BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 8190020)

  • 1. Trinucleotide repeats in neurologic diseases: an hypothesis concerning the pathogenesis of Huntington's disease, Kennedy's disease, and spinocerebellar ataxia type I.
    Cha JH; Dure LS
    Life Sci; 1994; 54(20):1459-64. PubMed ID: 8190020
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene.
    Hummerich H; Baxendale S; Mott R; Kirby SF; MacDonald ME; Gusella J; Lehrach H; Bates GP
    Hum Mol Genet; 1994 Jan; 3(1):73-8. PubMed ID: 8162055
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mouse models of human CAG repeat disorders.
    Burright EN; Orr HT; Clark HB
    Brain Pathol; 1997 Jul; 7(3):965-77. PubMed ID: 9217978
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase.
    Koshy B; Matilla T; Burright EN; Merry DE; Fischbeck KH; Orr HT; Zoghbi HY
    Hum Mol Genet; 1996 Sep; 5(9):1311-8. PubMed ID: 8872471
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The advances in research on phosphorylation of polyglutamine disease].
    Zhou YF; Jiang H; Tang JG; Tang BS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):414-7. PubMed ID: 18683139
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Trinucleotide repeat expansions and human genetic disease.
    Bates G; Lehrach H
    Bioessays; 1994 Apr; 16(4):277-84. PubMed ID: 8031305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cerebellar allografts survive and transiently alleviate ataxia in a transgenic model of spinocerebellar ataxia type-1.
    Kaemmerer WF; Low WC
    Exp Neurol; 1999 Aug; 158(2):301-11. PubMed ID: 10415138
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function.
    Chamberlain NL; Driver ED; Miesfeld RL
    Nucleic Acids Res; 1994 Aug; 22(15):3181-6. PubMed ID: 8065934
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genes with triplet repeats: a new class of mutations causing neurological diseases.
    Plassart E; Fontaine B
    Biomed Pharmacother; 1994; 48(5-6):191-7. PubMed ID: 7999979
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trinucleotide repeat disorders in humans: discussions of mechanisms and medical issues.
    Timchenko LT; Caskey CT
    FASEB J; 1996 Dec; 10(14):1589-97. PubMed ID: 9002550
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.
    Spiegel R; La Spada AR; Kress W; Fischbeck KH; Schmid W
    Hum Mutat; 1996; 8(1):32-7. PubMed ID: 8807333
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.
    Robitaille Y; Lopes-Cendes I; Becher M; Rouleau G; Clark AW
    Brain Pathol; 1997 Jul; 7(3):901-26. PubMed ID: 9217975
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Dynamic mutations in hereditary neurodegenerative disorders].
    Nilssen O
    Tidsskr Nor Laegeforen; 1999 Aug; 119(20):3021-7. PubMed ID: 10504853
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ectopic expression of the striatal-enriched GTPase Rhes elicits cerebellar degeneration and an ataxia phenotype in Huntington's disease.
    Swarnkar S; Chen Y; Pryor WM; Shahani N; Page DT; Subramaniam S
    Neurobiol Dis; 2015 Oct; 82():66-77. PubMed ID: 26048156
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trinucleotide repeats in neurogenetic disorders.
    Paulson HL; Fischbeck KH
    Annu Rev Neurosci; 1996; 19():79-107. PubMed ID: 8833437
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The Role of Mutant RNA in the Pathogenesis of Huntington's Disease and Other Polyglutamine Diseases].
    Bogomazova AN; Eremeev AV; Pozmogova GE; Lagarkova MA
    Mol Biol (Mosk); 2019; 53(6):954-967. PubMed ID: 31876275
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autophagy and Polyglutamine Disease.
    Ren H; Hao Z; Wang G
    Adv Exp Med Biol; 2020; 1207():149-161. PubMed ID: 32671744
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Growing genes cause neurological diseases].
    Johansson J; Holmgren G; Forsgren L; Holmberg M
    Lakartidningen; 1999 Feb; 96(8):897-900. PubMed ID: 10089735
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trinucleotide repeat expansion in neurological disease.
    La Spada AR; Paulson HL; Fischbeck KH
    Ann Neurol; 1994 Dec; 36(6):814-22. PubMed ID: 7998766
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unstable trinucleotide repeats and the diagnosis of neurodegenerative disease.
    Orr HT
    Hum Pathol; 1994 Jun; 25(6):598-601. PubMed ID: 8013951
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.