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Bernard Forget

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Bernard G Forget; H Franklin Bunn
Classification of the disorders of hemoglobin.
Hannah H Bogardus; Bernard G Forget; Yelena D Maksimova; Patrick G Gallagher
A de novo band 3 mutation in hereditary spherocytosis.
Bernard G Forget
Progress in understanding the hemoglobin switch.

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All Publications

2013: Bernard G Forget; H Franklin Bunn
Classification of the disorders of hemoglobin.
Cold Spring Harbor perspectives in medicine 2013;3(2):a011684.
2012: Hannah H Bogardus; Bernard G Forget; Yelena D Maksimova; Patrick G Gallagher
A de novo band 3 mutation in hereditary spherocytosis.
Pediatric blood & cancer 2012;58(6):1004.
2011: Bernard G Forget
Progress in understanding the hemoglobin switch.
The New England journal of medicine 2011;365(9):852-4.
2010: Bernard G Forget
Preface. Thalassemia.
Hematology/oncology clinics of North America 2010;24(6):xiii-xv.
2009: Han Lee; Jung Park; Bernard G Forget; Peter Gaines
Induced pluripotent stem cells in regenerative medicine: an argument for continued research on human embryonic stem cells.
Regenerative medicine 2009;4(5):759-69.
2008: Jose Sangerman; Yelena Maksimova; E Jennifer Edelman; Jon S Morrow; Bernard G Forget; Patrick G Gallagher
Ankyrin-linked hereditary spherocytosis in an African-American kindred.
American journal of hematology 2008;83(10):789-94.
2006: Bernard G Forget
De novo and acquired forms of alpha thalassemia.
Current hematology reports 2006;5(1):11-4.
2006: Hui Z Zhang; Barbara A Degar; Svetlana Rogoulina; Charles Resor; Carmen J Booth; Joseph Sinning; Philip J Gage; Bernard G Forget
Hematopoiesis following disruption of the Pitx2 homeodomain gene.
Experimental hematology 2006;34(2):167-78.
2006: AURELIE KIEUSSEIAN; Jalila Chagraoui; Cécile Kerdudo; Philippe-Emmanuel Mangeot; Philip J Gage; Nicole Navarro; Brigitte Izac; Georges Uzan; Bernard G Forget; Anne Dubart Kupperschmitt
Expression of Pitx2 in stromal cells is required for normal hematopoiesis.
Blood 2006;107(2):492-500.
2005: Daniel B Costa; Larisa Lozovatsky; Patrick G Gallagher; Bernard G Forget
A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.
Blood 2005;106(13):4367-9.
2005: Lei Wang; Murat O Arcasoy; Stephanie S Watowich; Bernard G Forget
Cytokine signals through STAT3 promote expression of granulocyte secondary granule proteins in 32D cells.
Experimental hematology 2005;33(3):308-17.
2004: Ellice Y Wong; Jolinta Lin; Bernard G Forget; David M Bodine; Patrick G Gallagher
Sequences downstream of the erythroid promoter are required for high level expression of the human alpha-spectrin gene.
The Journal of biological chemistry 2004;279(53):55024-33.
2004: Patrick G Gallagher; Zhushan Zhang; Jon S Morrow; Bernard G Forget
Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site.
Laboratory investigation; a journal of technical methods and pathology 2004;84(2):229-34.
2003: Jean-Francois Lambert; Meng Liu; Gerald A Colvin; Mark S Dooner; Christina I Mcauliffe; Pamela S Becker; Bernard G Forget; Sherman M Weissman; Peter J Quesenberry
Marrow stem cells shift gene expression and engraftment phenotype with cell cycle transit.
The Journal of experimental medicine 2003;197(11):1563-72.
2002: Murat O Arcasoy; Aysen F Karayal; Harvey M Segal; Joseph G Sinning; Bernard G Forget
A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis.
Blood 2002;99(8):3066-9.
2001: Murat O Arcasoy; Noel A Maun; L Perez; Bernard G Forget; Nancy Berliner
Erythropoietin mediates terminal granulocytic differentiation of committed myeloid cells with ectopic erythropoietin receptor expression.
European journal of haematology 2001;67(2):77-87.
2001: Barbara A Degar; N Baskaran; Ruud Hulspas; Peter J Quesenberry; Sherman M Weissman; Bernard G Forget
The homeodomain gene Pitx2 is expressed in primitive hematopoietic stem/progenitor cells but not in their differentiated progeny.
Experimental hematology 2001;29(7):894-902.
2000: Patrick G Gallagher; J D Ferreira; F F Costa; S T Saad; Bernard G Forget
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis.
