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Results: 1-25 | 26-35
Results: 1-25/35
SPECIALIZED KERATIN EXPRESSION PATTERN IN HUMAN RIDGED SKIN AS AN ADAPTATION TO HIGH PHYSICAL STRESS
Authors: SWENSSON O LANGBEIN L MCMILLAN JR STEVENS HP LEIGH IM MCLEAN WHI LANE EB EADY RAJ
Citation: O. Swensson et al., SPECIALIZED KERATIN EXPRESSION PATTERN IN HUMAN RIDGED SKIN AS AN ADAPTATION TO HIGH PHYSICAL STRESS, British journal of dermatology, 139(5), 1998, pp. 767-775
MUTATIONS IN THE HAIR CORTEX KERATIN HHB6 CAUSE THE INHERITED HAIR DISEASE MONILETHRIX
Authors: WINTER H ROGERS MA LANGBEIN L STEVENS HP LEIGH IM LABREZE C ROUL S TAIEB A KRIEG T SCHWEIZER J
Citation: H. Winter et al., MUTATIONS IN THE HAIR CORTEX KERATIN HHB6 CAUSE THE INHERITED HAIR DISEASE MONILETHRIX, Nature genetics, 16(4), 1997, pp. 372-374
LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING
Authors: LAASS MW HENNIES HC PREIS S STEVENS HP JUNG M LEIGH IM WIENKER TF REIS A
Citation: Mw. Laass et al., LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING, Human genetics, 101(3), 1997, pp. 376-382
A NEW MUTATION IN THE TYPE-II HAIR CORTEX KERATIN HHB1 INVOLVED IN THE INHERITED HAIR DISORDER MONILETHRIX
Authors: WINTER H ROGERS MA GEBHARDT M WOLLINA U BOXALL L CHITAYAT D BABULHIRJI R STEVENS HP ZLOTOGORSKI A SCHWEIZER J
Citation: H. Winter et al., A NEW MUTATION IN THE TYPE-II HAIR CORTEX KERATIN HHB1 INVOLVED IN THE INHERITED HAIR DISORDER MONILETHRIX, Human genetics, 101(2), 1997, pp. 165-169
CONNEXIN-26 MUTATIONS IN HEREDITARY NON-SYNDROMIC SENSORINEURAL DEAFNESS
Authors: KELSELL DP DUNLOP J STEVENS HP LENCH NJ LIANG JN PARRY G MUELLER RF LEIGH IM
Citation: Dp. Kelsell et al., CONNEXIN-26 MUTATIONS IN HEREDITARY NON-SYNDROMIC SENSORINEURAL DEAFNESS, Nature, 387(6628), 1997, pp. 80-83
MUTATIONS IN THE HAIR CORTEX KERATIN HHB6 CAUSE THE HEREDITARY HAIR DISEASE MONILETHRIX
Authors: SCHWEIZER J WINTER H ROGERS MA LANGBEIN L KRIEG T STEVENS HP LEIGH IM LABREZE CL ROUL S TAIEB A
Citation: J. Schweizer et al., MUTATIONS IN THE HAIR CORTEX KERATIN HHB6 CAUSE THE HEREDITARY HAIR DISEASE MONILETHRIX, Journal of investigative dermatology, 109(3), 1997, pp. 409-409
EXCLUSION OF TYPE-II KERATIN GENE-MUTATIONS IN DIFFUSE NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK) BY GENETIC AND IMMUNOHISTOCHEMICAL ANALYSIS
Authors: STEVENS HP DUNLOP J PURKIS PE LEIGH IM KELSELL DP
Citation: Hp. Stevens et al., EXCLUSION OF TYPE-II KERATIN GENE-MUTATIONS IN DIFFUSE NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK) BY GENETIC AND IMMUNOHISTOCHEMICAL ANALYSIS, Journal of investigative dermatology, 108(4), 1997, pp. 655-655
LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME (PLS) TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING
Authors: HENNIES HC LAASS MW PREIS S JUNG M STEVENS HP WIENKER TF REIS A
Citation: Hc. Hennies et al., LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME (PLS) TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING, American journal of human genetics, 61(4), 1997, pp. 64-64
TRANSGREDIENT AND FOCAL PALMOPLANTAR KERATODERMA - EVIDENCE FOR KERATIN FILAMENT ABNORMALITIES USING IMMUNOGOLD ELECTRON-MICROSCOPY
