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Results: 1-21 |
Results: 21
A novel keratin 5 mutation (K5V186L) in a family with EBS-K: a conservative substitution can lead to development of different disease phenotypes
Authors: Liovic, M Stojan, J Bowden, PE Gibbs, D Vahlquist, A Lane, EB Komel, R
Citation: M. Liovic et al., A novel keratin 5 mutation (K5V186L) in a family with EBS-K: a conservative substitution can lead to development of different disease phenotypes, J INVES DER, 116(6), 2001, pp. 964-969
A novel mutation in the keratin 13 gene causing oral white sponge nevus
Authors: Terrinoni, A Rugg, EL Lane, EB Melino, G Felix, DH Munro, CS McLean, WHI
Citation: A. Terrinoni et al., A novel mutation in the keratin 13 gene causing oral white sponge nevus, J DENT RES, 80(3), 2001, pp. 919-923
Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans
Authors: Porter, RM Corden, LD Lunny, DP Smith, FJD Lane, EB McLean, WHI
Citation: Rm. Porter et al., Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans, BR J DERM, 145(4), 2001, pp. 558-568
Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation
Authors: Irvine, AD Rugg, EL Lane, EB Hoare, S Peret, C Hughes, AE Heagerty, AH
Citation: Ad. Irvine et al., Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation, BR J DERM, 144(1), 2001, pp. 40-45
Expression of individual lamins in basal cell carcinomas of the skin
Authors: Venables, RS McLean, S Luny, D Moteleb, E Morley, S Quinlan, RA Lane, EB Hutchison, CJ
Citation: Rs. Venables et al., Expression of individual lamins in basal cell carcinomas of the skin, BR J CANC, 84(4), 2001, pp. 512-519
A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland
Authors: Gordon, KE Binas, B Chapman, RS Kurian, KM Clarkson, RWE Clark, AJ Lane, EB Watson, CJ
Citation: Ke. Gordon et al., A novel cell culture model for studying differentiation and apoptosis in the mouse mammary gland, BREAST CA R, 2(3), 2000, pp. 222-235
p53 is phosphorylated at the carboxyl terminus and promotes the differentiation of human HaCaT keratinocytes
Authors: Paramio, JM Segrelles, C Lain, S Gomez-Casero, E Lane, DP Lane, EB Jorcano, JL
Citation: Jm. Paramio et al., p53 is phosphorylated at the carboxyl terminus and promotes the differentiation of human HaCaT keratinocytes, MOL CARCINO, 29(4), 2000, pp. 251-262
DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplex
Authors: Rugg, EL Baty, D Shemanko, CS Magee, G Polak, S Bergman, R Kadar, T Boxer, M Falik-Zaccai, T Borochowitz, Z Lane, EB
Citation: El. Rugg et al., DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplex, PRENAT DIAG, 20(5), 2000, pp. 371-377
K15 expression implies lateral differentiation within stratified epithelial basal cells
Authors: Porter, RM Lunny, DP Ogden, PH Morley, SM McLean, WHI Evans, A Harrison, DL Rugg, EL Lane, EB
Citation: Rm. Porter et al., K15 expression implies lateral differentiation within stratified epithelial basal cells, LAB INV, 80(11), 2000, pp. 1701-1710
Supplementation of a mutant keratin by stable expression of desmin in cultured human EBS keratinocytes
Authors: Magin, TM Kaiser, HW Leitgeb, S Grund, C Leigh, IM Morley, SM Lane, EB
Citation: Tm. Magin et al., Supplementation of a mutant keratin by stable expression of desmin in cultured human EBS keratinocytes, J CELL SCI, 113(23), 2000, pp. 4231-4239
A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe disease
Authors: Batta, K Rugg, EL Wilson, NJ West, N Goodyear, H Lane, EB Gratian, M Dopping-Hepenstal, P Moss, C Eady, RAJ
