286 related articles for article (PubMed ID: 34054431)
1. Therapeutic Development for CGG Repeat Expansion-Associated Neurodegeneration.
Xu K; Li Y; Allen EG; Jin P
Front Cell Neurosci; 2021; 15():655568. PubMed ID: 34054431
[TBL] [Abstract][Full Text] [Related]
2. FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report.
Toko M; Ohshita T; Kurashige T; Morino H; Kume K; Yamashita H; Sobue G; Iwasaki Y; Sone J; Kawakami H; Maruyama H
BMC Neurol; 2021 Oct; 21(1):396. PubMed ID: 34641814
[TBL] [Abstract][Full Text] [Related]
3. TDP-43 suppresses CGG repeat-induced neurotoxicity through interactions with HnRNP A2/B1.
He F; Krans A; Freibaum BD; Taylor JP; Todd PK
Hum Mol Genet; 2014 Oct; 23(19):5036-51. PubMed ID: 24920338
[TBL] [Abstract][Full Text] [Related]
4. Piperine Modulates Protein Mediated Toxicity in Fragile X-Associated Tremor/Ataxia Syndrome through Interacting Expanded CGG Repeat (r(CGG)
Verma AK; Khan E; Mishra SK; Jain N; Kumar A
ACS Chem Neurosci; 2019 Aug; 10(8):3778-3788. PubMed ID: 31264835
[TBL] [Abstract][Full Text] [Related]
5. Upstream open reading frame with NOTCH2NLC GGC expansion generates polyglycine aggregates and disrupts nucleocytoplasmic transport: implications for polyglycine diseases.
Zhong S; Lian Y; Luo W; Luo R; Wu X; Ji J; Ji Y; Ding J; Wang X
Acta Neuropathol; 2021 Dec; 142(6):1003-1023. PubMed ID: 34694469
[TBL] [Abstract][Full Text] [Related]
6. Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease.
Ishiura H; Shibata S; Yoshimura J; Suzuki Y; Qu W; Doi K; Almansour MA; Kikuchi JK; Taira M; Mitsui J; Takahashi Y; Ichikawa Y; Mano T; Iwata A; Harigaya Y; Matsukawa MK; Matsukawa T; Tanaka M; Shirota Y; Ohtomo R; Kowa H; Date H; Mitsue A; Hatsuta H; Morimoto S; Murayama S; Shiio Y; Saito Y; Mitsutake A; Kawai M; Sasaki T; Sugiyama Y; Hamada M; Ohtomo G; Terao Y; Nakazato Y; Takeda A; Sakiyama Y; Umeda-Kameyama Y; Shinmi J; Ogata K; Kohno Y; Lim SY; Tan AH; Shimizu J; Goto J; Nishino I; Toda T; Morishita S; Tsuji S
Nat Genet; 2019 Aug; 51(8):1222-1232. PubMed ID: 31332380
[TBL] [Abstract][Full Text] [Related]
7. Long-read sequencing identified repeat expansions in the 5'UTR of the
Deng J; Gu M; Miao Y; Yao S; Zhu M; Fang P; Yu X; Li P; Su Y; Huang J; Zhang J; Yu J; Li F; Bai J; Sun W; Huang Y; Yuan Y; Hong D; Wang Z
J Med Genet; 2019 Nov; 56(11):758-764. PubMed ID: 31413119
[TBL] [Abstract][Full Text] [Related]
8. Neuronal intranuclear inclusion disease: recognition and update.
Lu X; Hong D
J Neural Transm (Vienna); 2021 Mar; 128(3):295-303. PubMed ID: 33599827
[TBL] [Abstract][Full Text] [Related]
9. Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome.
