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

Tanya M Teslovich

Showing results (1-10 of 60) with videos related to

Pageof 6
Sort By:
Nature Reviews. Genetics|March 2, 2005
The centrosome in human genetic diseaseJose L Badano, Tanya M Teslovich, Nicholas Katsanis
American Journal of Human Genetics|June 18, 2013
General framework for meta-analysis of rare variants in sequencing association studiesSeunggeun Lee, Tanya M Teslovich, Michael Boehnke, et al.
Bone|June 1, 2005
Dissection of the sets of genes that control the behavior of biglycan-deficient pre-osteoblasts using oligonucleotide microarraysXiao-Dong Chen, Xiaopeng Bian, Tanya M Teslovich, et al.
Current Biology : CB|February 21, 2003
Genome-wide analyses of steroid- and radiation-triggered programmed cell death in DrosophilaCheng-Yu Lee, Emily A Clough, Paula Yellon, et al.
Journal of Virology|December 14, 2007
Chronic CD4+ T-cell activation and depletion in human immunodeficiency virus type 1 infection: type I interferon-mediated disruption of T-cell dynamicsAhmad R Sedaghat, Jennifer German, Tanya M Teslovich, et al.
BMC Bioinformatics|November 29, 2002
Development and production of an oligonucleotide MuscleChip: use for validation of ambiguous ESTsRehannah H A Borup, Stefano Toppo, Yi-Wen Chen, et al.
Bioinformatics (Oxford, England)|July 17, 2010
LocusZoom: regional visualization of genome-wide association scan resultsRandall J Pruim, Ryan P Welch, Serena Sanna, et al.
Plos Genetics|July 31, 2007
Population bottlenecks as a potential major shaping force of human genome architectureAdrian Gherman, Peter E Chen, Tanya M Teslovich, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
American Journal of Human Genetics|January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autismDan E Arking, David J Cutler, Camille W Brune, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Nature Reviews. Genetics|March 2, 2005
The centrosome in human genetic diseaseJose L Badano, Tanya M Teslovich, Nicholas Katsanis
American Journal of Human Genetics|June 18, 2013
General framework for meta-analysis of rare variants in sequencing association studiesSeunggeun Lee, Tanya M Teslovich, Michael Boehnke, et al.
Bone|June 1, 2005
Dissection of the sets of genes that control the behavior of biglycan-deficient pre-osteoblasts using oligonucleotide microarraysXiao-Dong Chen, Xiaopeng Bian, Tanya M Teslovich, et al.
Current Biology : CB|February 21, 2003
Genome-wide analyses of steroid- and radiation-triggered programmed cell death in DrosophilaCheng-Yu Lee, Emily A Clough, Paula Yellon, et al.
Journal of Virology|December 14, 2007
Chronic CD4+ T-cell activation and depletion in human immunodeficiency virus type 1 infection: type I interferon-mediated disruption of T-cell dynamicsAhmad R Sedaghat, Jennifer German, Tanya M Teslovich, et al.
BMC Bioinformatics|November 29, 2002
Development and production of an oligonucleotide MuscleChip: use for validation of ambiguous ESTsRehannah H A Borup, Stefano Toppo, Yi-Wen Chen, et al.
Bioinformatics (Oxford, England)|July 17, 2010
LocusZoom: regional visualization of genome-wide association scan resultsRandall J Pruim, Ryan P Welch, Serena Sanna, et al.
Plos Genetics|July 31, 2007
Population bottlenecks as a potential major shaping force of human genome architectureAdrian Gherman, Peter E Chen, Tanya M Teslovich, et al.
Human Genetics|June 18, 2003
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13Lisbeth Tranebjaerg, Tanya M Teslovich, MaryPat Jones, et al.
American Journal of Human Genetics|January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autismDan E Arking, David J Cutler, Camille W Brune, et al.
Pageof 6