These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 32246618)

  • 21. Gene therapy for inherited retinal diseases.
    Nuzbrokh Y; Ragi SD; Tsang SH
    Ann Transl Med; 2021 Aug; 9(15):1278. PubMed ID: 34532415
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Microglial phagocytosis and activation underlying photoreceptor degeneration is regulated by CX3CL1-CX3CR1 signaling in a mouse model of retinitis pigmentosa.
    Zabel MK; Zhao L; Zhang Y; Gonzalez SR; Ma W; Wang X; Fariss RN; Wong WT
    Glia; 2016 Sep; 64(9):1479-91. PubMed ID: 27314452
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pigment epithelium-derived factor hinders photoreceptor cell death by reducing intracellular calcium in the degenerating retina.
    Comitato A; Subramanian P; Turchiano G; Montanari M; Becerra SP; Marigo V
    Cell Death Dis; 2018 May; 9(5):560. PubMed ID: 29752430
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Comprehensive strategy for retinal neuroprotection. Challenging the clinical application].
    Ishibashi T
    Nippon Ganka Gakkai Zasshi; 2012 Mar; 116(3):165-98; discussion 199. PubMed ID: 22568101
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Drug Discovery Strategies for Inherited Retinal Degenerations.
    Das A; Imanishi Y
    Biology (Basel); 2022 Sep; 11(9):. PubMed ID: 36138817
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dominant and recessive mutations in rhodopsin activate different cell death pathways.
    Comitato A; Di Salvo MT; Turchiano G; Montanari M; Sakami S; Palczewski K; Marigo V
    Hum Mol Genet; 2016 Jul; 25(13):2801-2812. PubMed ID: 27149983
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Naturally Occurring Inherited Forms of Retinal Degeneration in Vertebrate Animal Species: A Comparative and Evolutionary Perspective.
    Mowat FM
    Adv Exp Med Biol; 2019; 1185():239-243. PubMed ID: 31884618
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Using Stem Cells to Model Diseases of the Outer Retina.
    Yvon C; Ramsden CM; Lane A; Powner MB; da Cruz L; Coffey PJ; Carr AJ
    Comput Struct Biotechnol J; 2015; 13():382-9. PubMed ID: 26106463
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Simian lentiviral vector-mediated retinal gene transfer of pigment epithelium-derived factor protects retinal degeneration and electrical defect in Royal College of Surgeons rats.
    Miyazaki M; Ikeda Y; Yonemitsu Y; Goto Y; Sakamoto T; Tabata T; Ueda Y; Hasegawa M; Tobimatsu S; Ishibashi T; Sueishi K
    Gene Ther; 2003 Aug; 10(17):1503-11. PubMed ID: 12900766
    [TBL] [Abstract][Full Text] [Related]  

  • 30. An audit of genetic testing in diagnosis of inherited retinal disorders: a prerequisite for gene-specific intervention.
    Pradhan M; Hayes I; Vincent A
    Clin Exp Ophthalmol; 2009 Sep; 37(7):703-11. PubMed ID: 19788668
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Molecular-cellular mechanisms of retina pathology development in people of various age].
    Proniaeva VE; Lin'kova NS; Trofimova SV; D'iakonov MM
    Adv Gerontol; 2012; 25(2):232-8. PubMed ID: 23130512
    [TBL] [Abstract][Full Text] [Related]  

  • 32. In vivo phenotypic and molecular characterization of retinal degeneration in mouse models of three ciliopathies.
    Brun A; Yu X; Obringer C; Ajoy D; Haser E; Stoetzel C; Roux MJ; Messaddeq N; Dollfus H; Marion V
    Exp Eye Res; 2019 Sep; 186():107721. PubMed ID: 31302159
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice.
    Eblimit A; Agrawal SA; Thomas K; Anastassov IA; Abulikemu T; Moayedi Y; Mardon G; Chen R
    Exp Eye Res; 2018 Jan; 166():120-130. PubMed ID: 29100828
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A Mini Review: Moving iPSC-Derived Retinal Subtypes Forward for Clinical Applications for Retinal Degenerative Diseases.
    Cho C; Duong TT; Mills JA
    Adv Exp Med Biol; 2019; 1185():557-561. PubMed ID: 31884670
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Human umbilical tissue-derived cells rescue retinal pigment epithelium dysfunction in retinal degeneration.
    Cao J; Murat C; An W; Yao X; Lee J; Santulli-Marotto S; Harris IR; Inana G
    Stem Cells; 2016 Feb; 34(2):367-79. PubMed ID: 26523756
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia.
    Schön C; Asteriti S; Koch S; Sothilingam V; Garcia Garrido M; Tanimoto N; Herms J; Seeliger MW; Cangiano L; Biel M; Michalakis S
    Hum Mol Genet; 2016 Mar; 25(6):1165-75. PubMed ID: 26740549
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular genetics of Leber congenital amaurosis.
    Cremers FP; van den Hurk JA; den Hollander AI
    Hum Mol Genet; 2002 May; 11(10):1169-76. PubMed ID: 12015276
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Developing Cell-Based Therapies for RPE-Associated Degenerative Eye Diseases.
    Ben M'Barek K; Habeler W; Regent F; Monville C
    Adv Exp Med Biol; 2019; 1186():55-97. PubMed ID: 31654386
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mouse Models as Tools to Identify Genetic Pathways for Retinal Degeneration, as Exemplified by Leber's Congenital Amaurosis.
    Chang B
    Methods Mol Biol; 2016; 1438():417-30. PubMed ID: 27150101
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Retinal degeneration in retinitis pigmentosa and neuronal ceroid lipofuscinosis: An overview.
    Birch DG
    Mol Genet Metab; 1999 Apr; 66(4):356-66. PubMed ID: 10191129
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.