Cargando…

Comment on “Identification of Novel G Protein–Coupled Receptor 143 Ligands as Pharmacologic Tools for Investigating X-Linked Ocular Albinism”

Detalles Bibliográficos
Autores principales:	McKay, Brian S., Lynch, Ronald M., Stamer, W. Daniel
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Association for Research in Vision and Ophthalmology 2017
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600132/ https://www.ncbi.nlm.nih.gov/pubmed/28910826 http://dx.doi.org/10.1167/iovs.17-22660

Ejemplares similares

Author Response: Comment on “Identification of Novel G Protein–Coupled Receptor 143 Ligands as Pharmacologic Tools for Investigating X-Linked Ocular Albinism”
por: De Filippo, Elisabetta, et al.
Publicado: (2017)

Identification of Novel G Protein–Coupled Receptor 143 Ligands as Pharmacologic Tools for Investigating X-Linked Ocular Albinism
por: De Filippo, Elisabetta, et al.
Publicado: (2017)

Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism
por: Fang, Shaohua, et al.
Publicado: (2008)

A novel GPR143 mutation in a Chinese family with X-linked ocular albinism type 1
por: Gao, Xuhui, et al.
Publicado: (2020)

GPR143 mutations in Chinese patients with ocular albinism type 1
por: Jia, Xiuhua, et al.
Publicado: (2017)

Deep intronic GPR143 mutation in a Japanese family with ocular albinism
por: Naruto, Takuya, et al.
Publicado: (2015)

Comments on: Choroidal and retinal thickness variations in ocular albinism
por: Gioia, Marco, et al.
Publicado: (2023)

Response to comments on: Choroidal and retinal thickness variations in ocular albinism
por: Venkatesh, Ramesh, et al.
Publicado: (2023)

A Novel Nonsense Mutation of the GPR143 Gene Identified in a Chinese Pedigree with Ocular Albinism
por: Yan, Naihong, et al.
Publicado: (2012)

Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinism
por: Zou, Xuan, et al.
Publicado: (2017)

Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
por: Chan, Hwei Wuen, et al.
Publicado: (2021)

Retinal Vasoproliferative Tumor in Ocular Albinism
por: Alsakran, Wael A., et al.
Publicado: (2020)

Comment on: Photosensitivity and filter efficacy in albinism
por: Singh, Mahendra, et al.
Publicado: (2024)

The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells
por: Palmisano, Ilaria, et al.
Publicado: (2008)

The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells
por: Palmisano, Ilaria, et al.
Publicado: (2017)

Ocular albinism with bilateral ocular coloboma – A rare association
por: Raval, Vishal, et al.
Publicado: (2019)

L-DOPA Is an Endogenous Ligand for OA1
por: Lopez, Vanessa M, et al.
Publicado: (2008)

Albinism: Particular Attention to the Ocular Motor System
por: Hertle, Richard W.
Publicado: (2013)

Choroidal and retinal thickness variations in ocular albinism
por: Venkatesh, Ramesh, et al.
Publicado: (2022)

Ophthalmological Manifestations of Oculocutaneous and Ocular Albinism: Current Perspectives
por: Neveu, Magella M, et al.
Publicado: (2022)

CRISPR-AsCas12a Efficiently Corrects a GPR143 Intronic Mutation in Induced Pluripotent Stem Cells from an Ocular Albinism Patient
por: Torriano, Simona, et al.
Publicado: (2022)

A previously unidentified deletion in G protein-coupled receptor 143 causing X-linked congenital nystagmus in a Chinese family
por: Liu, Jing, et al.
Publicado: (2016)

Albinism, Partial Albinism, and Vitiligo
por: Kugelman, Thomas P., et al.
Publicado: (1961)

Ocular Albinism Type 1 Regulates Melanogenesis in Mouse Melanocytes
por: Chen, Tianzhi, et al.
Publicado: (2016)

Phenotypic variations in ocular features among siblings with oculocutaneous albinism
por: Bhate, Manjushree, et al.
Publicado: (2022)

GNAI3: Another Candidate Gene to Screen in Persons with Ocular Albinism
por: Young, Alejandra, et al.
Publicado: (2016)

A Molecular Link between Albinism and Visual Deficits
por: Gross, Liza
Publicado: (2008)

Eight previously unidentified mutations found in the OA1 ocular albinism gene
por: Mayeur, Hélène, et al.
Publicado: (2006)

Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism
por: Renugadevi, Kathirvel, et al.
Publicado: (2010)

A Case of a Newborn with Agenesis of the Corpus Callosum Complicated with Ocular Albinism
por: Miki, Michiko, et al.
Publicado: (2016)

Oculocutaneous albinism
por: Grønskov, Karen, et al.
Publicado: (2007)

The Many Faces of G Protein-Coupled Receptor 143, an Atypical Intracellular Receptor
por: Bueschbell, Beatriz, et al.
Publicado: (2022)

Ligand-Free Signaling of G-Protein-Coupled Receptors: Physiology, Pharmacology, and Genetics
por: Sadee, Wolfgang
Publicado: (2023)

Brown's syndrome with ocular albinism: Case report of a rare presentation and literature review
por: Nambiar, Soumya, et al.
Publicado: (2015)

Ocular Albinism Type 1 Regulates Deltamethrin Tolerance in Lymantria dispar and Drosophila melanogaster
por: Sun, Lili, et al.
Publicado: (2019)

Author response to ” Comment on: Photosensitivity and filter efficacy in albinism” JOPTOM-D-23-00096
por: Jordana, Joaquim Torner, et al.
Publicado: (2024)

Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinism
por: Preising, Markus N., et al.
Publicado: (2011)

GPR143 Gene Mutations in Five Chinese Families with X-linked Congenital Nystagmus
por: Han, Ruifang, et al.
Publicado: (2015)

Albin, Vasconcelos, Elizondo
por: Albin Zychlisky, Enrique, 1954-
Publicado: (1995)

Albinism: Images in ophthalmology
por: Sreelatha, O. K., et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_pdekufo1vr7eicms33esar048e