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

Ruth M Arkell

Showing results (31-40 of 37) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 37 results.
Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Plos One|March 8, 2013
Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseGeorgina Caruana, Peter G Farlie, Adam H Hart, et al.
Elife|May 5, 2021
Disruption of entire <i>Cables2</i> locus leads to embryonic lethality by diminished <i>Rps21</i> gene expression and enhanced p53 pathwayTra Thi Huong Dinh, Hiroyoshi Iseki, Seiya Mizuno, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2005
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screenDebora Bogani, Catherine Willoughby, Jennifer Davies, et al.
Plos Genetics|February 6, 2013
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesDawn E Watkins-Chow, Joanna Cooke, Ruth Pidsley, et al.
American Journal of Human Genetics|August 9, 2020
Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic DataSimon Easteal, Ruth M Arkell, Renzo F Balboa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 24, 2026
Expanding the phenotypic spectrum associated with ZIC1 variants: a neurodevelopmental disorder with and without craniosynostosisLaura M Watts, Michelle S M Chang, Elizabeth Lewis-Orr, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Plos One|March 8, 2013
Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseGeorgina Caruana, Peter G Farlie, Adam H Hart, et al.
Elife|May 5, 2021
Disruption of entire <i>Cables2</i> locus leads to embryonic lethality by diminished <i>Rps21</i> gene expression and enhanced p53 pathwayTra Thi Huong Dinh, Hiroyoshi Iseki, Seiya Mizuno, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2005
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screenDebora Bogani, Catherine Willoughby, Jennifer Davies, et al.
Plos Genetics|February 6, 2013
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesDawn E Watkins-Chow, Joanna Cooke, Ruth Pidsley, et al.
American Journal of Human Genetics|August 9, 2020
Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic DataSimon Easteal, Ruth M Arkell, Renzo F Balboa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 24, 2026
Expanding the phenotypic spectrum associated with ZIC1 variants: a neurodevelopmental disorder with and without craniosynostosisLaura M Watts, Michelle S M Chang, Elizabeth Lewis-Orr, et al.
Pageof 4