British journal of haematology 2000;111(4):1190-3.
2000: Patrick G Gallagher; M Romana; WT Tse; Samuel E Lux; Bernard G Forget
The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter.
Blood 2000;96(3):1136-43.
2000: Gerri Dooner; J E Barker; Patrick G Gallagher; Michelle E Debatis; A H Brown; Bernard G Forget; Pamela S Becker
Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro.
Experimental hematology 2000;28(7):765-74.
2000: Bernard G Forget; B A Degan; Murat O Arcasoy
Familial polycythemia due to truncations of the erythropoietin receptor.
Transactions of the American Clinical and Climatological Association 2000;111():38-44; discussion 44-5.
1999: Patrick G Gallagher; Denise E Sabatino; M Romana; Amanda P Cline; Lisa J Garrett; David M Bodine; Bernard G Forget
A human beta-spectrin gene promoter directs high level expression in erythroid but not muscle or neural cells.
The Journal of biological chemistry 1999;274(10):6062-73.
1999: Murat O Arcasoy; Kevin W Harris; Bernard G Forget
A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation.
Experimental hematology 1999;27(1):63-74.
1998: Patrick G Gallagher; Bernard G Forget
Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.
Blood cells, molecules & diseases 1998;24(4):539-43.
1998: Denise E Sabatino; Amanda P Cline; Patrick G Gallagher; Lisa J Garrett; G Stamatoyannopoulos; Bernard G Forget; David M Bodine
Substitution of the human beta-spectrin promoter for the human agamma-globin promoter prevents silencing of a linked human beta-globin gene in transgenic mice.
Molecular and cellular biology 1998;18(11):6634-40.
1998: Kevin W Harris; X J Hu; S Schultz; Murat O Arcasoy; Bernard G Forget; N Clare
The distal cytoplasmic domain of the erythropoietin receptor induces granulocytic differentiation in 32D cells.
Blood 1998;92(4):1219-24.
1998: Bernard G Forget
Molecular basis of hereditary persistence of fetal hemoglobin.
Annals of the New York Academy of Sciences 1998;850():38-44.
1998: Patrick G Gallagher; Bernard G Forget
An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene.
The Journal of biological chemistry 1998;273(3):1339-48.
1997: Patrick G Gallagher; Bernard G Forget
Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis.
Blood cells, molecules & diseases 1997;23(3):417-21.
1997: Patrick G Gallagher; M Romana; C Wong; Bernard G Forget
Genetic basis of the polymorphisms of the alphaI domain of spectrin.
American journal of hematology 1997;56(2):107-11.
1997: Patrick G Gallagher; WT Tse; A L Scarpa; Samuel E Lux; Bernard G Forget
Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing.
The Journal of biological chemistry 1997;272(31):19220-8.
1997: Murat O Arcasoy; Barbara A Degar; Kevin W Harris; Bernard G Forget
Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene.
Blood 1997;89(12):4628-35.
1997: Murat O Arcasoy; M Romana; Mary E Fabry; E Skarpidi; R L Nagel; Bernard G Forget
High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin.
Molecular and cellular biology 1997;17(4):2076-89.
1997: WT Tse; Patrick G Gallagher; P B Jenkins; Y Wang; L Benoit; D Speicher; J C Winkelmann; Peter Agre; Bernard G Forget; S L Marchesi
Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosis.
American journal of hematology 1997;54(3):233-41.
1997: Patrick G Gallagher; M J Petruzzi; S A Weed; Zhushan Zhang; S L Marchesi; N Mohandas; Jon S Morrow; Bernard G Forget
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.
The Journal of clinical investigation 1997;99(2):267-77.
1996: C Glele-Kakai; Michel Garbarz; Marie-Christine Lecomte; S Leborgne; Colette Galand; Odile Bournier; Isabelle Devaux; H Gautero; I Zohoun; Patrick G Gallagher; Bernard G Forget; Didier Dhermy
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin.
British journal of haematology 1996;95(1):57-66.
1996: Patrick G Gallagher; L Kotula; Y Wang; S L Marchesi; P J Curtis; David W Speicher; Bernard G Forget
Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.
American journal of human genetics 1996;59(2):351-9.
1996: Stefan W Eber; J M Gonzalez; M L Lux; A L Scarpa; WT Tse; M Dornwell; J Herbers; Wilfried Kugler; R Ozcan; Arnulf Pekrun; Patrick G Gallagher; W Schröter; Bernard G Forget; Samuel E Lux
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
Nature genetics 1996;13(2):214-8.
