AAAAAA

   
Results: 1-25 | 26-45
Results: 1-25/45
MUTATIONS IN THE HUMAN CONNEXIN GENE GJB3 CAUSE ERYTHROKERATODERMIA VARIABILIS
Authors: RICHARD G SMITH LE BAILEY RA ITIN P HOHL D EPSTEIN EH DIGIOVANNA JJ COMPTON JG BALE SJ
Citation: G. Richard et al., MUTATIONS IN THE HUMAN CONNEXIN GENE GJB3 CAUSE ERYTHROKERATODERMIA VARIABILIS, Nature genetics, 20(4), 1998, pp. 366-369
ACTIVATING SMOOTHENED MUTATIONS IN SPORADIC BASAL-CELL CARCINOMA
Authors: XIE JW MURONE M LUOH SM RYAN A GU QM ZHANG CH BONIFAS JM LAM CW HYNES M GODDARD A ROSENTHAL A EPSTEIN EH DESAUVAGE FJ
Citation: Jw. Xie et al., ACTIVATING SMOOTHENED MUTATIONS IN SPORADIC BASAL-CELL CARCINOMA, Nature, 391(6662), 1998, pp. 90-92
IDENTIFICATION OF MUTATIONS IN THE HUMAN PATCHED GENE IN SPORADIC BASAL-CELL CARCINOMAS AND IN PATIENTS WITH THE BASAL-CELL NEVUS SYNDROME
Authors: ASZTERBAUM M ROTHMAN A JOHNSON RL FISHER M XIE JW BONIFAS JM ZHANG XL SCOTT MP EPSTEIN EH
Citation: M. Aszterbaum et al., IDENTIFICATION OF MUTATIONS IN THE HUMAN PATCHED GENE IN SPORADIC BASAL-CELL CARCINOMAS AND IN PATIENTS WITH THE BASAL-CELL NEVUS SYNDROME, Journal of investigative dermatology, 110(6), 1998, pp. 885-888
CLONING OF MULTIPLE K16 GENES AND GENOTYPE-PHENOTYPE CORRELATION IN PACHYONYCHIA-CONGENITA TYPE-I AND FOCAL PPK
Authors: SMITH FJD STEIJLEN PM MCKENNA K HEALY E REES JL FISHER MP BONIFAS JM EPSTEIN EH MCKUSICK VA TAN E UITTO J MCLEAN WHI
Citation: Fjd. Smith et al., CLONING OF MULTIPLE K16 GENES AND GENOTYPE-PHENOTYPE CORRELATION IN PACHYONYCHIA-CONGENITA TYPE-I AND FOCAL PPK, Journal of investigative dermatology, 110(4), 1998, pp. 502-502
DETECTION OF PATCHED PROTEIN IN CUTANEOUS AND EXTRACUTANEOUS TUMORS VIA IMMUNOHISTOCHEMICAL STAINING
Authors: ASZTERBAUM M KERSCHMANN RL ABBEY N EPSTEIN EH
Citation: M. Aszterbaum et al., DETECTION OF PATCHED PROTEIN IN CUTANEOUS AND EXTRACUTANEOUS TUMORS VIA IMMUNOHISTOCHEMICAL STAINING, Journal of investigative dermatology, 110(4), 1998, pp. 611-611
UNTITLED
Authors: EPSTEIN EH
Citation: Eh. Epstein, UNTITLED, Comparative education review, 42(4), 1998, pp. 417-420
BASAL-CELL CARCINOMAS IN MICE OVEREXPRESSING SONIC HEDGEHOG
Authors: ORO AE HIGGINS KM HU ZL BONIFAS JM EPSTEIN EH SCOTT MP
Citation: Ae. Oro et al., BASAL-CELL CARCINOMAS IN MICE OVEREXPRESSING SONIC HEDGEHOG, Science, 276(5313), 1997, pp. 817-821
PARTIAL DOMINANCE OF A KERATIN-14 MUTATION IN EPIDERMOLYSIS-BULLOSA SIMPLEX - INCREASED SEVERITY OF DISEASE IN A HOMOZYGOTE
Authors: HU ZL SMITH L MARTINS S BONIFAS JM CHEN H EPSTEIN EH
