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Showing results (91-100 of 155) with videos related to

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The British Journal of Dermatology|March 5, 2004
Functional analysis of keratin components in the mouse hair follicle inner root sheathR M Porter, M Gandhi, N J Wilson, et al.
The Journal of Investigative Dermatology|December 1, 1991
Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14A Ishida-Yamamoto, J A McGrath, S J Chapman, et al.
The British Journal of Dermatology|November 13, 2001
Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humansR M Porter, L D Corden, D P Lunny, et al.
Cell Motility and the Cytoskeleton|October 24, 1998
Keratin filament deployment and cytoskeletal networking in a sensory epithelium that vibrates during hearingM M Mogensen, C G Henderson, J B Mackie, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
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 simplexE L Rugg, M O Rachet-Préhu, A Rochat, et al.
The American Journal of Pathology|March 1, 1989
Detection of basement membrane components and basal cell keratin 14 in noninvasive and invasive carcinomas of the breastR H Wetzels, R Holland, U J van Haelst, et al.
The Journal of Investigative Dermatology|July 1, 1992
Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)A Ishida-Yamamoto, J A McGrath, M R Judge, et al.
Journal of Cell Science|September 1, 1990
Antibody markers of basal cells in complex epitheliaP E Purkis, J B Steel, I C Mackenzie, et al.
Experimental Dermatology|May 8, 1999
Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythrodermaW H McLean, S M Morley, C Higgins, et al.
Molecular Carcinogenesis|February 15, 2001
p53 is phosphorylated at the carboxyl terminus and promotes the differentiation of human HaCaT keratinocytesJ M Paramio, C Segrelles, S Laín, et al.
Pageof 16

Showing results (91-100 of 155) with videos related to

Sort By:
Pageof 16
The British Journal of Dermatology|March 5, 2004
Functional analysis of keratin components in the mouse hair follicle inner root sheathR M Porter, M Gandhi, N J Wilson, et al.
The Journal of Investigative Dermatology|December 1, 1991
Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14A Ishida-Yamamoto, J A McGrath, S J Chapman, et al.
The British Journal of Dermatology|November 13, 2001
Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humansR M Porter, L D Corden, D P Lunny, et al.
Cell Motility and the Cytoskeleton|October 24, 1998
Keratin filament deployment and cytoskeletal networking in a sensory epithelium that vibrates during hearingM M Mogensen, C G Henderson, J B Mackie, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
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 simplexE L Rugg, M O Rachet-Préhu, A Rochat, et al.
The American Journal of Pathology|March 1, 1989
Detection of basement membrane components and basal cell keratin 14 in noninvasive and invasive carcinomas of the breastR H Wetzels, R Holland, U J van Haelst, et al.
The Journal of Investigative Dermatology|July 1, 1992
Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)A Ishida-Yamamoto, J A McGrath, M R Judge, et al.
Journal of Cell Science|September 1, 1990
Antibody markers of basal cells in complex epitheliaP E Purkis, J B Steel, I C Mackenzie, et al.
Experimental Dermatology|May 8, 1999
Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythrodermaW H McLean, S M Morley, C Higgins, et al.
Molecular Carcinogenesis|February 15, 2001
p53 is phosphorylated at the carboxyl terminus and promotes the differentiation of human HaCaT keratinocytesJ M Paramio, C Segrelles, S Laín, et al.
Pageof 16