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

H Shaikh

Showing results (221-230 of 236) with videos related to

Pageof 24
Sort By:
Cell Reports. Medicine|May 16, 2026
Understanding and overcoming innate and acquired MAPK inhibition resistance in anaplastic thyroid cancerPeter Y F Zeng, Jalna Meens, Amir Hossein Karimi, et al.
American Journal of Human Genetics|September 10, 2013
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1Hung-Chun Yu, Jennifer L Sloan, Gunter Scharer, et al.
Molecular Psychiatry|June 24, 2009
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genesJ Elia, X Gai, H M Xie, et al.
Ebiomedicine|March 6, 2025
Cohort-level clinical trajectory and molecular landscape of idiopathic subglottic stenosis for precision laryngology-a study of the Canadian Airways Research (CARE) groupR Jun Lin, Peter Y F Zeng, Kevin Fung, et al.
Nature Genetics|August 21, 2007
Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2Blake C Ballif, Sara A Hornor, Elizabeth Jenkins, et al.
Human Molecular Genetics|February 6, 2009
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome regionJustine Coppinger, Donna McDonald-McGinn, Elaine Zackai, et al.
Scientific Reports|September 20, 2024
A covalent creatine kinase inhibitor ablates glioblastoma migration and sensitizes tumors to oxidative stressJoshua L Katz, Yuheng Geng, Leah K Billingham, et al.
Nature|June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastomaSharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.
American Journal of Human Genetics|April 21, 2015
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion SyndromeElisabeth E Mlynarski, Molly B Sheridan, Michael Xie, et al.
Genome Research|July 14, 2009
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applicationsTamim H Shaikh, Xiaowu Gai, Juan C Perin, et al.
Pageof 24

Showing results (221-230 of 236) with videos related to

Sort By:
Pageof 24
Cell Reports. Medicine|May 16, 2026
Understanding and overcoming innate and acquired MAPK inhibition resistance in anaplastic thyroid cancerPeter Y F Zeng, Jalna Meens, Amir Hossein Karimi, et al.
American Journal of Human Genetics|September 10, 2013
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1Hung-Chun Yu, Jennifer L Sloan, Gunter Scharer, et al.
Molecular Psychiatry|June 24, 2009
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genesJ Elia, X Gai, H M Xie, et al.
Ebiomedicine|March 6, 2025
Cohort-level clinical trajectory and molecular landscape of idiopathic subglottic stenosis for precision laryngology-a study of the Canadian Airways Research (CARE) groupR Jun Lin, Peter Y F Zeng, Kevin Fung, et al.
Nature Genetics|August 21, 2007
Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2Blake C Ballif, Sara A Hornor, Elizabeth Jenkins, et al.
Human Molecular Genetics|February 6, 2009
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome regionJustine Coppinger, Donna McDonald-McGinn, Elaine Zackai, et al.
Scientific Reports|September 20, 2024
A covalent creatine kinase inhibitor ablates glioblastoma migration and sensitizes tumors to oxidative stressJoshua L Katz, Yuheng Geng, Leah K Billingham, et al.
Nature|June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastomaSharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.
American Journal of Human Genetics|April 21, 2015
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion SyndromeElisabeth E Mlynarski, Molly B Sheridan, Michael Xie, et al.
Genome Research|July 14, 2009
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applicationsTamim H Shaikh, Xiaowu Gai, Juan C Perin, et al.
Pageof 24