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

Veronica van Heyningen

Showing results (41-50 of 82) with videos related to

Pageof 9
Sort By:
Neuroimage|December 20, 2003
Quantitative MR image analysis in subjects with defects in the PAX6 geneSamantha L Free, Tejal N Mitchell, Kathleen A Williamson, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single centerChristina Gerth-Kahlert, Kathleen Williamson, Morad Ansari, et al.
Developmental Biology|October 4, 2006
Long-range downstream enhancers are essential for Pax6 expressionDirk A Kleinjan, Anne Seawright, Sebastien Mella, et al.
American Journal of Human Genetics|January 20, 2007
GDF6, a novel locus for a spectrum of ocular developmental anomaliesMika Asai-Coakwell, Curtis R French, Karyn M Berry, et al.
International Journal of Audiology|April 25, 2007
Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutationDoris-Eva Bamiou, Nicole G Campbell, Frank E Musiek, et al.
Annals of Clinical and Translational Neurology|May 28, 2016
PAX6, brain structure and function in human adults: advanced MRI in aniridiaMahinda Yogarajah, Mar Matarin, Christian Vollmar, et al.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
Plos Genetics|June 2, 2015
Functional assessment of disease-associated regulatory variants in vivo using a versatile dual colour transgenesis strategy in zebrafishShipra Bhatia, Christopher T Gordon, Robert G Foster, et al.
Plos Genetics|January 30, 2013
Sequencing of Pax6 loci from the elephant shark reveals a family of Pax6 genes in vertebrate genomes, forged by ancient duplications and divergencesVydianathan Ravi, Shipra Bhatia, Philippe Gautier, et al.
Human Molecular Genetics|January 5, 2002
Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and colobomaRobyn V Jamieson, Rahat Perveen, Bronwyn Kerr, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
Neuroimage|December 20, 2003
Quantitative MR image analysis in subjects with defects in the PAX6 geneSamantha L Free, Tejal N Mitchell, Kathleen A Williamson, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single centerChristina Gerth-Kahlert, Kathleen Williamson, Morad Ansari, et al.
Developmental Biology|October 4, 2006
Long-range downstream enhancers are essential for Pax6 expressionDirk A Kleinjan, Anne Seawright, Sebastien Mella, et al.
American Journal of Human Genetics|January 20, 2007
GDF6, a novel locus for a spectrum of ocular developmental anomaliesMika Asai-Coakwell, Curtis R French, Karyn M Berry, et al.
International Journal of Audiology|April 25, 2007
Auditory and verbal working memory deficits in a child with congenital aniridia due to a PAX6 mutationDoris-Eva Bamiou, Nicole G Campbell, Frank E Musiek, et al.
Annals of Clinical and Translational Neurology|May 28, 2016
PAX6, brain structure and function in human adults: advanced MRI in aniridiaMahinda Yogarajah, Mar Matarin, Christian Vollmar, et al.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
Plos Genetics|June 2, 2015
Functional assessment of disease-associated regulatory variants in vivo using a versatile dual colour transgenesis strategy in zebrafishShipra Bhatia, Christopher T Gordon, Robert G Foster, et al.
Plos Genetics|January 30, 2013
Sequencing of Pax6 loci from the elephant shark reveals a family of Pax6 genes in vertebrate genomes, forged by ancient duplications and divergencesVydianathan Ravi, Shipra Bhatia, Philippe Gautier, et al.
Human Molecular Genetics|January 5, 2002
Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and colobomaRobyn V Jamieson, Rahat Perveen, Bronwyn Kerr, et al.
Pageof 9