Morlé L - Search Results

1

A large deletion within the protein 4.1 gene associated with a stable truncated mRNA and an unaltered tissue-specific alternative splicing.

Venezia ND, Maillet P, Morlé L, Roda L, Delaunay J, Baklouti F. Venezia ND, et al. Among authors: morle l. Blood. 1998 Jun 1;91(11):4361-7. Blood. 1998. PMID: 9596685 Free article.

2

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: morle l. Blood. 1992 May 1;79(9):2464-70. Blood. 1992. PMID: 1571558 Free article.

3

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.

4

The genetic disorders of the red cell skeleton.

Delaunay J, Alloisio N, Morle L, Baklouti F. Delaunay J, et al. Among authors: morle l. Nouv Rev Fr Hematol (1978). 1991;33(2):63-70. Nouv Rev Fr Hematol (1978). 1991. PMID: 1766857 Review.

5

Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps.

Feddal S, Brunet G, Roda L, Chabanis S, Alloisio N, Morlé L, Ducluzeau MT, Maréchal J, Robert JM, Benz EJ Jr, et al. Feddal S, et al. Among authors: morle l. Blood. 1991 Oct 15;78(8):2113-9. Blood. 1991. PMID: 1912588 Free article.

6

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia.

Hayette S, Dhermy D, dos Santos ME, Bozon M, Drenckhahn D, Alloisio N, Texier P, Delaunay J, Morlé L. Hayette S, et al. Among authors: morle l. Blood. 1995 Jan 1;85(1):250-6. Blood. 1995. PMID: 7803799 Free article.

7

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.

8

Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis.

Maillet P, Alloisio N, Morlé L, Delaunay J. Maillet P, et al. Among authors: morle l. Hum Mutat. 1996;8(2):97-107. doi: 10.1002/(SICI)1098-1004(1996)8:2<97::AID-HUMU1>3.0.CO;2-M. Hum Mutat. 1996. PMID: 8844207

9

Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis.

Delaunay J, Alloisio N, Morle L, Baklouti F, Dalla Venezia N, Maillet P, Wilmotte R. Delaunay J, et al. Among authors: morle l. Ann Genet. 1996;39(4):209-21. Ann Genet. 1996. PMID: 9037349 Review.

10

Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis.

Alloisio N, Texier P, Vallier A, Ribeiro ML, Morlé L, Bozon M, Bursaux E, Maillet P, Gonçalves P, Tanner MJ, Tamagnini G, Delaunay J. Alloisio N, et al. Among authors: morle l. Blood. 1997 Jul 1;90(1):414-20. Blood. 1997. PMID: 9207478 Free article.

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