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Annals of Human Genetics|January 31, 2006
Golli-MBP copy number analysis by FISH, QMPSF and MAPH in 195 patients with hypomyelinating leukodystrophiesC Vaurs-Barriere, M-N Bonnet-Dupeyron, P Combes, et al.Human Mutation|October 15, 2008
Transcriptional behavior of DMD gene duplications in DMD/BMD malesF Gualandi, M Neri, M Bovolenta, et al.American Journal of Human Genetics|September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlationD Rodriguez, F Gauthier, E Bertini, et al.European Journal of Neurology|October 22, 2020
Clinical and radiological profile of patients with spinal muscular atrophy type 4P V S Souza, W B V R Pinto, A Ricarte, et al.Neurology|December 17, 2008
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletionC Cardoso, A Boys, E Parrini, et al.American Journal of Human Genetics|December 5, 1998
Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiencyV Tiranti, K Hoertnagel, R Carrozzo, et al.Cell Host & Microbe|January 12, 2018
The Marburgvirus-Neutralizing Human Monoclonal Antibody MR191 Targets a Conserved Site to Block Virus Receptor BindingLiam B King, Marnie L Fusco, Andrew I Flyak, et al.Nature Microbiology|August 27, 2016
Structures of Ebola virus GP and sGP in complex with therapeutic antibodiesJesper Pallesen, Charles D Murin, Natalia de Val, et al.Nature Structural & Molecular Biology|November 22, 2011
A shared structural solution for neutralizing ebolavirusesJoão M Dias, Ana I Kuehne, Dafna M Abelson, et al.Nature Genetics|August 31, 2001
Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1K Grohmann, M Schuelke, A Diers, et al.Pageof 29