205 related articles for article (PubMed ID: 34392981)
1. Analysis of NOTCH2NLC GGC repeat expansion in Taiwanese patients with amyotrophic lateral sclerosis.
Jih KY; Chou YT; Tsai PC; Liao YC; Lee YC
Neurobiol Aging; 2021 Dec; 108():210-212. PubMed ID: 34392981
[TBL] [Abstract][Full Text] [Related]
2. GGC Repeat Expansion of
Liao YC; Chang FP; Huang HW; Chen TB; Chou YT; Hsu SL; Jih KY; Liu YH; Hsiao CT; Fukukda H; Mizuguchi T; Lin KP; Lin CK; Matsumoto N; Kennerson M; Lee YC
Neurology; 2022 Jan; 98(2):e199-e206. PubMed ID: 34675106
[TBL] [Abstract][Full Text] [Related]
3.
Fan Y; Xu Y; Shi C
J Med Genet; 2022 Jan; 59(1):1-9. PubMed ID: 34675123
[TBL] [Abstract][Full Text] [Related]
4. NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients.
Manini A; Gagliardi D; Meneri M; Antognozzi S; Del Bo R; Comi GP; Corti S; Ronchi D
Sci Rep; 2023 Feb; 13(1):3187. PubMed ID: 36823368
[TBL] [Abstract][Full Text] [Related]
5. GGC repeat expansions in NOTCH2NLC causing a phenotype of lower motor neuron syndrome.
Zhang W; Ma J; Shi J; Huang S; Zhao R; Pang X; Wang J; Guo J; Chang X
J Neurol; 2022 Aug; 269(8):4469-4477. PubMed ID: 35366689
[TBL] [Abstract][Full Text] [Related]
6. Identification of GGC repeat expansion in the
Yuan Y; Liu Z; Hou X; Li W; Ni J; Huang L; Hu Y; Liu P; Hou X; Xue J; Sun Q; Tian Y; Jiao B; Duan R; Jiang H; Shen L; Tang B; Wang J
Neurology; 2020 Dec; 95(24):e3394-e3405. PubMed ID: 32989102
[TBL] [Abstract][Full Text] [Related]
7. Intermediate-Length GGC Repeat Expansion in NOTCH2NLC Was Identified in Chinese Patients with Amyotrophic Lateral Sclerosis.
Wan M; He J; Huo J; Sun C; Fu Y; Fan D
Brain Sci; 2023 Jan; 13(1):. PubMed ID: 36672065
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation.
Fan Y; Li MJ; Yang J; Li SJ; Hao XY; Li JD; Wang YC; Tang MB; Zhang C; Shi JJ; Ma DR; Guo MN; Liu F; Shen S; Yao DB; Zuo CY; Mao CY; Hu ZW; Zhang S; Yang ZH; Guo GY; Yang JH; Xia ZP; Xu YM; Shi CH
Brain; 2023 Aug; 146(8):3373-3391. PubMed ID: 36825461
[TBL] [Abstract][Full Text] [Related]
11. 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]
12.
Liao YC; Wei CY; Chang FP; Chou YT; Hsu SL; Chung CP; Mizuguchi T; Matsumoto N; Yet SF; Lee YC
Stroke; 2023 May; 54(5):1236-1245. PubMed ID: 36942588
[TBL] [Abstract][Full Text] [Related]
13. Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophy.
Fang P; Yu Y; Yao S; Chen S; Zhu M; Chen Y; Zou K; Wang L; Wang H; Xin L; Hong T; Hong D
Ann Clin Transl Neurol; 2020 Apr; 7(4):517-526. PubMed ID: 32250060
[TBL] [Abstract][Full Text] [Related]
14. Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia.
Hsu SL; Jih KY; Lin KP; Liao YC; Lee YC
Parkinsonism Relat Disord; 2022 Mar; 96():43-44. PubMed ID: 35180462
[TBL] [Abstract][Full Text] [Related]
15. NOTCH2NLC-related repeat expansion disorders: an expanding group of neurodegenerative disorders.
Cao L; Yan Y; Zhao G
Neurol Sci; 2021 Oct; 42(10):4055-4062. PubMed ID: 34333668
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review.
Huang XR; Tang BS; Jin P; Guo JF
Mol Neurobiol; 2022 Jan; 59(1):523-534. PubMed ID: 34718964
[TBL] [Abstract][Full Text] [Related]
18. Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort.
Chen Z; Xu Z; Cheng Q; Tan YJ; Ong HL; Zhao Y; Lim WK; Teo JX; Foo JN; Lee HY; Tan JMM; Hang L; Yu WY; Ting SKS; Tan EK; Lim TCC; Ng ASL
Clin Genet; 2020 Sep; 98(3):274-281. PubMed ID: 32602554
[TBL] [Abstract][Full Text] [Related]
19. Coexistence of neuronal intranuclear inclusion disease and amyotrophic lateral sclerosis: an autopsy case.
Sugiyama A; Takeda T; Koide M; Yokota H; Mukai H; Kitayama Y; Shibuya K; Araki N; Ishikawa A; Isose S; Ito K; Honda K; Yamanaka Y; Sano T; Saito Y; Arai K; Kuwabara S
BMC Neurol; 2021 Jul; 21(1):273. PubMed ID: 34243731
[TBL] [Abstract][Full Text] [Related]
20. Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy.
Liu YH; Chou YT; Chang FP; Lee WJ; Guo YC; Chou CT; Huang HC; Mizuguchi T; Chou CC; Yu HY; Yu KW; Wu HM; Tsai PC; Matsumoto N; Lee YC; Liao YC
Brain; 2022 Sep; 145(9):3010-3021. PubMed ID: 35411397
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