1996: P B Jenkins; Ghassan K Abou-Alfa; Didier Dhermy; E Bursaux; C Féo; A L Scarpa; Samuel E Lux; Michel Garbarz; Bernard G Forget; Patrick G Gallagher
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.
The Journal of clinical investigation 1996;97(2):373-80.
1996: Patrick G Gallagher; Bernard G Forget
Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis.
Blood cells, molecules & diseases 1996;22(3):254-8.
1995: Patrick G Gallagher; Bernard G Forget
Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary hydrocytosis.
The Journal of biological chemistry 1995;270(44):26358-63.
1995: Patrick G Gallagher; S A Weed; WT Tse; L Benoit; Jon S Morrow; S L Marchesi; N Mohandas; Bernard G Forget
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.
The Journal of clinical investigation 1995;95(3):1174-82.
1994: C R Lombardo; S A Weed; S P Kennedy; Bernard G Forget; Jon S Morrow
Beta II-spectrin (fodrin) and beta I epsilon 2-spectrin (muscle) contain NH2- and COOH-terminal membrane association domains (MAD1 and MAD2).
The Journal of biological chemistry 1994;269(46):29212-9.
1994: Patrick G Gallagher; Marie-Christine Lecomte; Colette Galand; Y P Wang; WT Tse; Bernard G Forget
Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB).
British journal of haematology 1994;88(2):413-4.
1994: J Starck; R Sarkar; M Romana; A Bhargava; A L Scarpa; M Tanaka; John W Chamberlain; S M Weissman; Bernard G Forget
Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region.
Blood 1994;84(5):1656-65.
1994: S P Kennedy; S A Weed; Bernard G Forget; Jon S Morrow
A partial structural repeat forms the heterodimer self-association site of all beta-spectrins.
The Journal of biological chemistry 1994;269(15):11400-8.
1994: M Upender; Patrick G Gallagher; Randall T Moon; David C Ward; Bernard G Forget
Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1994;66(1):39-41.
1993: P B Jenkins; Patrick G Gallagher; Bernard G Forget
Analysis of a PstI polymorphism of the human erythrocyte band 3 gene (EPB3).
British journal of haematology 1993;85(4):816-8.
1993: Patrick G Gallagher; W E Roberts; L Benoit; David W Speicher; S L Marchesi; Bernard G Forget
Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion.
Blood 1993;82(7):2210-5.
1993: Patrick G Gallagher; M Upender; David C Ward; Bernard G Forget
The gene for human erythrocyte membrane protein band 7.2 (EPB72) maps to 9q33-q34 centromeric to the Philadelphia chromosome translocation breakpoint region.
Genomics 1993;18(1):167-9.
1993: K M Amin; A L Scarpa; J C Winkelmann; P J Curtis; Bernard G Forget
The exon-intron organization of the human erythroid beta-spectrin gene.
Genomics 1993;18(1):118-25.
1993: J G Chang; A Scarpa; R L Eddy; M G Byers; A S Harris; Jon S Morrow; P Watkins; T B Shows; Bernard G Forget
Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin.
Genomics 1993;17(2):287-93.
1993: P S Becker; WT Tse; Samuel E Lux; Bernard G Forget
Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.
The Journal of clinical investigation 1993;92(2):612-6.
1993: J C Winkelmann; Bernard G Forget
Erythroid and nonerythroid spectrins.
Blood 1993;81(12):3173-85.
1993: Bernard G Forget
The pathophysiology and molecular genetics of beta thalassemia.
The Mount Sinai journal of medicine, New York 1993;60(2):95-103.
1993: Patrick G Gallagher; Bernard G Forget
Spectrin genes in health and disease.
Seminars in hematology 1993;30(1):4-20.
1992: Nicole Alloisio; R Wilmotte; Laurette Morlé; Faouzi Baklouti; J Maréchal; M T Ducluzeau; L Denoroy; C Féo; Bernard G Forget; R Kastally
Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site.
Blood 1992;80(3):809-15.
1992: J C Ward; K W Harris; L A Penny; Bernard G Forget; T Kitamura; J C Winkelmann
A structurally abnormal erythropoietin receptor gene in a human erythroleukemia cell line.
Experimental hematology 1992;20(3):371-3.
1992: Patrick G Gallagher; WT Tse; A L Scarpa; Samuel E Lux; Bernard G Forget
Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrin.
Transactions of the Association of American Physicians 1992;105():268-77.
1991: L A Penny; Bernard G Forget
Genomic organization of the human erythropoietin receptor gene.
Genomics 1991;11(4):974-80.
1991: S P Kennedy; SL Warren; Bernard G Forget; Jon S Morrow
Ankyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrin.
