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P Brooks

Showing results (791-800 of 854) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 28, 2009
Expression profiling during ocular development identifies 2 Nlz genes with a critical role in optic fissure closureJacob D Brown, Sunit Dutta, Kapil Bharti, et al.
Investigative Ophthalmology & Visual Science|October 3, 2025
Transgene-Induced Chromosomal Rearrangement With Aberrant Human Vascular Endothelial Growth Factor at the Optic Fissure Leads to Uveal Coloboma in MiceYuhong Anna Wang, Ramakrishna P Alur, Vijay Kalaskar, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 25, 2019
Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task ForceArlene V Drack, Virginia Miraldi Utz, Kai Wang, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Neuropsychological phenotypes of 76 individuals with Joubert syndrome evaluated at a single centerAngela C Summers, Joseph Snow, Edythe Wiggs, et al.
Human Molecular Genetics|March 19, 2020
The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphologyJennifer L Sloan, Nathan P Achilly, Madeline L Arnold, et al.
Ophthalmology|October 1, 2011
Ocular manifestations of trichothiodystrophyBrian P Brooks, Amy H Thompson, Janine A Clayton, et al.
Experimental Eye Research|March 26, 2026
Zfp503 haploinsufficiency causes optic nerve coloboma in miceJenna Wong-Fortunato, Benjamin Yang, Louise Lanoue, et al.
Human Molecular Genetics|February 25, 2016
A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant colobomaChunqiao Liu, Sonya A Widen, Kathleen A Williamson, et al.
Investigative Ophthalmology & Visual Science|April 27, 2022
ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt DiseaseZelia Corradi, Manar Salameh, Mubeen Khan, et al.
Circulation|September 12, 2001
Hypertensive end-organ damage and premature mortality are p38 mitogen-activated protein kinase-dependent in a rat model of cardiac hypertrophy and dysfunctionT M Behr, S S Nerurkar, A H Nelson, et al.
Pageof 86

Showing results (791-800 of 854) with videos related to

Sort By:
Pageof 86
Proceedings of the National Academy of Sciences of the United States of America|January 28, 2009
Expression profiling during ocular development identifies 2 Nlz genes with a critical role in optic fissure closureJacob D Brown, Sunit Dutta, Kapil Bharti, et al.
Investigative Ophthalmology & Visual Science|October 3, 2025
Transgene-Induced Chromosomal Rearrangement With Aberrant Human Vascular Endothelial Growth Factor at the Optic Fissure Leads to Uveal Coloboma in MiceYuhong Anna Wang, Ramakrishna P Alur, Vijay Kalaskar, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 25, 2019
Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task ForceArlene V Drack, Virginia Miraldi Utz, Kai Wang, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Neuropsychological phenotypes of 76 individuals with Joubert syndrome evaluated at a single centerAngela C Summers, Joseph Snow, Edythe Wiggs, et al.
Human Molecular Genetics|March 19, 2020
The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphologyJennifer L Sloan, Nathan P Achilly, Madeline L Arnold, et al.
Ophthalmology|October 1, 2011
Ocular manifestations of trichothiodystrophyBrian P Brooks, Amy H Thompson, Janine A Clayton, et al.
Experimental Eye Research|March 26, 2026
Zfp503 haploinsufficiency causes optic nerve coloboma in miceJenna Wong-Fortunato, Benjamin Yang, Louise Lanoue, et al.
Human Molecular Genetics|February 25, 2016
A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant colobomaChunqiao Liu, Sonya A Widen, Kathleen A Williamson, et al.
Investigative Ophthalmology & Visual Science|April 27, 2022
ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt DiseaseZelia Corradi, Manar Salameh, Mubeen Khan, et al.
Circulation|September 12, 2001
Hypertensive end-organ damage and premature mortality are p38 mitogen-activated protein kinase-dependent in a rat model of cardiac hypertrophy and dysfunctionT M Behr, S S Nerurkar, A H Nelson, et al.
Pageof 86