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 *

126 related articles for article (PubMed ID: 10969848)

  • 1. Heterozygous expansion of the GAA tract of the X25/frataxin gene is associated with insulin resistance in humans.
    Hebinck J; Hardt C; Schöls L; Vorgerd M; Briedigkeit L; Kahn CR; Ristow M
    Diabetes; 2000 Sep; 49(9):1604-7. PubMed ID: 10969848
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia.
    Bit-Avragim N; Perrot A; Schöls L; Hardt C; Kreuz FR; Zühlke C; Bubel S; Laccone F; Vogel HP; Dietz R; Osterziel KJ
    J Mol Med (Berl); 2001; 78(11):626-32. PubMed ID: 11269509
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients.
    De Castro M; García-Planells J; Monrós E; Cañizares J; Vázquez-Manrique R; Vílchez JJ; Urtasun M; Lucas M; Navarro G; Izquierdo G; Moltó MD; Palau F
    Hum Genet; 2000 Jan; 106(1):86-92. PubMed ID: 10982187
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Friedreich's ataxia and frataxin: molecular genetics, evolution and pathogenesis (Review).
    Palau F
    Int J Mol Med; 2001 Jun; 7(6):581-9. PubMed ID: 11351269
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sequence variation in GAA repeat expansions may cause differential phenotype display in Friedreich's ataxia.
    McDaniel DO; Keats B; Vedanarayanan VV; Subramony SH
    Mov Disord; 2001 Nov; 16(6):1153-8. PubMed ID: 11748752
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene.
    Ristow M; Giannakidou E; Hebinck J; Busch K; Vorgerd M; Kotzka J; Knebel B; Mueller-Berghaus J; Epplen C; Pfeiffer A; Kahn CR; Doria A; Krone W; Mueller-Wieland D
    Diabetes; 1998 May; 47(5):851-4. PubMed ID: 9588463
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Typical Friedreich's ataxia without GAA expansions and GAA expansion without typical Friedreich's ataxia.
    McCabe DJ; Ryan F; Moore DP; McQuaid S; King MD; Kelly A; Daly K; Barton DE; Murphy RP
    J Neurol; 2000 May; 247(5):346-55. PubMed ID: 10896266
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Central role and mechanisms of β-cell dysfunction and death in friedreich ataxia-associated diabetes.
    Cnop M; Igoillo-Esteve M; Rai M; Begu A; Serroukh Y; Depondt C; Musuaya AE; Marhfour I; Ladrière L; Moles Lopez X; Lefkaditis D; Moore F; Brion JP; Cooper JM; Schapira AH; Clark A; Koeppen AH; Marchetti P; Pandolfo M; Eizirik DL; Féry F
    Ann Neurol; 2012 Dec; 72(6):971-82. PubMed ID: 23280845
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Friedreich's ataxia. Revision of the phenotype according to molecular genetics.
    Schöls L; Amoiridis G; Przuntek H; Frank G; Epplen JT; Epplen C
    Brain; 1997 Dec; 120 ( Pt 12)():2131-40. PubMed ID: 9448568
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The GAA*TTC triplet repeat expanded in Friedreich's ataxia impedes transcription elongation by T7 RNA polymerase in a length and supercoil dependent manner.
    Grabczyk E; Usdin K
    Nucleic Acids Res; 2000 Jul; 28(14):2815-22. PubMed ID: 10908340
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.
    De Michele G; Cavalcanti F; Criscuolo C; Pianese L; Monticelli A; Filla A; Cocozza S
    Hum Mol Genet; 1998 Nov; 7(12):1901-6. PubMed ID: 9811933
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Friedreich ataxia: Detection of GAA repeat expansions and frataxin point mutations.
    Pandolfo M
    Methods Mol Med; 2006; 126():197-216. PubMed ID: 16930014
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Markedly different course of Friedreich's ataxia in sib pairs with similar GAA repeat expansions in the frataxin gene.
    Klopstock T; Chahrokh-Zadeh S; Holinski-Feder E; Meindl A; Gasser T; Pongratz D; Müller-Felber W
    Acta Neuropathol; 1999 Feb; 97(2):139-42. PubMed ID: 9928824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure.
    Bidichandani SI; Ashizawa T; Patel PI
    Am J Hum Genet; 1998 Jan; 62(1):111-21. PubMed ID: 9443873
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansion.
    Zhu D; Burke C; Leslie A; Nicholson GA
    Mov Disord; 2002 May; 17(3):585-9. PubMed ID: 12112211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frataxin knockin mouse.
    Miranda CJ; Santos MM; Ohshima K; Smith J; Li L; Bunting M; Cossée M; Koenig M; Sequeiros J; Kaplan J; Pandolfo M
    FEBS Lett; 2002 Feb; 512(1-3):291-7. PubMed ID: 11852098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 gene.
    Gellera C; Pareyson D; Castellotti B; Mazzucchelli F; Zappacosta B; Pandolfo M; Di Donato S
    Neurology; 1997 Oct; 49(4):1153-5. PubMed ID: 9339708
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Altered beta-cell characteristics in impaired glucose tolerant carriers of a GAA trinucleotide repeat polymorphism in the frataxin gene.
    t Hart LM; Ruige JB; Dekker JM; Stehouwer CD; Maassen JA; Heine RJ
    Diabetes; 1999 Apr; 48(4):924-6. PubMed ID: 10102715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differential stability of the (GAA)n tract in the Friedreich ataxia (STM7) gene.
    Epplen C; Epplen JT; Frank G; Miterski B; Santos EJ; Schöls L
    Hum Genet; 1997 Jun; 99(6):834-6. PubMed ID: 9187683
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of Friedreich's ataxia confirmed by DNA-analysis.
    Atanassov N; Markova V
    Folia Med (Plovdiv); 1998; 40(3):11-3. PubMed ID: 10658348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.