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Brian P Brooks

Showing results (41-50 of 158) with videos related to

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Pigment Cell & Melanoma Research|October 25, 2016
Oculocutaneous albinism type 1: link between mutations, tyrosinase conformational stability, and enzymatic activityMonika B Dolinska, Nicole J Kus, S Katie Farney, et al.
Journal of Pediatric Ophthalmology and Strabismus|May 29, 2010
Absent optic chiasm presenting with horizontal nystagmusDaniel J Salchow, Jürgen Kohlhase, Marijean Miller, et al.
Survey of Ophthalmology|June 21, 2011
Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literatureHema L Ramkumar, Brian P Brooks, Xiaoguang Cao, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Genomics in the era of molecular ophthalmology: reflections on the National Ophthalmic Disease Genotyping Network (eyeGENE)Brian P Brooks, Ian M Macdonald, Santa J Tumminia, et al.
Ophthalmology|January 31, 2016
Ophthalmic Manifestations and Long-Term Visual Outcomes in Patients with Cobalamin C DeficiencyBrian P Brooks, Amy H Thompson, Jennifer L Sloan, et al.
Ophthalmic Genetics|July 17, 2004
A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndromeBrian P Brooks, Sayoko E Moroi, Catherine A Downs, et al.
Plos One|July 9, 2014
aldh7a1 regulates eye and limb development in zebrafishHolly E Babcock, Sunit Dutta, Ramakrishna P Alur, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Genotype-Phenotype Association in ABCA4-Associated RetinopathyMaximilian Pfau, Wadih M Zein, Laryssa A Huryn, et al.
Stem Cell Reports|September 9, 2022
In vitro modeling and rescue of ciliopathy associated with IQCB1/NPHP5 mutations using patient-derived cellsKamil Kruczek, Zepeng Qu, Emily Welby, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 21, 2003
Mutation of the FOXC2 gene in familial distichiasisBrian P Brooks, Susan L Dagenais, Christine C Nelson, et al.
Pageof 16

Showing results (41-50 of 158) with videos related to

Sort By:
Pageof 16
Pigment Cell & Melanoma Research|October 25, 2016
Oculocutaneous albinism type 1: link between mutations, tyrosinase conformational stability, and enzymatic activityMonika B Dolinska, Nicole J Kus, S Katie Farney, et al.
Journal of Pediatric Ophthalmology and Strabismus|May 29, 2010
Absent optic chiasm presenting with horizontal nystagmusDaniel J Salchow, Jürgen Kohlhase, Marijean Miller, et al.
Survey of Ophthalmology|June 21, 2011
Ophthalmic manifestations and histopathology of xeroderma pigmentosum: two clinicopathological cases and a review of the literatureHema L Ramkumar, Brian P Brooks, Xiaoguang Cao, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Genomics in the era of molecular ophthalmology: reflections on the National Ophthalmic Disease Genotyping Network (eyeGENE)Brian P Brooks, Ian M Macdonald, Santa J Tumminia, et al.
Ophthalmology|January 31, 2016
Ophthalmic Manifestations and Long-Term Visual Outcomes in Patients with Cobalamin C DeficiencyBrian P Brooks, Amy H Thompson, Jennifer L Sloan, et al.
Ophthalmic Genetics|July 17, 2004
A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndromeBrian P Brooks, Sayoko E Moroi, Catherine A Downs, et al.
Plos One|July 9, 2014
aldh7a1 regulates eye and limb development in zebrafishHolly E Babcock, Sunit Dutta, Ramakrishna P Alur, et al.
Advances in Experimental Medicine and Biology|July 13, 2023
Genotype-Phenotype Association in ABCA4-Associated RetinopathyMaximilian Pfau, Wadih M Zein, Laryssa A Huryn, et al.
Stem Cell Reports|September 9, 2022
In vitro modeling and rescue of ciliopathy associated with IQCB1/NPHP5 mutations using patient-derived cellsKamil Kruczek, Zepeng Qu, Emily Welby, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 21, 2003
Mutation of the FOXC2 gene in familial distichiasisBrian P Brooks, Susan L Dagenais, Christine C Nelson, et al.
Pageof 16