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Results: 1-10 |
Results: 10
Characterization of the desmosomal cadherin gene family: Genomic organization of two desmoglein genes on human chromosome 18q12
Authors: Frank, J Cserhalmi-Friedman, PB Ahmad, W Panteleyev, AA Aita, VM Christiano, AM
Citation: J. Frank et al., Characterization of the desmosomal cadherin gene family: Genomic organization of two desmoglein genes on human chromosome 18q12, EXP DERMATO, 10(2), 2001, pp. 90-94
Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members
Authors: Cserhalmi-Friedman, PB Frank, JA Ahmad, W Panteleyev, AA Aita, VM Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members, EXP DERMATO, 10(2), 2001, pp. 95-99
Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix
Authors: Djabali, K Aita, VM Christiano, AM
Citation: K. Djabali et al., Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix, J CELL SCI, 114(2), 2001, pp. 367-376
Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from Chile
Authors: Frank, J Aita, VM Ahmad, W Lam, HM Wolff, C Christiano, AM
Citation: J. Frank et al., Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from Chile, HUMAN HERED, 51(3), 2001, pp. 160-168
A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions
Authors: Aita, VM Ahmad, W Panteleyev, AA Kozlowska, U Kozlowska, A Gilliam, TC Jablonska, S Christiano, AM
Citation: Vm. Aita et al., A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions, EXP DERMATO, 9(2), 2000, pp. 157-162
Settling the score on hairless
Authors: Aita, VM Zlotogorski, A Christiano, AM
Citation: Vm. Aita et al., Settling the score on hairless, J INVES DER, 115(4), 2000, pp. 761-762
Mapping complex traits in diseases of the hair and skin
Authors: Aita, VM Christiano, AM Gilliam, TC
Citation: Vm. Aita et al., Mapping complex traits in diseases of the hair and skin, EXP DERMATO, 8(6), 1999, pp. 439-452
Cloning and genomic organization of beclin 1, a candidate tumor suppressorgene on chromosome 17q21
Authors: Aita, VM Liang, XH Murty, VVVS Pincus, DL Yu, WP Cayanis, E Kalachikov, S Gilliam, TC Levine, B
Citation: Vm. Aita et al., Cloning and genomic organization of beclin 1, a candidate tumor suppressorgene on chromosome 17q21, GENOMICS, 59(1), 1999, pp. 59-65
Exposing the human nude phenotype
Authors: Frank, J Pignata, C Panteleyev, AA Prowse, DM Baden, H Weiner, L Gaetaniello, L Ahmad, W Pozzi, N Cserhalmi-Friedman, PB Aita, VM Uyttendaele, H Gordon, D Ott, J Brissette, JL Christiano, AM
Citation: J. Frank et al., Exposing the human nude phenotype, NATURE, 398(6727), 1999, pp. 473-474
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus
Authors: Aita, VM Liu, JJ Knowles, JA Terwilliger, JD Baltazar, R Grunn, A Loth, JE Kanyas, K Lerer, B Endicott, J Wang, ZY Penchaszadeh, G Gilliam, TC Baron, M
Citation: Vm. Aita et al., A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus, AM J HU GEN, 64(1), 1999, pp. 210-217
Risultati: 1-10 |