Literature DB >> 34584051

Retinal Degeneration Secondary to MERTK Mutations: Potential Candidate for Gene Therapy.

John H Shen-Sampas, Stephanie Duret, Jacque L Duncan.   

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Year:  2021        PMID： 34584051      PMCID： PMC8486302          DOI： 10.1097/IIO.0000000000000374

Source DB:  PubMed          Journal:  Int Ophthalmol Clin        ISSN： 0020-8167


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  29 in total

1.  Gene Therapy for MERTK-Associated Retinal Degenerations.

Authors:  Matthew M LaVail; Douglas Yasumura; Michael T Matthes; Haidong Yang; William W Hauswirth; Wen-Tao Deng; Douglas Vollrath
Journal:  Adv Exp Med Biol       Date:  2016       Impact factor: 2.622

2.  Essential role for MFG-E8 as ligand for alphavbeta5 integrin in diurnal retinal phagocytosis.

Authors:  Emeline F Nandrot; Monika Anand; Dena Almeida; Kamran Atabai; Dean Sheppard; Silvia C Finnemann
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-09       Impact factor: 11.205

Review 3.  A Comprehensive Review of Mutations in the MERTK Proto-Oncogene.

Authors:  Célia Parinot; Emeline F Nandrot
Journal:  Adv Exp Med Biol       Date:  2016       Impact factor: 2.622

4.  Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.

Authors:  A Gal; Y Li; D A Thompson; J Weir; U Orth; S G Jacobson; E Apfelstedt-Sylla; D Vollrath
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

5.  Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat.

Authors:  P M D'Cruz; D Yasumura; J Weir; M T Matthes; H Abderrahim; M M LaVail; D Vollrath
Journal:  Hum Mol Genet       Date:  2000-03-01       Impact factor: 6.150

Review 6.  Phagocytosis of retinal rod and cone photoreceptors.

Authors:  Brian M Kevany; Krzysztof Palczewski
Journal:  Physiology (Bethesda)       Date:  2010-02

7.  A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases.

Authors:  Elsebet Ostergaard; Morten Duno; Mustafa Batbayli; Kaj Vilhelmsen; Thomas Rosenberg
Journal:  Mol Vis       Date:  2011-06-04       Impact factor: 2.367

8.  Bi-Allelic Pathogenic Variations in MERTK Including Deletions Are Associated with an Early Onset Progressive Form of Retinitis Pigmentosa.

Authors:  Cathrine Jespersgaard; Mette Bertelsen; Farah Arif; Helene Gry Gellert-Kristensen; Mingyan Fang; Hanne Jensen; Thomas Rosenberg; Zeynep Tümer; Lisbeth Birk Møller; Karen Brøndum-Nielsen; Karen Grønskov
Journal:  Genes (Basel)       Date:  2020-12-18       Impact factor: 4.096

9.  Inherited retinal dystrophy in the rat.

Authors:  J E DOWLING; R L SIDMAN
Journal:  J Cell Biol       Date:  1962-07       Impact factor: 10.539

10.  The role of the pigment epithelium in the etiology of inherited retinal dystrophy in the rat.

Authors:  D Bok; M O Hall
Journal:  J Cell Biol       Date:  1971-06       Impact factor: 10.539
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