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Results: 1-17 |
Results: 17
Trans-species hair growth induction by human hair follicle dermal papillae
Authors: Jahoda, CAB Oliver, RF Reynolds, AJ Forrester, JC Gillespie, JW Cserhalmi-Friedman, PB Christiano, AM Horne, KA
Citation: Cab. Jahoda et al., Trans-species hair growth induction by human hair follicle dermal papillae, EXP DERMATO, 10(4), 2001, pp. 229-237
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
DNA based molecular analysis in the rapid diagnosis of Herlitz junctional epidermolysis bullosa
Authors: Cserhalmi-Friedman, PB Yeboa, KA Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., DNA based molecular analysis in the rapid diagnosis of Herlitz junctional epidermolysis bullosa, CLIN EXP D, 26(2), 2001, pp. 205-207
Maternal germline mosaicism in dominant dystrophic epidermolysis bullosa
Authors: Cserhalmi-Friedman, PB Garzon, MC Guzman, E Martinez-Mir, A Chung, WK Anyane-Yeboa, K Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Maternal germline mosaicism in dominant dystrophic epidermolysis bullosa, J INVES DER, 117(5), 2001, pp. 1327-1328
Diagnosis of autosomal recessive lamellar ichthyosis with mutations in theTGM1 gene
Authors: Cserhalmi-Friedman, PB Milstone, LM Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Diagnosis of autosomal recessive lamellar ichthyosis with mutations in theTGM1 gene, BR J DERM, 144(4), 2001, pp. 726-730
Structural analysis and mutation detection strategy for the human LamC3 gene
Authors: Cserhalmi-Friedman, PB Olson, PF Koch, M Champliaud, MF Brunken, WJ Burgeson, RE Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Structural analysis and mutation detection strategy for the human LamC3 gene, BIOC BIOP R, 280(1), 2001, pp. 39-44
Preimplantation genetic diagnosis in two families at risk for recurrence of Herlitz junctional epidermolysis bullosa
Authors: Cserhalmi-Friedman, PB Tang, Y Adler, A Krey, L Grifo, JA Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Preimplantation genetic diagnosis in two families at risk for recurrence of Herlitz junctional epidermolysis bullosa, EXP DERMATO, 9(4), 2000, pp. 290-297
Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene
Authors: Cserhalmi-Friedman, PB Squeo, R Gordon, D Garzon, M Schneiderman, P Grossman, ME Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene, CLIN EXP D, 25(3), 2000, pp. 241-243
Epidermolytic palmoplantar keratoderma in a Hispanic kindred resulting from a mutation in the keratin 9 gene
Authors: Warmuth, I Cserhalmi-Friedman, PB Schneiderman, P Grossman, ME Christiano, AM
Citation: I. Warmuth et al., Epidermolytic palmoplantar keratoderma in a Hispanic kindred resulting from a mutation in the keratin 9 gene, CLIN EXP D, 25(3), 2000, pp. 244-246
Analysis of the desmoplakin gene reveals striking conservation with other members of the plakin family of cytolinkers
Authors: Green, KJ Guy, SG Cserhalmi-Friedman, PB McLean, WHI Christiano, AM Wagner, RM
Citation: Kj. Green et al., Analysis of the desmoplakin gene reveals striking conservation with other members of the plakin family of cytolinkers, EXP DERMATO, 8(6), 1999, pp. 462-470
Identification of a de novo glycine substitution in the type VII collagen gene in a proband with mild dystrophic epidermolysis bullosa
Authors: Cserhalmi-Friedman, PB Grossman, J Karpati, S Ahmad, W Horvath, A Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Identification of a de novo glycine substitution in the type VII collagen gene in a proband with mild dystrophic epidermolysis bullosa, EXP DERMATO, 8(2), 1999, pp. 143-145
Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene
Authors: Moraru, R Cserhalmi-Friedman, PB Grossman, ME Schneiderman, P Christiano, AM
Citation: R. Moraru et al., Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene, CLIN EXP D, 24(5), 1999, pp. 412-415
Trans-gender induction of hair follicles
Authors: Reynolds, AJ Lawrence, C Cserhalmi-Friedman, PB Christiano, AM Jahoda, CAB
Citation: Aj. Reynolds et al., Trans-gender induction of hair follicles, NATURE, 402(6757), 1999, pp. 33-34
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
Restoration of open reading frame resulting from skipping of an exon with an internal deletion in the COL7A1 gene
Authors: Cserhalmi-Friedman, PB McGrath, JA Mellerio, JE Romero, R Salas-Alanis, JC Paller, AS Dietz, HC Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Restoration of open reading frame resulting from skipping of an exon with an internal deletion in the COL7A1 gene, LAB INV, 78(12), 1998, pp. 1483-1492
Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: Implications for geneticcounseling
Authors: Rouan, F Pulkkinen, L Jonkman, MF Bauer, JW Cserhalmi-Friedman, PB Christiano, AM Uitto, J
Citation: F. Rouan et al., Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: Implications for geneticcounseling, J INVES DER, 111(6), 1998, pp. 1210-1213
Risultati: 1-17 |