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Items: 1 to 20 of 710

1.

Unexpected formation of parallel duplex in GAA and TTC trinucleotide repeats of Friedreich's ataxia.

LeProust EM, Pearson CE, Sinden RR, Gao X.

J Mol Biol. 2000 Oct 6;302(5):1063-80. Erratum in: J Mol Biol 2001 Jan 9;306(1):133. Pearso, CE [corrected to Pearson, CE].

PMID:
11183775
2.

Alleviating transcript insufficiency caused by Friedreich's ataxia triplet repeats.

Grabczyk E, Usdin K.

Nucleic Acids Res. 2000 Dec 15;28(24):4930-7.

4.

Sticky DNA: self-association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich's ataxia.

Sakamoto N, Chastain PD, Parniewski P, Ohshima K, Pandolfo M, Griffith JD, Wells RD.

Mol Cell. 1999 Apr;3(4):465-75.

5.

The high-resolution structure of the triplex formed by the GAA/TTC triplet repeat associated with Friedreich's ataxia.

Mariappan SV, Catasti P, Silks LA 3rd, Bradbury EM, Gupta G.

J Mol Biol. 1999 Feb 5;285(5):2035-52.

PMID:
9925783
6.

GGA*TCC-interrupted triplets in long GAA*TTC repeats inhibit the formation of triplex and sticky DNA structures, alleviate transcription inhibition, and reduce genetic instabilities.

Sakamoto N, Larson JE, Iyer RR, Montermini L, Pandolfo M, Wells RD.

J Biol Chem. 2001 Jul 20;276(29):27178-87. Epub 2001 Apr 26.

7.
8.

Friedreich's ataxia GAA.TTC duplex and GAA.GAA.TTC triplex structures exclude nucleosome assembly.

Ruan H, Wang YH.

J Mol Biol. 2008 Nov 7;383(2):292-300. doi: 10.1016/j.jmb.2008.08.053. Epub 2008 Aug 27.

PMID:
18775729
9.
10.

GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseases.

Gacy AM, Goellner GM, Spiro C, Chen X, Gupta G, Bradbury EM, Dyer RB, Mikesell MJ, Yao JZ, Johnson AJ, Richter A, Melançon SB, McMurray CT.

Mol Cell. 1998 Mar;1(4):583-93.

11.
12.

Structure-dependent recombination hot spot activity of GAA.TTC sequences from intron 1 of the Friedreich's ataxia gene.

Napierala M, Dere R, Vetcher A, Wells RD.

J Biol Chem. 2004 Feb 20;279(8):6444-54. Epub 2003 Nov 18.

13.

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.

PMID:
10982187
14.

Energetics of strand-displacement reactions in triple helices: a spectroscopic study.

Mills M, Arimondo PB, Lacroix L, Garestier T, Hélène C, Klump H, Mergny JL.

J Mol Biol. 1999 Sep 3;291(5):1035-54.

PMID:
10518941
15.

Structure-specific recognition of Friedreich's ataxia (GAA)n repeats by benzoquinoquinoxaline derivatives.

Bergquist H, Nikravesh A, Fernández RD, Larsson V, Nguyen CH, Good L, Zain R.

Chembiochem. 2009 Nov 2;10(16):2629-37. doi: 10.1002/cbic.200900263.

PMID:
19746387
16.

Fragile X syndrome and Friedreich's ataxia: two different paradigms for repeat induced transcript insufficiency.

Grabczyk E, Kumari D, Usdin K.

Brain Res Bull. 2001 Oct-Nov 1;56(3-4):367-73. Review.

PMID:
11719274
17.

Sticky DNA formation in vivo alters the plasmid dimer/monomer ratio.

Vetcher AA, Wells RD.

J Biol Chem. 2004 Feb 20;279(8):6434-43. Epub 2003 Nov 18.

18.

Sticky DNA, a self-associated complex formed at long GAA*TTC repeats in intron 1 of the frataxin gene, inhibits transcription.

Sakamoto N, Ohshima K, Montermini L, Pandolfo M, Wells RD.

J Biol Chem. 2001 Jul 20;276(29):27171-7. Epub 2001 May 4.

19.

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.

PMID:
11269509
20.

Sticky DNA, a long GAA.GAA.TTC triplex that is formed intramolecularly, in the sequence of intron 1 of the frataxin gene.

Vetcher AA, Napierala M, Iyer RR, Chastain PD, Griffith JD, Wells RD.

J Biol Chem. 2002 Oct 18;277(42):39217-27. Epub 2002 Aug 2.

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