Todd PK; Oh SY; Krans A; Pandey UB; Di Prospero NA; Min KT; Taylor JP; Paulson HL
PLoS Genet; 2010 Dec; 6(12):e1001240. PubMed ID: 21170301
[TBL] [Abstract][Full Text] [Related]
10. CGG Repeats in the 5'UTR of FMR1 RNA Regulate Translation of Other RNAs Localized in the Same RNA Granules.
Rovozzo R; Korza G; Baker MW; Li M; Bhattacharyya A; Barbarese E; Carson JH
PLoS One; 2016; 11(12):e0168204. PubMed ID: 28005950
[TBL] [Abstract][Full Text] [Related]
11. Neurodegenerative diseases associated with non-coding CGG tandem repeat expansions.
Zhou ZD; Jankovic J; Ashizawa T; Tan EK
Nat Rev Neurol; 2022 Mar; 18(3):145-157. PubMed ID: 35022573
[TBL] [Abstract][Full Text] [Related]
12. Neuronal intranuclear inclusion disease tremor-dominant subtype: A mimicker of essential tremor.
Yang D; Cen Z; Wang L; Chen X; Liu P; Wang H; Ouyang Z; Chen Y; Zhang F; Xie F; Wang B; Wu S; Yin H; Jiang B; Wang Z; Ji J; Luo W
Eur J Neurol; 2022 Feb; 29(2):450-458. PubMed ID: 34750918
[TBL] [Abstract][Full Text] [Related]
13.
Fan Y; Xu Y; Shi C
J Med Genet; 2022 Jan; 59(1):1-9. PubMed ID: 34675123
[TBL] [Abstract][Full Text] [Related]
14. Small Molecule Screening Discovers Compounds that Reduce FMRpolyG Protein Aggregates and Splicing Defect Toxicity in Fragile X-Associated Tremor/Ataxia Syndrome.
Verma AK; Khan E; Mishra SK; Kumar A
Mol Neurobiol; 2022 Mar; 59(3):1992-2007. PubMed ID: 35040038
[TBL] [Abstract][Full Text] [Related]
15. Potential pathogenic mechanisms underlying Fragile X Tremor Ataxia Syndrome: RAN translation and/or RNA gain-of-function?
Boivin M; Willemsen R; Hukema RK; Sellier C
Eur J Med Genet; 2018 Nov; 61(11):674-679. PubMed ID: 29223504
[TBL] [Abstract][Full Text] [Related]
16. Unstable mutations in the FMR1 gene and the phenotypes.
Loesch D; Hagerman R
Adv Exp Med Biol; 2012; 769():78-114. PubMed ID: 23560306
[TBL] [Abstract][Full Text] [Related]
17. Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.
Arocena DG; Iwahashi CK; Won N; Beilina A; Ludwig AL; Tassone F; Schwartz PH; Hagerman PJ
Hum Mol Genet; 2005 Dec; 14(23):3661-71. PubMed ID: 16239243
[TBL] [Abstract][Full Text] [Related]
18. Secondary structural choice of DNA and RNA associated with CGG/CCG trinucleotide repeat expansion rationalizes the RNA misprocessing in FXTAS.
Ajjugal Y; Kolimi N; Rathinavelan T
Sci Rep; 2021 Apr; 11(1):8163. PubMed ID: 33854084
[TBL] [Abstract][Full Text] [Related]
19. Association of NOTCH2NLC Repeat Expansions With Parkinson Disease.
Ma D; Tan YJ; Ng ASL; Ong HL; Sim W; Lim WK; Teo JX; Ng EYL; Lim EC; Lim EW; Chan LL; Tan LCS; Yi Z; Tan EK
JAMA Neurol; 2020 Dec; 77(12):1559-1563. PubMed ID: 32852534
[TBL] [Abstract][Full Text] [Related]
20. Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders.
Tian Y; Wang JL; Huang W; Zeng S; Jiao B; Liu Z; Chen Z; Li Y; Wang Y; Min HX; Wang XJ; You Y; Zhang RX; Chen XY; Yi F; Zhou YF; Long HY; Zhou CJ; Hou X; Wang JP; Xie B; Liang F; Yang ZY; Sun QY; Allen EG; Shafik AM; Kong HE; Guo JF; Yan XX; Hu ZM; Xia K; Jiang H; Xu HW; Duan RH; Jin P; Tang BS; Shen L
Am J Hum Genet; 2019 Jul; 105(1):166-176. PubMed ID: 31178126
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