Citation: K. Batta et al., A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe disease, BR J DERM, 143(3), 2000, pp. 621-627
Laryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential
Authors: Shemanko, CS Horn, HM Keohane, SG Hepburn, N Kerr, AIG Atherton, DJ Tidman, MJ Lane, EB
Citation: Cs. Shemanko et al., Laryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential, BR J DERM, 142(2), 2000, pp. 315-320
Women's ways of knowing in nursing and critical thinking
Authors: Nelms, TP Lane, EB
Citation: Tp. Nelms et Eb. Lane, Women's ways of knowing in nursing and critical thinking, J PROF NURS, 15(3), 1999, pp. 179-186
Identification of two novel mutations in keratin 13 as the cause of white sponge naevus
Authors: Rugg, EL Magee, GJ Wilson, NJ Brandrup, F Hamburger, J Lane, EB
Citation: El. Rugg et al., Identification of two novel mutations in keratin 13 as the cause of white sponge naevus, ORAL DIS, 5(4), 1999, pp. 321-324
Donor splice site mutation in keratin 5 causes in-frame removal of 22 amino acids of H1 and 1A rod domains in Dowling-Meara epidermolysis bullosa simplex
Authors: Rugg, EL Rachet-Prehu, MO Rochat, A Barrandon, Y Goossens, M Lane, EB Hovnanian, A
Citation: El. Rugg et al., Donor splice site mutation in keratin 5 causes in-frame removal of 22 amino acids of H1 and 1A rod domains in Dowling-Meara epidermolysis bullosa simplex, EUR J HUM G, 7(3), 1999, pp. 293-300
Effects on normal fibroblasts and neuroblastoma cells of the activation ofthe p53 response by the nuclear export inhibitor leptomycin B
Authors: Smart, P Lane, EB Lane, DP Midgley, C Vojtesek, B Lain, S
Citation: P. Smart et al., Effects on normal fibroblasts and neuroblastoma cells of the activation ofthe p53 response by the nuclear export inhibitor leptomycin B, ONCOGENE, 18(51), 1999, pp. 7378-7386
Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythroderma
Authors: McLean, WHI Morley, SM Higgins, C Bowden, PE White, M Leigh, IM Lane, EB
Citation: Whi. Mclean et al., Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythroderma, EXP DERMATO, 8(2), 1999, pp. 120-123
Modulation of cell proliferation by cytokeratins K10 and K16
Authors: Paramio, JM Casanova, ML Segrelles, C Mittnacht, S Lane, EB Jorcano, JL
Citation: Jm. Paramio et al., Modulation of cell proliferation by cytokeratins K10 and K16, MOL CELL B, 19(4), 1999, pp. 3086-3094
Binding of integrin alpha 6 beta 4 to plectin prevents plectin associationwith F-actin but does not interfere with intermediate filament binding
Authors: Geerts, D Fontao, L Nievers, MG Schaapveld, RQJ Purkis, PE Wheeler, GN Lane, EB Leigh, IM Sonnenberg, A
Citation: D. Geerts et al., Binding of integrin alpha 6 beta 4 to plectin prevents plectin associationwith F-actin but does not interfere with intermediate filament binding, J CELL BIOL, 147(2), 1999, pp. 417-434
An inhibitor of nuclear export activates the p53 response and induces the localization of HDM2 and p53 to U1A-positive nuclear bodies associated withthe PODs
Authors: Lain, S Midgley, C Sparks, A Lane, EB Lane, DP
Citation: S. Lain et al., An inhibitor of nuclear export activates the p53 response and induces the localization of HDM2 and p53 to U1A-positive nuclear bodies associated withthe PODs, EXP CELL RE, 248(2), 1999, pp. 457-472
An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1
Authors: Kremer, H Lavrijsen, APM McLean, WHI Lane, EB Melchers, D Ruiter, DJ Mariman, ECM Steijlen, PM
Citation: H. Kremer et al., An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1, J INVES DER, 111(6), 1998, pp. 1224-1226
Risultati: 1-21 |