These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 17331881)

  • 1. Trinucleotide repeat disorders.
    Lutz RE
    Semin Pediatr Neurol; 2007 Mar; 14(1):26-33. PubMed ID: 17331881
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. Argonaute-2-dependent rescue of a Drosophila model of FXTAS by FRAXE premutation repeat.
    Sofola OA; Jin P; Botas J; Nelson DL
    Hum Mol Genet; 2007 Oct; 16(19):2326-32. PubMed ID: 17635840
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fragile sites and human disease.
    Debacker K; Kooy RF
    Hum Mol Genet; 2007 Oct; 16 Spec No. 2():R150-8. PubMed ID: 17567780
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rearrangements in the flanking sequences of the triplet repeat of the FMR1 gene give clues to the mechanisms involved in repeat instability in fragile X.
    Mononen T; von Koskull H; Airaksinen RL; Juvonen V
    DNA Repair (Amst); 2008 May; 7(5):684-5. PubMed ID: 18337192
    [No Abstract]   [Full Text] [Related]  

  • 6. Expression of the GABAergic system in animal models for fragile X syndrome and fragile X associated tremor/ataxia syndrome (FXTAS).
    D'Hulst C; Heulens I; Brouwer JR; Willemsen R; De Geest N; Reeve SP; De Deyn PP; Hassan BA; Kooy RF
    Brain Res; 2009 Feb; 1253():176-83. PubMed ID: 19070606
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Expansion of trinucleotide repeats].
    Siianova EIu; Mirkin SM
    Mol Biol (Mosk); 2001; 35(2):208-23. PubMed ID: 11357405
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Variation on a trinucleotide theme.
    Yvert G; Mandel JL
    Nat Med; 1999 Apr; 5(4):383-4. PubMed ID: 10202924
    [No Abstract]   [Full Text] [Related]  

  • 9. [Molecular basis of spinocerebellar ataxias subtype caused by nucleotide repeat expansion in noncoding region].
    Wang JL; Tang BS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Jun; 25(3):293-6. PubMed ID: 18543219
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of triplet-repeat DNA by capillary electrophoresis.
    Kiba Y; Baba Y
    Methods Mol Biol; 2001; 163():221-9. PubMed ID: 11242947
    [No Abstract]   [Full Text] [Related]  

  • 11. Unstable triplet repeat diseases.
    Monckton DG; Caskey CT
    Circulation; 1995 Jan; 91(2):513-20. PubMed ID: 7805257
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fragile X--a challenge to models of the mind and to best clinical practice.
    Hay DA
    Cortex; 2008 Jun; 44(6):626-7. PubMed ID: 18472032
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CREB-binding protein modulates repeat instability in a Drosophila model for polyQ disease.
    Jung J; Bonini N
    Science; 2007 Mar; 315(5820):1857-9. PubMed ID: 17332375
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Candidate gene approach for polyglutamine disease: isolation and characterization of human brain cDNAs containing CAG repeats].
    Igarashi S; Amaya N; Tsuji S
    Tanpakushitsu Kakusan Koso; 2001 Dec; 46(16 Suppl):2295-8. PubMed ID: 11802382
    [No Abstract]   [Full Text] [Related]  

  • 15. [Spinocerebellar degeneration].
    Sugai Y
    Ryoikibetsu Shokogun Shirizu; 2003; (40):272-4. PubMed ID: 14626118
    [No Abstract]   [Full Text] [Related]  

  • 16. A-overhang-dependent repeat expansion determination (ADRED).
    Achmüller C; Köhler A; Bösch S; Schneider R
    Biotechniques; 2008 Nov; 45(5):577-80. PubMed ID: 19007342
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CAG repeat disorder models and human neuropathology: similarities and differences.
    Yamada M; Sato T; Tsuji S; Takahashi H
    Acta Neuropathol; 2008 Jan; 115(1):71-86. PubMed ID: 17786457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of the fragile X syndrome among Estonian mentally retarded and the entire children's population.
    Puusepp H; Kahre T; Sibul H; Soo V; Lind I; Raukas E; Ounap K
    J Child Neurol; 2008 Dec; 23(12):1400-5. PubMed ID: 19073844
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.
    Guruju MR; Lavanya K; Thelma BK; Sujatha M; OmSai VR; Nagarathna V; Amarjyothi P; Jyothi A; Anandaraj MP
    J Clin Neurosci; 2009 Oct; 16(10):1305-10. PubMed ID: 19560928
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Altered expression of Autism-associated genes in the brain of Fragile X mouse model.
    Zhang A; Shen CH; Ma SY; Ke Y; El Idrissi A
    Biochem Biophys Res Commun; 2009 Feb; 379(4):920-3. PubMed ID: 19138667
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.