Vaula G - Search Results

1

Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease.

Rogaev EI, Lukiw WJ, Vaula G, Haines JL, Rogaeva EA, Tsuda T, Alexandrova N, Liang Y, Mortilla M, Amaducci L, Bergamini L, Bruni AC, Foncin JF, Macciardi F, Montesi M, Sorbi S, Rainero I, Pinessi L, Polinsky RJ, Frommelt P, Duara R, Lopez R, Pollen D, Gusella JF, Tanzi R, MacLachlan D, Crapper D, St George-Hyslop PH, et al. Rogaev EI, et al. Among authors: vaula g. Neurology. 1993 Nov;43(11):2275-9. doi: 10.1212/wnl.43.11.2275. Neurology. 1993. PMID: 8232942

2

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.

St George-Hyslop P, Haines J, Rogaev E, Mortilla M, Vaula G, Pericak-Vance M, Foncin JF, Montesi M, Bruni A, Sorbi S, Rainero I, Pinessi L, Pollen D, Polinsky R, Nee L, Kennedy J, Macciardi F, Rogaeva E, Liang Y, Alexandrova N, Lukiw W, Schlumpf K, Tanzi R, Tsuda T, Farrer L, Cantu JM, Duara R, Amaducci L, Bergamini L, Gusella J, Roses A, Crapper McLachlan D, et al. St George-Hyslop P, et al. Among authors: vaula g. Nat Genet. 1992 Dec;2(4):330-4. doi: 10.1038/ng1292-330. Nat Genet. 1992. PMID: 1303289 Free article.

3

A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene.

Vaula G, Mortilla M, Tupler R, Lukiw W, Tanzi R, Nee L, Polinsky R, Foncin JF, Bruni AC, Montesi MP, et al. Vaula G, et al. Neurosci Lett. 1992 Sep 14;144(1-2):46-8. doi: 10.1016/0304-3940(92)90712-g. Neurosci Lett. 1992. PMID: 1436713

4

Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene.

Karlinsky H, Vaula G, Haines JL, Ridgley J, Bergeron C, Mortilla M, Tupler RG, Percy ME, Robitaille Y, Noldy NE, et al. Karlinsky H, et al. Among authors: vaula g. Neurology. 1992 Aug;42(8):1445-53. doi: 10.1212/wnl.42.8.1445. Neurology. 1992. PMID: 1520398

5

Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease cases.

Tanzi RE, Vaula G, Romano DM, Mortilla M, Huang TL, Tupler RG, Wasco W, Hyman BT, Haines JL, Jenkins BJ, et al. Tanzi RE, et al. Among authors: vaula g. Am J Hum Genet. 1992 Aug;51(2):273-82. Am J Hum Genet. 1992. PMID: 1642228 Free PMC article.

6

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: vaula g. 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

7

A new Italian pedigree with early-onset Alzheimer's disease.

Rainero I, Bergamini L, Bruni AC, Ferini-Strambi L, Foncin JF, Gei G, Macciardi F, Montesi MP, Pinessi L, Vaula G. Rainero I, et al. Among authors: vaula g. J Geriatr Psychiatry Neurol. 1994 Jan-Mar;7(1):28-32. J Geriatr Psychiatry Neurol. 1994. PMID: 8192827

8

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: vaula g. Neurology. 1994 Feb;44(2):347-9. doi: 10.1212/wnl.44.2.347. Neurology. 1994. PMID: 8309590

9

A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) gene.

Tupler R, Rogaeva E, Vaula G, Mortilla M, Lukiw W, Liang Y, Hancock R, Rogaev E, St George-Hyslop P. Tupler R, et al. Among authors: vaula g. Hum Mol Genet. 1993 May;2(5):620. doi: 10.1093/hmg/2.5.620. Hum Mol Genet. 1993. PMID: 8518820 No abstract available.

10

An informative microsatellite repeat polymorphism in the human neurofilament light polypeptide (NEFL) gene.

Rogaev E, Rogaeva E, Lukiw WJ, Vaula G, Liang Y, Hancock R, McLachlan DC, St George-Hyslop PH. Rogaev E, et al. Among authors: vaula g. Hum Mol Genet. 1992 Dec;1(9):781. doi: 10.1093/hmg/1.9.781. Hum Mol Genet. 1992. PMID: 1302625 No abstract available.

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