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E B Lane

Showing results (141-150 of 155) with videos related to

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Differentiation; Research in Biological Diversity|May 1, 1989
Expression of intermediate filament proteins in fetal and adult human lung tissuesJ L Broers, L de Leij, M K Rot, et al.
Genes & Development|November 1, 1994
A functional "knockout" of human keratin 14E L Rugg, W H McLean, E B Lane, et al.
The British Journal of Dermatology|August 2, 2003
Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutationsS M Morley, M D'Alessandro, C Sexton, et al.
Human Mutation|April 29, 1998
Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplexL D Corden, J E Mellerio, M J Gratian, et al.
Nature Genetics|March 1, 1995
Keratin 16 and keratin 17 mutations cause pachyonychia congenitaW H McLean, E L Rugg, D P Lunny, et al.
Muscle & Nerve|September 13, 2006
Plectin defects in epidermolysis bullosa simplex with muscular dystrophyJ R McMillan, M Akiyama, F Rouan, et al.
The American Journal of Pathology|December 1, 1991
Cytokeratin expression patterns in metastatic transitional cell carcinoma of the urinary tract. An immunohistochemical study comparing local tumor and autologous metastasesH E Schaafsma, F C Ramaekers, G N van Muijen, et al.
The British Journal of Dermatology|July 28, 2011
Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitisS C S Cai, H Chen, W-P Koh, et al.
Journal of Clinical Pathology|November 1, 1982
Use of monoclonal antibodies for the histopathological diagnosis of human malignancyK C Gatter, Z Abdulaziz, P Beverley, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
Pageof 16

Showing results (141-150 of 155) with videos related to

Sort By:
Pageof 16
Differentiation; Research in Biological Diversity|May 1, 1989
Expression of intermediate filament proteins in fetal and adult human lung tissuesJ L Broers, L de Leij, M K Rot, et al.
Genes & Development|November 1, 1994
A functional "knockout" of human keratin 14E L Rugg, W H McLean, E B Lane, et al.
The British Journal of Dermatology|August 2, 2003
Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutationsS M Morley, M D'Alessandro, C Sexton, et al.
Human Mutation|April 29, 1998
Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplexL D Corden, J E Mellerio, M J Gratian, et al.
Nature Genetics|March 1, 1995
Keratin 16 and keratin 17 mutations cause pachyonychia congenitaW H McLean, E L Rugg, D P Lunny, et al.
Muscle & Nerve|September 13, 2006
Plectin defects in epidermolysis bullosa simplex with muscular dystrophyJ R McMillan, M Akiyama, F Rouan, et al.
The American Journal of Pathology|December 1, 1991
Cytokeratin expression patterns in metastatic transitional cell carcinoma of the urinary tract. An immunohistochemical study comparing local tumor and autologous metastasesH E Schaafsma, F C Ramaekers, G N van Muijen, et al.
The British Journal of Dermatology|July 28, 2011
Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitisS C S Cai, H Chen, W-P Koh, et al.
Journal of Clinical Pathology|November 1, 1982
Use of monoclonal antibodies for the histopathological diagnosis of human malignancyK C Gatter, Z Abdulaziz, P Beverley, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
Pageof 16