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Items: 1 to 20 of 126

1.

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.

Biancalana V, Serville F, Pommier J, Julien J, Hanauer A, Mandel JL.

Hum Mol Genet. 1992 Jul;1(4):255-8.

PMID:
1303195
2.

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
3.

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.

La Spada AR, Roling DB, Harding AE, Warner CL, Spiegel R, Hausmanowa-Petrusewicz I, Yee WC, Fischbeck KH.

Nat Genet. 1992 Dec;2(4):301-4.

PMID:
1303283
4.

Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability.

La Spada AR, Peterson KR, Meadows SA, McClain ME, Jeng G, Chmelar RS, Haugen HA, Chen K, Singer MJ, Moore D, Trask BJ, Fischbeck KH, Clegg CH, McKnight GS.

Hum Mol Genet. 1998 Jun;7(6):959-67.

PMID:
9580659
5.
6.

Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy.

Belsham DD, Yee WC, Greenberg CR, Wrogemann K.

J Neurol Sci. 1992 Oct;112(1-2):133-8.

PMID:
1469423
7.

CAG repeat length variation in sperm from a patient with Kennedy's disease.

Zhang L, Fischbeck KH, Arnheim N.

Hum Mol Genet. 1995 Feb;4(2):303-5.

PMID:
7757084
8.

A novel primer extension method to detect the number of CAG repeats in the androgen receptor gene in families with X-linked spinal and bulbar muscular atrophy.

Yamamoto Y, Kawai H, Nakahara K, Osame M, Nakatsuji Y, Kishimoto T, Sakoda S.

Biochem Biophys Res Commun. 1992 Jan 31;182(2):507-13.

PMID:
1734865
9.

Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals.

Kuhlenbäumer G, Kress W, Ringelstein EB, Stögbauer F.

J Neurol. 2001 Jan;248(1):23-6.

PMID:
11266016
10.

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH.

Nature. 1991 Jul 4;352(6330):77-9.

PMID:
2062380
11.

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.

Snow K, Tester DJ, Kruckeberg KE, Schaid DJ, Thibodeau SN.

Hum Mol Genet. 1994 Sep;3(9):1543-51.

PMID:
7833909
12.

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
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
14.

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy.

Igarashi S, Tanno Y, Onodera O, Yamazaki M, Sato S, Ishikawa A, Miyatani N, Nagashima M, Ishikawa Y, Sahashi K, et al.

Neurology. 1992 Dec;42(12):2300-2.

PMID:
1461383
15.

CAG-repeat expansion in androgen receptor in Kennedy's disease is not a loss of function mutation.

Neuschmid-Kaspar F, Gast A, Peterziel H, Schneikert J, Muigg A, Ransmayr G, Klocker H, Bartsch G, Cato AC.

Mol Cell Endocrinol. 1996 Mar 25;117(2):149-56.

PMID:
8737374
16.
17.

Mitotic and meiotic stability of the CAG repeat in the X-linked spinal and bulbar muscular atrophy gene.

Watanabe M, Abe K, Aoki M, Yasuo K, Itoyama Y, Shoji M, Ikeda Y, Iizuka T, Ikeda M, Shizuka M, Mizushima K, Hirai S.

Clin Genet. 1996 Sep;50(3):133-7.

PMID:
8946111
18.

Spinal and bulbar muscular atrophy (SBMA): somatic stability of an expanded CAG repeat in fetal tissues.

Jedele KB, Wahl D, Chahrokh-Zadeh S, Wirtz A, Murken J, Holinski-Feder E.

Clin Genet. 1998 Aug;54(2):148-51.

PMID:
9761394
19.

The mutation properties of spinal and bulbar muscular atrophy disease alleles.

Grewal RP, Leeflang EP, Zhang L, Arnheim N.

Neurogenetics. 1998 Aug;1(4):249-52.

PMID:
10732798
20.

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