad; Andrey Panteleyev; Vincent M Aita; Angela M Christiano
Characterization of the desmosomal cadherin gene family: genomic organization of two desmoglein genes on human chromosome 18q12.
Experimental dermatology 2001;10(2):90-4.
2001: J Frank; Vincent M Aita; Wasim Ahmad; HaMut Lam; C Wolff; Angela M Christiano
Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from chile.
Human heredity 2001;51(3):160-8.
2001: Karima Djabali; Vincent M Aita; Angela M Christiano
Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix.
Journal of cell science 2001;114(Pt 2):367-76.
2000: Vincent M Aita; Abraham Zlotogorski; Angela M Christiano
Settling the score on hairless.
The Journal of investigative dermatology 2000;115(4):761-4.
2000: Vincent M Aita; Wasim Ahmad; Andrey Panteleyev; U Kozlowska; A Kozlowska; T Conrad Gilliam; S Jablonska; Angela M Christiano
A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions.
Experimental dermatology 2000;9(2):157-62.
1999: Vincent M Aita; Angela M Christiano; T Conrad Gilliam
Mapping complex traits in diseases of the hair and skin.
Experimental dermatology 1999;8(6):439-52.
1999: Vincent M Aita; Xiao Huan Liang; Vundavalli Murty; David L Pincus; W Yu; Eftihia Cayanis; Sergey Kalachikov; T Conrad Gilliam; Beth Levine
Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21.
Genomics 1999;59(1):59-65.
1999: Jorge Frank; Claudio Pignata; Andrey Panteleyev; David Prowse; Howard P Baden; Lorin Weiner; L Gaetaniello; Wasim Ahmad; N Pozzi; Peter B Cserhalmi-Friedman; Vincent M Aita; Hendrik Uyttendaele; D Gordon; Jurg Ott; Janice L Brissette; Angela M Christiano
Exposing the human nude phenotype.
Nature 1999;398(6727):473-4.
1999: Vincent M Aita; Jianjun Liu; James A Knowles; Joseph D Terwilliger; R Baltazar; Adina Grunn; JE Loth; Kyra Sarner Kanyas; Bernard Lerer; Jean Endicott; Z Wang; Graciela Penchaszadeh; T Conrad Gilliam; M Baron
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus.
American journal of human genetics 1999;64(1):210-7.
1998: J Frank; Xiao-Jing Wang; H M Lam; Vincent M Aita; Frank K Jugert; G Goerz; Hans F Merk; Maureen B Poh-Fitzpatrick; Angela M Christiano
C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria.
Annals of human genetics 1998;62(Pt 3):225-30.
1998: Wasim Ahmad; V Brancolini; M F ul Faiyaz; HaMut Lam; S ul Haque; M Haider; A Maimon; Vincent M Aita; J Owen; D Brown; D J Zegarelli; M Ahmad; Jurg Ott; Angela M Christiano
A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.
American journal of human genetics 1998;62(4):987-91.
1998: Wasim Ahmad; Muhammad Faiyaz-Ul-Haque; V Brancolini; HC Tsou; S ul Haque; HaMut Lam; Vincent M Aita; J Owen; M deBlaquiere; J Frank; Peter B Cserhalmi-Friedman; A Leask; John A McGrath; M Peacocke; M Ahmad; Jurg Ott; Angela M Christiano
Alopecia universalis associated with a mutation in the human hairless gene.
Science (New York, N.Y.) 1998;279(5351):720-4.