Cuisset L - Search Results

1

New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.

Dodé C, Le Dû N, Cuisset L, Letourneur F, Berthelot JM, Vaudour G, Meyrier A, Watts RA, Scott DG, Nicholls A, Granel B, Frances C, Garcier F, Edery P, Boulinguez S, Domergues JP, Delpech M, Grateau G. Dodé C, et al. Among authors: cuisset l. Am J Hum Genet. 2002 Jun;70(6):1498-506. doi: 10.1086/340786. Epub 2002 Apr 25. Am J Hum Genet. 2002. PMID: 11992256 Free PMC article.

2

Characterization, purification and cDNA cloning of a rat perchloric-acid-soluble 23-kDa protein present only in liver and kidney.

Levy-Favatier F, Cuisset L, Nedelec B, Tichonicky L, Kruh J, Delpech M. Levy-Favatier F, et al. Among authors: cuisset l. Eur J Biochem. 1993 Mar 15;212(3):665-73. doi: 10.1111/j.1432-1033.1993.tb17704.x. Eur J Biochem. 1993. PMID: 8385007 Free article.

3

The effects of sodium butyrate on transcription are mediated through activation of a protein phosphatase.

Cuisset L, Tichonicky L, Jaffray P, Delpech M. Cuisset L, et al. J Biol Chem. 1997 Sep 26;272(39):24148-53. doi: 10.1074/jbc.272.39.24148. J Biol Chem. 1997. PMID: 9305863 Free article.

4

A protein phosphatase is involved in the inhibition of histone deacetylation by sodium butyrate.

Cuisset L, Tichonicky L, Delpech M. Cuisset L, et al. Biochem Biophys Res Commun. 1998 May 29;246(3):760-4. doi: 10.1006/bbrc.1998.8698. Biochem Biophys Res Commun. 1998. PMID: 9618285

5

Potential pitfall in Prader-Willi syndrome and Angelman syndrome molecular diagnosis.

Cuisset L, Vasseur C, Jeanpierre M, Delpech M, Noséda G, Ponsot G. Cuisset L, et al. Am J Med Genet. 1998 Dec 28;80(5):543-5. Am J Med Genet. 1998. PMID: 9880230 No abstract available.

6

Quantitative analysis of histone H1 degrees protein synthesis in HTC cells.

Cuisset L, Tichonicky L, Delpech M. Cuisset L, et al. Eur J Biochem. 1999 May;261(3):593-9. doi: 10.1046/j.1432-1327.1999.00331.x. Eur J Biochem. 1999. PMID: 10215874 Free article.

7

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

Drenth JP, Cuisset L, Grateau G, Vasseur C, van de Velde-Visser SD, de Jong JG, Beckmann JS, van der Meer JW, Delpech M. Drenth JP, et al. Among authors: cuisset l. Nat Genet. 1999 Jun;22(2):178-81. doi: 10.1038/9696. Nat Genet. 1999. PMID: 10369262

8

Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.

Cuisset L, Drenth JP, Berthelot JM, Meyrier A, Vaudour G, Watts RA, Scott DG, Nicholls A, Pavek S, Vasseur C, Beckmann JS, Delpech M, Grateau G. Cuisset L, et al. Am J Hum Genet. 1999 Oct;65(4):1054-9. doi: 10.1086/302589. Am J Hum Genet. 1999. PMID: 10486324 Free PMC article.

9

Breakthroughs in the genetics of hereditary fevers.

Grateau G, Cuisset L, Dodé C, Delpech M. Grateau G, et al. Among authors: cuisset l. Eur J Intern Med. 2000 Oct;11(5):242-244. doi: 10.1016/s0953-6205(00)00104-7. Eur J Intern Med. 2000. PMID: 11025247 No abstract available.

10

Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome.

Cuisset L, Drenth JP, Simon A, Vincent MF, van der Velde Visser S, van der Meer JW, Grateau G, Delpech M; International Hyper-IgD Study Group. Cuisset L, et al. Eur J Hum Genet. 2001 Apr;9(4):260-6. doi: 10.1038/sj.ejhg.5200614. Eur J Hum Genet. 2001. PMID: 11313769

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