The Journal of cell biology 1991;115(1):267-77.
1991: P B Floyd; Patrick G Gallagher; L A Valentino; M Davis; S L Marchesi; Bernard G Forget
Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide.
Blood 1991;78(5):1364-72.
1991: Patrick G Gallagher; WT Tse; F Costa; A Scarpa; P Boivin; J Delaunay; Bernard G Forget
A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain.
The Journal of biological chemistry 1991;266(23):15154-9.
1991: WT Tse; J C Menninger; TL Yang-Feng; U Francke; K E Sahr; Samuel E Lux; David C Ward; Bernard G Forget
Isolation and chromosomal localization of a novel nonerythroid ankyrin gene.
Genomics 1991;10(4):858-66.
1991: WT Tse; Patrick G Gallagher; B Pothier; F F Costa; A Scarpa; J Delaunay; Bernard G Forget
An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216).
Blood 1991;78(2):517-23.
1991: Michel Garbarz; WT Tse; Patrick G Gallagher; C Picat; Marie-Christine Lecomte; Francis Galibert; Didier Dhermy; Bernard G Forget
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.
The Journal of clinical investigation 1991;88(1):76-81.
1991: Nadya Lumelsky; Bernard G Forget
Negative regulation of globin gene expression during megakaryocytic differentiation of a human erythroleukemic cell line.
Molecular and cellular biology 1991;11(7):3528-36.
1991: J A Bollekens; Bernard G Forget
Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
Hematology/oncology clinics of North America 1991;5(3):399-422.
1991: Patrick G Gallagher; WT Tse; S L Marchesi; H S Zarkowsky; Bernard G Forget
A defect in alpha-spectrin mRNA accumulation in hereditary pyropoikilocytosis.
Transactions of the Association of American Physicians 1991;104():32-9.
1991: L Kotula; L D Laury-Kleintop; Louise C Showe; K Sahr; A J Linnenbach; Bernard G Forget; P J Curtis
The exon-intron organization of the human erythrocyte alpha-spectrin gene.
Genomics 1991;9(1):131-40.
1990: J C Winkelmann; F F Costa; B L Linzie; Bernard G Forget
Beta spectrin in human skeletal muscle. Tissue-specific differential processing of 3' beta spectrin pre-mRNA generates a beta spectrin isoform with a unique carboxyl terminus.
The Journal of biological chemistry 1990;265(33):20449-54.
1990: F F Costa; Peter Agre; P C Watkins; J C Winkelmann; T K Tang; K M John; Samuel E Lux; Bernard G Forget
Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.
The New England journal of medicine 1990;323(15):1046-50.
1990: Patrick G Gallagher; WT Tse; Bernard G Forget
Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton.
Seminars in perinatology 1990;14(5):351-67.
1990: D Guetarni; A F Roux; Nicole Alloisio; François Morlé; M T Ducluzeau; Bernard G Forget; P Colonna; Jean Delaunay; Jacqueline Godet
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele.
Human genetics 1990;85(6):627-30.
1990: WT Tse; Marie-Christine Lecomte; F F Costa; Michel Garbarz; C Feo; P Boivin; Didier Dhermy; Bernard G Forget
Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
The Journal of clinical investigation 1990;86(3):909-16.
1990: Laurette Morlé; A F Roux; Nicole Alloisio; B Pothier; Joëlle Starck; L Denoroy; François Morlé; R C Rudigoz; Bernard G Forget; Jean Delaunay
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).
The Journal of clinical investigation 1990;86(2):548-54.
1990: J C Winkelmann; J G Chang; WT Tse; A L Scarpa; V T Marchesi; Bernard G Forget
Full-length sequence of the cDNA for human erythroid beta-spectrin.
The Journal of biological chemistry 1990;265(20):11827-32.
1990: J C Winkelmann; L A Penny; L L Deaven; Bernard G Forget; R B Jenkins
The gene for the human erythropoietin receptor: analysis of the coding sequence and assignment to chromosome 19p.
Blood 1990;76(1):24-30.
1990: WT Tse; Bernard G Forget
Reverse transcription and direct amplification of cellular RNA transcripts by Taq polymerase.
Gene 1990;88(2):293-6.
1990: C A Stolle; L A Penny; S Ivory; Bernard G Forget; Edward J Benz
Sequence analysis of the gamma-globin gene locus from a patient with the deletion form of hereditary persistence of fetal hemoglobin.
Blood 1990;75(2):499-504.
1990: M Tanaka; J A Nolan; A K Bhargava; K Rood; Francis S Collins; S M Weissman; Bernard G Forget; John W Chamberlain
Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobin.
