Laplanche JL - Search Results

1

Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov.

Elsen JM, Amigues Y, Schelcher F, Ducrocq V, Andreoletti O, Eychenne F, Khang JV, Poivey JP, Lantier F, Laplanche JL. Elsen JM, et al. Among authors: laplanche jl. Arch Virol. 1999;144(3):431-45. doi: 10.1007/s007050050516. Arch Virol. 1999. PMID: 10226611

2

Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie.

Clouscard C, Beaudry P, Elsen JM, Milan D, Dussaucy M, Bounneau C, Schelcher F, Chatelain J, Launay JM, Laplanche JL. Clouscard C, et al. Among authors: laplanche jl. J Gen Virol. 1995 Aug;76 ( Pt 8):2097-101. doi: 10.1099/0022-1317-76-8-2097. J Gen Virol. 1995. PMID: 7636494

3

Genetic heterogeneity versus molecular analysis of prion susceptibility in neuroblasma N2a sublines.

Chasseigneaux S, Pastore M, Britton-Davidian J, Manié E, Stern MH, Callebert J, Catalan J, Casanova D, Belondrade M, Provansal M, Zhang Y, Bürkle A, Laplanche JL, Sévenet N, Lehmann S. Chasseigneaux S, et al. Among authors: laplanche jl. Arch Virol. 2008;153(9):1693-702. doi: 10.1007/s00705-008-0177-8. Epub 2008 Aug 12. Arch Virol. 2008. PMID: 18696008

4

PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresis.

Laplanche JL, Chatelain J, Westaway D, Thomas S, Dussaucy M, Brugere-Picoux J, Launay JM. Laplanche JL, et al. Genomics. 1993 Jan;15(1):30-7. doi: 10.1006/geno.1993.1006. Genomics. 1993. PMID: 8094373

5

Fluorine 18-labeled fluorodeoxyglucose positron emission tomography in familial Creutzfeldt-Jakob disease.

Renard D, Collombier L, Castelnovo G, Remy A, Laplanche JL, Labauge P. Renard D, et al. Among authors: laplanche jl. Arch Neurol. 2008 Oct;65(10):1390-1. doi: 10.1001/archneur.65.10.1390. Arch Neurol. 2008. PMID: 18852360 No abstract available.

6

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.

7

Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene.

Hauw JJ, Sazdovitch V, Laplanche JL, Peoc'h K, Kopp N, Kemeny J, Privat N, Delasnerie-Lauprêtre N, Brandel JP, Deslys JP, Dormont D, Alpérovitch A. Hauw JJ, et al. Among authors: laplanche jl. Neurology. 2000 Apr 25;54(8):1641-6. doi: 10.1212/wnl.54.8.1641. Neurology. 2000. PMID: 10762506

8

[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.

9

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.

Laplanche JL, Delasnerie-Lauprêtre N, Brandel JP, Chatelain J, Beaudry P, Alpérovitch A, Launay JM. Laplanche JL, et al. Neurology. 1994 Dec;44(12):2347-51. doi: 10.1212/wnl.44.12.2347. Neurology. 1994. PMID: 7991124

10

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease.

Ripoll L, Laplanche JL, Salzmann M, Jouvet A, Planques B, Dussaucy M, Chatelain J, Beaudry P, Launay JM. Ripoll L, et al. Among authors: laplanche jl. Neurology. 1993 Oct;43(10):1934-8. doi: 10.1212/wnl.43.10.1934. Neurology. 1993. PMID: 8105421

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