Laplanche JL - Search Results

1

[Unconventional transmissible agents and prion protein: is something still missing?].

Laplanche JL. Laplanche JL. Ann Biol Clin (Paris). 1997 Sep-Oct;55(5):395-407. Ann Biol Clin (Paris). 1997. PMID: 9347006 Free article. Review. French.

2

[Prion protein: structure, functions and polymorphisms associated with human spongiform encephalopathies].

Laplanche JL, Beaudry P, Ripoll L, Launay JM. Laplanche JL, et al. Pathol Biol (Paris). 1995 Feb;43(2):104-13. Pathol Biol (Paris). 1995. PMID: 7777379 Review. French.

3

[Human transmissible dementia: prion diseases?].

Dreux C, Laplanche JL, Chatelain J. Dreux C, et al. Among authors: laplanche jl. Bull Acad Natl Med. 1992 Nov;176(8):1279-88; discussion 1289-91. Bull Acad Natl Med. 1992. PMID: 1300226 Review. French.

4

[Proteins, genes and early diagnosis of Alzheimer's disease].

Laplanche JL, Chatelain J, Launay JM, Dreux C. Laplanche JL, et al. Ann Biol Clin (Paris). 1990;48(5):281-5. Ann Biol Clin (Paris). 1990. PMID: 2195924 Review. French.

5

[Molecular genetics of familial and sporadic forms of human prion diseases].

Laplanche JL, Launay JM, Dreux C. Laplanche JL, et al. Ann Pharm Fr. 1995;53(5):193-200. Ann Pharm Fr. 1995. PMID: 7503507 Review. French.

6

[Molecular basis of familial and sporadic forms of human prion diseases].

Laplanche JL. Laplanche JL. Transfus Clin Biol. 1994;1(5):345-53. doi: 10.1016/s1246-7820(06)80016-9. Transfus Clin Biol. 1994. PMID: 7812461 French.

7

First report of polymorphisms in the prion-like protein gene (PRND): implications for human prion diseases.

Peoc'h K, Guérin C, Brandel JP, Launay JM, Laplanche JL. Peoc'h K, et al. Among authors: laplanche jl. Neurosci Lett. 2000 Jun 2;286(2):144-8. doi: 10.1016/s0304-3940(00)01100-9. Neurosci Lett. 2000. PMID: 10825657

8

Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.

Peoc'h K, Manivet P, Beaudry P, Attane F, Besson G, Hannequin D, Delasnerie-Lauprêtre N, Laplanche JL. Peoc'h K, et al. Among authors: laplanche jl. Hum Mutat. 2000 May;15(5):482. doi: 10.1002/(SICI)1098-1004(200005)15:5<482::AID-HUMU16>3.0.CO;2-1. Hum Mutat. 2000. PMID: 10790216

9

Prion-like protein Doppel expression is not modified in scrapie-infected cells and in the brains of patients with Creutzfeldt-Jakob disease.

Peoc'h K, Volland H, De Gassart A, Beaudry P, Sazdovitch V, Sorgato MC, Creminon C, Laplanche JL, Lehmann S. Peoc'h K, et al. Among authors: laplanche jl. FEBS Lett. 2003 Feb 11;536(1-3):61-5. doi: 10.1016/s0014-5793(03)00012-7. FEBS Lett. 2003. PMID: 12586339 Free article.

10

V180I mutation of the prion protein gene associated with atypical PrPSc glycosylation.

Chasseigneaux S, Haïk S, Laffont-Proust I, De Marco O, Lenne M, Brandel JP, Hauw JJ, Laplanche JL, Peoc'h K. Chasseigneaux S, et al. Among authors: laplanche jl. Neurosci Lett. 2006 Nov 20;408(3):165-9. doi: 10.1016/j.neulet.2006.08.008. Epub 2006 Oct 9. Neurosci Lett. 2006. PMID: 17029785

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