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Results: 1-25 | 26-50 | 51-75 | 76-88
Results: 1-25/88
HOMOZYGOUS NONSENSE MUTATION IN HELIX-2 OF K14 CAUSES SEVERE RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX
Authors: CORDEN LD MELLERIO JE GRATIAN MJ EADY RAJ HARPER JI LACOUR M MAGEE G LANE EB MCGRATH JA MCLEAN WHI
Citation: Ld. Corden et al., HOMOZYGOUS NONSENSE MUTATION IN HELIX-2 OF K14 CAUSES SEVERE RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX, Human mutation, 11(4), 1998, pp. 279-285
DIFFERENTIAL EXPRESSION AND FUNCTIONALLY COOPERATIVE ROLES FOR THE RETINOBLASTOMA FAMILY OF PROTEINS IN EPIDERMAL DIFFERENTIATION
Authors: PARAMIO JM LAIN S SEGRELLES C LANE EB JORCANO JL
Citation: Jm. Paramio et al., DIFFERENTIAL EXPRESSION AND FUNCTIONALLY COOPERATIVE ROLES FOR THE RETINOBLASTOMA FAMILY OF PROTEINS IN EPIDERMAL DIFFERENTIATION, Oncogene, 17(8), 1998, pp. 949-957
KERATIN FILAMENT DEPLOYMENT AND CYTOSKELETAL NETWORKING IN A SENSORY EPITHELIUM THAT VIBRATES DURING HEARING
Authors: MOGENSEN MM HENDERSON CG MACKLE JB LANE EB GARROD DR TUCKER JB
Citation: Mm. Mogensen et al., KERATIN FILAMENT DEPLOYMENT AND CYTOSKELETAL NETWORKING IN A SENSORY EPITHELIUM THAT VIBRATES DURING HEARING, Cell motility and the cytoskeleton, 41(2), 1998, pp. 138-153
THE DEVELOPMENT OF EPITHELIAL PHENOTYPES IN THE HUMAN FETAL AND INFANT BREAST
Authors: ANBAZHAGAN R OSIN PP BARTKOVA J NATHAN B LANE EB GUSTERSON BA
Citation: R. Anbazhagan et al., THE DEVELOPMENT OF EPITHELIAL PHENOTYPES IN THE HUMAN FETAL AND INFANT BREAST, Journal of pathology, 184(2), 1998, pp. 197-206
GENOMIC ORGANIZATION AND FINE MAPPING OF THE KERATIN 2E GENE (KRT2E) - K2E V1 DOMAIN POLYMORPHISM AND NOVEL MUTATIONS IN ICHTHYOSIS BULLOSAOF SIEMENS
Authors: SMITH FJD MAINGI C COVELLO SP HIGGINS C SCHMIDT M LANE EB UITTO J LEIGH IM MCLEAN WHI
Citation: Fjd. Smith et al., GENOMIC ORGANIZATION AND FINE MAPPING OF THE KERATIN 2E GENE (KRT2E) - K2E V1 DOMAIN POLYMORPHISM AND NOVEL MUTATIONS IN ICHTHYOSIS BULLOSAOF SIEMENS, Journal of investigative dermatology, 111(5), 1998, pp. 817-821
SEVERE PALMOPLANTAR HYPERKERATOSIS IN DOWLING-MEARA EPIDERMOLYSIS-BULLOSA SIMPLEX CAUSED BY A MUTATION IN THE KERATIN-14 GENE (KRT14)
Authors: SHEMANKO CS MELLERIO JE TIDMAN MJ LANE EB EADY RAJ
Citation: Cs. Shemanko et al., SEVERE PALMOPLANTAR HYPERKERATOSIS IN DOWLING-MEARA EPIDERMOLYSIS-BULLOSA SIMPLEX CAUSED BY A MUTATION IN THE KERATIN-14 GENE (KRT14), Journal of investigative dermatology, 111(5), 1998, pp. 893-895
THE RELATIONSHIP BETWEEN HYPERPROLIFERATION AND EPIDERMAL THICKENING IN A MOUSE MODEL FOR BCIE
Authors: PORTER RM REICHELT J LUNNY DP MAGIN TM LANE EB
Citation: Rm. Porter et al., THE RELATIONSHIP BETWEEN HYPERPROLIFERATION AND EPIDERMAL THICKENING IN A MOUSE MODEL FOR BCIE, Journal of investigative dermatology, 110(6), 1998, pp. 951-957
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
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 PLAKOPHILIN-1 GENE RESULT IN ECTODERMAL DYSPLASIA SKIN FRAGILITY SYNDROME
Authors: MCGRATH JA MCMILLAN JR SHEMANKO CS RUNSWICK SK LEIGHT IM LANE EB GARROD DR EADY RAJ
Citation: Ja. Mcgrath et al., MUTATIONS IN THE PLAKOPHILIN-1 GENE RESULT IN ECTODERMAL DYSPLASIA SKIN FRAGILITY SYNDROME, Nature genetics, 17(2), 1997, pp. 240-244
CELL-CYCLE CHANGES IN A-TYPE LAMIN ASSOCIATIONS DETECTED IN HUMAN DERMAL FIBROBLASTS USING MONOCLONAL-ANTIBODIES
Authors: DYER JA KILL IR PUGH G QUINLAN RA LANE EB HUTCHISON CJ
Citation: Ja. Dyer et al., CELL-CYCLE CHANGES IN A-TYPE LAMIN ASSOCIATIONS DETECTED IN HUMAN DERMAL FIBROBLASTS USING MONOCLONAL-ANTIBODIES, Chromosome research, 5(6), 1997, pp. 383-394