Authors: SWENSSON O MCMILLAN JR RATNAVEL RC STEVENS HP LANGBEIN L GRIFFITHS WAD LEIGH IM EADY RAJ
Citation: O. Swensson et al., TRANSGREDIENT AND FOCAL PALMOPLANTAR KERATODERMA - EVIDENCE FOR KERATIN FILAMENT ABNORMALITIES USING IMMUNOGOLD ELECTRON-MICROSCOPY, Journal of investigative dermatology, 107(2), 1996, pp. 21-21
LINKAGE OF MONILETHRIX TO THE TRICHOCYTE AND EPITHELIAL KERATIN GENE-CLUSTER ON 12Q11-Q13
Authors: STEVENS HP KELSELL DP BRYANT SP BISHOP DT DAWBER RPR SPURR NK LEIGH IM
Citation: Hp. Stevens et al., LINKAGE OF MONILETHRIX TO THE TRICHOCYTE AND EPITHELIAL KERATIN GENE-CLUSTER ON 12Q11-Q13, Journal of investigative dermatology, 106(4), 1996, pp. 795-797
PUNCTATE PALMOPLANTAR KERATODERMA AND MALIGNANCY IN A 4-GENERATION FAMILY
Authors: STEVENS HP KELSELL DP LEIGH IM OSTLERE LS MACDERMOT KD RUSTIN MHA
Citation: Hp. Stevens et al., PUNCTATE PALMOPLANTAR KERATODERMA AND MALIGNANCY IN A 4-GENERATION FAMILY, British journal of dermatology, 134(4), 1996, pp. 720-726
LINKAGE OF AN AMERICAN PEDIGREE WITH PALMOPLANTAR KERATODERMA AND MALIGNANCY (PALMOPLANTAR ECTODERMAL DYSPLASIA TYPE-III) TO 17Q24 - LITERATURE SURVEY AND PROPOSED UPDATED CLASSIFICATION OF THE KERATODERMAS
Authors: STEVENS HP KELSELL DP BRYANT SP BISHOP T SPURR NK WEISSENBACH J MARGER D MARGER RS LEIGH IM
Citation: Hp. Stevens et al., LINKAGE OF AN AMERICAN PEDIGREE WITH PALMOPLANTAR KERATODERMA AND MALIGNANCY (PALMOPLANTAR ECTODERMAL DYSPLASIA TYPE-III) TO 17Q24 - LITERATURE SURVEY AND PROPOSED UPDATED CLASSIFICATION OF THE KERATODERMAS, Archives of dermatology, 132(6), 1996, pp. 640-651
GENETIC-LINKAGE STUDIES IN NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA- EVIDENCE FOR HETEROGENEITY
Authors: KELSELL DP STEVENS HP RATNAVEL R BRYANT SP BISHOP DT LEIGH IM SPURR NK
Citation: Dp. Kelsell et al., GENETIC-LINKAGE STUDIES IN NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA- EVIDENCE FOR HETEROGENEITY, Human molecular genetics, 4(6), 1995, pp. 1021-1025
NOVEL MUTATIONS IN KERATIN-16 GENE UNDERLY FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK) IN 2 FAMILIES
Authors: SHAMSHER MK NAVSARIA HA STEVENS HP RATNAVEL RC PURKIS PE KELSELL DP MCLEAN WHI COOK LJ GRIFFITHS WAD GSCHMEISSNER S SPURR N LEIGH IM
Citation: Mk. Shamsher et al., NOVEL MUTATIONS IN KERATIN-16 GENE UNDERLY FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK) IN 2 FAMILIES, Human molecular genetics, 4(10), 1995, pp. 1875-1881
BOWEL EVANS-SYNDROME IS LIKED TO 17Q24 BUT AN IDENTICAL CUTANEOUS PHENOTYPE CAN RESULT FROM K16 MUTATIONS
Authors: STEVENS HP KELSELL DP SHAMSHER M RATNAVEL R NAVSARIA HA SPURR N BISHOP DT BRYANT SP MARGER D MARGER FS GRIFFITHS WAD LEIGH IM
Citation: Hp. Stevens et al., BOWEL EVANS-SYNDROME IS LIKED TO 17Q24 BUT AN IDENTICAL CUTANEOUS PHENOTYPE CAN RESULT FROM K16 MUTATIONS, Journal of investigative dermatology, 105(3), 1995, pp. 456-456
HPV-16 IMMORTALIZED KERATINOCYTES FROM PATIENTS WITH FOCAL PALMOPLANTAR KERATODERMA (PPK) EXPRESS KERATIN-16 MUTATIONS
Authors: PURKIS PE STEVENS HP SHAMSHER M NAVSARIA H PRICE K LEIGHT IM
