Morlé 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: morle f. 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: morle l. Blood. 1992 Aug 1;80(3):809-15. Blood. 1992. PMID: 1638030 Free article.

3

Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans.

Alloisio N, Morlé L, Maréchal J, Roux AF, Ducluzeau MT, Guetarni D, Pothier B, Baklouti F, Ghanem A, Kastally R, Delaunay J, et al. Alloisio N, et al. Among authors: morle l. J Clin Invest. 1991 Jun;87(6):2169-77. doi: 10.1172/JCI115250. J Clin Invest. 1991. PMID: 2040699 Free PMC article.

4

Occurrence of the alpha I 22 Arg----His (CGT----CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis.

Baklouti F, Marechal J, Morle L, Alloisio N, Wilmotte R, Pothier B, Ducluzeau MT, Kastally R, Delaunay J. Baklouti F, et al. Among authors: morle l. Br J Haematol. 1991 May;78(1):108-13. doi: 10.1111/j.1365-2141.1991.tb04391.x. Br J Haematol. 1991. PMID: 2043465

5

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution.

Pothier B, Alloisio N, Maréchal J, Morlé L, Ducluzeau MT, Caldani C, Philippe N, Delaunay J. Pothier B, et al. Among authors: morle l. Blood. 1990 May 15;75(10):2061-9. Blood. 1990. PMID: 2337674 Free article.

6

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: morle f. Blood. 1989 Aug 1;74(2):828-32. Blood. 1989. PMID: 2568861 Free article.

7

Two distinct variants of erythrocyte spectrin beta IV domain.

Pothier B, Alloisio N, Morlé L, Maréchal J, Barthélemy H, Ducluzeau MT, Dorier A, Delaunay J. Pothier B, et al. Among authors: morle l. Hum Genet. 1989 Nov;83(4):373-6. doi: 10.1007/BF00291384. Hum Genet. 1989. PMID: 2807277

8

Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state.

Alloisio N, Morlé L, Pothier B, Roux AF, Maréchal J, Ducluzeau MT, Benhadji-Zouaoui Z, Delaunay J. Alloisio N, et al. Among authors: morle l. Blood. 1988 Apr;71(4):1039-47. Blood. 1988. PMID: 2895677 Free article.

9

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state.

Morlé L, Alloisio N, Ducluzeau MT, Pothier B, Blibech R, Kastally R, Delaunay J. Morlé L, et al. Blood. 1988 Feb;71(2):508-11. Blood. 1988. PMID: 3337911 Free article.

10

Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.

Lorenzo F, Dalla Venezia N, Morlé L, Baklouti F, Alloisio N, Ducluzeau MT, Roda L, Lefrançois P, Delaunay J. Lorenzo F, et al. Among authors: morle l. J Clin Invest. 1994 Oct;94(4):1651-6. doi: 10.1172/JCI117508. J Clin Invest. 1994. PMID: 7929842 Free PMC article.

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