Chartier-Harlin MC - Search Results

1

No pathogenic mutations in the persyn gene in Parkinson's disease.

Lincoln S, Gwinn-Hardy K, Goudreau J, Chartier-Harlin MC, Baker M, Mouroux V, Richard F, Destée A, Becquet E, Amouyel P, Lynch T, Hardy J, Farrer M. Lincoln S, et al. Neurosci Lett. 1999 Jan 4;259(1):65-6. doi: 10.1016/s0304-3940(98)00901-x. Neurosci Lett. 1999. PMID: 10027558

2

Crosstalk between the Hippo Pathway and the Wnt Pathway in Huntington's Disease and Other Neurodegenerative Disorders.

Sileo P, Simonin C, Melnyk P, Chartier-Harlin MC, Cotelle P. Sileo P, et al. Among authors: chartier harlin mc. Cells. 2022 Nov 16;11(22):3631. doi: 10.3390/cells11223631. Cells. 2022. PMID: 36429058 Free PMC article. Review.

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

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

6

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

7

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

8

[Huntington disease: disclosing the gene].

Destée A, Chartier-Harlin MC. Destée A, et al. Presse Med. 1995 Feb 11;24(6):312-6. Presse Med. 1995. PMID: 7899393 Review. French.

9

Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease.

Wavrant-DeVrièze F, Pérez-Tur J, Lambert JC, Frigard B, Pasquier F, Delacourte A, Amouyel P, Hardy J, Chartier-Harlin MC. Wavrant-DeVrièze F, et al. Neurosci Lett. 1997 May 9;227(1):68-70. doi: 10.1016/s0304-3940(97)00304-2. Neurosci Lett. 1997. PMID: 9178861

10

Distortion of allelic expression of apolipoprotein E in Alzheimer's disease.

Lambert JC, Pérez-Tur J, Dupire MJ, Galasko D, Mann D, Amouyel P, Hardy J, Delacourte A, Chartier-Harlin MC. Lambert JC, et al. Hum Mol Genet. 1997 Nov;6(12):2151-4. doi: 10.1093/hmg/6.12.2151. Hum Mol Genet. 1997. PMID: 9328480

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