146 related articles for article (PubMed ID: 32676850)
1. Factors Associated with Intergenerational Instability of ATXN3 CAG Repeat and Genetic Anticipation in Chinese Patients with Spinocerebellar Ataxia Type 3.
Du YC; Ma Y; Shao YR; Gan SR; Dong Y; Wu ZY
Cerebellum; 2020 Dec; 19(6):902-906. PubMed ID: 32676850
[TBL] [Abstract][Full Text] [Related]
2. Selective forces acting on spinocerebellar ataxia type 3/Machado-Joseph disease recurrency: A systematic review and meta-analysis.
Sena LS; Dos Santos Pinheiro J; Saraiva-Pereira ML; Jardim LB
Clin Genet; 2021 Mar; 99(3):347-358. PubMed ID: 33219521
[TBL] [Abstract][Full Text] [Related]
3. Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population.
Gan SR; Ni W; Dong Y; Wang N; Wu ZY
PLoS One; 2015; 10(8):e0134405. PubMed ID: 26266536
[TBL] [Abstract][Full Text] [Related]
4. RAN Translation of the Expanded CAG Repeats in the SCA3 Disease Context.
Jazurek-Ciesiolka M; Ciesiolka A; Komur AA; Urbanek-Trzeciak MO; Krzyzosiak WJ; Fiszer A
J Mol Biol; 2020 Dec; 432(24):166699. PubMed ID: 33157084
[TBL] [Abstract][Full Text] [Related]
5. APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han population.
Peng H; Wang C; Chen Z; Sun Z; Jiao B; Li K; Huang F; Hou X; Wang J; Shen L; Xia K; Tang B; Jiang H
Neurobiol Aging; 2014 Sep; 35(9):2179.e15-8. PubMed ID: 24746364
[TBL] [Abstract][Full Text] [Related]
6. Spinocerebellar ataxia type 3/Machado-Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions.
Souza GN; Kersting N; Krum-Santos AC; Santos AS; Furtado GV; Pacheco D; Gonçalves TA; Saute JA; Schuler-Faccini L; Mattos EP; Saraiva-Pereira ML; Jardim LB
Clin Genet; 2016 Aug; 90(2):134-40. PubMed ID: 26693702
[TBL] [Abstract][Full Text] [Related]
7. Alteration of methylation status in the ATXN3 gene promoter region is linked to the SCA3/MJD.
Wang C; Peng H; Li J; Ding D; Chen Z; Long Z; Peng Y; Zhou X; Ye W; Li K; Xu Q; Ai S; Song C; Weng L; Qiu R; Xia K; Tang B; Jiang H
Neurobiol Aging; 2017 May; 53():192.e5-192.e10. PubMed ID: 28094059
[TBL] [Abstract][Full Text] [Related]
8. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
9. Age is an important independent modifier of SCA3 phenotype severity.
Jiao S; Wang P; Chen Z; Wang C; Shi Y; Qiu R; Tang B; Jiang H
Neurosci Lett; 2021 Jan; 741():135510. PubMed ID: 33221475
[TBL] [Abstract][Full Text] [Related]
10. Variation in DNA Repair System Gene as an Additional Modifier of Age at Onset in Spinocerebellar Ataxia Type 3/Machado-Joseph Disease.
Mergener R; Furtado GV; de Mattos EP; Leotti VB; Jardim LB; Saraiva-Pereira ML
Neuromolecular Med; 2020 Mar; 22(1):133-138. PubMed ID: 31587151
[TBL] [Abstract][Full Text] [Related]
11. Homozygous spinocerebellar ataxia type 3 in China: a case report.
Chen Y; Li D; Wei M; Zhou M; Zhang L; Yu J; Qiu M; Jin Y; Lu X
J Int Med Res; 2021 Jun; 49(6):3000605211021370. PubMed ID: 34167352
[TBL] [Abstract][Full Text] [Related]
12. Genotype-phenotype correlation in 667 Chinese families with spinocerebellar ataxia type 3.
Du YC; Dong Y; Cheng HL; Li QF; Yang L; Shao YR; Ma Y; Ni W; Gan SR; Wu ZY
Parkinsonism Relat Disord; 2020 Sep; 78():116-121. PubMed ID: 32814229
[TBL] [Abstract][Full Text] [Related]
13. Yemenite-Jewish families with Machado-Joseph disease (MJD/SCA3) share a recent common ancestor.
Sharony R; Martins S; Costa IPD; Zaltzman R; Amorim A; Sequeiros J; Gordon CR
Eur J Hum Genet; 2019 Nov; 27(11):1731-1737. PubMed ID: 31189928
[TBL] [Abstract][Full Text] [Related]
14. Chinese homozygous Machado-Joseph disease (MJD)/SCA3: a case report.
Zeng S; Zeng J; He M; Zeng X; Zhou Y; Liu Z; Jiang H; Tang B; Wang J
J Hum Genet; 2015 Mar; 60(3):157-60. PubMed ID: 25566755
[TBL] [Abstract][Full Text] [Related]
15. CRISPR/Cas9-Targeted Deletion of Polyglutamine in Spinocerebellar Ataxia Type 3-Derived Induced Pluripotent Stem Cells.
Ouyang S; Xie Y; Xiong Z; Yang Y; Xian Y; Ou Z; Song B; Chen Y; Xie Y; Li H; Sun X
Stem Cells Dev; 2018 Jun; 27(11):756-770. PubMed ID: 29661116
[TBL] [Abstract][Full Text] [Related]
16. Childhood-Onset Spinocerebellar Ataxia 3: Tongue Dystonia as an Early Manifestation.
Mitchell N; LaTouche GA; Nelson B; Figueroa KP; Walker RH; Sobering AK
Tremor Other Hyperkinet Mov (N Y); 2019; 9():. PubMed ID: 31565539
[TBL] [Abstract][Full Text] [Related]
17. [Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].
Jiang M; Jin CL; Lin CK; Qiu GR; Liu ZL; Wang CX; Sun KL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):83-5. PubMed ID: 14767919
[TBL] [Abstract][Full Text] [Related]
18. Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3.
Li QF; Cheng HL; Yang L; Ma Y; Zhao JJ; Dong Y; Wu ZY
Mol Genet Genomic Med; 2020 Sep; 8(9):e1314. PubMed ID: 32643267
[TBL] [Abstract][Full Text] [Related]
19. Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease.
Chen Z; Wang C; Zheng C; Long Z; Cao L; Li X; Shang H; Yin X; Zhang B; Liu J; Ding D; Peng Y; Peng H; Ye W; Qiu R; Pan Q; Xia K; Chen S; Sequeiros J; Ashizawa T; Tang B; Jiang H;
Brain; 2017 Apr; 140(4):e25. PubMed ID: 28334945
[No Abstract] [Full Text] [Related]
20. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M
Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