Citation: Pe. Purkis et al., HPV-16 IMMORTALIZED KERATINOCYTES FROM PATIENTS WITH FOCAL PALMOPLANTAR KERATODERMA (PPK) EXPRESS KERATIN-16 MUTATIONS, Journal of investigative dermatology, 105(3), 1995, pp. 488-488
CHARACTERIZATION OF PARANEOPLASTIC PEMPHIGUS AUTOANTIGENS BY IMMUNOBLOT ANALYSIS
Authors: HASHIMOTO T AMAGAI M WATANABE K CHORZELSKI TP BHOGAL BS BLACK MM STEVENS HP BOORSMA DM KORMAN NJ GAMOU S SHIMIZU N NISHIKAWA T
Citation: T. Hashimoto et al., CHARACTERIZATION OF PARANEOPLASTIC PEMPHIGUS AUTOANTIGENS BY IMMUNOBLOT ANALYSIS, Journal of investigative dermatology, 104(5), 1995, pp. 829-834
IDENTIFICATION OF NOVEL MUTATIONS IN KERATIN-16 GENE IN 2-FAMILIES WITH FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK)
Authors: LEIGH M SHAMSHER M STEVENS HP RATNAVEL R PURKIS PE GRIFFITHS WAD MCLEAN WHI
Citation: M. Leigh et al., IDENTIFICATION OF NOVEL MUTATIONS IN KERATIN-16 GENE IN 2-FAMILIES WITH FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK), Journal of investigative dermatology, 104(4), 1995, pp. 582-582
PALMOPLANTAR KERATODERMA (PPK) AND CARCINOMA OF THE ESOPHAGUS - LINKAGE ANALYSIS AND DESCRIPTION OF A UNIQUE PHENOTYPE
Authors: STEVENS HP KELSELL DP SPURR NK BRYANT SP MARGER D MARGER RS BISHOP DT LEIGH IM
Citation: Hp. Stevens et al., PALMOPLANTAR KERATODERMA (PPK) AND CARCINOMA OF THE ESOPHAGUS - LINKAGE ANALYSIS AND DESCRIPTION OF A UNIQUE PHENOTYPE, Journal of investigative dermatology, 104(4), 1995, pp. 605-605
GENETIC-ANALYSIS OF FAMILIES WITH FOCAL PALMOPLANTAR KERATODERMA WITHOR WITHOUT MALIGNANCY
Authors: KELSELL DP STEVENS HP BRYANT SP MARGER D MARGER RS LEIGH IM BISHOP DT WEISSENBACH J SPURR NK
Citation: Dp. Kelsell et al., GENETIC-ANALYSIS OF FAMILIES WITH FOCAL PALMOPLANTAR KERATODERMA WITHOR WITHOUT MALIGNANCY, American journal of human genetics, 57(4), 1995, pp. 112-112
PARANEOPLASTIC PEMPHIGUS AS A PRESENTING FEATURE OF AN OCCULT LYMPHOMA
Authors: STEVENS HP OSTLERE LS BLACK MM NISHIKAWA T HASHIMOTO T BHOGAL BS RUSTIN MHA
Citation: Hp. Stevens et al., PARANEOPLASTIC PEMPHIGUS AS A PRESENTING FEATURE OF AN OCCULT LYMPHOMA, EJD. European journal of dermatology, 4(1), 1994, pp. 26-29
FIBROBLASTIC RHEUMATISM
Authors: OSTLERE LS STEVENS HP JARMULOWICZ M HIGGENS C BLACK C RUSTIN MHA
Citation: Ls. Ostlere et al., FIBROBLASTIC RHEUMATISM, Clinical and experimental dermatology, 19(3), 1994, pp. 268-270
CHRONIC RASH ASSOCIATED WITH CONGENITAL-RUBELLA
Authors: OSTLERE LS STEVENS HP DILLON MJ ATHERTON D VANSOMEREN V RUSTIN MHA HARRIS D
Citation: Ls. Ostlere et al., CHRONIC RASH ASSOCIATED WITH CONGENITAL-RUBELLA, Journal of the Royal Society of Medicine, 87(4), 1994, pp. 242-243
KERATIN GENE-MUTATIONS IN HUMAN SKIN-DISEASE
Authors: STEVENS HP RUSTIN MHA
Citation: Hp. Stevens et Mha. Rustin, KERATIN GENE-MUTATIONS IN HUMAN SKIN-DISEASE, Postgraduate medical journal, 70(829), 1994, pp. 775-779
KERATOSIS PUNCTATA PALMARIS ET PLANTARIS - AN AUTOSOMAL DOMINANTLY INHERITED KERATODERMA ASSOCIATED WITH MALIGNANCY
Authors: STEVENS HP RUSTIN MHA MACDERMOT K
Citation: Hp. Stevens et al., KERATOSIS PUNCTATA PALMARIS ET PLANTARIS - AN AUTOSOMAL DOMINANTLY INHERITED KERATODERMA ASSOCIATED WITH MALIGNANCY, Journal of Medical Genetics, 31(2), 1994, pp. 168-168
Risultati: 1-25 | 26-35