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Results: 1-25 | 26-39
Results: 1-25/39
REFINED GENETIC-MAPPING OF THE DARIER LOCUS TO A LESS-THAN-1-CM REGION OF CHROMOSOME 12Q24.1, AND CONSTRUCTION OF A COMPLETE, HIGH-RESOLUTION P1 ARTIFICIAL CHROMOSOME BACTERIAL ARTIFICIAL CHROMOSOME CONTIG OF THE CRITICAL REGION
Authors: MONK S SAKUNTABHAI A CARTER SA BRYCE SD COX R HARRINGTON L LEVY E RUIZPEREZ VL KATSANTONI E KODVAWALA A MUNRO CS BURGE S LARREGUE M NAGY G REES JL LATHROP M MONACO AP STRACHAN T HOVNANIAN A
Citation: S. Monk et al., REFINED GENETIC-MAPPING OF THE DARIER LOCUS TO A LESS-THAN-1-CM REGION OF CHROMOSOME 12Q24.1, AND CONSTRUCTION OF A COMPLETE, HIGH-RESOLUTION P1 ARTIFICIAL CHROMOSOME BACTERIAL ARTIFICIAL CHROMOSOME CONTIG OF THE CRITICAL REGION, American journal of human genetics, 62(4), 1998, pp. 890-903
EPIDERMAL MOSAICISM PRODUCING LOCALIZED ACNE - SOMATIC MUTATION IN FGFR2
Authors: MUNRO CS WILKIE AOM
Citation: Cs. Munro et Aom. Wilkie, EPIDERMAL MOSAICISM PRODUCING LOCALIZED ACNE - SOMATIC MUTATION IN FGFR2, Lancet, 352(9129), 1998, pp. 704-705
A MUTATIONAL HOTSPOT IN THE 2B DOMAIN OF HUMAN HAIR BASIC KERATIN-6 (HHB6) IN MONILETHRIX PATIENTS
Authors: KORGE BP HEALY E MUNRO CS PUNTER C BIRCHMACHIN M HOLMES SC DARLINGTON S HAMM H MESSENGER AG REES JL TRAUPE H
Citation: Bp. Korge et al., A MUTATIONAL HOTSPOT IN THE 2B DOMAIN OF HUMAN HAIR BASIC KERATIN-6 (HHB6) IN MONILETHRIX PATIENTS, Journal of investigative dermatology, 111(5), 1998, pp. 896-899
KERATIN-17 MUTATIONS CAUSE EITHER STEATOCYSTOMA MULTIPLEX OR PACHYONYCHIA-CONGENITA TYPE-2
Authors: COVELLO SP SMITH FJD COLEMAN CS SMITT JHS PALLER AS TENCONI R MUNRO CS UITTO J MCLEAN WHI
Citation: Sp. Covello et al., KERATIN-17 MUTATIONS CAUSE EITHER STEATOCYSTOMA MULTIPLEX OR PACHYONYCHIA-CONGENITA TYPE-2, Journal of investigative dermatology, 110(4), 1998, pp. 614-614
POPULATION PREVALENCE AND MUTATION DETECTION IN EPIDERMOLYTIC PALMOPLANTAR KERATODERMA
Authors: IRVINE AD COVELLO SP MCKENNA KE COLEMAN CS MUNRO CS UITTO J MCLEAN WHI
Citation: Ad. Irvine et al., POPULATION PREVALENCE AND MUTATION DETECTION IN EPIDERMOLYTIC PALMOPLANTAR KERATODERMA, Journal of investigative dermatology, 110(4), 1998, pp. 618-618
KERATIN-17 MUTATIONS CAUSE EITHER STEATOCYSTOMA MULTIPLEX OR PACHYONYCHIA-CONGENITA TYPE-2
Authors: COVELLO SP SMITH FJD SMITT JHS PALLER AS MUNRO CS JONKMAN MF UITTO J MCLEAN WHI
Citation: Sp. Covello et al., KERATIN-17 MUTATIONS CAUSE EITHER STEATOCYSTOMA MULTIPLEX OR PACHYONYCHIA-CONGENITA TYPE-2, British journal of dermatology, 139(3), 1998, pp. 475-480
TREATMENT OF MINOCYCLINE-INDUCED PIGMENTATION WITH THE NEODYMIUM-YAG LASER
Authors: WOOD B MUNRO CS BILSLAND D
Citation: B. Wood et al., TREATMENT OF MINOCYCLINE-INDUCED PIGMENTATION WITH THE NEODYMIUM-YAG LASER, British journal of dermatology, 139(3), 1998, pp. 562-562
NAIL AND SCALP LESIONS IN A MAN WITH DIABETES-INSIPIDUS
Authors: MUNRO CS MORTON R
Citation: Cs. Munro et R. Morton, NAIL AND SCALP LESIONS IN A MAN WITH DIABETES-INSIPIDUS, Archives of dermatology, 134(11), 1998, pp. 1478
ACNE
Authors: MUNRO CS
