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Items: 1 to 20 of 117

1.

Haplotype background, repeat length evolution, and Huntington's disease.

Falush D.

Am J Hum Genet. 2009 Dec;85(6):939-42. doi: 10.1016/j.ajhg.2009.11.002. No abstract available.

2.

Response to Falush: a role for cis-element polymorphisms in HD.

Warby SC, Visscher H, Butland S, Pearson CE, Hayden MR.

Am J Hum Genet. 2009 Dec;85(6):942-5. doi: 10.1016/j.ajhg.2009.11.006. No abstract available.

3.

[Analysis of the IT15 gene in Huntington's disease families].

[No authors listed]

Genetika. 2004 Aug;40(8):1123-30. Russian.

PMID:
15523851
4.

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.

5.

Huntington disease mutation in Venezuela: age of onset, haplotype analyses and geographic aggregation.

Paradisi I, Hernández A, Arias S.

J Hum Genet. 2008;53(2):127-35. Epub 2007 Dec 22. Erratum in: J Hum Genet. 2008;53(4):376.

PMID:
18157708
6.

Update on genetics of Huntington's disease: availability of direct and accurate predictive test.

Squitieri F, Campanella G, Hayden MR.

Ital J Neurol Sci. 1996 Jun;17(3):185-7. No abstract available.

PMID:
8856407
7.

Correlation of CAG repeat length between the maternal and paternal allele of the Huntingtin gene: evidence for assortative mating.

Nopoulos P, Epping EA, Wassink T, Schlaggar BL, Perlmutter J.

Behav Brain Funct. 2011 Oct 18;7:45. doi: 10.1186/1744-9081-7-45.

8.

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease.

Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, Gellera C, Soliveri P, Lange HW, Weirich-Schwaiger H, Wenning GK, Melegh B, Havasi V, Balikó L, Wieczorek S, Arning L, Zaremba J, Sulek A, Hoffman-Zacharska D, Basak AN, Ersoy N, Zidovska J, Kebrdlova V, Pandolfo M, Ribaï P, Kadasi L, Kvasnicova M, Weber BH, Kreuz F, Dose M, Stuhrmann M, Riess O.

Neurogenetics. 2006 Mar;7(1):27-30. Epub 2005 Dec 21.

PMID:
16369839
9.

Images in neuroscience. Clinical genetics, I. Huntington's disease: from disease to gene.

Tamminga CA, Schwarcz R, MacDonald ME.

Am J Psychiatry. 1997 Jun;154(6):725. No abstract available.

PMID:
9167497
10.

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
11.

Identification and characterization of the miniature pig Huntington's disease gene homolog: evidence for conservation and polymorphism in the CAG triplet repeat.

Matsuyama N, Hadano S, Onoe K, Osuga H, Showguchi-Miyata J, Gondo Y, Ikeda JE.

Genomics. 2000 Oct 1;69(1):72-85.

PMID:
11013077
12.

Caudate glucose hypometabolism in a subject carrying an unstable allele of intermediate CAG(33) repeat length in the Huntington's disease gene.

Squitieri F, Esmaeilzadeh M, Ciarmiello A, Jankovic J.

Mov Disord. 2011 Apr;26(5):925-7. doi: 10.1002/mds.23623. Epub 2011 Mar 2. No abstract available.

PMID:
21370274
13.

Autopsy-proven Huntington's disease with 29 trinucleotide repeats.

Kenney C, Powell S, Jankovic J.

Mov Disord. 2007 Jan;22(1):127-30.

PMID:
17115386
14.

Intergenerational CAG repeat instability is highly heritable in Huntington's disease.

Aziz NA, van Belzen MJ, Roos RA.

J Med Genet. 2008 Nov;45(11):766. doi: 10.1136/jmg.2008.062133. No abstract available.

PMID:
18978336
15.

Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.

García-Planells J, Burguera JA, Solís P, Millán JM, Ginestar D, Palau F, Espinós C.

Hum Mutat. 2005 May;25(5):453-9.

PMID:
15832309
16.

CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup.

Warby SC, Montpetit A, Hayden AR, Carroll JB, Butland SL, Visscher H, Collins JA, Semaka A, Hudson TJ, Hayden MR.

Am J Hum Genet. 2009 Mar;84(3):351-66. doi: 10.1016/j.ajhg.2009.02.003. Epub 2009 Feb 26.

17.

Characterising the Huntington's disease gene product.

Wood J, MacMillan JC, Thomas P, Lowenstein PR, Harper PS, Jones AL.

Biochem Soc Trans. 1995 Nov;23(4):595S. No abstract available.

PMID:
8654780
18.

How does the Huntington's disease mutation damage cells?

Rubinsztein DC.

Sci Aging Knowledge Environ. 2003 Sep 17;2003(37):PE26. Review.

PMID:
13679594
19.

Analysis of short tandem repeat markers by capillary array electrophoresis.

Mansfield ES, Wilson RB, Fortina P.

Methods Mol Biol. 2001;163:151-61. No abstract available.

PMID:
11242940
20.

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

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