Denoroy L - Search Results

1

Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).

Morlé L, Roux AF, Alloisio N, Pothier B, Starck J, Denoroy L, Morlé F, Rudigoz RC, Forget BG, Delaunay J, et al. Morlé L, et al. Among authors: denoroy l. J Clin Invest. 1990 Aug;86(2):548-54. doi: 10.1172/JCI114743. J Clin Invest. 1990. PMID: 2384601 Free PMC article.

2

Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site.

Alloisio N, Wilmotte R, Morlé L, Baklouti F, Maréchal J, Ducluzeau MT, Denoroy L, Féo C, Forget BG, Kastally R, et al. Alloisio N, et al. Among authors: denoroy l. Blood. 1992 Aug 1;80(3):809-15. Blood. 1992. PMID: 1638030 Free article.

3

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain.

Morlé L, Morlé F, Roux AF, Godet J, Forget BG, Denoroy L, Garbarz M, Dhermy D, Kastally R, Delaunay J. Morlé L, et al. Among authors: denoroy l. Blood. 1989 Aug 1;74(2):828-32. Blood. 1989. PMID: 2568861 Free article.

4

Elliptocytogenic alpha I/36 spectrin Sfax lacks nine amino acids in helix 3 of repeat 4. Evidence for the activation of a cryptic 5'-splice site in exon 8 of spectrin alpha-gene.

Baklouti F, Maréchal J, Wilmotte R, Alloisio N, Morlé L, Ducluzeau MT, Denoroy L, Mrad A, Ben Aribia MH, Kastally R, et al. Baklouti F, et al. Among authors: denoroy l. Blood. 1992 May 1;79(9):2464-70. Blood. 1992. PMID: 1571558 Free article.

5

Elliptopoikilocytosis associated with the alpha 469 His-->Pro mutation in spectrin Barcelona (alpha I/50-46b).

Dalla Venezia N, Alloisio N, Forissier A, Denoroy L, Aymerich M, Vives-Corrons JL, Besalduch J, Besson I, Delaunay J. Dalla Venezia N, et al. Among authors: denoroy l. Blood. 1993 Sep 1;82(5):1661-5. Blood. 1993. PMID: 8364215 Free article.

6

A splice site mutation of alpha-spectrin gene causing skipping of exon 18 in hereditary elliptocytosis.

Alloisio N, Wilmotte R, Maréchal J, Texier P, Denoroy L, Féo C, Benhadji-Zouaoui Z, Delaunay J. Alloisio N, et al. Among authors: denoroy l. Blood. 1993 May 15;81(10):2791-8. Blood. 1993. PMID: 8490186 Free article.

7

The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum.

Alloisio N, Texier P, Denoroy L, Berger C, Miraglia del Giudice E, Perrotta S, Iolascon A, Gilsanz F, Berger G, Guichard J. Alloisio N, et al. Among authors: denoroy l. Blood. 1996 May 15;87(10):4433-9. Blood. 1996. PMID: 8639805 Free article.

8

Primary structure of a variable region of the V kappa I subgroup (ISE) in light chain deposition disease.

Rocca A, Khamlichi AA, Aucouturier P, Noël LH, Denoroy L, Preud'homme JL, Cogné M. Rocca A, et al. Among authors: denoroy l. Clin Exp Immunol. 1993 Mar;91(3):506-9. doi: 10.1111/j.1365-2249.1993.tb05932.x. Clin Exp Immunol. 1993. PMID: 7680298 Free PMC article.

9

Monoclonal Ig L chain and L chain V domain fragment crystallization in myeloma-associated Fanconi's syndrome.

Aucouturier P, Bauwens M, Khamlichi AA, Denoroy L, Spinelli S, Touchard G, Preud'homme JL, Cogné M. Aucouturier P, et al. Among authors: denoroy l. J Immunol. 1993 Apr 15;150(8 Pt 1):3561-8. J Immunol. 1993. PMID: 8468490

10

Synergistic hemolytic activity of Staphylococcus lugdunensis is mediated by three peptides encoded by a non-agr genetic locus.

Donvito B, Etienne J, Denoroy L, Greenland T, Benito Y, Vandenesch F. Donvito B, et al. Among authors: denoroy l. Infect Immun. 1997 Jan;65(1):95-100. doi: 10.1128/iai.65.1.95-100.1997. Infect Immun. 1997. PMID: 8975897 Free PMC article.

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