V. Aita

发表

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

J. Ott, J. Owen, J. McGrath, 1998, Science.

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

T. Gilliam, W. Ahmad, V. Aita, 2000, Experimental dermatology.

Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions.

A. Christiano, A. Zlotogorski, V. Aita, 2001, The Journal of investigative dermatology.

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

D L Pincus, V V Murty, T. Gilliam, 1999, Genomics.

Mapping complex traits in diseases of the hair and skin

T. Gilliam, V. Aita, A. Christiano, 1999, Experimental dermatology.

Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene

J. Sundberg, A. Christiano, W. Ahmad, 2002, Laboratory animals.

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

A. Christiano, W. Ahmad, V. Aita, 2001, Experimental dermatology.

Settling the score on hairless.

A. Christiano, A. Zlotogorski, V. Aita, 2000, The Journal of investigative dermatology.

Exposing the human nude phenotype

J. Ott, C. Pignata, D. Gordon, 1999, Nature.

Characterization of the desmosomal cadherin gene family: Genomic organization of two desmoglein genes on human chromosome 18q12

A. Christiano, W. Ahmad, J. Frank, 2001, Experimental dermatology.

Identification of a Founder Mutation in the Protoporphyrinogen Oxidase Gene in Variegate Porphyria Patients from Chile

A. Christiano, W. Ahmad, J. Frank, 2001, Human Heredity.

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

P. Sieving, J. Ott, M. Devoto, 1996, American journal of human genetics.

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

J. Ott, J. Owen, A. Christiano, 1998, American journal of human genetics.

Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris

J. Ott, T. Gilliam, J. Sundberg, 2003, Cell.

The genetics of alopecia areata

V. Aita, A. Christiano, 2001 .

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

J. Terwilliger, T. Gilliam, J. Endicott, 1999, American journal of human genetics.

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

A. Christiano, V. Aita, K. Djabali, 2001, Journal of cell science.

A Recombination Outside theBBDeletion Refines theLocation of theX-Linked Retinitis Pigmentosa LocusRP3

M. Devoto, R. Fujita, V. Aita, 1996 .