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

Richard Holt

Showing results (131-140 of 146) with videos related to

Pageof 15
Sort By:
Nature Communications|October 25, 2024
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye developmentFabiola Ceroni, Munevver B Cicekdal, Richard Holt, et al.
Ophthalmic Genetics|January 25, 2023
Individuals with heterozygous variants in the Wnt-signalling pathway gene <i>FZD5</i> delineate a phenotype characterized by isolated coloboma and variable expressivityRichard Holt, David Goudie, Alejandra Damián Verde, et al.
BMC Nephrology|September 17, 2021
Clinical practice guidelines standardisation of immunosuppressive and anti-infective drug regimens in UK paediatric renal transplantation: the harmonisation programmeJan Dudley, Martin Christian, Alice Andrews, et al.
Nature Genetics|May 20, 2003
Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthmaYouming Zhang, Nicholas I Leaves, Gavin G Anderson, et al.
Trials|February 13, 2016
Evaluating the clinical and cost effectiveness of a behaviour change intervention for lowering cardiovascular disease risk for people with severe mental illnesses in primary care (PRIMROSE study): study protocol for a cluster randomised controlled trialDavid Osborn, Alexandra Burton, Kate Walters, et al.
European Journal of Human Genetics : EJHG|April 29, 2025
GJA8-associated developmental eye disorders: a new multicentre study highlights mutational hotspots and genotype-phenotype correlationsSolomon S Merepa, Linda M Reis, Alejandra Damián, et al.
Nature Genetics|October 21, 2003
Positional cloning of a novel gene influencing asthma from chromosome 2q14Maxine Allen, Andrea Heinzmann, Emiko Noguchi, et al.
British Journal of Sports Medicine|March 4, 2026
Harmful anachronism: World Athletics reinstates gene testing to participate in women's competitionsSilvia Camporesi, Shane M Heffernan, Pascal Borry, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 24, 2023
Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor betaVéronique Caron, Nicolas Chassaing, Nicola Ragge, et al.
Pageof 15

Showing results (131-140 of 146) with videos related to

Sort By:
Pageof 15
Nature Communications|October 25, 2024
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye developmentFabiola Ceroni, Munevver B Cicekdal, Richard Holt, et al.
Ophthalmic Genetics|January 25, 2023
Individuals with heterozygous variants in the Wnt-signalling pathway gene <i>FZD5</i> delineate a phenotype characterized by isolated coloboma and variable expressivityRichard Holt, David Goudie, Alejandra Damián Verde, et al.
BMC Nephrology|September 17, 2021
Clinical practice guidelines standardisation of immunosuppressive and anti-infective drug regimens in UK paediatric renal transplantation: the harmonisation programmeJan Dudley, Martin Christian, Alice Andrews, et al.
Nature Genetics|May 20, 2003
Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthmaYouming Zhang, Nicholas I Leaves, Gavin G Anderson, et al.
Trials|February 13, 2016
Evaluating the clinical and cost effectiveness of a behaviour change intervention for lowering cardiovascular disease risk for people with severe mental illnesses in primary care (PRIMROSE study): study protocol for a cluster randomised controlled trialDavid Osborn, Alexandra Burton, Kate Walters, et al.
European Journal of Human Genetics : EJHG|April 29, 2025
GJA8-associated developmental eye disorders: a new multicentre study highlights mutational hotspots and genotype-phenotype correlationsSolomon S Merepa, Linda M Reis, Alejandra Damián, et al.
Nature Genetics|October 21, 2003
Positional cloning of a novel gene influencing asthma from chromosome 2q14Maxine Allen, Andrea Heinzmann, Emiko Noguchi, et al.
British Journal of Sports Medicine|March 4, 2026
Harmful anachronism: World Athletics reinstates gene testing to participate in women's competitionsSilvia Camporesi, Shane M Heffernan, Pascal Borry, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 24, 2023
Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor betaVéronique Caron, Nicolas Chassaing, Nicola Ragge, et al.
Pageof 15