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Results: 1 to 20 of 128

1.

Unusual structures are present in DNA fragments containing super-long Huntingtin CAG repeats.

Duzdevich D, Li J, Whang J, Takahashi H, Takeyasu K, Dryden DT, Morton AJ, Edwardson JM.

PLoS One. 2011 Feb 11;6(2):e17119. doi: 10.1371/journal.pone.0017119.

PMID:
21347256
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Paradoxical delay in the onset of disease caused by super-long CAG repeat expansions in R6/2 mice.

Morton AJ, Glynn D, Leavens W, Zheng Z, Faull RL, Skepper JN, Wight JM.

Neurobiol Dis. 2009 Mar;33(3):331-41. doi: 10.1016/j.nbd.2008.11.015. Epub 2008 Dec 11.

PMID:
19130884
[PubMed - indexed for MEDLINE]
3.

Quantification of age-dependent somatic CAG repeat instability in Hdh CAG knock-in mice reveals different expansion dynamics in striatum and liver.

Lee JM, Pinto RM, Gillis T, St Claire JC, Wheeler VC.

PLoS One. 2011;6(8):e23647. doi: 10.1371/journal.pone.0023647. Epub 2011 Aug 29.

PMID:
21897851
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

A critical window of CAG repeat-length correlates with phenotype severity in the R6/2 mouse model of Huntington's disease.

Cummings DM, Alaghband Y, Hickey MA, Joshi PR, Hong SC, Zhu C, Ando TK, André VM, Cepeda C, Watson JB, Levine MS.

J Neurophysiol. 2012 Jan;107(2):677-91. doi: 10.1152/jn.00762.2011. Epub 2011 Nov 9.

PMID:
22072510
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice.

Lloret A, Dragileva E, Teed A, Espinola J, Fossale E, Gillis T, Lopez E, Myers RH, MacDonald ME, Wheeler VC.

Hum Mol Genet. 2006 Jun 15;15(12):2015-24. Epub 2006 May 10.

PMID:
16687439
[PubMed - indexed for MEDLINE]
Free Article
6.

Counting CAG repeats in the Huntington's disease gene by restriction endonuclease EcoP15I cleavage.

Möncke-Buchner E, Reich S, Mücke M, Reuter M, Messer W, Wanker EE, Krüger DH.

Nucleic Acids Res. 2002 Aug 15;30(16):e83.

PMID:
12177311
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Transcription elongation and tissue-specific somatic CAG instability.

Goula AV, Stys A, Chan JP, Trottier Y, Festenstein R, Merienne K.

PLoS Genet. 2012;8(11):e1003051. doi: 10.1371/journal.pgen.1003051. Epub 2012 Nov 29.

PMID:
23209427
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.

Masuda N, Goto J, Murayama N, Watanabe M, Kondo I, Kanazawa I.

J Med Genet. 1995 Sep;32(9):701-5.

PMID:
8544189
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length.

Hansson O, Castilho RF, Korhonen L, Lindholm D, Bates GP, Brundin P.

J Neurochem. 2001 Aug;78(4):694-703.

PMID:
11520890
[PubMed - indexed for MEDLINE]
10.

MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.

Tomé S, Manley K, Simard JP, Clark GW, Slean MM, Swami M, Shelbourne PF, Tillier ER, Monckton DG, Messer A, Pearson CE.

PLoS Genet. 2013;9(2):e1003280. doi: 10.1371/journal.pgen.1003280. Epub 2013 Feb 28.

PMID:
23468640
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

Mangiarini L, Sathasivam K, Mahal A, Mott R, Seller M, Bates GP.

Nat Genet. 1997 Feb;15(2):197-200.

PMID:
9020849
[PubMed - indexed for MEDLINE]
12.

Expansion of a (CAG)n repeat region in a sporadic case of HD.

Bozza A, Malagù S, Calzolari E, Novelletto A, Pavoni M, del Senno L.

Acta Neurol Scand. 1995 Aug;92(2):132-4.

PMID:
7484060
[PubMed - indexed for MEDLINE]
13.

Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease.

Reddy PH, Charles V, Williams M, Miller G, Whetsell WO Jr, Tagle DA.

Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):1035-45.

PMID:
10434303
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Patterns of meiotic variability of the (CAG)n repeat in the Huntington disease gene.

Lucotte G, Gérard N, Aouizérate A, Loirat F, Hazout S.

Genet Couns. 1997;8(2):77-81.

PMID:
9219003
[PubMed - indexed for MEDLINE]
15.

Weight loss in Huntington disease increases with higher CAG repeat number.

Aziz NA, van der Burg JM, Landwehrmeyer GB, Brundin P, Stijnen T; EHDI Study Group, Roos RA.

Neurology. 2008 Nov 4;71(19):1506-13. doi: 10.1212/01.wnl.0000334276.09729.0e.

PMID:
18981372
[PubMed - indexed for MEDLINE]
16.

Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standard.

Bruland O, Almqvist EW, Goldberg YP, Boman H, Hayden MR, Knappskog PM.

Clin Genet. 1999 Mar;55(3):198-202.

PMID:
10334474
[PubMed - indexed for MEDLINE]
17.

Premutation huntingtin allele adopts a non-B conformation and contains a hot spot for DNA damage.

Jarem DA, Delaney S.

Biochem Biophys Res Commun. 2011 Dec 9;416(1-2):146-52. doi: 10.1016/j.bbrc.2011.11.013. Epub 2011 Nov 11.

PMID:
22100810
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients.

Sathasivam K, Woodman B, Mahal A, Bertaux F, Wanker EE, Shima DT, Bates GP.

Hum Mol Genet. 2001 Oct 1;10(21):2425-35.

PMID:
11689489
[PubMed - indexed for MEDLINE]
Free Article
19.

The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease.

Klempíř J, Zidovská J, Stochl J, Ing VK, Uhrová T, Roth J.

Mov Disord. 2011 Jan;26(1):125-9. doi: 10.1002/mds.23436. Epub 2010 Nov 10.

PMID:
21322024
[PubMed - indexed for MEDLINE]
20.

Solution structures of the Huntington's disease DNA triplets, (CAG)n.

Mariappan SV, Silks LA 3rd, Chen X, Springer PA, Wu R, Moyzis RK, Bradbury EM, Garcia AE, Gupta G.

J Biomol Struct Dyn. 1998 Feb;15(4):723-44.

PMID:
9514249
[PubMed - indexed for MEDLINE]

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