Blanquet-Grossard F - Search Results

1

X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene.

Ressot C, Latour P, Blanquet-Grossard F, Sturtz F, Duthel S, Battin J, Corbillon E, Ollagnon E, Serville F, Vandenberghe A, Dautigny A, Pham-Dinh D. Ressot C, et al. Among authors: blanquet grossard f. Hum Genet. 1996 Aug;98(2):172-5. doi: 10.1007/s004390050183. Hum Genet. 1996. PMID: 8698335

2

Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO gene.

Blanquet-Grossard F, Pham-Dinh D, Dautigny A, Latour P, Bonnebouche C, Corbillon E, Chazot G, Vandenberghe A. Blanquet-Grossard F, et al. Clin Genet. 1995 Dec;48(6):281-3. doi: 10.1111/j.1399-0004.1995.tb04109.x. Clin Genet. 1995. PMID: 8835320

3

Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po.

Blanquet-Grossard F, Pham-Dinh D, Dautigny A, Latour P, Bonnebouche C, Diraison P, Chapon F, Chazot G, Vandenberghe A. Blanquet-Grossard F, et al. Hum Mutat. 1996;8(2):185-6. doi: 10.1002/(SICI)1098-1004(1996)8:2<185::AID-HUMU13>3.0.CO;2-Z. Hum Mutat. 1996. PMID: 8844219 No abstract available.

4

New mutations in the X-linked form of Charcot-Marie-Tooth disease.

Latour P, Fabreguette A, Ressot C, Blanquet-Grossard F, Antoine JC, Calvas P, Chapon F, Corbillon E, Ollagnon E, Sturtz F, Boucherat M, Chazot G, Dautigny A, Pham-Dinh D, Vandenberghe A. Latour P, et al. Among authors: blanquet grossard f. Eur Neurol. 1997;37(1):38-42. doi: 10.1159/000117403. Eur Neurol. 1997. PMID: 9018031 Review.

5

Complement protein C1q recognizes a conformationally modified form of the prion protein.

Blanquet-Grossard F, Thielens NM, Vendrely C, Jamin M, Arlaud GJ. Blanquet-Grossard F, et al. Biochemistry. 2005 Mar 22;44(11):4349-56. doi: 10.1021/bi047370a. Biochemistry. 2005. PMID: 15766264

6

Epithelial and endothelial expression of the green fluorescent protein reporter gene under the control of bovine prion protein (PrP) gene regulatory sequences in transgenic mice.

Lemaire-Vieille C, Schulze T, Podevin-Dimster V, Follet J, Bailly Y, Blanquet-Grossard F, Decavel JP, Heinen E, Cesbron JY. Lemaire-Vieille C, et al. Among authors: blanquet grossard f. Proc Natl Acad Sci U S A. 2000 May 9;97(10):5422-7. doi: 10.1073/pnas.080081197. Proc Natl Acad Sci U S A. 2000. PMID: 10792029 Free PMC article.

7

PrP expression and replication by Schwann cells: implications in prion spreading.

Follet J, Lemaire-Vieille C, Blanquet-Grossard F, Podevin-Dimster V, Lehmann S, Chauvin JP, Decavel JP, Varea R, Grassi J, Fontès M, Cesbron JY. Follet J, et al. Among authors: blanquet grossard f. J Virol. 2002 Mar;76(5):2434-9. doi: 10.1128/jvi.76.5.2434-2439.2002. J Virol. 2002. PMID: 11836421 Free PMC article.

8

Prion protein (PrPc) immunocytochemistry and expression of the green fluorescent protein reporter gene under control of the bovine PrP gene promoter in the mouse brain.

Bailly Y, Haeberlé AM, Blanquet-Grossard F, Chasserot-Golaz S, Grant N, Schulze T, Bombarde G, Grassi J, Cesbron JY, Lemaire-Vieille C. Bailly Y, et al. Among authors: blanquet grossard f. J Comp Neurol. 2004 May 24;473(2):244-69. doi: 10.1002/cne.20117. J Comp Neurol. 2004. PMID: 15101092

9

Prion protein is not detectable in dental pulp from patients with Creutzfeldt-Jakob disease.

Blanquet-Grossard F, Sazdovitch V, Jean A, Deslys JP, Dormont D, Hauw JJ, Marion D, Brown P, Cesbron JY. Blanquet-Grossard F, et al. J Dent Res. 2000 Feb;79(2):700. doi: 10.1177/00220345000790020101. J Dent Res. 2000. PMID: 10728969 No abstract available.

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