Demaille J - Search Results

1

Spatial and temporal expression of the cystathionine beta-synthase gene during early human development.

Quéré I, Paul V, Rouillac C, Janbon C, London J, Demaille J, Kamoun P, Dufier JL, Abitbol M, Chassé JF. Quéré I, et al. Among authors: demaille j. Biochem Biophys Res Commun. 1999 Jan 8;254(1):127-37. doi: 10.1006/bbrc.1998.9079. Biochem Biophys Res Commun. 1999. PMID: 9920745

2

In vitro creation of amyloid fibrils from native and Arg124Cys mutated betaIGH3((110-131)) peptides, and its relevance for lattice corneal amyloid dystrophy type I.

Schmitt-Bernard CF, Chavanieu A, Derancourt J, Arnaud B, Demaille JG, Calas B, Argiles A. Schmitt-Bernard CF, et al. Among authors: demaille jg. Biochem Biophys Res Commun. 2000 Jul 5;273(2):649-53. doi: 10.1006/bbrc.2000.2955. Biochem Biophys Res Commun. 2000. PMID: 10873659

3

Localization of human cell cycle regulatory genes CDC25C to 5q31 and WEE1 to 11p15.3-11p15.1 by fluorescence in situ hybridization.

Taviaux SA, Demaille JG. Taviaux SA, et al. Among authors: demaille jg. Genomics. 1993 Jan;15(1):194-6. doi: 10.1006/geno.1993.1032. Genomics. 1993. PMID: 8432534

4

The myosin light chain kinase gene is not duplicated in mouse: partial structure and chromosomal localization of Mylk.

Giorgi D, Ferraz C, Mattéi MG, Demaille J, Rouquier S. Giorgi D, et al. Among authors: demaille j. Genomics. 2001 Jul;75(1-3):49-56. doi: 10.1006/geno.2001.6571. Genomics. 2001. PMID: 11472067

5

A genomic region encompassing a cluster of olfactory receptor genes and a myosin light chain kinase (MYLK) gene is duplicated on human chromosome regions 3q13-q21 and 3p13.

Brand-Arpon V, Rouquier S, Massa H, de Jong PJ, Ferraz C, Ioannou PA, Demaille JG, Trask BJ, Giorgi D. Brand-Arpon V, et al. Among authors: demaille jg. Genomics. 1999 Feb 15;56(1):98-110. doi: 10.1006/geno.1998.5690. Genomics. 1999. PMID: 10036190

6

[Expression and localization of dystrophin during human skeletal, cardiac and smooth muscle development].

Chevron MP, Demaille J. Chevron MP, et al. Among authors: demaille j. C R Seances Soc Biol Fil. 1994;188(5-6):575-84. C R Seances Soc Biol Fil. 1994. PMID: 7780798 French.

7

BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro.

Schmitt-Bernard CF, Chavanieu A, Herrada G, Subra G, Arnaud B, Demaille JG, Calas B, Argilés A. Schmitt-Bernard CF, et al. Eur J Biochem. 2002 Nov;269(21):5149-56. doi: 10.1046/j.1432-1033.2002.03205.x. Eur J Biochem. 2002. PMID: 12392546 Free article.

8

BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.

Schmitt-Bernard CF, Guittard C, Arnaud B, Demaille J, Argiles A, Claustres M, Tuffery-Giraud S. Schmitt-Bernard CF, et al. Among authors: demaille j. Invest Ophthalmol Vis Sci. 2000 May;41(6):1302-8. Invest Ophthalmol Vis Sci. 2000. PMID: 10798644

9

Beta 2 microglobulin isoforms in healthy individuals and in amyloid deposits.

Argilés A, García-García M, Derancourt J, Mourad G, Demaille JG. Argilés A, et al. Among authors: demaille jg. Kidney Int. 1995 Nov;48(5):1397-405. doi: 10.1038/ki.1995.428. Kidney Int. 1995. PMID: 8544395 Free article.

10

Lattice corneal dystrophy.

Schmitt-Bernard CF, Claustres M, Arnaud B, Demaille J, Argiles A. Schmitt-Bernard CF, et al. Among authors: demaille j. Ophthalmology. 2000 Sep;107(9):1613-4. doi: 10.1016/s0161-6420(00)00055-5. Ophthalmology. 2000. PMID: 10964807 No abstract available.

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