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

David Sargan

Showing results (11-20 of 21) with videos related to

Pageof 3
Sort By:
BMC Veterinary Research|May 24, 2019
Health-related welfare prioritisation of canine disorders using electronic health records in primary care practice in the UKJennifer F Summers, Dan G O'Neill, David Church, et al.
The Veterinary Record|November 4, 2008
LUPA - studying human diseases using dog geneticsHannah Copeland, Jo Dukes-McEwan, David Sargan, et al.
Plos One|July 8, 2022
Development and application of a next-generation sequencing protocol and bioinformatics pipeline for the comprehensive analysis of the canine immunoglobulin repertoireJonah N Cullen, Jolyon Martin, Albert J Vilella, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 11, 2005
Karyotype of canine soft tissue sarcomas: a multi-colour, multi-species approach to canine chromosome paintingBruce S Milne, Tess Hoather, Patricia C M O'Brien, et al.
Genes|November 27, 2021
A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (<i>BBS2</i>) Leads to a Novel Syndromic Retinal Degeneration in the Shetland SheepdogRebekkah J Hitti-Malin, Louise M Burmeister, Frode Lingaas, et al.
Veterinary Ophthalmology|November 5, 2011
ADAMTS17 mutation associated with primary lens luxation is widespread among breedsDavid Gould, Louise Pettitt, Bryan McLaughlin, et al.
BMC Genetics|September 7, 2020
A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogsRebekkah J Hitti-Malin, Louise M Burmeister, Sally L Ricketts, et al.
Scientific Reports|April 6, 2018
Prevalence, duration and risk factors for appendicular osteoarthritis in a UK dog population under primary veterinary careKatharine L Anderson, Dan G O'Neill, David C Brodbelt, et al.
European Journal of Human Genetics : EJHG|May 5, 2005
Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndromeIsabella Borg, Kristine Freude, Sabine Kübart, et al.
Genes|May 24, 2019
Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes <i>NECAP1</i> as a Novel Candidate Gene for Retinal DegenerationRebekkah J Hitti, James A C Oliver, Ellen C Schofield, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
BMC Veterinary Research|May 24, 2019
Health-related welfare prioritisation of canine disorders using electronic health records in primary care practice in the UKJennifer F Summers, Dan G O'Neill, David Church, et al.
The Veterinary Record|November 4, 2008
LUPA - studying human diseases using dog geneticsHannah Copeland, Jo Dukes-McEwan, David Sargan, et al.
Plos One|July 8, 2022
Development and application of a next-generation sequencing protocol and bioinformatics pipeline for the comprehensive analysis of the canine immunoglobulin repertoireJonah N Cullen, Jolyon Martin, Albert J Vilella, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 11, 2005
Karyotype of canine soft tissue sarcomas: a multi-colour, multi-species approach to canine chromosome paintingBruce S Milne, Tess Hoather, Patricia C M O'Brien, et al.
Genes|November 27, 2021
A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (<i>BBS2</i>) Leads to a Novel Syndromic Retinal Degeneration in the Shetland SheepdogRebekkah J Hitti-Malin, Louise M Burmeister, Frode Lingaas, et al.
Veterinary Ophthalmology|November 5, 2011
ADAMTS17 mutation associated with primary lens luxation is widespread among breedsDavid Gould, Louise Pettitt, Bryan McLaughlin, et al.
BMC Genetics|September 7, 2020
A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogsRebekkah J Hitti-Malin, Louise M Burmeister, Sally L Ricketts, et al.
Scientific Reports|April 6, 2018
Prevalence, duration and risk factors for appendicular osteoarthritis in a UK dog population under primary veterinary careKatharine L Anderson, Dan G O'Neill, David C Brodbelt, et al.
European Journal of Human Genetics : EJHG|May 5, 2005
Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndromeIsabella Borg, Kristine Freude, Sabine Kübart, et al.
Genes|May 24, 2019
Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes <i>NECAP1</i> as a Novel Candidate Gene for Retinal DegenerationRebekkah J Hitti, James A C Oliver, Ellen C Schofield, et al.
Pageof 3