Search research articles
Contact Us
Filters
Showing results (61-70 of 73) with videos related to
Page
of 8
Sort By:
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 mutations
Amanda L Aloia, Nicholas S Eyre, Stuart Black, et al.
Emerging Infectious Diseases
|
January 23, 2014
Monitoring human babesiosis emergence through vector surveillance New England, USA
Maria 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 blood
Lindsay 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 theory
J 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 palsy
Mark 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 palsy
Mark 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 leukodystrophy
Cas Simons, David Dyment, Stephen J Bent, et al.
Nature Neuroscience
|
May 2, 2017
Mural lymphatic endothelial cells regulate meningeal angiogenesis in the zebrafish
Neil 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 Infancy
Huifang Yan, Guy Helman, Swetha E Murthy, et al.
Neurogenetics
|
August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1
Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 73) with videos related to
Sort By:
Page
of 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 mutations
Amanda L Aloia, Nicholas S Eyre, Stuart Black, et al.
Emerging Infectious Diseases
|
January 23, 2014
Monitoring human babesiosis emergence through vector surveillance New England, USA
Maria 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 blood
Lindsay 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 theory
J 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 palsy
Mark 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 palsy
Mark 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 leukodystrophy
Cas Simons, David Dyment, Stephen J Bent, et al.
Nature Neuroscience
|
May 2, 2017
Mural lymphatic endothelial cells regulate meningeal angiogenesis in the zebrafish
Neil 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 Infancy
Huifang Yan, Guy Helman, Swetha E Murthy, et al.
Neurogenetics
|
August 27, 2017
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1
Noriko Miyake, Nicole I Wolf, Ferdy K Cayami, et al.
Page
of 8