Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Drew

Showing results (91-100 of 108) with videos related to

Pageof 11
Sort By:
Human Molecular Genetics|January 9, 2013
A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) geneMarina L Kennerson, Eppie M Yiu, David T Chuang, et al.
Emerging Infectious Diseases|July 14, 2011
Severe leptospirosis similar to pandemic (H1N1) 2009, Florida and Missouri, USAYi-Chun Lo, Kristina W Kintziger, Henry J Carson, et al.
Msystems|October 31, 2019
Changes in the Composition of the Gut Microbiota and the Blood Transcriptome in Preterm Infants at Less than 29 Weeks Gestation Diagnosed with Bronchopulmonary DysplasiaFeargal J Ryan, Damian P Drew, Chloe Douglas, et al.
Journal of Virology|October 7, 2011
Rift Valley fever virus vaccine lacking the NSs and NSm genes is safe, nonteratogenic, and confers protection from viremia, pyrexia, and abortion following challenge in adult and pregnant sheepBrian H Bird, Louis H Maartens, Shelley Campbell, et al.
Plos Genetics|July 21, 2016
Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3Megan H Brewer, Rabia Chaudhry, Jessica Qi, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathyAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2018
Response to Brodehl et alAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Blood|January 25, 2020
Leveraging gene expression subgroups to classify DLBCL patients and select for clinical benefit from a novel agentAlberto Risueño, Patrick R Hagner, Fadi Towfic, et al.
Plos One|September 7, 2012
The pox in the North American backyard: Volepox virus pathogenesis in California mice (Peromyscus californicus)Nadia F Gallardo-Romero, Clifton P Drew, Sonja L Weiss, et al.
Pageof 11

Showing results (91-100 of 108) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|January 9, 2013
A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) geneMarina L Kennerson, Eppie M Yiu, David T Chuang, et al.
Emerging Infectious Diseases|July 14, 2011
Severe leptospirosis similar to pandemic (H1N1) 2009, Florida and Missouri, USAYi-Chun Lo, Kristina W Kintziger, Henry J Carson, et al.
Msystems|October 31, 2019
Changes in the Composition of the Gut Microbiota and the Blood Transcriptome in Preterm Infants at Less than 29 Weeks Gestation Diagnosed with Bronchopulmonary DysplasiaFeargal J Ryan, Damian P Drew, Chloe Douglas, et al.
Journal of Virology|October 7, 2011
Rift Valley fever virus vaccine lacking the NSs and NSm genes is safe, nonteratogenic, and confers protection from viremia, pyrexia, and abortion following challenge in adult and pregnant sheepBrian H Bird, Louis H Maartens, Shelley Campbell, et al.
Plos Genetics|July 21, 2016
Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3Megan H Brewer, Rabia Chaudhry, Jessica Qi, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathyAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2018
Response to Brodehl et alAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Blood|January 25, 2020
Leveraging gene expression subgroups to classify DLBCL patients and select for clinical benefit from a novel agentAlberto Risueño, Patrick R Hagner, Fadi Towfic, et al.
Plos One|September 7, 2012
The pox in the North American backyard: Volepox virus pathogenesis in California mice (Peromyscus californicus)Nadia F Gallardo-Romero, Clifton P Drew, Sonja L Weiss, et al.
Pageof 11