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Results: 1 to 20 of 173

1.

CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.

Nielsen JE, Koefoed P, Abell K, Hasholt L, Eiberg H, Fenger K, Niebuhr E, Sørensen SA.

Hum Mol Genet. 1997 Oct;6(11):1811-6.

PMID:
9302257
[PubMed - indexed for MEDLINE]
Free Article
2.

An expanded CAG repeat sequence in spinocerebellar ataxia type 7.

Lindblad K, Savontaus ML, Stevanin G, Holmberg M, Digre K, Zander C, Ehrsson H, David G, Benomar A, Nikoskelainen E, Trottier Y, Holmgren G, Ptacek LJ, Anttinen A, Brice A, Schalling M.

Genome Res. 1996 Oct;6(10):965-71.

PMID:
8908515
[PubMed - indexed for MEDLINE]
Free Article
3.

Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation.

Del-Favero J, Goossens D, De Jonghe P, Benson K, Michalik A, Van den Bossche D, Horwitz M, Van Broeckhoven C.

Hum Genet. 1999 Sep;105(3):217-25.

PMID:
10987648
[PubMed - indexed for MEDLINE]
4.

No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24.

Zander C, Yuan QP, Lindblad K, Stevanin G, Dürr A, Davoine CS, Hazan J, Fontaine B, Brice A, Schalling M.

Neurosci Lett. 2000 Jan 21;279(1):41-4.

PMID:
10670783
[PubMed - indexed for MEDLINE]
5.

CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients.

Benson KF, Horwitz M, Wolff J, Friend K, Thompson E, White S, Richards RI, Raskind WH, Bird TD.

Hum Mol Genet. 1998 Oct;7(11):1779-86.

PMID:
9736780
[PubMed - indexed for MEDLINE]
Free Article
6.

Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.

Pujana MA, Volpini V, Gratacós M, Corral J, Banchs I, Sánchez A, Genís D, Cervera C, Estivill X.

J Med Genet. 1998 Feb;35(2):99-102.

PMID:
9507387
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.

Koshy BT, Zoghbi HY.

Brain Pathol. 1997 Jul;7(3):927-42. Review.

PMID:
9217976
[PubMed - indexed for MEDLINE]
8.

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.

Ishikawa K, Tanaka H, Saito M, Ohkoshi N, Fujita T, Yoshizawa K, Ikeuchi T, Watanabe M, Hayashi A, Takiyama Y, Nishizawa M, Nakano I, Matsubayashi K, Miwa M, Shoji S, Kanazawa I, Tsuji S, Mizusawa H.

Am J Hum Genet. 1997 Aug;61(2):336-46.

PMID:
9311738
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study.

Nielsen JE, Krabbe K, Jennum P, Koefoed P, Jensen LN, Fenger K, Eiberg H, Hasholt L, Werdelin L, Sørensen SA.

J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):61-6.

PMID:
9436729
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

[Growing genes cause neurological diseases].

Johansson J, Holmgren G, Forsgren L, Holmberg M.

Lakartidningen. 1999 Feb 24;96(8):897-900. Review. Swedish.

PMID:
10089735
[PubMed - indexed for MEDLINE]
11.

[Genomic instability and neurodegenerative disease].

Miki T, Yamagata H.

Rinsho Byori. 1999 Jan;47(1):37-45. Japanese.

PMID:
10067364
[PubMed - indexed for MEDLINE]
12.

CAG-encoded polyglutamine length polymorphism in the human genome.

Butland SL, Devon RS, Huang Y, Mead CL, Meynert AM, Neal SJ, Lee SS, Wilkinson A, Yang GS, Yuen MM, Hayden MR, Holt RA, Leavitt BR, Ouellette BF.

BMC Genomics. 2007 May 22;8:126.

PMID:
17519034
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Trinucleotide repeat expansion in neurological disease.

La Spada AR, Paulson HL, Fischbeck KH.

Ann Neurol. 1994 Dec;36(6):814-22. Review.

PMID:
7998766
[PubMed - indexed for MEDLINE]
14.

A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.

Hazan J, Davoine CS, Mavel D, Fonknechten N, Paternotte C, Fizames C, Cruaud C, Samson D, Muselet D, Vega-Czarny N, Brice A, Gyapay G, Heilig R, Fontaine B, Weissenbach J.

Genomics. 1999 Sep 15;60(3):309-19.

PMID:
10493830
[PubMed - indexed for MEDLINE]
15.

Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.

Spiegel R, La Spada AR, Kress W, Fischbeck KH, Schmid W.

Hum Mutat. 1996;8(1):32-7.

PMID:
8807333
[PubMed - indexed for MEDLINE]
16.

Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder.

Hedera P, Rainier S, Zhao XP, Schalling M, Lindblad K, Yuan QP, Ikeuchi T, Trobe J, Wald JJ, Eldevik OP, Kluin K, Fink JK.

Neurology. 2002 Feb 12;58(3):411-6.

PMID:
11839840
[PubMed - indexed for MEDLINE]
17.
18.

Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias.

Matilla T, Volpini V, Genís D, Rosell J, Corral J, Dávalos A, Molins A, Estivill X.

Hum Mol Genet. 1993 Dec;2(12):2123-8.

PMID:
8111382
[PubMed - indexed for MEDLINE]
19.

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.

Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A.

Hum Genet. 1996 Sep;98(3):371-5.

PMID:
8707310
[PubMed - indexed for MEDLINE]
20.

[Molecular genetics of Huntington's disease].

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

Rinsho Shinkeigaku. 1995 Dec;35(12):1529-31. Japanese.

PMID:
8752453
[PubMed - indexed for MEDLINE]

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