Citation: Cs. Munro, ACNE, Journal of the Royal College of Physicians of London, 31(4), 1997, pp. 360-363
LORICRIN MUTATION IN VOHWINKELS KERATODERMA IS UNIQUE TO THE VARIANT WITH ICHTHYOSIS
Authors: KORGE BP ISHIDAYAMAMOTO A PUNTER C DOPPINGHEPENSTAL PJC IIZUKA H STEPHENSON A EADY RAJ MUNRO CS
Citation: Bp. Korge et al., LORICRIN MUTATION IN VOHWINKELS KERATODERMA IS UNIQUE TO THE VARIANT WITH ICHTHYOSIS, Journal of investigative dermatology, 109(4), 1997, pp. 604-610
MONILETHRIX IS CAUSED BY MUTATION IN THE HELIX TERMINATION PEPTIDE OFHUMAN TYPE-II HAIR KERATIN HHB6 IN 3 FAMILIES
Authors: KORGE BP HEALY E TRAUPE H PUNTER C MAUCH C HAMM H BIRCHMACHIN MA BELGAID CE STEPHENSON AM HOLMES SC DARLINGTON S MESSENGER AG REES JL MUNRO CS
Citation: Bp. Korge et al., MONILETHRIX IS CAUSED BY MUTATION IN THE HELIX TERMINATION PEPTIDE OFHUMAN TYPE-II HAIR KERATIN HHB6 IN 3 FAMILIES, Journal of investigative dermatology, 109(3), 1997, pp. 409-409
ABNORMAL KERATINIZATION AND LORICRIN MUTATION IN VOHWINKELS-SYNDROME (VS) WITH ICHTHYOSIS
Authors: ISHIDAYAMAMOTO A KORGE BP PUENTER C DOPPINGHEPENSTAL T HOHL D IIZUKA H STEPHENSON AM EADY RAJ MUNRO CS
Citation: A. Ishidayamamoto et al., ABNORMAL KERATINIZATION AND LORICRIN MUTATION IN VOHWINKELS-SYNDROME (VS) WITH ICHTHYOSIS, Journal of investigative dermatology, 108(4), 1997, pp. 642-642
MISSENSE MUTATIONS IN KERATIN-17 CAUSE EITHER PACHYONYCHIA-CONGENITA TYPE-2 OR A PHENOTYPE RESEMBLING STEATOCYSTOMA MULTIPLEX
Authors: SMITH FJD CORDEN LD RUGG EL RATNAVEL R LEIGH IM MOSS C TIDMAN MJ HOHL D HUBER M KUNKELER L MUNRO CS LANE EB MCLEAN WHI
Citation: Fjd. Smith et al., MISSENSE MUTATIONS IN KERATIN-17 CAUSE EITHER PACHYONYCHIA-CONGENITA TYPE-2 OR A PHENOTYPE RESEMBLING STEATOCYSTOMA MULTIPLEX, Journal of investigative dermatology, 108(2), 1997, pp. 220-223
TREATMENT OF PSORIASIS WITH INTERMITTENT SHORT-COURSE CYCLOSPORINE (NEORAL(R)) - A MULTICENTER STUDY
Authors: BERTHJONES J HENDERSON CA MUNRO CS ROGERS S CHALMERS RJG BOFFA MJ NORRIS PG FRIEDMANN PS GRAHAMBROWN RAC DOWD PM MARKS R SUMNER MJ
Citation: J. Berthjones et al., TREATMENT OF PSORIASIS WITH INTERMITTENT SHORT-COURSE CYCLOSPORINE (NEORAL(R)) - A MULTICENTER STUDY, British journal of dermatology, 136(4), 1997, pp. 527-530
SYSTEMIC LUPUS-ERYTHEMATOSUS COMPLICATING COMPLEMENT TYPE-2 DEFICIENCY - SUCCESSFUL TREATMENT WITH FRESH-FROZEN PLASMA
Authors: HUDSONPEACOCK MJ JOSEPH SA COX J MUNRO CS SIMPSON NB
Citation: Mj. Hudsonpeacock et al., SYSTEMIC LUPUS-ERYTHEMATOSUS COMPLICATING COMPLEMENT TYPE-2 DEFICIENCY - SUCCESSFUL TREATMENT WITH FRESH-FROZEN PLASMA, British journal of dermatology, 136(3), 1997, pp. 388-392
EB SIMPLEX AND THE GROWING FAMILY OF KERATIN DISEASES
Authors: MCLEAN WHI RUGG EL SMITH FJD MORLEY SM SHEMANKO CC CORDEN LD MUNRO CS LEIGH IM EADY RAJ LANE EB
Citation: Whi. Mclean et al., EB SIMPLEX AND THE GROWING FAMILY OF KERATIN DISEASES, Journal of investigative dermatology, 107(5), 1996, pp. 8-8
EVIDENCE OF GENETIC-HETEROGENEITY IN VOHWINKELS KERATODERMA
Authors: KORGE BP PUNTER C STEPHENSON A MUNRO CS
Citation: Bp. Korge et al., EVIDENCE OF GENETIC-HETEROGENEITY IN VOHWINKELS KERATODERMA, Journal of investigative dermatology, 107(3), 1996, pp. 200-200
