Chartier-Harlin MC - Search Results

1

No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease.

Wavrant-DeVrièze F, Rudrasingham V, Lambert JC, Chakraverty S, Kehoe P, Crook R, Amouyel P, Wu W, Holmans P, Rice F, Pérez-Tur J, Frigard B, Morris JC, Carty S, Cottel D, Tunstall N, Lovestone S, Petersen RC, Chartier-Harlin MC, Goate A, Owen MJ, Williams J, Hardy J. Wavrant-DeVrièze F, et al. Neurosci Lett. 1999 Mar 5;262(2):137-9. doi: 10.1016/s0304-3940(99)00035-x. Neurosci Lett. 1999. PMID: 10203250

2

A polymorphic dinucleotide repeat in intron 2 of the human cystatin-C gene.

Hughes D, Brown J, Hardy J, Chartier-Harlin MC. Hughes D, et al. Hum Mol Genet. 1992 May;1(2):143. doi: 10.1093/hmg/1.2.143. Hum Mol Genet. 1992. PMID: 1301159 No abstract available.

3

Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile.

Fidani L, Rooke K, Chartier-Harlin MC, Hughes D, Tanzi R, Mullan M, Roques P, Rossor M, Hardy J, Goate A. Fidani L, et al. Hum Mol Genet. 1992 Jun;1(3):165-8. doi: 10.1093/hmg/1.3.165. Hum Mol Genet. 1992. PMID: 1303172

4

Alzheimer disease: the new agenda.

Hardy J, Chartier-Harlin MC, Mullan M. Hardy J, et al. Am J Hum Genet. 1992 Mar;50(3):648-51. Am J Hum Genet. 1992. PMID: 1539602 Free PMC article. No abstract available.

5

Alzheimer's--a correction.

Crawford F, Chartier-Harlin MC, Mullan M, Hardy J, Delacourte A, Arnott G. Crawford F, et al. Nature. 1992 Apr 2;356(6368):390. doi: 10.1038/356390b0. Nature. 1992. PMID: 1557118 No abstract available.

6

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.

Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, Giuffra L, Haynes A, Irving N, James L, et al. Goate A, et al. Nature. 1991 Feb 21;349(6311):704-6. doi: 10.1038/349704a0. Nature. 1991. PMID: 1671712

7

Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequence.

Crawford F, Hardy J, Mullan M, Goate A, Hughes D, Fidani L, Roques P, Rossor M, Chartier-Harlin MC. Crawford F, et al. Neurosci Lett. 1991 Nov 25;133(1):1-2. doi: 10.1016/0304-3940(91)90042-r. Neurosci Lett. 1991. PMID: 1791986

8

Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's disease.

Chartier-Harlin MC, Crawford F, Hamandi K, Mullan M, Goate A, Hardy J, Backhovens H, Martin JJ, Broeckhoven CV. Chartier-Harlin MC, et al. Neurosci Lett. 1991 Aug 5;129(1):134-5. doi: 10.1016/0304-3940(91)90738-f. Neurosci Lett. 1991. PMID: 1922963

9

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene.

Chartier-Harlin MC, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J, et al. Chartier-Harlin MC, et al. Nature. 1991 Oct 31;353(6347):844-6. doi: 10.1038/353844a0. Nature. 1991. PMID: 1944558

10

Alzheimer's disease: A beta or ApoE amyloidosis?

Buée L, Permanne B, Pérez-Tur J, Chartier-Harlin MC, Delacourte A. Buée L, et al. Lancet. 1995 Jul 1;346(8966):59. doi: 10.1016/s0140-6736(95)92694-1. Lancet. 1995. PMID: 7603172 No abstract available.

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