163 related articles for article (PubMed ID: 26427420)
1. A Comprehensive Review of Mutations in the MERTK Proto-Oncogene.
Parinot C; Nandrot EF
Adv Exp Med Biol; 2016; 854():259-65. PubMed ID: 26427420
[TBL] [Abstract][Full Text] [Related]
2. Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk.
Vollrath D; Feng W; Duncan JL; Yasumura D; D'Cruz PM; Chappelow A; Matthes MT; Kay MA; LaVail MM
Proc Natl Acad Sci U S A; 2001 Oct; 98(22):12584-9. PubMed ID: 11592982
[TBL] [Abstract][Full Text] [Related]
3. Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.
Gal A; Li Y; Thompson DA; Weir J; Orth U; Jacobson SG; Apfelstedt-Sylla E; Vollrath D
Nat Genet; 2000 Nov; 26(3):270-1. PubMed ID: 11062461
[TBL] [Abstract][Full Text] [Related]
4. Ectopic synaptogenesis during retinal degeneration in the royal college of surgeons rat.
Peng YW; Senda T; Hao Y; Matsuno K; Wong F
Neuroscience; 2003; 119(3):813-20. PubMed ID: 12809702
[TBL] [Abstract][Full Text] [Related]
5. CERKL gene knockout disturbs photoreceptor outer segment phagocytosis and causes rod-cone dystrophy in zebrafish.
Yu S; Li C; Biswas L; Hu X; Liu F; Reilly J; Liu X; Liu Y; Huang Y; Lu Z; Han S; Wang L; Yu Liu J; Jiang T; Shu X; Wong F; Tang Z; Liu M
Hum Mol Genet; 2017 Jun; 26(12):2335-2345. PubMed ID: 28398482
[TBL] [Abstract][Full Text] [Related]
6. Tyro3 Modulates Mertk-Associated Retinal Degeneration.
Vollrath D; Yasumura D; Benchorin G; Matthes MT; Feng W; Nguyen NM; Sedano CD; Calton MA; LaVail MM
PLoS Genet; 2015 Dec; 11(12):e1005723. PubMed ID: 26656104
[TBL] [Abstract][Full Text] [Related]
7. Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat.
D'Cruz PM; Yasumura D; Weir J; Matthes MT; Abderrahim H; LaVail MM; Vollrath D
Hum Mol Genet; 2000 Mar; 9(4):645-51. PubMed ID: 10699188
[TBL] [Abstract][Full Text] [Related]
8. Gene Therapy for MERTK-Associated Retinal Degenerations.
LaVail MM; Yasumura D; Matthes MT; Yang H; Hauswirth WW; Deng WT; Vollrath D
Adv Exp Med Biol; 2016; 854():487-93. PubMed ID: 26427450
[TBL] [Abstract][Full Text] [Related]
9. Retinal pigment epithelial cells use a MerTK-dependent mechanism to limit the phagocytic particle binding activity of αvβ5 integrin.
Nandrot EF; Silva KE; Scelfo C; Finnemann SC
Biol Cell; 2012 Jun; 104(6):326-41. PubMed ID: 22289110
[TBL] [Abstract][Full Text] [Related]
10. MERTK arginine-844-cysteine in a patient with severe rod-cone dystrophy: loss of mutant protein function in transfected cells.
McHenry CL; Liu Y; Feng W; Nair AR; Feathers KL; Ding X; Gal A; Vollrath D; Sieving PA; Thompson DA
Invest Ophthalmol Vis Sci; 2004 May; 45(5):1456-63. PubMed ID: 15111602
[TBL] [Abstract][Full Text] [Related]
11. Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy.
Tschernutter M; Schlichtenbrede FC; Howe S; Balaggan KS; Munro PM; Bainbridge JW; Thrasher AJ; Smith AJ; Ali RR
Gene Ther; 2005 Apr; 12(8):694-701. PubMed ID: 15660111
[TBL] [Abstract][Full Text] [Related]
12. Outer segment phagocytosis by cultured retinal pigment epithelial cells requires Gas6.
Hall MO; Prieto AL; Obin MS; Abrams TA; Burgess BL; Heeb MJ; Agnew BJ
Exp Eye Res; 2001 Oct; 73(4):509-20. PubMed ID: 11825022
[TBL] [Abstract][Full Text] [Related]
13. Mertk in daily retinal phagocytosis: a history in the making.
Nandrot EF; Dufour EM
Adv Exp Med Biol; 2010; 664():133-40. PubMed ID: 20238011
[TBL] [Abstract][Full Text] [Related]
14. Expression pattern of Ccr2 and Cx3cr1 in inherited retinal degeneration.
Kohno H; Koso H; Okano K; Sundermeier TR; Saito S; Watanabe S; Tsuneoka H; Sakai T
J Neuroinflammation; 2015 Oct; 12():188. PubMed ID: 26458944
[TBL] [Abstract][Full Text] [Related]
15. Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene.
Tschernutter M; Jenkins SA; Waseem NH; Saihan Z; Holder GE; Bird AC; Bhattacharya SS; Ali RR; Webster AR
Br J Ophthalmol; 2006 Jun; 90(6):718-23. PubMed ID: 16714263
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations in MERTK associated with childhood onset rod-cone dystrophy.
Mackay DS; Henderson RH; Sergouniotis PI; Li Z; Moradi P; Holder GE; Waseem N; Bhattacharya SS; Aldahmesh MA; Alkuraya FS; Meyer B; Webster AR; Moore AT
Mol Vis; 2010 Mar; 16():369-77. PubMed ID: 20300561
[TBL] [Abstract][Full Text] [Related]
17. Mertk triggers uptake of photoreceptor outer segments during phagocytosis by cultured retinal pigment epithelial cells.
Feng W; Yasumura D; Matthes MT; LaVail MM; Vollrath D
J Biol Chem; 2002 May; 277(19):17016-22. PubMed ID: 11861639
[TBL] [Abstract][Full Text] [Related]
18. Inflammation of the retinal pigment epithelium drives early-onset photoreceptor degeneration in
Mercau ME; Akalu YT; Mazzoni F; Gyimesi G; Alberto EJ; Kong Y; Hafler BP; Finnemann SC; Rothlin CV; Ghosh S
Sci Adv; 2023 Jan; 9(3):eade9459. PubMed ID: 36662852
[TBL] [Abstract][Full Text] [Related]
19. Preclinical potency and safety studies of an AAV2-mediated gene therapy vector for the treatment of MERTK associated retinitis pigmentosa.
Conlon TJ; Deng WT; Erger K; Cossette T; Pang JJ; Ryals R; Clément N; Cleaver B; McDoom I; Boye SE; Peden MC; Sherwood MB; Abernathy CR; Alkuraya FS; Boye SL; Hauswirth WW
Hum Gene Ther Clin Dev; 2013 Mar; 24(1):23-8. PubMed ID: 23692380
[TBL] [Abstract][Full Text] [Related]
20. TUDCA Promotes Phagocytosis by Retinal Pigment Epithelium via MerTK Activation.
Murase H; Tsuruma K; Shimazawa M; Hara H
Invest Ophthalmol Vis Sci; 2015 Apr; 56(4):2511-8. PubMed ID: 25804419
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]