REFINED LOCALIZATION OF THE DARIERS-DISEASE AND SPINOCEREBELLAR ATAXIA TYPE-2 GENES AT CHROMOSOME 12Q24.1 - CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THESE GENES
Authors: BRYCE SD CARTER SA PANG JT TWELLS R RENAULT B SCHLEICHNORTE B ALLOTEY R ROSS CJD KATSANTONIA E WEISSENBACH J KUCHERLAPATI RS REES JL MUNRO CS CHAMBERLAIN S STRACHAN T
Citation: Sd. Bryce et al., REFINED LOCALIZATION OF THE DARIERS-DISEASE AND SPINOCEREBELLAR ATAXIA TYPE-2 GENES AT CHROMOSOME 12Q24.1 - CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THESE GENES, Journal of investigative dermatology, 107(3), 1996, pp. 210-210
THE EFFECT OF A MUTATION IN K16 ON KERATIN FILAMENT DYNAMICS IN-VITRO
Authors: RUGG EL MCLEAN WHI PRESCOTT AR RATNAVEL R LEIGH IM MUNRO CS LANE EB
Citation: El. Rugg et al., THE EFFECT OF A MUTATION IN K16 ON KERATIN FILAMENT DYNAMICS IN-VITRO, Journal of investigative dermatology, 106(4), 1996, pp. 46-46
MUTATIONS IN KERATIN-17 CAUSE STEATOCYSTOMA MULTIPLEX
Authors: SMITH FJD CORDEN LD RUGG EL MORLEY SM LANE EB HUBER M HOHL D MUNRO CS MCLEAN WHI
Citation: Fjd. Smith et al., MUTATIONS IN KERATIN-17 CAUSE STEATOCYSTOMA MULTIPLEX, Journal of investigative dermatology, 106(4), 1996, pp. 225-225
KERATIN-16 AND KERATIN-17 MUTATIONS CAUSE PACHYONYCHIA-CONGENITA
Authors: MCLEAN WHI RUGG EL LUNNY DP MORLEY SM LANE EB SWENSSON O DOPPINGHEPENSTAL PJC GRIFFITHS WAD EADY RAJ HIGGINS C NAVSARIA HA LEIGH IM STRACHAN T KUNKELER L MUNRO CS
Citation: Whi. Mclean et al., KERATIN-16 AND KERATIN-17 MUTATIONS CAUSE PACHYONYCHIA-CONGENITA, Nature genetics, 9(3), 1995, pp. 273-278
A MUTATION IN THE MUCOSAL KERATIN K4 IS ASSOCIATED WITH ORAL WHITE SPONGE NEVUS
Authors: RUGG EL MCLEAN WHI ALLISON WE LUNNY DP MACLEOD RI FELIX DH LANE EB MUNRO CS
Citation: El. Rugg et al., A MUTATION IN THE MUCOSAL KERATIN K4 IS ASSOCIATED WITH ORAL WHITE SPONGE NEVUS, Nature genetics, 11(4), 1995, pp. 450-452
A GENE FOR MONILETHRIX IS CLOSELY LINKED TO THE TYPE-II KERATIN GENE-CLUSTER AT 12Q13
Authors: HEALY E HOLMES SC BELGAID CE STEPHENSON AM MCLEAN WHI REES JL MUNRO CS
Citation: E. Healy et al., A GENE FOR MONILETHRIX IS CLOSELY LINKED TO THE TYPE-II KERATIN GENE-CLUSTER AT 12Q13, Human molecular genetics, 4(12), 1995, pp. 2399-2402
AN OPEN AND SINGLE-BLIND COMPARATIVE-ASSESSMENT OF UNGUENTUM COCOIS COMPOUND IN THE TREATMENT OF PSORIASIS OF THE SCALP
Authors: MONK BE MASON RBS MUNRO CS DARLEY CR
Citation: Be. Monk et al., AN OPEN AND SINGLE-BLIND COMPARATIVE-ASSESSMENT OF UNGUENTUM COCOIS COMPOUND IN THE TREATMENT OF PSORIASIS OF THE SCALP, Journal of dermatological treatment, 6(3), 1995, pp. 159-161
PACHYONYCHIA-CONGENITA IS CAUSED BY MUTATIONS IN KERATIN-16 AND KERATIN-17
Authors: MCLEAN WHI SMITH FJD CORDEN L RUGG EL LUNNY DP MORLEY SM SWENSSON O DOPPINGHEPENSTAL PJC GRIFFITHS WAD EADY RAJ RATNAVEL R HIGGINS C NAVSARIA H LEIGH IM MOSS C MCKENNA KE BINGHAM EA KUNKELER L MUNRO CS LANE EB
Citation: Whi. Mclean et al., PACHYONYCHIA-CONGENITA IS CAUSED BY MUTATIONS IN KERATIN-16 AND KERATIN-17, Journal of investigative dermatology, 105(3), 1995, pp. 454-454
Risultati: 1-25 | 26-39