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Results: 1-12 |
Results: 12
Discovery of a novel murine keratin 6 (K6) isoform explains the absence ofhair and nail defects in mice deficient for K6a and K6b
Authors: Wojcik, SM Longley, MA Roop, DR
Citation: Sm. Wojcik et al., Discovery of a novel murine keratin 6 (K6) isoform explains the absence ofhair and nail defects in mice deficient for K6a and K6b, J CELL BIOL, 154(3), 2001, pp. 619-630
Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders
Authors: Arin, MJ Longley, MA Wang, XJ Roop, DR
Citation: Mj. Arin et al., Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders, J CELL BIOL, 152(3), 2001, pp. 645-649
An inducible mouse model for epidermolysis bullosa simplex: Implications for gene therapy
Authors: Cao, TY Longley, MA Wang, XJ Roop, DR
Citation: Ty. Cao et al., An inducible mouse model for epidermolysis bullosa simplex: Implications for gene therapy, J CELL BIOL, 152(3), 2001, pp. 651-656
Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis
Authors: Arin, MJ Longley, MA Epstein, EH Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis, EXP DERMATO, 9(1), 2000, pp. 16-19
Lessons from loricrin-deficient mice: Compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope protein
Authors: Koch, PJ de Viragh, PA Scharer, E Bundman, D Longley, MA Bickenbach, J Kawachi, Y Suga, Y Zhou, ZJ Huber, M Hohl, D Kartasova, T Jarnik, M Steven, AC Roop, DR
Citation: Pj. Koch et al., Lessons from loricrin-deficient mice: Compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope protein, J CELL BIOL, 151(2), 2000, pp. 389-400
Transgenic mice expressing a mutant form of loricrin reveal the molecular basis of the skin diseases, Vohwinkel syndrome and progressive symmetric erythrokeratoderma
Authors: Suga, Y Jarnik, M Attar, PS Longley, MA Bundman, D Steven, AC Koch, PJ Roop, DR
Citation: Y. Suga et al., Transgenic mice expressing a mutant form of loricrin reveal the molecular basis of the skin diseases, Vohwinkel syndrome and progressive symmetric erythrokeratoderma, J CELL BIOL, 151(2), 2000, pp. 401-412
An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis
Authors: Arin, MJ Longley, MA Kuster, W Huber, M Hohl, D Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis, EXP DERMATO, 8(2), 1999, pp. 124-127
Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
Authors: Wojcik, SM Imakado, S Seki, T Longley, MA Petherbridge, L Bundman, DS Bickenbach, JR Rothnagel, JA Roop, DR
Citation: Sm. Wojcik et al., Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle, DIFFERENTIA, 65(2), 1999, pp. 97-112
The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
Authors: Rothnagel, JA Seki, T Ogo, M Longley, MA Wojcik, SM Bundman, DS Bickenbach, JR Roop, DR
Citation: Ja. Rothnagel et al., The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis, DIFFERENTIA, 65(2), 1999, pp. 119-130
Characterization of loricrin regulation in vitro and in transgenic mice
Authors: DiSepio, D Bickenbach, JR Longley, MA Bundman, DS Rothnagel, JA Roop, DR
Citation: D. Disepio et al., Characterization of loricrin regulation in vitro and in transgenic mice, DIFFERENTIA, 64(4), 1999, pp. 225-235
A novel substitution in keratin 10 in epidermolytic hyperkeratosis
Authors: Arin, MJ Longley, MA Anton-Lamprech, I Kurze, G Huber, M Hohl, D Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., A novel substitution in keratin 10 in epidermolytic hyperkeratosis, J INVES DER, 112(4), 1999, pp. 506-508
A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens
Authors: Arin, MJ Longley, MA Epstein, EH Scott, G Goldsmith, LA Rothnagel, JA Roop, DR
Citation: Mj. Arin et al., A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens, J INVES DER, 112(3), 1999, pp. 380-382
Risultati: 1-12 |