Rubinsztein DC - Search Results

1

Candidate gene association studies of genes involved in neuronal cholinergic transmission in Alzheimer's disease suggests choline acetyltransferase as a candidate deserving further study.

Cook LJ, Ho LW, Wang L, Terrenoire E, Brayne C, Evans JG, Xuereb J, Cairns NJ, Turic D, Hollingworth P, Moore PJ, Jehu L, Archer N, Walter S, Foy C, Edmondson A, Powell J, Lovestone S, Williams J, Rubinsztein DC. Cook LJ, et al. Among authors: rubinsztein dc. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):5-8. doi: 10.1002/ajmg.b.30068. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15690550

2

Apo E genotypes in multiple sclerosis, Parkinson's disease, schwannomas and late-onset Alzheimer's disease.

Rubinsztein DC, Hanlon CS, Irving RM, Goodburn S, Evans DG, Kellar-Wood H, Xuereb JH, Bandmann O, Harding AE. Rubinsztein DC, et al. Mol Cell Probes. 1994 Dec;8(6):519-25. doi: 10.1006/mcpr.1994.1073. Mol Cell Probes. 1994. PMID: 7700274

3

Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia.

Rubinsztein DC, Leggo J, Goodburn S, Crow TJ, Lofthouse R, DeLisi LE, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. J Med Genet. 1994 Sep;31(9):690-3. doi: 10.1136/jmg.31.9.690. J Med Genet. 1994. PMID: 7815437 Free PMC article.

4

The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years.

Tysoe C, Robinson D, Brayne C, Dening T, Paykel ES, Huppert FA, Rubinsztein DC. Tysoe C, et al. Among authors: rubinsztein dc. J Med Genet. 1996 Dec;33(12):1002-6. doi: 10.1136/jmg.33.12.1002. J Med Genet. 1996. PMID: 9004131 Free PMC article.

5

Analysis of the apo E/apo C-I, angiotensin converting enzyme and methylenetetrahydrofolate reductase genes as candidates affecting human longevity.

Galinsky D, Tysoe C, Brayne CE, Easton DF, Huppert FA, Dening TR, Paykel ES, Rubinsztein DC. Galinsky D, et al. Among authors: rubinsztein dc. Atherosclerosis. 1997 Mar 21;129(2):177-83. doi: 10.1016/s0021-9150(96)06027-3. Atherosclerosis. 1997. PMID: 9105559

6

Presenilin-1 intron 8 polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's disease.

Tysoe C, Whittaker J, Cairns NJ, Atkinson PF, Harrington CR, Xuereb J, Wilcock G, Rubinsztein DC. Tysoe C, et al. Among authors: rubinsztein dc. Neurosci Lett. 1997 Jan 24;222(1):68-9. doi: 10.1016/s0304-3940(97)13339-0. Neurosci Lett. 1997. PMID: 9121726

7

Analysis of alpha-1 antichymotrypsin, presenilin-1, angiotensin-converting enzyme, and methylenetetrahydrofolate reductase loci as candidates for dementia.

Tysoe C, Galinsky D, Robinson D, Brayne CE, Easton DF, Huppert FA, Dening T, Paykel ES, Rubinsztein DC. Tysoe C, et al. Among authors: rubinsztein dc. Am J Med Genet. 1997 Apr 18;74(2):207-12. doi: 10.1002/(sici)1096-8628(19970418)74:2<207::aid-ajmg20>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9129727

8

Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats.

Rubinsztein DC, Leggo J. Rubinsztein DC, et al. J Med Genet. 1997 Mar;34(3):234-6. doi: 10.1136/jmg.34.3.234. J Med Genet. 1997. PMID: 9132496 Free PMC article.

9

Analysis of the 5' upstream sequence of the Huntington's disease (HD) gene shows six new rare alleles which are unrelated to the age at onset of HD.

Coles R, Leggo J, Rubinsztein DC. Coles R, et al. Among authors: rubinsztein dc. J Med Genet. 1997 May;34(5):371-4. doi: 10.1136/jmg.34.5.371. J Med Genet. 1997. PMID: 9152833 Free PMC article.

10

The genetics of Alzheimer's disease.

Rubinsztein DC. Rubinsztein DC. Prog Neurobiol. 1997 Aug;52(6):447-54. doi: 10.1016/s0301-0082(97)00014-2. Prog Neurobiol. 1997. PMID: 9316155 Review.

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