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Results: 1-25 | 26-26
Results: 1-25/26
CDNA CLONING, EXPRESSION, AND ASSEMBLY CHARACTERISTICS OF MOUSE KERATIN-16
Authors: PORTER RM HUTCHESON AM RUGG EL QUINLAN RA LANE EB
Citation: Rm. Porter et al., CDNA CLONING, EXPRESSION, AND ASSEMBLY CHARACTERISTICS OF MOUSE KERATIN-16, The Journal of biological chemistry, 273(48), 1998, pp. 32265-32272
THE EFFECTS OF KERATIN MUTATIONS ON FILAMENT STRUCTURE AND FUNCTION IN CULTURED KERATINOCYTES
Authors: MORLEY SM RUGG EL SHEMANKO CS SEXTON CJ NAVSARIA HA LEIGH IM LANE EB
Citation: Sm. Morley et al., THE EFFECTS OF KERATIN MUTATIONS ON FILAMENT STRUCTURE AND FUNCTION IN CULTURED KERATINOCYTES, Journal of investigative dermatology, 108(4), 1997, pp. 358-358
TAKING EBS FROM MUTATION ANALYSIS TO PRENATAL-DIAGNOSIS
Authors: RUGG EL SHEMANKO CS MAGEE GJ BATY D BOXER M LANE EB
Citation: El. Rugg et al., TAKING EBS FROM MUTATION ANALYSIS TO PRENATAL-DIAGNOSIS, Journal of investigative dermatology, 108(4), 1997, pp. 359-359
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
PLECTIN DEFICIENCY RESULTS IN MUSCULAR-DYSTROPHY WITH EPIDERMOLYSIS-BULLOSA
Authors: SMITH FJD EADY RAJ LEIGH IM MCMILLAN JR RUGG EL KELSELL DP BRYANT SP SPURR NK GEDDES JF KIRTSCHIG G MILANA G DEBONO AG OWARIBE K WICHE G PULKKINEN L UITTO J MCLEAN WHI LANE EB
Citation: Fjd. Smith et al., PLECTIN DEFICIENCY RESULTS IN MUSCULAR-DYSTROPHY WITH EPIDERMOLYSIS-BULLOSA, Nature genetics, 13(4), 1996, pp. 450-457
LOSS OF PLECTIN CAUSES EPIDERMOLYSIS-BULLOSA WITH MUSCULAR-DYSTROPHY - CDNA CLONING AND GENOMIC ORGANIZATION
Authors: MCLEAN WHI PULKKINEN L SMITH FJD RUGG EL LANE EB BULLRICH F BURGESON RE AMANO S HUDSON DL OWARIBE K MCGRATH JA MCMILLAN JR EADY RAJ LEIGH IM CHRISTIANO AM UITTO J
Citation: Whi. Mclean et al., LOSS OF PLECTIN CAUSES EPIDERMOLYSIS-BULLOSA WITH MUSCULAR-DYSTROPHY - CDNA CLONING AND GENOMIC ORGANIZATION, Genes & development, 10(14), 1996, pp. 1724-1735
CLONING AND SEQUENCING OF THE HUMAN PLECTIN GENE
Authors: MCLEAN WHI SMITH FJD RUGG EL PULKKINEN L LEIGH IM EADY RAJ UITTO J LANE EB
Citation: Whi. Mclean et al., CLONING AND SEQUENCING OF THE HUMAN PLECTIN GENE, Journal of investigative dermatology, 107(5), 1996, pp. 5-5
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
COMPLETE CDNA SEQUENCE, GENOMIC ORGANIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PLECTIN GENE
Authors: MCLEAN WHI SMITH FJD RUGG EL PULKKINEN L BULLRICH F LEIGH IM EADY RAJ LANE EB UITTO J
Citation: Whi. Mclean et al., COMPLETE CDNA SEQUENCE, GENOMIC ORGANIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN PLECTIN GENE, Journal of investigative dermatology, 107(3), 1996, pp. 1-1
KERATIN MESSENGER-RNA AND PROTEIN EXPRESSION PATTERNS DEMONSTRATE KERATINOCYTE DIVERSITY IN NORMAL EPIDERMIS OF PALMS AND SOLES
Authors: PITERA R PITERA JE SWENSSON O MCLEAN WHI RUGG EL LANE EB LEIGH JM MCMILLAN JR CHURCHILL LJ LANGBEIN L EADY RAJ
Citation: R. Pitera et al., KERATIN MESSENGER-RNA AND PROTEIN EXPRESSION PATTERNS DEMONSTRATE KERATINOCYTE DIVERSITY IN NORMAL EPIDERMIS OF PALMS AND SOLES, Journal of investigative dermatology, 107(3), 1996, pp. 20-20
CLONING OF THE MURINE PLECTIN CDNA REVEALS HIGH EVOLUTIONARY CONSERVATION OF THIS CYTOSKELETAL-ASSOCIATED PROTEIN
Authors: SMITH FJD MCLEAN WHI RUGG EL LEIGH IM EADY RAJ UITTO J LANE EB
