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

Carole Ober

Showing results (81-90 of 296) with videos related to

Pageof 30
Sort By:
Nucleic Acids Research|October 1, 2015
Ultra-fast local-haplotype variant calling using paired-end DNA-sequencing data reveals somatic mosaicism in tumor and normal blood samplesSubhajit Sengupta, Kamalakar Gulukota, Yitan Zhu, et al.
American Journal of Human Genetics|December 19, 2003
Evidence for extensive transmission distortion in the human genomeSebastian Zöllner, Xiaoquan Wen, Neil A Hanchard, et al.
Plos One|March 13, 2014
Seasonal variation in human gut microbiome compositionEmily R Davenport, Orna Mizrahi-Man, Katelyn Michelini, et al.
Molecular Human Reproduction|September 25, 2012
The maternal HLA-G 1597ΔC null mutation is associated with increased risk of pre-eclampsia and reduced HLA-G expression during pregnancy in African-American womenDagan A Loisel, Christine Billstrand, Kathleen Murray, et al.
Human Immunology|June 2, 2012
HLA-G polymorphisms and soluble HLA-G protein levels in women with recurrent pregnancy loss from Basrah province in IraqRaghed M Jassem, Wafaa Sadoon Shani, Dagan A Loisel, et al.
Plos One|November 4, 2015
Genome-Wide Association Studies of the Human Gut MicrobiotaEmily R Davenport, Darren A Cusanovich, Katelyn Michelini, et al.
HGG Advances|September 4, 2023
Revealing polygenic pleiotropy using genetic risk scores for asthmaMatthew Dapas, Yu Lin Lee, William Wentworth-Sheilds, et al.
Obstetrics and Gynecology|June 12, 2003
Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivationAmy E Sullivan, Tracey Lewis, Mary Stephenson, et al.
European Journal of Human Genetics : EJHG|May 26, 2011
A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US HutteritesJessica X Chong, A Afşin Oktay, Zunyan Dai, et al.
Respiratory Research|December 13, 2005
Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopyJoseph Donfack, Daniel H Schneider, Zheng Tan, et al.
Pageof 30

Showing results (81-90 of 296) with videos related to

Sort By:
Pageof 30
Nucleic Acids Research|October 1, 2015
Ultra-fast local-haplotype variant calling using paired-end DNA-sequencing data reveals somatic mosaicism in tumor and normal blood samplesSubhajit Sengupta, Kamalakar Gulukota, Yitan Zhu, et al.
American Journal of Human Genetics|December 19, 2003
Evidence for extensive transmission distortion in the human genomeSebastian Zöllner, Xiaoquan Wen, Neil A Hanchard, et al.
Plos One|March 13, 2014
Seasonal variation in human gut microbiome compositionEmily R Davenport, Orna Mizrahi-Man, Katelyn Michelini, et al.
Molecular Human Reproduction|September 25, 2012
The maternal HLA-G 1597ΔC null mutation is associated with increased risk of pre-eclampsia and reduced HLA-G expression during pregnancy in African-American womenDagan A Loisel, Christine Billstrand, Kathleen Murray, et al.
Human Immunology|June 2, 2012
HLA-G polymorphisms and soluble HLA-G protein levels in women with recurrent pregnancy loss from Basrah province in IraqRaghed M Jassem, Wafaa Sadoon Shani, Dagan A Loisel, et al.
Plos One|November 4, 2015
Genome-Wide Association Studies of the Human Gut MicrobiotaEmily R Davenport, Darren A Cusanovich, Katelyn Michelini, et al.
HGG Advances|September 4, 2023
Revealing polygenic pleiotropy using genetic risk scores for asthmaMatthew Dapas, Yu Lin Lee, William Wentworth-Sheilds, et al.
Obstetrics and Gynecology|June 12, 2003
Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivationAmy E Sullivan, Tracey Lewis, Mary Stephenson, et al.
European Journal of Human Genetics : EJHG|May 26, 2011
A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US HutteritesJessica X Chong, A Afşin Oktay, Zunyan Dai, et al.
Respiratory Research|December 13, 2005
Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopyJoseph Donfack, Daniel H Schneider, Zheng Tan, et al.
Pageof 30