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 *

74 related articles for article (PubMed ID: 29742619)

  • 1. Loss-of-function mutation in Hippo suppressed enlargement of lysosomes and neurodegeneration caused by dFIG4 knockdown.
    Kushimura Y; Azuma Y; Mizuta I; Muraoka Y; Kyotani A; Yoshida H; Tokuda T; Mizuno T; Yamaguchi M
    Neuroreport; 2018 Jul; 29(10):856-862. PubMed ID: 29742619
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic screening of the genes interacting with Drosophila FIG4 identified a novel link between CMT-causing gene and long noncoding RNAs.
    Muraoka Y; Nakamura A; Tanaka R; Suda K; Azuma Y; Kushimura Y; Lo Piccolo L; Yoshida H; Mizuta I; Tokuda T; Mizuno T; Nakagawa M; Yamaguchi M
    Exp Neurol; 2018 Dec; 310():1-13. PubMed ID: 30165075
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hippo, Drosophila MST, is a novel modifier of motor neuron degeneration induced by knockdown of Caz, Drosophila FUS.
    Azuma Y; Tokuda T; Kushimura Y; Yamamoto I; Mizuta I; Mizuno T; Nakagawa M; Ueyama M; Nagai Y; Iwasaki Y; Yoshida M; Pan D; Yoshida H; Yamaguchi M
    Exp Cell Res; 2018 Oct; 371(2):311-321. PubMed ID: 30092221
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Knockdown of the Drosophila FIG4 induces deficient locomotive behavior, shortening of motor neuron, axonal targeting aberration, reduction of life span and defects in eye development.
    Kyotani A; Azuma Y; Yamamoto I; Yoshida H; Mizuta I; Mizuno T; Nakagawa M; Tokuda T; Yamaguchi M
    Exp Neurol; 2016 Mar; 277():86-95. PubMed ID: 26708557
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of CR43467 encoding a long non-coding RNA as a novel genetic interactant with dFIG4, a CMT-causing gene.
    Shimada S; Muraoka Y; Ibaraki K; Takano-Shimizu-Kouno T; Yoshida H; Yamaguchi M
    Exp Cell Res; 2020 Jan; 386(1):111711. PubMed ID: 31704059
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FIG4 regulates lysosome membrane homeostasis independent of phosphatase function.
    Bharadwaj R; Cunningham KM; Zhang K; Lloyd TE
    Hum Mol Genet; 2016 Feb; 25(4):681-92. PubMed ID: 26662798
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel genetic link between the ATP-binding cassette subfamily A gene and hippo gene in Drosophila.
    Ueoka I; Takai A; Yamaguchi M; Chiyonobu T; Yoshida H; Yamaguchi M
    Exp Cell Res; 2020 Jan; 386(2):111733. PubMed ID: 31751555
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4J.
    Lenk GM; Ferguson CJ; Chow CY; Jin N; Jones JM; Grant AE; Zolov SN; Winters JJ; Giger RJ; Dowling JJ; Weisman LS; Meisler MH
    PLoS Genet; 2011 Jun; 7(6):e1002104. PubMed ID: 21655088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases.
    Niehues S; Bussmann J; Steffes G; Erdmann I; Köhrer C; Sun L; Wagner M; Schäfer K; Wang G; Koerdt SN; Stum M; Jaiswal S; RajBhandary UL; Thomas U; Aberle H; Burgess RW; Yang XL; Dieterich D; Storkebaum E
    Nat Commun; 2015 Jul; 6():7520. PubMed ID: 26138142
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A New Mutation in FIG4 Causes a Severe Form of CMT4J Involving TRPV4 in the Pathogenic Cascade.
    Gentil BJ; O'Ferrall E; Chalk C; Santana LF; Durham HD; Massie R
    J Neuropathol Exp Neurol; 2017 Sep; 76(9):789-799. PubMed ID: 28859335
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2.
    Bian X; Lin P; Li J; Long F; Duan R; Yuan Q; Li Y; Gao F; Gao S; Wei S; Li X; Sun W; Gong Y; Yan C; Liu Q
    Neurodegener Dis; 2018; 18(2-3):74-83. PubMed ID: 29587262
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy.
    Vaccari I; Carbone A; Previtali SC; Mironova YA; Alberizzi V; Noseda R; Rivellini C; Bianchi F; Del Carro U; D'Antonio M; Lenk GM; Wrabetz L; Giger RJ; Meisler MH; Bolino A
    Hum Mol Genet; 2015 Jan; 24(2):383-96. PubMed ID: 25187576
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
    Chow CY; Zhang Y; Dowling JJ; Jin N; Adamska M; Shiga K; Szigeti K; Shy ME; Li J; Zhang X; Lupski JR; Weisman LS; Meisler MH
    Nature; 2007 Jul; 448(7149):68-72. PubMed ID: 17572665
    [TBL] [Abstract][Full Text] [Related]  

  • 15. AAV9-mediated FIG4 delivery prolongs life span in Charcot-Marie-Tooth disease type 4J mouse model.
    Presa M; Bailey RM; Davis C; Murphy T; Cook J; Walls R; Wilpan H; Bogdanik L; Lenk GM; Burgess RW; Gray SJ; Lutz C
    J Clin Invest; 2021 Jun; 131(11):. PubMed ID: 33878035
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of Rpd3 as a novel epigenetic regulator of Drosophila FIG 4, a Charcot-Marie-Tooth disease-causing gene.
    Muraoka Y; Nikaido A; Kowada R; Kimura H; Yamaguchi M; Yoshida H
    Neuroreport; 2021 May; 32(7):562-568. PubMed ID: 33850086
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification and functional characterization of two missense mutations in NDRG1 associated with Charcot-Marie-Tooth disease type 4D.
    Li LX; Liu GL; Liu ZJ; Lu C; Wu ZY
    Hum Mutat; 2017 Nov; 38(11):1569-1578. PubMed ID: 28776325
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reduction of Rpd3 suppresses defects in locomotive ability and neuronal morphology induced by the knockdown of Drosophila SLC25A46 via an epigenetic pathway.
    Suda K; Muraoka Y; Ortega-Yáñez A; Yoshida H; Kizu F; Hochin T; Kimura H; Yamaguchi M
    Exp Cell Res; 2019 Dec; 385(2):111673. PubMed ID: 31614134
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Drosophila Charcot-Marie-Tooth Disease Models.
    Yamaguchi M; Takashima H
    Adv Exp Med Biol; 2018; 1076():97-117. PubMed ID: 29951817
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic and systems level analysis of Drosophila sticky/citron kinase and dFmr1 mutants reveals common regulation of genetic networks.
    Bauer CR; Epstein AM; Sweeney SJ; Zarnescu DC; Bosco G
    BMC Syst Biol; 2008 Nov; 2():101. PubMed ID: 19032789
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.