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

Diane Hu

Showing results (61-70 of 75) with videos related to

Pageof 8
Sort By:
The Journal of Thoracic and Cardiovascular Surgery|May 15, 2022
Quantifying the effects of circulatory arrest on acute kidney injury in aortic surgeryDiane Hu, David Blitzer, Yanling Zhao, et al.
Development (Cambridge, England)|February 20, 2014
Embryonic bauplans and the developmental origins of facial diversity and constraintNathan M Young, Diane Hu, Alexis J Lainoff, et al.
BMC Genomics|October 4, 2005
Identification of disease causing loci using an array-based genotyping approach on pooled DNADavid W Craig, Matthew J Huentelman, Diane Hu-Lince, et al.
Tissue Engineering. Part A|February 3, 2016
Promoting Endochondral Bone Repair Using Human Osteoarthritic Articular ChondrocytesChelsea S Bahney, Linsey Jacobs, Robert Tamai, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 26, 2006
High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35Demetra S Stamm, Evadnie Rampersaud, Susan H Slifer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2004
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of functionErik G Puffenberger, Diane Hu-Lince, Jennifer M Parod, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15Abee L Boyles, David S Enterline, Preston H Hammock, et al.
Nature Genetics|November 6, 2007
A survey of genetic human cortical gene expressionAmanda J Myers, J Raphael Gibbs, Jennifer A Webster, et al.
American Journal of Human Genetics|November 4, 2008
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOELars Bertram, Christoph Lange, Kristina Mullin, et al.
The Journal of Clinical Psychiatry|May 4, 2007
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's diseaseKeith D Coon, Amanda J Myers, David W Craig, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
The Journal of Thoracic and Cardiovascular Surgery|May 15, 2022
Quantifying the effects of circulatory arrest on acute kidney injury in aortic surgeryDiane Hu, David Blitzer, Yanling Zhao, et al.
Development (Cambridge, England)|February 20, 2014
Embryonic bauplans and the developmental origins of facial diversity and constraintNathan M Young, Diane Hu, Alexis J Lainoff, et al.
BMC Genomics|October 4, 2005
Identification of disease causing loci using an array-based genotyping approach on pooled DNADavid W Craig, Matthew J Huentelman, Diane Hu-Lince, et al.
Tissue Engineering. Part A|February 3, 2016
Promoting Endochondral Bone Repair Using Human Osteoarthritic Articular ChondrocytesChelsea S Bahney, Linsey Jacobs, Robert Tamai, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 26, 2006
High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35Demetra S Stamm, Evadnie Rampersaud, Susan H Slifer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2004
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of functionErik G Puffenberger, Diane Hu-Lince, Jennifer M Parod, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15Abee L Boyles, David S Enterline, Preston H Hammock, et al.
Nature Genetics|November 6, 2007
A survey of genetic human cortical gene expressionAmanda J Myers, J Raphael Gibbs, Jennifer A Webster, et al.
American Journal of Human Genetics|November 4, 2008
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOELars Bertram, Christoph Lange, Kristina Mullin, et al.
The Journal of Clinical Psychiatry|May 4, 2007
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's diseaseKeith D Coon, Amanda J Myers, David W Craig, et al.
Pageof 8