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World Journal of Microbiology & Biotechnology|August 12, 2024
Occurrence, serotypes and virulence characteristics of Shiga toxin-producing and Enteropathogenic Escherichia coli isolates from dairy cattle in South AfricaAlaba S Olawole, Mogaugedi N Malahlela, Thierry Y Fonkui, et al.Virus Research|November 8, 2012
African swine fever virus serodiagnosis: a general review with a focus on the analyses of African serum samplesCarolina Cubillos, Silvia Gómez-Sebastian, Noelia Moreno, et al.Molecular Ecology|April 14, 2011
A lectin-mediated resistance of higher fungi against predators and parasitesS Bleuler-Martínez, A Butschi, M Garbani, et al.Orthopaedics & Traumatology, Surgery & Research : OTSR|August 21, 2012
Minimally invasive management of thoraco-lumbar fractures: combined percutaneous fixation and balloon kyphoplastyF Zairi, C Court, P Tropiano, et al.Human Genetics|July 29, 2000
Multi-allelic origin of congenital disorder of glycosylation (CDG)-IcT Imbach, S Grünewald, B Schenk, et al.The Journal of Biological Chemistry|August 16, 2001
The CWH8 gene encodes a dolichyl pyrophosphate phosphatase with a luminally oriented active site in the endoplasmic reticulum of Saccharomyces cerevisiaeF Fernandez, J S Rush, D A Toke, et al.The Journal of Clinical Investigation|January 22, 2000
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type IeT Imbach, B Schenk, E Schollen, et al.Ticks and Tick-Borne Diseases|November 17, 2025
Prevalence of heartwater in Guadeloupe (2024): stable endemicity and evidence of spread to Les SaintesVictor Dufleit, Laure Guerrini, Mélanie Dhune, et al.The Journal of Clinical Investigation|December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfB Schenk, T Imbach, C G Frank, et al.Psychological Medicine|April 13, 2010
Predictability of oppositional defiant disorder and symptom dimensions in children and adolescents with ADHD combined typeM Aebi, U C Müller, P Asherson, et al.Pageof 22