Citation: Zl. Hu et al., PARTIAL DOMINANCE OF A KERATIN-14 MUTATION IN EPIDERMOLYSIS-BULLOSA SIMPLEX - INCREASED SEVERITY OF DISEASE IN A HOMOZYGOTE, Journal of investigative dermatology, 109(3), 1997, pp. 360-364
HEDGEHOG SIGNALING PATHWAY - ACTIVATION IN DIVERSE CANCERS BY MUTATIONS IN DIVERSE GENES
Authors: ASZTERBAUM M HU ZL XIE JW BONIFAS JM FISHER M EPSTEIN EH
Citation: M. Aszterbaum et al., HEDGEHOG SIGNALING PATHWAY - ACTIVATION IN DIVERSE CANCERS BY MUTATIONS IN DIVERSE GENES, Journal of investigative dermatology, 108(4), 1997, pp. 43-43
UNTITLED
Authors: EPSTEIN EH
Citation: Eh. Epstein, UNTITLED, Comparative education review, 41(1), 1997, pp. 1-2
MUTATIONS OF THE PATCHED GENE IN SEVERAL TYPES OF SPORADIC EXTRACUTANEOUS TUMORS
Authors: XIE JW JOHNSON RL ZHANG XL BARE JW WALDMAN FM COGEN PH MENON AG WARREN RS CHEN LC SCOTT MP EPSTEIN EH
Citation: Jw. Xie et al., MUTATIONS OF THE PATCHED GENE IN SEVERAL TYPES OF SPORADIC EXTRACUTANEOUS TUMORS, Cancer research, 57(12), 1997, pp. 2369-2372
MISSENSE OR IN-FRAME DELETION MUTATIONS IN HUMAN KERATIN-16 CAN CAUSEVARIABLE PHENOTYPES OF PACHYONYCHIA AND OR PALMOPLANTAR KERATODERMA/
Authors: SMITH FJD FISHER MP HEALY E REES JL MCKUSICK VA BONIFAS JM EPSTEIN EH UITTO J MCLEAN WHI
Citation: Fjd. Smith et al., MISSENSE OR IN-FRAME DELETION MUTATIONS IN HUMAN KERATIN-16 CAN CAUSEVARIABLE PHENOTYPES OF PACHYONYCHIA AND OR PALMOPLANTAR KERATODERMA/, American journal of human genetics, 61(4), 1997, pp. 2032-2032
THE GENETICS OF HUMAN SKIN DISEASES
Authors: EPSTEIN EH
Citation: Eh. Epstein, THE GENETICS OF HUMAN SKIN DISEASES, Current opinion in genetics & development, 6(3), 1996, pp. 295-300
GENETIC-BASIS OF BARTS-SYNDROME - A GLYCINE SUBSTITUTION MUTATION IN THE TYPE-VII COLLAGEN GENE (VOL 106, PG 778, 1996)
Authors: CHRISTIANO AM BART BJ EPSTEIN EH UITTO J
Citation: Am. Christiano et al., GENETIC-BASIS OF BARTS-SYNDROME - A GLYCINE SUBSTITUTION MUTATION IN THE TYPE-VII COLLAGEN GENE (VOL 106, PG 778, 1996), Journal of investigative dermatology, 106(6), 1996, pp. 1339-1342
INCREASED SEVERITY OF AUTOSOMAL-DOMINANT EPIDERMOLYSIS-BULLOSA SIMPLEX IN A PATIENT HOMOZYGOUS FOR A KERATIN-14 MUTATION
Authors: HU ZI BONIFAS JM MARTINS S CHEN H EPSTEIN EH
Citation: Zi. Hu et al., INCREASED SEVERITY OF AUTOSOMAL-DOMINANT EPIDERMOLYSIS-BULLOSA SIMPLEX IN A PATIENT HOMOZYGOUS FOR A KERATIN-14 MUTATION, Journal of investigative dermatology, 106(4), 1996, pp. 224-224
GENETIC-BASIS OF BARTS-SYNDROME - A GLYCINE SUBSTITUTION MUTATION IN THE TYPE-VII COLLAGEN GENE
Authors: CHRISTIANO AM BART BJ EPSTEIN EH UITTO J
