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Results: 1 to 20 of 138

Similar articles for PubMed (Select 22262734)

1.

Effects of Friedreich's ataxia GAA repeats on DNA replication in mammalian cells.

Chandok GS, Patel MP, Mirkin SM, Krasilnikova MM.

Nucleic Acids Res. 2012 May;40(9):3964-74. doi: 10.1093/nar/gks021. Epub 2012 Jan 19.

2.

GAA triplet-repeats cause nucleosome depletion in the human genome.

Zhao H, Xing Y, Liu G, Chen P, Zhao X, Li G, Cai L.

Genomics. 2015 Jun 20. pii: S0888-7543(15)30014-8. doi: 10.1016/j.ygeno.2015.06.010. [Epub ahead of print]

PMID:
26100357
3.

Identification of genes containing expanded purine repeats in the human genome and their apparent protective role against cancer.

Singh HN, Rajeswari MR.

J Biomol Struct Dyn. 2015 Jun 25:1-16. [Epub ahead of print]

PMID:
25990537
4.

Friedreich's ataxia - a case of aberrant transcription termination?

Butler JS, Napierala M.

Transcription. 2015 Mar 15;6(2):33-6. doi: 10.1080/21541264.2015.1026538. Epub 2015 Apr 1.

PMID:
25831023
5.

Expanded GAA repeats impair FXN gene expression and reposition the FXN locus to the nuclear lamina in single cells.

Silva AM, Brown JM, Buckle VJ, Wade-Martins R, Lufino MM.

Hum Mol Genet. 2015 Jun 15;24(12):3457-71. doi: 10.1093/hmg/ddv096. Epub 2015 Mar 26.

PMID:
25814655
6.

Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population.

Zeng J, Wang J, Zeng S, He M, Zeng X, Zhou Y, Liu Z, Jiang H, Tang B.

J Neurol Sci. 2015 Apr 15;351(1-2):124-6. doi: 10.1016/j.jns.2015.03.002. Epub 2015 Mar 6.

PMID:
25765228
7.

Excision of Expanded GAA Repeats Alleviates the Molecular Phenotype of Friedreich's Ataxia.

Li Y, Polak U, Bhalla AD, Rozwadowska N, Butler JS, Lynch DR, Dent SY, Napierala M.

Mol Ther. 2015 Jun;23(6):1055-65. doi: 10.1038/mt.2015.41. Epub 2015 Mar 11.

PMID:
25758173
8.

A novel GAA-repeat-expansion-based mouse model of Friedreich's ataxia.

Anjomani Virmouni S, Ezzatizadeh V, Sandi C, Sandi M, Al-Mahdawi S, Chutake Y, Pook MA.

Dis Model Mech. 2015 Mar;8(3):225-35. doi: 10.1242/dmm.018952. Epub 2015 Feb 13.

9.

Coupling transcriptional state to large-scale repeat expansions in yeast.

Shah KA, McGinty RJ, Egorova VI, Mirkin SM.

Cell Rep. 2014 Dec 11;9(5):1594-602. doi: 10.1016/j.celrep.2014.10.048. Epub 2014 Nov 20.

10.

MutLα heterodimers modify the molecular phenotype of Friedreich ataxia.

Ezzatizadeh V, Sandi C, Sandi M, Anjomani-Virmouni S, Al-Mahdawi S, Pook MA.

PLoS One. 2014 Jun 27;9(6):e100523. doi: 10.1371/journal.pone.0100523. eCollection 2014.

11.

Mitochondrial disease: gene therapy protects heart in Friedreich's ataxia.

Flemming A.

Nat Rev Drug Discov. 2014 Jun;13(6):416-7. doi: 10.1038/nrd4346. Epub 2014 May 23. No abstract available.

PMID:
24854410
12.

Altered nucleosome positioning at the transcription start site and deficient transcriptional initiation in Friedreich ataxia.

Chutake YK, Costello WN, Lam C, Bidichandani SI.

J Biol Chem. 2014 May 30;289(22):15194-202. doi: 10.1074/jbc.M114.566414. Epub 2014 Apr 15.

13.

Base excision repair of chemotherapeutically-induced alkylated DNA damage predominantly causes contractions of expanded GAA repeats associated with Friedreich's ataxia.

Lai Y, Beaver JM, Lorente K, Melo J, Ramjagsingh S, Agoulnik IU, Zhang Z, Liu Y.

PLoS One. 2014 Apr 1;9(4):e93464. doi: 10.1371/journal.pone.0093464. eCollection 2014.

14.

FXN GAA repeat expansions in amyotrophic lateral sclerosis.

Rizik N, Freischmidt A, Ludolph AC, Weishaupt JH.

J Clin Neurosci. 2014 Aug;21(8):1319-22. doi: 10.1016/j.jocn.2013.10.029. Epub 2014 Jan 27.

PMID:
24613765
15.

Molecular and clinical investigation of Iranian patients with Friedreich ataxia.

Salehi MH, Houshmand M, Aryani O, Kamalidehghan B, Khalili E.

Iran Biomed J. 2014;18(1):28-33.

16.

Combined bidimensional electrophoresis and electron microscopy to study specific plasmid DNA replication intermediates in human cells.

Follonier C, Lopes M.

Methods Mol Biol. 2014;1094:209-19. doi: 10.1007/978-1-62703-706-8_16.

PMID:
24162990
17.

Friedreich ataxia patient tissues exhibit increased 5-hydroxymethylcytosine modification and decreased CTCF binding at the FXN locus.

Al-Mahdawi S, Sandi C, Mouro Pinto R, Pook MA.

PLoS One. 2013 Sep 4;8(9):e74956. doi: 10.1371/journal.pone.0074956. eCollection 2013.

18.

A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like.

Maalej M, Mkaouar-Rebai E, Mnif M, Mezghani N, Ben Ayed I, Chamkha I, Abid M, Fakhfakh F.

Pathol Biol (Paris). 2014 Feb;62(1):41-8. doi: 10.1016/j.patbio.2013.07.013. Epub 2013 Sep 4.

PMID:
24011957
19.

Quantitative profiling and identification of differentially expressed plasma proteins in Friedreich's ataxia.

Swarup V, Srivastava AK, Padma MV, Rajeswari MR.

J Neurosci Res. 2013 Nov;91(11):1483-91. doi: 10.1002/jnr.23262. Epub 2013 Aug 30.

PMID:
23996585
20.

A GAA repeat expansion reporter model of Friedreich's ataxia recapitulates the genomic context and allows rapid screening of therapeutic compounds.

Lufino MM, Silva AM, Németh AH, Alegre-Abarrategui J, Russell AJ, Wade-Martins R.

Hum Mol Genet. 2013 Dec 20;22(25):5173-87. doi: 10.1093/hmg/ddt370. Epub 2013 Aug 13.

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