183 related articles for article (PubMed ID: 30165075)
1. 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]
2. 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]
3. 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]
4. 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]
5. Genetic link between Cabeza, a Drosophila homologue of Fused in Sarcoma (FUS), and the EGFR signaling pathway.
Shimamura M; Kyotani A; Azuma Y; Yoshida H; Binh Nguyen T; Mizuta I; Yoshida T; Mizuno T; Nakagawa M; Tokuda T; Yamaguchi M
Exp Cell Res; 2014 Aug; 326(1):36-45. PubMed ID: 24928275
[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. 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]
8. RNAi of arcRNA hsrω affects sub-cellular localization of Drosophila FUS to drive neurodiseases.
Lo Piccolo L; Yamaguchi M
Exp Neurol; 2017 Jun; 292():125-134. PubMed ID: 28342748
[TBL] [Abstract][Full Text] [Related]
9. Identification of ter94, Drosophila VCP, as a strong modulator of motor neuron degeneration induced by knockdown of Caz, Drosophila FUS.
Azuma Y; Tokuda T; Shimamura M; Kyotani A; Sasayama H; Yoshida T; Mizuta I; Mizuno T; Nakagawa M; Fujikake N; Ueyama M; Nagai Y; Yamaguchi M
Hum Mol Genet; 2014 Jul; 23(13):3467-80. PubMed ID: 24497576
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.
Higuchi Y; Okunushi R; Hara T; Hashiguchi A; Yuan J; Yoshimura A; Murayama K; Ohtake A; Ando M; Hiramatsu Y; Ishihara S; Tanabe H; Okamoto Y; Matsuura E; Ueda T; Toda T; Yamashita S; Yamada K; Koide T; Yaguchi H; Mitsui J; Ishiura H; Yoshimura J; Doi K; Morishita S; Sato K; Nakagawa M; Yamaguchi M; Tsuji S; Takashima H
Brain; 2018 Jun; 141(6):1622-1636. PubMed ID: 29718187
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Motor neuron apoptosis and neuromuscular junction perturbation are prominent features in a Drosophila model of Fus-mediated ALS.
Xia R; Liu Y; Yang L; Gal J; Zhu H; Jia J
Mol Neurodegener; 2012 Mar; 7():10. PubMed ID: 22443542
[TBL] [Abstract][Full Text] [Related]
14. Novel Drosophila model for mitochondrial diseases by targeting of a solute carrier protein SLC25A46.
Suda K; Ueoka I; Azuma Y; Muraoka Y; Yoshida H; Yamaguchi M
Brain Res; 2018 Jun; 1689():30-44. PubMed ID: 29604258
[TBL] [Abstract][Full Text] [Related]
15. Clinical features of homozygous FIG4-p.Ile41Thr Charcot-Marie-Tooth 4J patients.
Lafontaine M; Lia AS; Bourthoumieu S; Beauvais-Dzugan H; Derouault P; Arné-Bes MC; Sarret C; Laffargue F; Magot A; Sturtz F; Magy L; Magdelaine C
Ann Clin Transl Neurol; 2021 Feb; 8(2):471-476. PubMed ID: 33405357
[TBL] [Abstract][Full Text] [Related]
16. Over-expression of Hsp83 in grossly depleted
Ray M; Acharya S; Shambhavi S; Lakhotia SC
J Biosci; 2019 Jun; 44(2):. PubMed ID: 31180049
[TBL] [Abstract][Full Text] [Related]
17. Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot-Marie-Tooth disease.
Menezes MP; Waddell L; Lenk GM; Kaur S; MacArthur DG; Meisler MH; Clarke NF
Neuromuscul Disord; 2014 Aug; 24(8):666-70. PubMed ID: 24878229
[TBL] [Abstract][Full Text] [Related]
18. Epigenetic Regulation of ALS and CMT: A Lesson from
Yamaguchi M; Omori K; Asada S; Yoshida H
Int J Mol Sci; 2021 Jan; 22(2):. PubMed ID: 33419039
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A dysfunctional endolysosomal pathway common to two sub-types of demyelinating Charcot-Marie-Tooth disease.
Edgar JR; Ho AK; Laurá M; Horvath R; Reilly MM; Luzio JP; Roberts RC
Acta Neuropathol Commun; 2020 Oct; 8(1):165. PubMed ID: 33059769
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
