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Frank Baas

Showing results (201-210 of 231) with videos related to

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Brain : a Journal of Neurology|October 19, 2010
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasiaYasmin Namavar, Peter G Barth, Paul R Kasher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 2, 2024
Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhageJulie W Rutten, Minne N Cerfontaine, Kyra L Dijkstra, et al.
Plos One|February 2, 2011
A sensitive assay for virus discovery in respiratory clinical samplesMichel de Vries, Martin Deijs, Marta Canuti, et al.
Nature Genetics|July 15, 2014
Mutations in ZBTB20 cause Primrose syndromeViviana Cordeddu, Bert Redeker, Emilia Stellacci, et al.
Journal of Virology|October 24, 2014
Clonal evolution of CD8+ T cell responses against latent viruses: relationship among phenotype, localization, and functionEster B M Remmerswaal, Paul L Klarenbeek, Nuno L Alves, et al.
The Lancet. Neurology|September 11, 2007
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyMichael A van Es, Paul W Van Vught, Hylke M Blauw, et al.
Nature Genetics|December 18, 2007
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosisMichael A van Es, Paul W J van Vught, Hylke M Blauw, et al.
Annals of Neurology|February 2, 2019
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1AFeifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
American Journal of Human Genetics|September 27, 2016
Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset EncephalopathyElisabetta Flex, Marcello Niceta, Serena Cecchetti, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 22, 2009
The establishment of the GENEQOL consortium to investigate the genetic disposition of patient-reported quality-of-life outcomesMirjam A G Sprangers, Jeff A Sloan, Ruut Veenhoven, et al.
Pageof 24

Showing results (201-210 of 231) with videos related to

Sort By:
Pageof 24
Brain : a Journal of Neurology|October 19, 2010
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasiaYasmin Namavar, Peter G Barth, Paul R Kasher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 2, 2024
Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhageJulie W Rutten, Minne N Cerfontaine, Kyra L Dijkstra, et al.
Plos One|February 2, 2011
A sensitive assay for virus discovery in respiratory clinical samplesMichel de Vries, Martin Deijs, Marta Canuti, et al.
Nature Genetics|July 15, 2014
Mutations in ZBTB20 cause Primrose syndromeViviana Cordeddu, Bert Redeker, Emilia Stellacci, et al.
Journal of Virology|October 24, 2014
Clonal evolution of CD8+ T cell responses against latent viruses: relationship among phenotype, localization, and functionEster B M Remmerswaal, Paul L Klarenbeek, Nuno L Alves, et al.
The Lancet. Neurology|September 11, 2007
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyMichael A van Es, Paul W Van Vught, Hylke M Blauw, et al.
Nature Genetics|December 18, 2007
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosisMichael A van Es, Paul W J van Vught, Hylke M Blauw, et al.
Annals of Neurology|February 2, 2019
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1AFeifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
American Journal of Human Genetics|September 27, 2016
Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset EncephalopathyElisabetta Flex, Marcello Niceta, Serena Cecchetti, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 22, 2009
The establishment of the GENEQOL consortium to investigate the genetic disposition of patient-reported quality-of-life outcomesMirjam A G Sprangers, Jeff A Sloan, Ruut Veenhoven, et al.
Pageof 24