Citation: Fjd. Smith et al., CLONING OF THE MURINE PLECTIN CDNA REVEALS HIGH EVOLUTIONARY CONSERVATION OF THIS CYTOSKELETAL-ASSOCIATED PROTEIN, Journal of investigative dermatology, 107(3), 1996, pp. 199-199
MUTATIONS IN THE PLECTIN GENE CAUSE EPIDERMOLYSIS-BULLOSA WITH MUSCULAR-DYSTROPHY
Authors: MCLEAN WHI PULKKINEN L SMITH FJD RUGG EL BULLRICH F BURGESON RE AMANO S HUDSON DL OWARIBE K MCGRATH JA EADY RAJ LEIGH IM LANE EB CHRISTIANO AM UITTO J
Citation: Whi. Mclean et al., MUTATIONS IN THE PLECTIN GENE CAUSE EPIDERMOLYSIS-BULLOSA WITH MUSCULAR-DYSTROPHY, Journal of investigative dermatology, 107(1), 1996, pp. 144-144
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
CLONING AND SEQUENCING OF THE HUMAN PLECTIN GENE
Authors: MCLEAN WHI SMITH FJD RUGG EL STOREY A LEIGH IM EADY RAJ PULKKINEN L UITTO J LANE EB
Citation: Whi. Mclean et al., CLONING AND SEQUENCING OF THE HUMAN PLECTIN GENE, Journal of investigative dermatology, 106(4), 1996, pp. 223-223
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
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
WHITE SPONGE NEVUS - A DISORDER OF MUCOSAL KERATINS
Authors: RUGG EL MCLEAN WHI MACLEOD RI FELIX DH TIDMAN MJ LANE EB MUNRO CS
Citation: El. Rugg et al., WHITE SPONGE NEVUS - A DISORDER OF MUCOSAL KERATINS, Journal of investigative dermatology, 105(3), 1995, pp. 456-456
THE H1 DOMAIN OF KERATIN-5 IS A HOTSPOT FOR MUTATIONS ASSOCIATED WITHEPIDERMOLYSIS-BULLOSA SIMPLEX WEBER-COCKAYNE
Authors: RUGG EL DUNNILL MGS EADY RAJ LANE EB
Citation: El. Rugg et al., THE H1 DOMAIN OF KERATIN-5 IS A HOTSPOT FOR MUTATIONS ASSOCIATED WITHEPIDERMOLYSIS-BULLOSA SIMPLEX WEBER-COCKAYNE, Journal of investigative dermatology, 104(4), 1995, pp. 632-632
MOLECULAR-BASIS OF PACHYONYCHIA-CONGENITA - MUTATIONS IN KERATIN-16 AND KERATIN-17
Authors: MCLEAN WHI RUGG EL LUNNY DP MORLEY SM LANE EB SWENSSON O DOPPINGHEPENSTAL PJC
Citation: Whi. Mclean et al., MOLECULAR-BASIS OF PACHYONYCHIA-CONGENITA - MUTATIONS IN KERATIN-16 AND KERATIN-17, Journal of investigative dermatology, 104(4), 1995, pp. 632-632
WHITE SPONGE NEVUS (WSN) IS CAUSED BY MUTATIONS IN MUCOSAL KERATIN K4
Authors: RUGG EL MCLEAN WHI ALLISON WE LUNNY DP LANE EB MACLEOD RI FELIX DH MUNRO CS
Citation: El. Rugg et al., WHITE SPONGE NEVUS (WSN) IS CAUSED BY MUTATIONS IN MUCOSAL KERATIN K4, American journal of human genetics, 57(4), 1995, pp. 237-237
PACHYONYCHIA-CONGENITA IS CAUSED BY MUTATIONS IN KERATINS K16 AND K17
Authors: MCLEAN WHI SMITH FJD CORDEN L RUGG EL EADY RAJ LEIGH IM MOSS C MCKENNA DI BINGHAM EA KUNKELER L MUNRO CS LANE EB
Citation: Whi. Mclean et al., PACHYONYCHIA-CONGENITA IS CAUSED BY MUTATIONS IN KERATINS K16 AND K17, American journal of human genetics, 57(4), 1995, pp. 238-238
A FUNCTIONAL KNOCKOUT OF HUMAN KERATIN-14
Authors: RUGG EL MCLEAN WHI LANE EB PITERA R MCMILLAN JR DOPPINGHEPENSTAL PJC NAVSARIA HA LEIGH IM EADY RAJ
Citation: El. Rugg et al., A FUNCTIONAL KNOCKOUT OF HUMAN KERATIN-14, Genes & development, 8(21), 1994, pp. 2563-2573
RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX CAUSED BY A FUNCTIONAL KNOCKOUT OF KERATIN-14
Authors: RUGG EL MCLEAN WHI PITERA R MCMILLAN JR DOPPINGHEPENSTAL PJC NAVSARIA HA LEIGH IM LANE EB EADY RAJ
Citation: El. Rugg et al., RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX CAUSED BY A FUNCTIONAL KNOCKOUT OF KERATIN-14, Journal of investigative dermatology, 103(3), 1994, pp. 438-438
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