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The Journal of Investigative Dermatology|September 1, 1997
A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skinN Hammami-Hauasli, D U Kalinke, H Schumann, et al.The Journal of Hospital Infection|September 1, 2015
Preoperative hair removal and surgical site infections: network meta-analysis of randomized controlled trialsA Lefebvre, P Saliou, J C Lucet, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|March 5, 2003
[Early study of myocardial perfusion with MRI in revascularized infarcts]K Rezaizadeh-Bourdariat, A Lalande, D Ben Salem, et al.Leukemia & Lymphoma|March 1, 1997
Heterogenous expression of CD15 in acute lymphoblastic leukemia: a study of ten anti-CD15 monoclonal antibodies in 158 patientsM Maynadié, L Campos, P Moskovtchenko, et al.Journal De Mycologie Medicale|November 27, 2012
Dynamics of fungal colonization in a new medical mycology laboratoryM Sautour, I Fournel, F Dalle, et al.The American Journal of Pathology|June 17, 1998
Collagenase-3 (matrix metalloproteinase-13) expression is induced in oral mucosal epithelium during chronic inflammationV J Uitto, K Airola, M Vaalamo, et al.Journal of Cell Science|August 9, 2001
trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiationF Rouan, T W White, N Brown, et al.The British Journal of Dermatology|April 1, 1996
First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus samplingJ A McGrath, M G Dunnill, A M Christiano, et al.American Journal of Human Genetics|November 1, 1989
Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen geneR G Knowlton, E J Weaver, A F Struyk, et al.American Journal of Human Genetics|October 27, 1997
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formationA Hovnanian, A Rochat, C Bodemer, et al.Pageof 67