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Molecular Nutrition & Food Research|February 26, 2011
Microbial food cultures--opinion of the Senate Commission on Food Safety (SKLM) of the German Research Foundation (DFG)Rudi F Vogel, Walter P Hammes, Michael Habermeyer, et al.Applied and Environmental Microbiology|January 5, 2000
Homogeneity of Danish environmental and clinical isolates of Shewanella algaeB F Vogel, H M Holt, P Gerner-Smidt, et al.Journal of Medical Genetics|October 1, 1992
Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13qC A Brandt, J M Hertz, M B Petersen, et al.International Journal of Biological Macromolecules|September 24, 2017
Characterization of β-glucan formation by Lactobacillus brevis TMW 1.2112 isolated from slimy spoiled beerMarion E Fraunhofer, Andreas J Geissler, Daniel Wefers, et al.Journal of Proteome Research|September 2, 2017
Quantitative Proteomics for the Comprehensive Analysis of Stress Responses of Lactobacillus paracasei subsp. paracasei F19Ann-Sophie Schott, Jürgen Behr, Andreas J Geißler, et al.The Journal of Antimicrobial Chemotherapy|July 1, 1995
Treatment of acute bacterial exacerbations of chronic obstructive pulmonary disease in hospitalised patients--a comparison of meropenem and imipenem/cilastatin. COPD Study GroupJ Hamacher, F Vogel, J Lichey, et al.Applied and Environmental Microbiology|May 5, 2006
High-pressure-mediated survival of Clostridium botulinum and Bacillus amyloliquefaciens endospores at high temperatureDirk Margosch, Matthias A Ehrmann, Roman Buckow, et al.American Journal of Human Genetics|June 23, 1998
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteriaR Kruse, A Rütten, C Lamberti, et al.American Journal of Human Genetics|April 16, 1998
A gene for universal congenital alopecia maps to chromosome 8p21-22M M Nöthen, S Cichon, I R Vogt, et al.Nature Genetics|March 4, 2000
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type BM Oldridge, A M Fortuna, M Maringa, et al.Pageof 80