DEMONSTRATION OF THE IMPACT OF KERATIN MUTATIONS ON MOTILITY AND RESISTANCE TO OSMOTIC STRESSES IN CULTURED KERATINOCYTES
Authors: MORLEY SM NOMAN A JAMES J LANE EB
Citation: Sm. Morley et al., DEMONSTRATION OF THE IMPACT OF KERATIN MUTATIONS ON MOTILITY AND RESISTANCE TO OSMOTIC STRESSES IN CULTURED KERATINOCYTES, Journal of investigative dermatology, 109(3), 1997, pp. 428-428
RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX WITH RESPIRATORY COMPLICATIONS CAUSED BY MUTATIONS IN THE PLECTIN GENE
Authors: MELLERIO JE SMITH FJD MCLEAN WHI MCGRATH JA MORRISON GAJ TIERNEY P ALBERT DM PULKKINEN L MCMILLAN JR LANE EB LEIGH IM GEDDES JF UITLO J EADY RAJ
Citation: Je. Mellerio et al., RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX WITH RESPIRATORY COMPLICATIONS CAUSED BY MUTATIONS IN THE PLECTIN GENE, Journal of investigative dermatology, 108(4), 1997, pp. 151-151
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
HOMOZYGOUS NONSENSE MUTATION IN THE HELIX-2 DOMAIN OF K14 CAUSES RECESSIVE EBS
Authors: CORDEN LD MELLERIO JE GRATIAN MJ EADY RAJ HARPER JI LACOUR M MAGEE G LANE EB MCLEAN WHI MCGRATH JA
Citation: Ld. Corden et al., HOMOZYGOUS NONSENSE MUTATION IN THE HELIX-2 DOMAIN OF K14 CAUSES RECESSIVE EBS, Journal of investigative dermatology, 108(4), 1997, pp. 662-662
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
DISTINCT NUCLEAR ASSEMBLY PATHWAYS FOR LAMIN-A AND LAMIN-C LEAD TO THEIR INCREASE DURING QUIESCENCE IN SWISS 3T3 CELLS
Authors: PUGH GE COATES PJ LANE EB RAYMOND Y QUINLAN RA
Citation: Ge. Pugh et al., DISTINCT NUCLEAR ASSEMBLY PATHWAYS FOR LAMIN-A AND LAMIN-C LEAD TO THEIR INCREASE DURING QUIESCENCE IN SWISS 3T3 CELLS, Journal of Cell Science, 110, 1997, pp. 2483-2493
OUT OF BALANCE - CONSEQUENCES OF A PARTIAL KERATIN-10 KNOCKOUT
Authors: REICHELT J BAUER C PORTER RM LANE EB HERZOG V MAGIN TM
Citation: J. Reichelt et al., OUT OF BALANCE - CONSEQUENCES OF A PARTIAL KERATIN-10 KNOCKOUT, Journal of Cell Science, 110, 1997, pp. 2175-2186
RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX ASSOCIATED WITH PLECTIN MUTATIONS - INFANTILE RESPIRATORY COMPLICATIONS IN 2 UNRELATED CASES
Authors: MELLERIO JE SMITH FJD MCMILLAN JR MCLEAN WHI MCGRATH JA MORRISON GAJ TIERNEY P ALBERT DM WICHE G LEIGH IM GEDDES JF LANE EB UITTO J EADY RAJ
Citation: Je. Mellerio et al., RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX ASSOCIATED WITH PLECTIN MUTATIONS - INFANTILE RESPIRATORY COMPLICATIONS IN 2 UNRELATED CASES, British journal of dermatology, 137(6), 1997, pp. 898-906
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
KERATIN-14 AND KERATIN-19 EXPRESSION IN NORMAL, DYSPLASTIC AND MALIGNANT ORAL EPITHELIA - A STUDY USING IN-SITU HYBRIDIZATION AND IMMUNOHISTOCHEMISTRY
Authors: SU L MORGAN PR LANE EB
Citation: L. Su et al., KERATIN-14 AND KERATIN-19 EXPRESSION IN NORMAL, DYSPLASTIC AND MALIGNANT ORAL EPITHELIA - A STUDY USING IN-SITU HYBRIDIZATION AND IMMUNOHISTOCHEMISTRY, Journal of oral pathology & medicine, 25(6), 1996, pp. 293-301
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
THE UTILITY OF CYTOKERATIN PROFILES FOR DETECTING ORAL-CANCER USING EXFOLIATIVE CYTOLOGY
Authors: OGDEN GR CHISHOLM DM LANE EB
Citation: Gr. Ogden et al., THE UTILITY OF CYTOKERATIN PROFILES FOR DETECTING ORAL-CANCER USING EXFOLIATIVE CYTOLOGY, British journal of oral & maxillofacial surgery, 34(5), 1996, pp. 461-466
EXPRESSION OF CYTOKERATIN MESSENGER-RNA VERSUS PROTEIN IN THE NORMAL MAMMARY-GLAND AND IN BREAST-CANCER
Authors: SU L MORGAN PR LANE EB
Citation: L. Su et al., EXPRESSION OF CYTOKERATIN MESSENGER-RNA VERSUS PROTEIN IN THE NORMAL MAMMARY-GLAND AND IN BREAST-CANCER, Human pathology, 27(8), 1996, pp. 800-806
Risultati: 1-25 | 26-50 | 51-75 | 76-88