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Robyn V Jamieson

Showing results (41-50 of 78) with videos related to

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Clinical & Experimental Ophthalmology|March 5, 2024
Natural history and biomarkers of KCNV2-associated retinopathyDhimas H Sakti, Elisa E Cornish, Haipha Ali, et al.
Human Molecular Genetics|March 7, 2003
A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA bindingMary F Lyon, Robyn V Jamieson, Rahat Perveen, et al.
Development (Cambridge, England)|April 12, 2008
Dkk1 and Wnt3 interact to control head morphogenesis in the mouseSamara L Lewis, Poh-Lynn Khoo, R Andrea De Young, et al.
Gene Expression Patterns : GEP|January 24, 2007
Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse developmentStephen J Palmer, Enoch S E Tay, Nicole Santucci, et al.
Ophthalmic Epidemiology|September 14, 2022
Eye Abnormalities in Children with Fetal Alcohol Spectrum Disorders: A Systematic ReviewTracey W Tsang, Amy Finlay-Jones, Kerrin Perry, 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.
JAMA Ophthalmology|November 2, 2013
Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrumSimon E Skalicky, Andrew J R White, John R Grigg, et al.
American Journal of Ophthalmology|January 31, 2015
Primary congenital glaucoma outcomes: lessons from 23 years of follow-upSophia L Zagora, Charlotte L Funnell, Frank J Martin, et al.
Clinical & Experimental Ophthalmology|July 26, 2014
Value of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patientsIvan Prokudin, Dong Li, Sijie He, et al.
Journal of Personalized Medicine|March 25, 2022
Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic <i>RPGR</i> Variant Assessment for Therapy SuitabilityFidelle Chahine Karam, To Ha Loi, Alan Ma, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
Clinical & Experimental Ophthalmology|March 5, 2024
Natural history and biomarkers of KCNV2-associated retinopathyDhimas H Sakti, Elisa E Cornish, Haipha Ali, et al.
Human Molecular Genetics|March 7, 2003
A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA bindingMary F Lyon, Robyn V Jamieson, Rahat Perveen, et al.
Development (Cambridge, England)|April 12, 2008
Dkk1 and Wnt3 interact to control head morphogenesis in the mouseSamara L Lewis, Poh-Lynn Khoo, R Andrea De Young, et al.
Gene Expression Patterns : GEP|January 24, 2007
Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse developmentStephen J Palmer, Enoch S E Tay, Nicole Santucci, et al.
Ophthalmic Epidemiology|September 14, 2022
Eye Abnormalities in Children with Fetal Alcohol Spectrum Disorders: A Systematic ReviewTracey W Tsang, Amy Finlay-Jones, Kerrin Perry, 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.
JAMA Ophthalmology|November 2, 2013
Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrumSimon E Skalicky, Andrew J R White, John R Grigg, et al.
American Journal of Ophthalmology|January 31, 2015
Primary congenital glaucoma outcomes: lessons from 23 years of follow-upSophia L Zagora, Charlotte L Funnell, Frank J Martin, et al.
Clinical & Experimental Ophthalmology|July 26, 2014
Value of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patientsIvan Prokudin, Dong Li, Sijie He, et al.
Journal of Personalized Medicine|March 25, 2022
Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic <i>RPGR</i> Variant Assessment for Therapy SuitabilityFidelle Chahine Karam, To Ha Loi, Alan Ma, et al.
Pageof 8