Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene-Reference-Cited by-同舟云学术

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Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene

Published:2019-03-08 Issue:1 Volume:19 Page:
ISSN:1471-2148
Container-title:BMC Evolutionary Biology
language:en
Short-container-title:BMC Evol Biol

Author:

Seemab Suman,Pervaiz Nashaiman,Zehra Rabail,Anwar Saneela,Bao Yiming,Abbasi Amir Ali

Funder

Scientific Research and Technology Development Program of Guangxi

13th Five-year Informatization Plan of Chinese Academy of Sciences

Publisher

Springer Science and Business Media LLC

Subject

Ecology, Evolution, Behavior and Systematics

Link

http://link.springer.com/content/pdf/10.1186/s12862-019-1400-9.pdf

Reference56 articles.

1. Venkatakrishnan A, Deupi X, Lebon G, Tate CG, Schertler GF, Babu MM. Molecular signatures of G-protein-coupled receptors. Nature. 2013;494(7436):185.

2. Millar RP, Newton CL. The year in G protein-coupled receptor research. Mol Endocrinol. 2010;24(1):261–74.

3. Terrillon S, Bouvier M. Roles of G-protein-coupled receptor dimerization: from ontogeny to signalling regulation. EMBO Rep. 2004;5(1):30–4.

4. Fredriksson R, Lagerström MC, Lundin L-G, Schiöth HB. The G-protein-coupled receptors in the human genome form five main families. Phylogenetic analysis, paralogon groups, and fingerprints. Mol Pharmacol. 2003;63(6):1256–72.

5. Hanyaloglu AC, Zastrow M. Regulation of GPCRs by endocytic membrane trafficking and its potential implications. Annu Rev Pharmacol Toxicol. 2008;48:537–68.

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1. FZD4 in a Large Chinese Population With Familial Exudative Vitreoretinopathy: Molecular Characteristics and Clinical Manifestations;Investigative Opthalmology & Visual Science;2022-04-08

2. Ocular phenotype and genetical analysis in patients with retinopathy of prematurity;BMC Ophthalmology;2022-01-12

3. Whole-Gene Deletions of FZD4 Cause Familial Exudative Vitreoretinopathy;Genes;2021-06-27

4. Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR);Ophthalmic Genetics;2020-12-10

5. Molecular evolutionary and structural analysis of human UCHL1 gene demonstrates the relevant role of intragenic epistasis in Parkinson’s disease and other neurological disorders;BMC Evolutionary Biology;2020-10-07

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