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

N Robinson

Showing results (1171-1180 of 1,318) with videos related to

Pageof 132
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|August 28, 2020
4-Hydroxyacetophenone modulates the actomyosin cytoskeleton to reduce metastasisDarren S Bryan, Melinda Stack, Katarzyna Krysztofiak, et al.
Bone Marrow Transplantation|January 26, 2006
A novel triple purge strategy for eliminating chronic myelogenous leukemia (CML) cells from autograftsH Yang, C Eaves, M de Lima, et al.
Contemporary Clinical Trials|April 14, 2015
Clinical trial management of participant recruitment, enrollment, engagement, and retention in the SMART study using a Marketing and Information Technology (MARKIT) modelAnjali Gupta, Karen J Calfas, Simon J Marshall, et al.
Human Mutation|December 30, 2014
Recessive inheritance of population-specific intronic LINE-1 insertion causes a rotor syndrome phenotypeTatehiro Kagawa, Akira Oka, Yoshinao Kobayashi, et al.
Surgical Endoscopy|June 21, 2015
Structured simulation improves learning of the Fundamental Use of Surgical Energy™ curriculum: a multicenter randomized controlled trialAmin Madani, Yusuke Watanabe, Nicole Townsend, et al.
Briefings in Bioinformatics|October 1, 2015
The digital revolution in phenotypingAnika Oellrich, Nigel Collier, Tudor Groza, et al.
Genome Research|September 3, 2013
Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutationsDaniel M Ibrahim, Peter Hansen, Christian Rödelsperger, et al.
Orphanet Journal of Rare Diseases|September 28, 2024
Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseasesClara D M van Karnebeek, Anne O'Donnell-Luria, Gareth Baynam, et al.
BMC Genomics|November 9, 2015
Crowdsourced direct-to-consumer genomic analysis of a family quartetManuel Corpas, Willy Valdivia-Granda, Nazareth Torres, et al.
European Journal of Human Genetics : EJHG|June 4, 2015
Towards a European consensus for reporting incidental findings during clinical NGS testingJayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, et al.
Pageof 132

Showing results (1171-1180 of 1,318) with videos related to

Sort By:
Pageof 132
Proceedings of the National Academy of Sciences of the United States of America|August 28, 2020
4-Hydroxyacetophenone modulates the actomyosin cytoskeleton to reduce metastasisDarren S Bryan, Melinda Stack, Katarzyna Krysztofiak, et al.
Bone Marrow Transplantation|January 26, 2006
A novel triple purge strategy for eliminating chronic myelogenous leukemia (CML) cells from autograftsH Yang, C Eaves, M de Lima, et al.
Contemporary Clinical Trials|April 14, 2015
Clinical trial management of participant recruitment, enrollment, engagement, and retention in the SMART study using a Marketing and Information Technology (MARKIT) modelAnjali Gupta, Karen J Calfas, Simon J Marshall, et al.
Human Mutation|December 30, 2014
Recessive inheritance of population-specific intronic LINE-1 insertion causes a rotor syndrome phenotypeTatehiro Kagawa, Akira Oka, Yoshinao Kobayashi, et al.
Surgical Endoscopy|June 21, 2015
Structured simulation improves learning of the Fundamental Use of Surgical Energy™ curriculum: a multicenter randomized controlled trialAmin Madani, Yusuke Watanabe, Nicole Townsend, et al.
Briefings in Bioinformatics|October 1, 2015
The digital revolution in phenotypingAnika Oellrich, Nigel Collier, Tudor Groza, et al.
Genome Research|September 3, 2013
Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutationsDaniel M Ibrahim, Peter Hansen, Christian Rödelsperger, et al.
Orphanet Journal of Rare Diseases|September 28, 2024
Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseasesClara D M van Karnebeek, Anne O'Donnell-Luria, Gareth Baynam, et al.
BMC Genomics|November 9, 2015
Crowdsourced direct-to-consumer genomic analysis of a family quartetManuel Corpas, Willy Valdivia-Granda, Nazareth Torres, et al.
European Journal of Human Genetics : EJHG|June 4, 2015
Towards a European consensus for reporting incidental findings during clinical NGS testingJayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, et al.
Pageof 132