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

R Wilcox

Showing results (601-610 of 627) with videos related to

Pageof 63
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2016
The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastatElfrida R Benjamin, Maria Cecilia Della Valle, Xiaoyang Wu, et al.
Global Change Biology|October 10, 2023
Accounting for herbaceous communities in process-based models will advance our understanding of "grassy" ecosystemsKevin R Wilcox, Anping Chen, Meghan L Avolio, et al.
The Pediatric Infectious Disease Journal|October 1, 2021
Applicability of the GAIA Maternal and Neonatal Outcome Case Definitions for the Evaluation of Adverse Events Following Vaccination in Pregnancy in High-income CountriesGabriella Watson, Caitlin Dodd, Flor M Munoz, et al.
The Lancet. Child & Adolescent Health|November 20, 2023
Vosoritide therapy in children with achondroplasia aged 3-59 months: a multinational, randomised, double-blind, placebo-controlled, phase 2 trialRavi Savarirayan, William R Wilcox, Paul Harmatz, et al.
Med (New York, N.Y.)|December 31, 2024
Sustained growth-promoting effects of vosoritide in children with achondroplasia from an ongoing phase 3 extension studyRavi Savarirayan, Melita Irving, William R Wilcox, et al.
Nature Genetics|November 11, 2008
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golginHans Christian Hennies, Uwe Kornak, Haikuo Zhang, et al.
American Journal of Human Genetics|July 7, 2009
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39Julie M Schultz, Shaheen N Khan, Zubair M Ahmed, et al.
Global Change Biology|October 29, 2018
Ambient changes exceed treatment effects on plant species abundance in global change experimentsJ Adam Langley, Samantha K Chapman, Kimberly J La Pierre, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
Nature Genetics|February 19, 2002
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell functionKiyoto Kurima, Linda M Peters, Yandan Yang, et al.
Pageof 63

Showing results (601-610 of 627) with videos related to

Sort By:
Pageof 63
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 23, 2016
The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastatElfrida R Benjamin, Maria Cecilia Della Valle, Xiaoyang Wu, et al.
Global Change Biology|October 10, 2023
Accounting for herbaceous communities in process-based models will advance our understanding of "grassy" ecosystemsKevin R Wilcox, Anping Chen, Meghan L Avolio, et al.
The Pediatric Infectious Disease Journal|October 1, 2021
Applicability of the GAIA Maternal and Neonatal Outcome Case Definitions for the Evaluation of Adverse Events Following Vaccination in Pregnancy in High-income CountriesGabriella Watson, Caitlin Dodd, Flor M Munoz, et al.
The Lancet. Child & Adolescent Health|November 20, 2023
Vosoritide therapy in children with achondroplasia aged 3-59 months: a multinational, randomised, double-blind, placebo-controlled, phase 2 trialRavi Savarirayan, William R Wilcox, Paul Harmatz, et al.
Med (New York, N.Y.)|December 31, 2024
Sustained growth-promoting effects of vosoritide in children with achondroplasia from an ongoing phase 3 extension studyRavi Savarirayan, Melita Irving, William R Wilcox, et al.
Nature Genetics|November 11, 2008
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golginHans Christian Hennies, Uwe Kornak, Haikuo Zhang, et al.
American Journal of Human Genetics|July 7, 2009
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39Julie M Schultz, Shaheen N Khan, Zubair M Ahmed, et al.
Global Change Biology|October 29, 2018
Ambient changes exceed treatment effects on plant species abundance in global change experimentsJ Adam Langley, Samantha K Chapman, Kimberly J La Pierre, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
Nature Genetics|February 19, 2002
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell functionKiyoto Kurima, Linda M Peters, Yandan Yang, et al.
Pageof 63