McLachlan DR - Search Results

1

Machado-Joseph disease in pedigrees of Azorean descent is linked to chromosome 14.

St George-Hyslop P, Rogaeva E, Huterer J, Tsuda T, Santos J, Haines JL, Schlumpf K, Rogaev EI, Liang Y, McLachlan DR, et al. St George-Hyslop P, et al. Among authors: mclachlan dr. Am J Hum Genet. 1994 Jul;55(1):120-5. Am J Hum Genet. 1994. PMID: 8023841 Free PMC article.

2

Are the associations between Alzheimer's disease and polymorphisms in the apolipoprotein E and the apolipoprotein CII genes due to linkage disequilibrium?

Tsuda T, Lopez R, Rogaeva EA, Freedman M, Rogaev E, Drachman D, Pollen D, Haines J, Liang Y, McLachlan DR, et al. Tsuda T, et al. Among authors: mclachlan dr. Ann Neurol. 1994 Jul;36(1):97-100. doi: 10.1002/ana.410360118. Ann Neurol. 1994. PMID: 8024269

3

Protein-DNA interactions in the promoter region of the amyloid precursor protein (APP) gene in human neocortex.

Lukiw WJ, Rogaev EI, Wong L, Vaula G, McLachlan DR, St George Hyslop P. Lukiw WJ, et al. Among authors: mclachlan dr. Brain Res Mol Brain Res. 1994 Mar;22(1-4):121-31. doi: 10.1016/0169-328x(94)90039-6. Brain Res Mol Brain Res. 1994. PMID: 8015372

4

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, Voskresenskaya N, Mayeux R, Growden J, Fried VA, Myers RH, Nee L, Backhovens H, Martin JJ, Rossor M, Owen MJ, Mullan M, Percy ME, Karlinsky H, Rich S, Heston L, Montesi M, Mortilla M, Nacmias N, Gusella JF, Hardy JA; FAD Collaborative Study Group, et al. St George-Hyslop PH, et al. Among authors: mclachlan dr. Nature. 1990 Sep 13;347(6289):194-7. doi: 10.1038/347194a0. Nature. 1990. PMID: 2395471

5

A prospective study of the clinical utility of ApoE genotype in the prediction of outcome in patients with memory impairment.

Tierney MC, Szalai JP, Snow WG, Fisher RH, Tsuda T, Chi H, McLachlan DR, St George-Hyslop PH. Tierney MC, et al. Among authors: mclachlan dr. Neurology. 1996 Jan;46(1):149-54. doi: 10.1212/wnl.46.1.149. Neurology. 1996. PMID: 8559365

6

Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosis.

Tsuda T, Munthasser S, Fraser PE, Percy ME, Rainero I, Vaula G, Pinessi L, Bergamini L, Vignocchi G, McLachlan DR, et al. Tsuda T, et al. Among authors: mclachlan dr. Neuron. 1994 Sep;13(3):727-36. doi: 10.1016/0896-6273(94)90039-6. Neuron. 1994. PMID: 7917302

7

Age-associated chromosome 21 loss in Down syndrome: possible relevance to mosaicism and Alzheimer disease.

Percy ME, Markovic VD, Dalton AJ, McLachlan DR, Berg JM, Rusk AC, Somerville MJ, Chodakowski B, Andrews DF. Percy ME, et al. Among authors: mclachlan dr. Am J Med Genet. 1993 Mar 1;45(5):584-8. doi: 10.1002/ajmg.1320450513. Am J Med Genet. 1993. PMID: 8456829

8

Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: II. Further cytogenetic analysis of the marker and characterization of the high-level repeat sequences using fluorescence in situ hybridization.

Percy ME, Dearie TG, Jabs EW, Bauer SJ, Chodakowski B, Somerville MJ, Lennox A, McLachlan DR, Baldini A, Miller DA. Percy ME, et al. Among authors: mclachlan dr. Am J Med Genet. 1993 Aug 1;47(1):14-9. doi: 10.1002/ajmg.1320470104. Am J Med Genet. 1993. PMID: 7690182

9

Red cell superoxide dismutase, glutathione peroxidase and catalase in Down syndrome patients with and without manifestations of Alzheimer disease.

Percy ME, Dalton AJ, Markovic VD, McLachlan DR, Hummel JT, Rusk AC, Andrews DF. Percy ME, et al. Among authors: mclachlan dr. Am J Med Genet. 1990 Apr;35(4):459-67. doi: 10.1002/ajmg.1320350403. Am J Med Genet. 1990. PMID: 2139757

10

SOD1 missense mutation in an Italian family with ALS.

Rainero I, Pinessi L, Tsuda T, Vignocchi MG, Vaula G, Calvi L, Cerrato P, Rossi B, Bergamini L, McLachlan DR, et al. Rainero I, et al. Among authors: mclachlan dr. Neurology. 1994 Feb;44(2):347-9. doi: 10.1212/wnl.44.2.347. Neurology. 1994. PMID: 8309590

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