Showing results (481-490 of 533) with videos related to
Sort By:
Pageof 54
The British Journal of Dermatology|April 23, 2002
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approachA M Hillmer, R Kruse, F Macciardi, et al.The Journal of Investigative Dermatology|September 21, 2001
Role of integrin alphaE(CD103)beta7 for tissue-specific epidermal localization of CD8+ T lymphocytesK Pauls, M Schön, R C Kubitza, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|March 12, 2015
Non-invasive diagnosis of sweat gland dysplasia using optical coherence tomography and reflectance confocal microscopy in a family with anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome)M Reinholz, G G Gauglitz, K Giehl, et al.Journal of Bacteriology|February 11, 1998
Two separate regulatory systems participate in control of swarming motility of Serratia liquefaciens MG1M Givskov, J Ostling, L Eberl, et al.Annual Review of Microbiology|January 1, 1993
Suicidal genetic elements and their use in biological containment of bacteriaS Molin, L Boe, L B Jensen, et al.Journal of Bacteriology|June 15, 2000
Inactivation of gltB abolishes expression of the assimilatory nitrate reductase gene (nasB) in Pseudomonas putida KT2442L Eberl, A Ammendola, M H Rothballer, et al.Applied and Environmental Microbiology|February 7, 2001
gfp-based N-acyl homoserine-lactone sensor systems for detection of bacterial communicationJ B Andersen, A Heydorn, M Hentzer, et al.Archives of Dermatology|April 1, 1990
Efficiency of acitretin in combination with UV-B in the treatment of severe psoriasisT Ruzicka, C Sommerburg, O Braun-Falco, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|October 6, 2011
[Galli-Galli disease. Clinical and histopathological investigation using a case series of 18 patients]S Hanneken, A Rütten, S Eigelshoven, et al.Human Genetics|December 1, 1996
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?R Kruse, C Lamberti, Y Wang, et al.Pageof 54