Citation: Am. Christiano et al., GENETIC-BASIS OF BARTS-SYNDROME - A GLYCINE SUBSTITUTION MUTATION IN THE TYPE-VII COLLAGEN GENE, Journal of investigative dermatology, 106(4), 1996, pp. 778-780
LOCALIZATION OF THE DARIER-DISEASE GENE TO A 2-CM PORTION OF 12Q23-24.1
Authors: WAKEM P IKEDA S HAAKE A POLAKOWSKA R EWING N SARRET Y DUVIC M BERG D BASSETT A KENNEDY JL TUSKIS A EPSTEIN EH GOLDSMITH LA
Citation: P. Wakem et al., LOCALIZATION OF THE DARIER-DISEASE GENE TO A 2-CM PORTION OF 12Q23-24.1, Journal of investigative dermatology, 106(2), 1996, pp. 365-367
KERATIN-14 GENE-MUTATIONS IN PATIENTS WITH EPIDERMOLYSIS-BULLOSA SIMPLEX
Authors: CHEN H BONIFAS JM MATSUMURA K IKEDA S LEYDEN WA EPSTEIN EH
Citation: H. Chen et al., KERATIN-14 GENE-MUTATIONS IN PATIENTS WITH EPIDERMOLYSIS-BULLOSA SIMPLEX, Journal of investigative dermatology, 105(4), 1995, pp. 629-632
EVIDENCE FOR CONSTITUTIONAL MUTATIONS IN PATIENTS WITH MULTIPLE BCCS
Authors: BONIFAS JM KERSCHMANN RL SNYDER RA LEYDEN WA EPSTEIN EH
Citation: Jm. Bonifas et al., EVIDENCE FOR CONSTITUTIONAL MUTATIONS IN PATIENTS WITH MULTIPLE BCCS, Journal of investigative dermatology, 104(4), 1995, pp. 574-574
HAILEY-HAILEY DISEASE - SUBLOCALIZATION OF THE GENE ON CHROMOSOME 3Q AND IDENTIFICATION OF A KINDRED WITH AN APPARENT DELETION
Authors: PELUSO AM BONIFAS J IKEDA S EPSTEIN EH
Citation: Am. Peluso et al., HAILEY-HAILEY DISEASE - SUBLOCALIZATION OF THE GENE ON CHROMOSOME 3Q AND IDENTIFICATION OF A KINDRED WITH AN APPARENT DELETION, Journal of investigative dermatology, 104(4), 1995, pp. 598-598
ANALYSIS OF THE FACC AND XPAC GENES AS CANDIDATE GENES FOR THE BASAL-CELL NEVUS SYNDROME
Authors: BARE JW XIE JW QUINN AG EPSTEIN EH
Citation: Jw. Bare et al., ANALYSIS OF THE FACC AND XPAC GENES AS CANDIDATE GENES FOR THE BASAL-CELL NEVUS SYNDROME, Journal of investigative dermatology, 104(4), 1995, pp. 604-604
FURTHER SUBLOCALIZATION OF THE DARIERS-DISEASE GENE
Authors: WAKEM P IKEDA S HAAKE A POLAKOWSKA R EWING N SARRET Y TRATTNER A SHOHAT B SCHROEDER DW BERG D BASSETT A KENNEDY JL EPSTEIN EH GOLDSMITH LA
Citation: P. Wakem et al., FURTHER SUBLOCALIZATION OF THE DARIERS-DISEASE GENE, Journal of investigative dermatology, 104(4), 1995, pp. 674-674
UNTITLED
Authors: EPSTEIN EH
Citation: Eh. Epstein, UNTITLED, Comparative education review, 39(4), 1995, pp. 421-422
UNTITLED
Authors: EPSTEIN EH
Citation: Eh. Epstein, UNTITLED, Comparative education review, 39(3), 1995, pp. 253-254
UNTITLED
Authors: EPSTEIN EH
Citation: Eh. Epstein, UNTITLED, Comparative education review, 39(2), 1995, pp. 167-168
Risultati: 1-25 | 26-45