Chartier-Harlin MC - Search Results

1

No pathogenic mutations in the beta-synuclein gene in Parkinson's disease.

Lincoln S, Crook R, Chartier-Harlin MC, Gwinn-Hardy K, Baker M, Mouroux V, Richard F, Becquet E, Amouyel P, Destée A, Hardy J, Farrer M. Lincoln S, et al. Neurosci Lett. 1999 Jul 9;269(2):107-9. doi: 10.1016/s0304-3940(99)00420-6. Neurosci Lett. 1999. PMID: 10430516

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

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.

4

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

5

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.

6

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

7

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

8

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

9

[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.

10

The Cystatin-C gene is not linked to early onset familial Alzheimer's disease.

Parfitt M, Crook R, Roques P, Rossor M, Chartier-Harlin MC. Parfitt M, et al. Neurosci Lett. 1993 May 14;154(1-2):81-3. doi: 10.1016/0304-3940(93)90176-l. Neurosci Lett. 1993. PMID: 8361651

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