BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 33219521)

  • 1. 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]  

  • 2. 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]  

  • 3. Machado Joseph-Disease Is Rare in the Peruvian Population.
    Cornejo-Olivas M; Solis-Ponce L; Araujo-Aliaga I; Milla-Neyra K; Ortega O; Illanes-Manrique M; Mazzetti P; Manrique-Enciso C; Cubas-Montecino D; Saraiva-Pereira ML; Jardim LB; Sarapura-Castro E
    Cerebellum; 2023 Dec; 22(6):1192-1199. PubMed ID: 36323979
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Spinocerebellar ataxia type 2 from an evolutionary perspective: Systematic review and meta-analysis.
    Sena LS; Dos Santos Pinheiro J; Hasan A; Saraiva-Pereira ML; Jardim LB
    Clin Genet; 2021 Sep; 100(3):258-267. PubMed ID: 33960424
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression.
    Shi Y; Wang C; Huang F; Chen Z; Sun Z; Wang J; Tang B; Ashizawa T; Klockgether T; Jiang H
    Cerebellum; 2015 Dec; 14(6):677-81. PubMed ID: 25869927
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients.
    Long Z; Chen Z; Wang C; Huang F; Peng H; Hou X; Ding D; Ye W; Wang J; Pan Q; Li J; Xia K; Tang B; Ashizawa T; Jiang H
    PLoS One; 2015; 10(2):e0117488. PubMed ID: 25689313
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.
    Takiyama Y; Igarashi S; Rogaeva EA; Endo K; Rogaev EI; Tanaka H; Sherrington R; Sanpei K; Liang Y; Saito M
    Hum Mol Genet; 1995 Jul; 4(7):1137-46. PubMed ID: 8528200
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of Machado-Joseph disease/Spinocerebellar Ataxia Type 3 in Taiwan: early detection of expanded ataxin-3.
    Tsai HF; Liu CS; Chen GD; Lin ML; Li C; Chen YY; Wang BT; Hsieh M
    J Clin Lab Anal; 2003; 17(5):195-200. PubMed ID: 12938149
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.
    Bettencourt C; Santos C; Coutinho P; Rizzu P; Vasconcelos J; Kay T; Cymbron T; Raposo M; Heutink P; Lima M
    BMC Neurol; 2011 Oct; 11():131. PubMed ID: 22023810
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Machado-Joseph disease/spinocerebellar ataxia type 3.
    Paulson H
    Handb Clin Neurol; 2012; 103():437-49. PubMed ID: 21827905
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Planning Future Clinical Trials for Machado-Joseph Disease.
    Saute JAM; Jardim LB
    Adv Exp Med Biol; 2018; 1049():321-348. PubMed ID: 29427112
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variants in Genes of Calpain System as Modifiers of Spinocerebellar Ataxia Type 3 Phenotype.
    Martins AC; Rieck M; Leotti VB; Saraiva-Pereira ML; Jardim LB
    J Mol Neurosci; 2021 Sep; 71(9):1906-1913. PubMed ID: 34191270
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis.
    Ikeuchi T; Igarashi S; Takiyama Y; Onodera O; Oyake M; Takano H; Koide R; Tanaka H; Tsuji S
    Am J Hum Genet; 1996 Apr; 58(4):730-3. PubMed ID: 8644735
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.