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Brian P Brooks

Showing results (111-120 of 158) with videos related to

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Cell Reports|July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 MutationsHiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, et al.
Communications Medicine|April 24, 2025
Artificial intelligence assisted clinical fluorescence imaging achieves in vivo cellular resolution comparable to adaptive optics ophthalmoscopyJoanne Li, Jianfei Liu, Vineeta Das, et al.
Ophthalmology Science|November 7, 2022
Investigating Determinants and Evaluating Deep Learning Training Approaches for Visual Acuity in Foveal HypoplasiaVolha V Malechka, Dat Duong, Keyla D Bordonada, et al.
Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Analysis of ocular hypopigmentation in Rab38cht/cht miceBrian P Brooks, Denise M Larson, Chi-Chao Chan, et al.
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.
Journal of the American Academy of Dermatology|January 3, 2009
Skin cancers, blindness, and anterior tongue mass in African brothersPriya Mahindra, John J DiGiovanna, Deborah Tamura, et al.
Pageof 16

Showing results (111-120 of 158) with videos related to

Sort By:
Pageof 16
Cell Reports|July 13, 2017
In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 MutationsHiroko Shimada, Quanlong Lu, Christine Insinna-Kettenhofen, et al.
Communications Medicine|April 24, 2025
Artificial intelligence assisted clinical fluorescence imaging achieves in vivo cellular resolution comparable to adaptive optics ophthalmoscopyJoanne Li, Jianfei Liu, Vineeta Das, et al.
Ophthalmology Science|November 7, 2022
Investigating Determinants and Evaluating Deep Learning Training Approaches for Visual Acuity in Foveal HypoplasiaVolha V Malechka, Dat Duong, Keyla D Bordonada, et al.
Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Analysis of ocular hypopigmentation in Rab38cht/cht miceBrian P Brooks, Denise M Larson, Chi-Chao Chan, et al.
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.
Journal of the American Academy of Dermatology|January 3, 2009
Skin cancers, blindness, and anterior tongue mass in African brothersPriya Mahindra, John J DiGiovanna, Deborah Tamura, et al.
Pageof 16