Mallet J - Search Results

1

Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.

Brice A, Boch AL, Stevanin G, Khati C, Dubois B, Agid Y, Campion D, Clerget F, Mallet J, Bellis M, et al. Brice A, et al. Among authors: mallet j. J Neurol Neurosurg Psychiatry. 1993 Jan;56(1):112-3. doi: 10.1136/jnnp.56.1.112-a. J Neurol Neurosurg Psychiatry. 1993. PMID: 8429314 Free PMC article. No abstract available.

2

No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients.

Carter D, Campion D, d'Amato T, Jay M, Brice A, Bellis M, Mallet J, Agid Y. Carter D, et al. Among authors: mallet j. Hum Mol Genet. 1993 Mar;2(3):321. doi: 10.1093/hmg/2.3.321. Hum Mol Genet. 1993. PMID: 8499923 No abstract available.

3

More missense in amyloid gene.

Carter DA, Desmarais E, Bellis M, Campion D, Clerget-Darpoux F, Brice A, Agid Y, Jaillard-Serradt A, Mallet J. Carter DA, et al. Among authors: mallet j. Nat Genet. 1992 Dec;2(4):255-6. doi: 10.1038/ng1292-255. Nat Genet. 1992. PMID: 1303275 No abstract available.

4

Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study Group.

Brice A, Tardieu S, Campion D, Le Guern E, Martinez M, Carpentier A, Penet C, Dubois B, Bellis M, Mallet J, et al. Brice A, et al. Among authors: mallet j. Am J Med Genet. 1995 Apr 24;60(2):91-3. doi: 10.1002/ajmg.1320600202. Am J Med Genet. 1995. PMID: 7485257

5

[Genetics of dominant autosomal forms of Alzheimer disease: 3 genes and one phenotype. Groupe de Recherche Francais sur la Maladie d'Alzheimer].

Brice A, Dubois B, Agid Y, Campion D, Martinez M, Clerger-Darpoux F, Bellis M, Mallet J, Frebourg T, Hannequin D, Puel M, Ledoze F, Pasquier F, Zimmerman MA, Thomas-Anterion C, Moreaud O, Goas JY. Brice A, et al. Among authors: mallet j. Rev Neurol (Paris). 1996 Dec;152(12):725-6. Rev Neurol (Paris). 1996. PMID: 9205694 French. No abstract available.

6

Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.

Martinez M, Campion D, Babron MC, Hannequin D, Agid Y, Bellis M, Brice A, Mallet J, Michon A, Thomas-Anterion C, Clerget-Darpoux F. Martinez M, et al. Among authors: mallet j. Am J Med Genet. 1996 Feb 16;67(1):9-12. doi: 10.1002/ajmg.1320670102. Am J Med Genet. 1996. PMID: 8678122

7

[Molecular genetics: a new approach of clinical neurosciences].

Brice A, Mallet J. Brice A, et al. Among authors: mallet j. Rev Neurol (Paris). 1991;147(1):1-16. Rev Neurol (Paris). 1991. PMID: 2014378 Review. French.

8

Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q11.2 by nonradioactive in situ hybridization.

Viegas-Péquignot E, Berrard S, Brice A, Apiou F, Mallet J. Viegas-Péquignot E, et al. Among authors: mallet j. Genomics. 1991 Jan;9(1):210-2. doi: 10.1016/0888-7543(91)90242-7. Genomics. 1991. PMID: 2004764 No abstract available.

9

Localization of the choline acetyltransferase (CHAT) gene to human chromosome 10.

Cohen-Haguenauer O, Brice A, Berrard S, Nguyen VC, Mallet J, Frézal J. Cohen-Haguenauer O, et al. Among authors: mallet j. Genomics. 1990 Feb;6(2):374-8. doi: 10.1016/0888-7543(90)90579-j. Genomics. 1990. PMID: 2307477

10

Molecular genetic approach to the study of mammalian choline acetyltransferase.

Berrard S, Brice A, Mallet J. Berrard S, et al. Among authors: mallet j. Brain Res Bull. 1989 Jan;22(1):147-53. doi: 10.1016/0361-9230(89)90139-1. Brain Res Bull. 1989. PMID: 2713713

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