Page 1 | Search Results | Blood | American Society of Hematology

1-9 of 9

Sort by

Sort Order Select

Journal Articles

A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

N. Dalla Venezia, P. Maillet, L. Morlé, L. Roda, J. Delaunay, F. Baklouti

Blood (1998) 91 (11): 4361–4367.

https://doi.org/10.1182/blood.V91.11.4361

Published: 1998

Journal Articles

Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas)

N Alloisio, P Maillet, G Carre, P Texier, A Vallier, F Baklouti, N Philippe, J Delaunay

Blood (1996) 88 (3): 1062–1069.

https://doi.org/10.1182/blood.V88.3.1062.1062

Published: 1996

Journal Articles

Asynchronous regulation of splicing events within protein 4.1 pre-mRNA during erythroid differentiation

F Baklouti, SC Huang, TK Tang, J Delaunay, VT Marchesi, EJ Jr Benz

Blood (1996) 87 (9): 3934–3941.

https://doi.org/10.1182/blood.V87.9.3934.bloodjournal8793934

Published: 1996

Journal Articles

Prevalent skipping of an individual exon accounts for shortened protein 4.1 Presles

S Feddal, S Hayette, F Baklouti, R Rimokh, R Wilmotte, JP Magaud, J Maréchal, EJ Benz, Jr, R Girot, J Delaunay, L Morlé

Blood (1992) 80 (11): 2925–2930.

https://doi.org/10.1182/blood.V80.11.2925.2925

Published: 1992

Journal Articles

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

N Alloisio, R Wilmotte, L Morlé, F Baklouti, J Maréchal, MT Ducluzeau, L Denoroy, C Féo, BG Forget, R Kastally, J Delaunay

Blood (1992) 80 (3): 809–815.

https://doi.org/10.1182/blood.V80.3.809.809

Published: 1992

Journal Articles

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

F Baklouti, J Maréchal, R Wilmotte, N Alloisio, L Morlé, MT Ducluzeau, L Denoroy, A Mrad, MH Ben Aribia, R Kastally, J Delaunay

Blood (1992) 79 (9): 2464–2470.

https://doi.org/10.1182/blood.V79.9.2464.2464

Published: 1992

Journal Articles

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

S Feddal, G Brunet, L Roda, S Chabanis, N Alloisio, L Morle, MT Ducluzeau, J Marechal, JM Robert, EJ Benz, Jr, J Delaunay, F Baklouti

Blood (1991) 78 (8): 2113–2119.

https://doi.org/10.1182/blood.V78.8.2113.2113

Published: 1991

Journal Articles

Beta+-thalassemia in cis of a sickle cell gene: occurrence of a promoter mutation on a beta s chromosome

F Baklouti, R Ouazana, C Gonnet, A Lapillonne, J Delaunay, J Godet

Blood (1989) 74 (5): 1817–1822.

https://doi.org/10.1182/blood.V74.5.1817.1817

Published: 1989

Journal Articles

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

F Baklouti, E Dorleac, L Morle, P Laselve, D Peyramond, M Aubry, J Godet, J Delaunay

Blood (1986) 67 (4): 957–961.

https://doi.org/10.1182/blood.V67.4.957.957

Published: 1986

NARROW

A Large Deletion Within the Protein 4.1 Gene Associated With a Stable Truncated mRNA and an Unaltered Tissue-Specific Alternative Splicing

Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas)

Asynchronous regulation of splicing events within protein 4.1 pre-mRNA during erythroid differentiation

Prevalent skipping of an individual exon accounts for shortened protein 4.1 Presles

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

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

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

Beta+-thalassemia in cis of a sickle cell gene: occurrence of a promoter mutation on a beta s chromosome

Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only