BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 15223312)

  • 21. DNA-labelled cytidine assay for the quantification of CAG repeats.
    Pérez-Bello D; Xu ZH; Higginson-Clarke D; Rojas AM; Le W; Rodríguez-Tanty C
    J Neurosci Methods; 2008 Mar; 169(1):201-7. PubMed ID: 18261802
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project.
    Akçimen F; Ross JP; Liao C; Spiegelman D; Dion PA; Rouleau GA
    Mov Disord; 2021 Feb; 36(2):514-518. PubMed ID: 33159825
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
    Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Tang JG
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Oct; 31(5):702-5. PubMed ID: 17062934
    [TBL] [Abstract][Full Text] [Related]  

  • 24. In Vitro Expansion of CAG, CAA, and Mixed CAG/CAA Repeats.
    Figura G; Koscianska E; Krzyzosiak WJ
    Int J Mol Sci; 2015 Aug; 16(8):18741-51. PubMed ID: 26270660
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [CAG trinucleotide mutation detection in patients with hereditary spinocerebellar ataxia].
    Tang B; Xia J; Wang D; Tang X; Shen L; Liu C; Dai H; Yan X; Pan Q; Xiao J; Zhang B; Ou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct; 16(5):281-4. PubMed ID: 10514531
    [TBL] [Abstract][Full Text] [Related]  

  • 26. FAT10 protein binds to polyglutamine proteins and modulates their solubility.
    Nagashima Y; Kowa H; Tsuji S; Iwata A
    J Biol Chem; 2011 Aug; 286(34):29594-600. PubMed ID: 21757738
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: a correlation with CAG repeat length.
    Hasegawa A; Ikeuchi T; Koike R; Matsubara N; Tsuchiya M; Nozaki H; Homma A; Idezuka J; Nishizawa M; Onodera O
    Mov Disord; 2010 Aug; 25(11):1694-700. PubMed ID: 20589872
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Triplet repeats in transcripts: structural insights into RNA toxicity.
    Galka-Marciniak P; Urbanek MO; Krzyzosiak WJ
    Biol Chem; 2012 Nov; 393(11):1299-315. PubMed ID: 23052488
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Allele-selective inhibition of mutant atrophin-1 expression by duplex and single-stranded RNAs.
    Hu J; Liu J; Narayanannair KJ; Lackey JG; Kuchimanchi S; Rajeev KG; Manoharan M; Swayze EE; Lima WF; Prakash TP; Xiang Q; Martinez C; Corey DR
    Biochemistry; 2014 Jul; 53(28):4510-8. PubMed ID: 24981774
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias.
    Safaei S; Houshmand M; Banoei MM; Panahi MS; Nafisi S; Parivar K; Rostami M; Shariati P
    Neurodegener Dis; 2009; 6(1-2):16-22. PubMed ID: 19066432
    [TBL] [Abstract][Full Text] [Related]  

  • 31. DRPLA transgenic mouse substrains carrying single copy of full-length mutant human DRPLA gene with variable sizes of expanded CAG repeats exhibit CAG repeat length- and age-dependent changes in behavioral abnormalities and gene expression profiles.
    Suzuki K; Zhou J; Sato T; Takao K; Miyagawa T; Oyake M; Yamada M; Takahashi H; Takahashi Y; Goto J; Tsuji S
    Neurobiol Dis; 2012 May; 46(2):336-50. PubMed ID: 22342974
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Structural Insights Reveal the Dynamics of the Repeating r(CAG) Transcript Found in Huntington's Disease (HD) and Spinocerebellar Ataxias (SCAs).
    Tawani A; Kumar A
    PLoS One; 2015; 10(7):e0131788. PubMed ID: 26148061
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype.
    Rodrigues GR; Walker RH; Bader B; Danek A; Brice A; Cazeneuve C; Russaouen O; Lopes-Cendes I; Marques W; Tumas V
    Arq Neuropsiquiatr; 2011 Jun; 69(3):419-23. PubMed ID: 21755114
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Preparation of human cDNas encoding expanded polyglutamine repeats.
    Peters MF; Ross CA
    Neurosci Lett; 1999 Nov; 275(2):129-32. PubMed ID: 10568516
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Haplotype study in Dutch SCA3 and SCA6 families: evidence for common founder mutations.
    Verbeek DS; Piersma SJ; Hennekam EF; Ippel EF; Pearson PL; Sinke RJ
    Eur J Hum Genet; 2004 Jun; 12(6):441-6. PubMed ID: 15026782
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Molecular analysis of the CAG repeat among patients with Type-2 spinocerebellar ataxia in the Mexican population].
    Magaña JJ; Vergara MD; Sierra-Martínez M; García-Jiménez E; Rodríguez-Antonio F; Gómez Mdel R; Valdés-Flores M; Cisneros B
    Gac Med Mex; 2008; 144(5):413-8. PubMed ID: 19043961
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
    Jiang H; Tang B; Xia K; Zhou Y; Xu B; Zhao G; Li H; Shen L; Pan Q; Cai F
    J Neurol Sci; 2005 Sep; 236(1-2):25-9. PubMed ID: 15979648
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Role of context in RNA structure: flanking sequences reconfigure CAG motif folding in huntingtin exon 1 transcripts.
    Busan S; Weeks KM
    Biochemistry; 2013 Nov; 52(46):8219-25. PubMed ID: 24199621
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spinocerebellar ataxia type 7.
    Martin JJ
    Handb Clin Neurol; 2012; 103():475-91. PubMed ID: 21827908
    [TBL] [Abstract][Full Text] [Related]  

  • 40. CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 alleles.
    Zühlke C; Hellenbroich Y; Schaaff F; Gehlken U; Wessel K; Schubert T; Cervos-Navarro J; Pickartz H; Schwinger E
    Hum Genet; 1997 Sep; 100(3-4):339-44. PubMed ID: 9272152
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.