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J Bent

Showing results (61-70 of 73) with videos related to

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Antiviral Therapy|September 16, 2014
Generation of a chimeric hepatitis C replicon encoding a genotype-6a NS3 protease and assessment of boceprevir (SCH503034) sensitivity and drug-associated mutationsAmanda L Aloia, Nicholas S Eyre, Stuart Black, et al.
Emerging Infectious Diseases|January 23, 2014
Monitoring human babesiosis emergence through vector surveillance New England, USAMaria A Diuk-Wasser, Yuchen Liu, Tanner K Steeves, et al.
Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)|October 11, 2013
Quantitative PCR for detection of Babesia microti in Ixodes scapularis ticks and in human bloodLindsay Rollend, Stephen J Bent, Peter J Krause, et al.
Science (New York, N.Y.)|September 23, 2003
Neutron-mapping polymer flow: scattering, flow visualization, and molecular theoryJ Bent, L R Hutchings, R W Richards, et al.
NPJ Genomic Medicine|December 20, 2018
Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
NPJ Genomic Medicine|June 25, 2019
Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
Brain : a Journal of Neurology|November 30, 2017
A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophyCas Simons, David Dyment, Stephen J Bent, et al.
Nature Neuroscience|May 2, 2017
Mural lymphatic endothelial cells regulate meningeal angiogenesis in the zebrafishNeil I Bower, Katarzyna Koltowska, Cathy Pichol-Thievend, et al.
American Journal of Human Genetics|October 8, 2019
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during InfancyHuifang Yan, Guy Helman, Swetha E Murthy, et al.
Neurogenetics|August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Antiviral Therapy|September 16, 2014
Generation of a chimeric hepatitis C replicon encoding a genotype-6a NS3 protease and assessment of boceprevir (SCH503034) sensitivity and drug-associated mutationsAmanda L Aloia, Nicholas S Eyre, Stuart Black, et al.
Emerging Infectious Diseases|January 23, 2014
Monitoring human babesiosis emergence through vector surveillance New England, USAMaria A Diuk-Wasser, Yuchen Liu, Tanner K Steeves, et al.
Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)|October 11, 2013
Quantitative PCR for detection of Babesia microti in Ixodes scapularis ticks and in human bloodLindsay Rollend, Stephen J Bent, Peter J Krause, et al.
Science (New York, N.Y.)|September 23, 2003
Neutron-mapping polymer flow: scattering, flow visualization, and molecular theoryJ Bent, L R Hutchings, R W Richards, et al.
NPJ Genomic Medicine|December 20, 2018
Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
NPJ Genomic Medicine|June 25, 2019
Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
Brain : a Journal of Neurology|November 30, 2017
A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophyCas Simons, David Dyment, Stephen J Bent, et al.
Nature Neuroscience|May 2, 2017
Mural lymphatic endothelial cells regulate meningeal angiogenesis in the zebrafishNeil I Bower, Katarzyna Koltowska, Cathy Pichol-Thievend, et al.
American Journal of Human Genetics|October 8, 2019
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during InfancyHuifang Yan, Guy Helman, Swetha E Murthy, et al.
Neurogenetics|August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Pageof 8