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Nature Communications|August 25, 2015
Loss of lamin A function increases chromatin dynamics in the nuclear interiorI Bronshtein, E Kepten, I Kanter, et al.Acta Dermato-Venereologica|June 23, 2004
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutationD Koss-Harnes, B Høyheim, M F Jonkman, et al.The American Journal of Pathology|February 13, 2001
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyJ W Bauer, F Rouan, B Kofler, et al.Muscle & Nerve|September 13, 2006
Plectin defects in epidermolysis bullosa simplex with muscular dystrophyJ R McMillan, M Akiyama, F Rouan, et al.Oncogene|May 9, 2007
The transcription factor ZEB1 (deltaEF1) promotes tumour cell dedifferentiation by repressing master regulators of epithelial polarityK Aigner, B Dampier, L Descovich, et al.The British Journal of Dermatology|February 21, 1998
Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated casesJ E Mellerio, F J Smith, J R McMillan, et al.Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.Pageof 11