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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

309 related items for PubMed ID: 24239381

  • 21.
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  • 22. Rab18 Collaborates with Rab7 to Modulate Lysosomal and Autophagy Activities in the Nervous System: an Overlapping Mechanism for Warburg Micro Syndrome and Charcot-Marie-Tooth Neuropathy Type 2B.
    Nian FS, Li LL, Cheng CY, Wu PC, Lin YT, Tang CY, Ren BS, Tai CY, Fann MJ, Kao LS, Hong CJ, Tsai JW.
    Mol Neurobiol; 2019 Sep; 56(9):6095-6105. PubMed ID: 30721447
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  • 23. Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1: a case report.
    Khalesi R, Razmara E, Asgaritarghi G, Tavasoli AR, Riazalhosseini Y, Auld D, Garshasbi M.
    BMC Neurol; 2021 Apr 28; 21(1):180. PubMed ID: 33910511
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  • 25. A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton.
    Carpanini SM, McKie L, Thomson D, Wright AK, Gordon SL, Roche SL, Handley MT, Morrison H, Brownstein D, Wishart TM, Cousin MA, Gillingwater TH, Aligianis IA, Jackson IJ.
    Dis Model Mech; 2014 Jun 28; 7(6):711-22. PubMed ID: 24764192
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  • 26. TBC1D20 mediates autophagy as a key regulator of autophagosome maturation.
    Sidjanin DJ, Park AK, Ronchetti A, Martins J, Jackson WT.
    Autophagy; 2016 Oct 02; 12(10):1759-1775. PubMed ID: 27487390
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  • 27.
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  • 28. Rab18: new insights into the function of an essential protein.
    Dejgaard SY, Presley JF.
    Cell Mol Life Sci; 2019 May 02; 76(10):1935-1945. PubMed ID: 30830238
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  • 32. RAB18, a protein associated with Warburg Micro syndrome, controls neuronal migration in the developing cerebral cortex.
    Wu Q, Sun X, Yue W, Lu T, Ruan Y, Chen T, Zhang D.
    Mol Brain; 2016 Feb 16; 9():19. PubMed ID: 26879639
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  • 33. [Warburg-Micro syndrome caused by 1q43-q44 deletion: genotypic and phenotypic analysis in a child].
    Li HH, Shan L, Wang B, DU L, Jia FY.
    Zhongguo Dang Dai Er Ke Za Zhi; 2018 Jul 16; 20(7):585-587. PubMed ID: 30022763
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  • 35. Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome.
    Handley MT, Morris-Rosendahl DJ, Brown S, Macdonald F, Hardy C, Bem D, Carpanini SM, Borck G, Martorell L, Izzi C, Faravelli F, Accorsi P, Pinelli L, Basel-Vanagaite L, Peretz G, Abdel-Salam GM, Zaki MS, Jansen A, Mowat D, Glass I, Stewart H, Mancini G, Lederer D, Roscioli T, Giuliano F, Plomp AS, Rolfs A, Graham JM, Seemanova E, Poo P, García-Cazorla A, Edery P, Jackson IJ, Maher ER, Aligianis IA.
    Hum Mutat; 2013 May 16; 34(5):686-96. PubMed ID: 23420520
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  • 39. [Analysis of a case of Warburg micro syndrome type 1 due to variant of RAB3GAP1 gene].
    Yang D, Wang X, Yang J, Liu D, Li D.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec 10; 37(12):1384-1386. PubMed ID: 33306828
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  • 40.
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