Annals of the New York Academy of Sciences 1990;612():167-78.
1990: Y Fukushima; M G Byers; P C Watkins; J C Winkelmann; Bernard G Forget; TB Shows
Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridization.
Cytogenetics and cell genetics 1990;53(4):232-3.
1990: WT Tse; J C Menninger; David C Ward; R R Chilcote; K M John; Samuel E Lux; Bernard G Forget
Demonstration of the deletion of a copy of the ankyrin gene in a patient with hereditary spherocytosis by in situ hybridization.
Transactions of the Association of American Physicians 1990;103():242-8.
1990: Bernard G Forget
Developmental control of human globin gene expression.
Progress in clinical and biological research 1990;352():313-22.
1989: E A Feingold; Bernard G Forget
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.
Blood 1989;74(6):2178-86.
1989: K E Sahr; T Tobe; A Scarpa; K Laughinghouse; S L Marchesi; Peter Agre; A J Linnenbach; V T Marchesi; Bernard G Forget
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
The Journal of clinical investigation 1989;84(4):1243-52.
1989: Laurette Morlé; François Morlé; A F Roux; Jacqueline Godet; Bernard G Forget; L Denoroy; Michel Garbarz; Didier Dhermy; R Kastally; Jean Delaunay
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.
Blood 1989;74(2):828-32.
1989: A F Roux; François Morlé; D Guetarni; P Colonna; K Sahr; Bernard G Forget; Jean Delaunay; Jacqueline Godet
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.
Blood 1989;73(8):2196-201.
1989: J E Metherall; F P Gillespie; Bernard G Forget
Nuclear proteins of a human erythroleukemic cell line that bind to the promoter region of normal and nondeletion HPFH gamma-globin genes.
Progress in clinical and biological research 1989;316A():247-60.
1989: Michel Garbarz; Isabelle Devaux; Bernard Grandchamp; C Picat; Didier Dhermy; Marie-Christine Lecomte; P Boivin; K E Sahr; Bernard G Forget
[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant].
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1989;308(2):43-8.
1989: C J Cohen; L Penny; Bernard G Forget
Point mutations or polymorphisms? A sequence analysis of the enhancer 3' to the A gamma-globin gene.
Progress in clinical and biological research 1989;316B():395-401.
1989: L A Penny; Bernard G Forget
A conserved gene 3' to the HPFH-1 deletion breakpoint may have an effect on fetal globin gene expression in HPFH-1.
Progress in clinical and biological research 1989;316B():133-41.
1988: J C Winkelmann; T L Leto; P C Watkins; R Eddy; T B Shows; A J Linnenbach; K E Sahr; navneet kathuria; V T Marchesi; Bernard G Forget
Molecular cloning of the cDNA for human erythrocyte beta-spectrin.
Blood 1988;72(1):328-34.
1988: J E Metherall; F P Gillespie; Bernard G Forget
Analyses of linked beta-globin genes suggest that nondeletion forms of hereditary persistence of fetal hemoglobin are bona fide switching mutants.
American journal of human genetics 1988;42(3):476-81.
1988: Bernard G Forget; J G Chang; E Coupal; P Stanislovitis; F F Costa; J C Winkelmann; Peter Agre; V T Marchesi; P C Watkins
Molecular genetics of the human beta-spectrin gene.
Transactions of the Association of American Physicians 1988;101():149-54.
1987: C J Stoeckert; J E Metherall; M Yamakawa; J M Eisenstadt; S M Weissman; Bernard G Forget
Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin.
Molecular and cellular biology 1987;7(8):2999-3003.
1987: N Hoffman; P Stanislovitis; P C Watkins; Katherine W Klinger; A J Linnenbach; Bernard G Forget
Three RFLPs are detected by an alpha spectrin genomic clone.
Nucleic acids research 1987;15(11):4696.
1987: J E Metherall; C J Stoeckert; F P Gillespie; S M Weissman; Bernard G Forget
Support for the causal relationship between gamma globin gene promoter mutations and nondeletion forms of hereditary persistence of fetal hemoglobin.
Progress in clinical and biological research 1987;251():347-61.
1985: E A Feingold; Francis S Collins; J E Metherall; C J Stoeckert; S M Weissman; Bernard G Forget
Analysis of mutations associated with deletion and nondeletion hereditary persistence of fetal hemoglobin.
Progress in clinical and biological research 1985;191():107-24.
1985: E A Feingold; Francis S Collins; J E Metherall; C J Stoeckert; S M Weissman; Bernard G Forget
Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia.
Annals of the New York Academy of Sciences 1985;445():159-69.