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Journal Articles

Spectrin St Louis and the alpha LELY allele [letter]

PG Gallagher, BG Forget

Blood (1994) 84 (5): 1686–1687.

https://doi.org/10.1182/blood.V84.5.1686.1686

Published: 1994

Journal Articles

Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region

J Starck, R Sarkar, M Romana, A Bhargava, AL Scarpa, M Tanaka, JW Chamberlain, SM Weissman, BG Forget

Blood (1994) 84 (5): 1656–1665.

https://doi.org/10.1182/blood.V84.5.1656.1656

Published: 1994

Journal Articles

Increased expression of the G gamma and A gamma globin genes associated with a mutation in the A gamma enhancer

G Balta, HE Brickner, S Takegawa, HH Kazazian, Jr, T Papayannopoulou, BG Forget, GF Atweh

Blood (1994) 83 (12): 3727–3737.

https://doi.org/10.1182/blood.V83.12.3727.3727

Published: 1994

Journal Articles

Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion

PG Gallagher, WE Roberts, L Benoit, DW Speicher, SL Marchesi, BG Forget

Blood (1993) 82 (7): 2210–2215.

https://doi.org/10.1182/blood.V82.7.2210.2210

Published: 1993

Journal Articles

Erythroid and nonerythroid spectrins

JC Winkelmann, BG Forget

Blood (1993) 81 (12): 3173–3185.

https://doi.org/10.1182/blood.V81.12.3173.3173

Published: 1993

Journal Articles

Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene [letter]

PG Gallagher, WT Tse, BG Forget

Blood (1992) 80 (7): 1856–1857.

https://doi.org/10.1182/blood.V80.7.1856.1856

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

Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide

PB Floyd, PG Gallagher, LA Valentino, M Davis, SL Marchesi, BG Forget

Blood (1991) 78 (5): 1364–1372.

https://doi.org/10.1182/blood.V78.5.1364.1364

Published: 1991

Journal Articles

An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216)

WT Tse, PG Gallagher, B Pothier, FF Costa, A Scarpa, J Delaunay, BG Forget

Blood (1991) 78 (2): 517–523.

https://doi.org/10.1182/blood.V78.2.517.517

Published: 1991

Journal Articles

The gene for the human erythropoietin receptor: analysis of the coding sequence and assignment to chromosome 19p

JC Winkelmann, LA Penny, LL Deaven, BG Forget, RB Jenkins

Blood (1990) 76 (1): 24–30.

https://doi.org/10.1182/blood.V76.1.24.24

Published: 1990

Journal Articles

Sequence analysis of the gamma-globin gene locus from a patient with the deletion form of hereditary persistence of fetal hemoglobin

CA Stolle, LA Penny, S Ivory, BG Forget, EJ Jr Benz

Blood (1990) 75 (2): 499–504.

https://doi.org/10.1182/blood.V75.2.499.499

Published: 1990

Journal Articles

The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster

EA Feingold, BG Forget

Blood (1989) 74 (6): 2178–2186.

https://doi.org/10.1182/blood.V74.6.2178.2178

Published: 1989

Journal Articles

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

L Morle, F Morle, AF Roux, J Godet, BG Forget, L Denoroy, M Garbarz, D Dhermy, R Kastally, J Delaunay

Blood (1989) 74 (2): 828–832.

https://doi.org/10.1182/blood.V74.2.828.828

Published: 1989

Journal Articles

Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families

AF Roux, F Morle, D Guetarni, P Colonna, K Sahr, BG Forget, J Delaunay, J Godet

Blood (1989) 73 (8): 2196–2201.

https://doi.org/10.1182/blood.V73.8.2196.2196

Published: 1989

Journal Articles

Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene

C Wong, SE Antonarakis, SC Goff, SH Orkin, BG Forget, DG Nathan, PJ Giardina, HH Jr Kazazian

Blood (1989) 73 (4): 914–918.

https://doi.org/10.1182/blood.V73.4.914.914

Published: 1989

Journal Articles

Molecular cloning of the cDNA for human erythrocyte beta-spectrin

JC Winkelmann, TL Leto, PC Watkins, R Eddy, TB Shows, AJ Linnenbach, KE Sahr, N Kathuria, VT Marchesi, BG Forget

Blood (1988) 72 (1): 328–334.

https://doi.org/10.1182/blood.V72.1.328.328

Published: 1988

Journal Articles

The beta-globin gene on the Chinese delta beta-thalassemia chromosome carries a promoter mutation

GF Atweh, XX Zhu, HE Brickner, CH Dowling, HH Jr Kazazian, BG Forget

Blood (1987) 70 (5): 1470–1474.

https://doi.org/10.1182/blood.V70.5.1470.1470

Published: 1987

Journal Articles

A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing

GF Atweh, C Wong, R Reed, SE Antonarakis, D Zhu, PK Ghosh, T Maniatis, BG Forget, HH Jr Kazazian

Blood (1987) 70 (1): 147–151.

https://doi.org/10.1182/blood.V70.1.147.147

Published: 1987

Journal Articles

A novel basis for delta beta-thalassemia in a Chinese family

GF Atweh, DE Zhu, BG Forget

Blood (1986) 68 (5): 1108–1113.

https://doi.org/10.1182/blood.V68.5.1108.1108

Published: 1986

Journal Articles

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks

PG Waber, MA Bender, RE Gelinas, C Kattamis, A Karaklis, K Sofroniadou, G Stamatoyannopoulos, FS Collins, BG Forget, HH Jr Kazazian

Blood (1986) 67 (2): 551–554.

https://doi.org/10.1182/blood.V67.2.551.551

Published: 1986

NARROW

Spectrin St Louis and the alpha LELY allele [letter]

Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region

Increased expression of the G gamma and A gamma globin genes associated with a mutation in the A gamma enhancer

Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion

Erythroid and nonerythroid spectrins

Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene [letter]

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

Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide

An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216)

The gene for the human erythropoietin receptor: analysis of the coding sequence and assignment to chromosome 19p

Sequence analysis of the gamma-globin gene locus from a patient with the deletion form of hereditary persistence of fetal hemoglobin

The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster

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

Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families

Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene

Molecular cloning of the cDNA for human erythrocyte beta-spectrin

The beta-globin gene on the Chinese delta beta-thalassemia chromosome carries a promoter mutation

A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing

A novel basis for delta beta-thalassemia in a Chinese family

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks

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American Society of Hematology

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American Society of Hematology

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