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Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society
|
December 29, 2023
Gene therapy in bestrophinopathies: Insights from preclinical studies in preparation for clinical trials
Alessia Amato, Nida Wongchaisuwat, Andrew Lamborn, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
December 22, 2022
Two-Color Dark-Adapted Perimetry Implemented With a Commercially Available Perimeter to Characterize Rod-Pathway Sensitivity
Austin D Igelman, Jason C Park, Robert A Hyde, et al.
Ocular Oncology and Pathology
|
April 13, 2019
Metastatic Cutaneous Melanoma Presenting with Choroidal Metastasis Simulating Primary Uveal Melanoma
Lesley Everett, Bertil E Damato, Michele M Bloomer, et al.
Molecular and Cellular Biology
|
July 30, 2014
Absence of a red blood cell phenotype in mice with hematopoietic deficiency of SEC23B
Rami Khoriaty, Matthew P Vasievich, Morgan Jones, et al.
British Journal of Haematology
|
May 24, 2019
Genome-wide linkage analysis and whole-exome sequencing identifies an ITGA2B mutation in a family with thrombocytopenia
Rami Khoriaty, Ayse B Ozel, Shweta Ramdas, et al.
American Journal of Ophthalmology Case Reports
|
January 1, 2024
Optical coherence tomography angiography of choroidal neovascularization in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)
Nida Wongchaisuwat, Jie Wang, Paul Yang, et al.
Scientific Reports
|
June 15, 2016
Pancreatic SEC23B deficiency is sufficient to explain the perinatal lethality of germline SEC23B deficiency in mice
Rami Khoriaty, Lesley Everett, Jennifer Chase, et al.
Molecular Biology of the Cell
|
May 26, 2017
SEC23B is required for pancreatic acinar cell function in adult mice
Rami Khoriaty, Nancy Vogel, Mark J Hoenerhoff, et al.
Ophthalmic Genetics
|
January 30, 2024
A proposal for an updated staging system for LCHADD retinopathy
Nida Wongchaisuwat, Melanie B Gillingham, Paul Yang, et al.
American Journal of Human Genetics
|
January 3, 2009
Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS
Clement Y Chow, John E Landers, Sarah K Bergren, et al.
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of 3
Search research articles
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Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society
|
December 29, 2023
Gene therapy in bestrophinopathies: Insights from preclinical studies in preparation for clinical trials
Alessia Amato, Nida Wongchaisuwat, Andrew Lamborn, et al.
Ophthalmic Surgery, Lasers & Imaging Retina
|
December 22, 2022
Two-Color Dark-Adapted Perimetry Implemented With a Commercially Available Perimeter to Characterize Rod-Pathway Sensitivity
Austin D Igelman, Jason C Park, Robert A Hyde, et al.
Ocular Oncology and Pathology
|
April 13, 2019
Metastatic Cutaneous Melanoma Presenting with Choroidal Metastasis Simulating Primary Uveal Melanoma
Lesley Everett, Bertil E Damato, Michele M Bloomer, et al.
Molecular and Cellular Biology
|
July 30, 2014
Absence of a red blood cell phenotype in mice with hematopoietic deficiency of SEC23B
Rami Khoriaty, Matthew P Vasievich, Morgan Jones, et al.
British Journal of Haematology
|
May 24, 2019
Genome-wide linkage analysis and whole-exome sequencing identifies an ITGA2B mutation in a family with thrombocytopenia
Rami Khoriaty, Ayse B Ozel, Shweta Ramdas, et al.
American Journal of Ophthalmology Case Reports
|
January 1, 2024
Optical coherence tomography angiography of choroidal neovascularization in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)
Nida Wongchaisuwat, Jie Wang, Paul Yang, et al.
Scientific Reports
|
June 15, 2016
Pancreatic SEC23B deficiency is sufficient to explain the perinatal lethality of germline SEC23B deficiency in mice
Rami Khoriaty, Lesley Everett, Jennifer Chase, et al.
Molecular Biology of the Cell
|
May 26, 2017
SEC23B is required for pancreatic acinar cell function in adult mice
Rami Khoriaty, Nancy Vogel, Mark J Hoenerhoff, et al.
Ophthalmic Genetics
|
January 30, 2024
A proposal for an updated staging system for LCHADD retinopathy
Nida Wongchaisuwat, Melanie B Gillingham, Paul Yang, et al.
American Journal of Human Genetics
|
January 3, 2009
Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS
Clement Y Chow, John E Landers, Sarah K Bergren, et al.
Page
of 3