B. Forget

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Disorders of Hemoglobin: THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS

D. Weatherall, D. Higgs, M. Steinberg, 2009 .

Disorders of Hemoglobin: THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS

D. Weatherall, D. Higgs, M. Steinberg, 2009 .

The structure and evolution of the human β-globin gene family

Tom Maniatis, Sherman M. Weissman, Francisco E. Baralle, 1980, Cell.

Progress in understanding the hemoglobin switch.

B. Forget, 2011, The New England journal of medicine.

A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred.

B. Forget, P. Gallagher, D. B. Costa, 2005, Blood.

Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis

B. Forget, P. Gallagher, A. Pekrun, 1996, Nature Genetics.

Cytokine signals through STAT3 promote expression of granulocyte secondary granule proteins in 32D cells.

M. Arcasoy, B. Forget, S. Watowich, 2005, Experimental hematology.

G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.

F. Collins, S. Weissman, C. Stoeckert, 1984, Proceedings of the National Academy of Sciences of the United States of America.

An Alternate Promoter Directs Expression of a Truncated, Muscle-specific Isoform of the Human Ankyrin 1 Gene*

B. Forget, P. Gallagher, 1998, The Journal of Biological Chemistry.

The structure and evolution of the human beta-globin gene family.

S. Weissman, T. Maniatis, R. Spritz, 1980, Cell.

Full-length sequence of the cDNA for human erythroid beta-spectrin.

V. Marchesi, Jan-Gowth Chang, B. Forget, 1990, The Journal of biological chemistry.

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).

F. Morlé, J. Starck, L. Denoroy, 1990, The Journal of clinical investigation.

Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis.

B. Forget, P. Gallagher, 1996, Blood cells, molecules & diseases.

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

B. Forget, P. Gallagher, I. Devaux, 1996, British journal of haematology.

Induced pluripotent stem cells in regenerative medicine: an argument for continued research on human embryonic stem cells.

J. Park, B. Forget, P. Gaines, 2009, Regenerative medicine.

Prenatal diagnosis of homozygous alpha-thalassemia.

Y. Kan, B. Forget, M. Mahoney, 1979, JAMA.

The Prevention of Thalassemia Antonio Cao and Yuet Wai Kan Classification of the Disorders of Hemoglobin

S. Orkin, S. Philipsen, D. Schaer, 2013 .

Absence of Messenger RNA for Beta Globin Chain in β°-Thalassaemia

D. Housman, A. Skoultchi, C. Baglioni, 1974, Nature.

Disorders of Hemoglobin: The Normal Structure and Regulation of Human Globin Gene Clusters

R. Hardison, B. Forget, 2009 .

Hemoglobin: Molecular, Genetic and Clinical Aspects

H. Bunn, B. Forget, 1984 .

Concordance of a Point Mutation 5 ’ to the “ y Globin Gene With G # y + Hereditary Persistence of Fetal Hemoglobin in the Black Population

F. Collins, C. Stoeckert, H. Kazazian, 2005 .

High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin

R. Nagel, M. Arcasoy, B. Forget, 1997, Molecular and cellular biology.

Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing β‐Thalassemia a

F. Collins, S. Weissman, E. Feingold, 1985, Annals of the New York Academy of Sciences.

Expression of Pitx2 in stromal cells is required for normal hematopoiesis.

P. Mangeot, A. Dubart-Kupperschmitt, B. Forget, 2006, Blood.

Molecular genetics of human hemoglobin synthesis.

B. Forget, 1979, Annals of internal medicine.

Absence of messenger RNA and gene DNA for β-globin chains in hereditary persistence of fetal hemoglobin

H. Lazarus, D. Housman, C. Caskey, 1976, Cell.

Nonsense mutations of the α-spectrin gene in hereditary pyropoikilocytosis

B. Forget, P. Gallagher, Y. Maksimova, 2008, Haematologica.

Disorders of Hemoglobin: THE β THALASSEMIAS

D. Weatherall, D. Higgs, M. Steinberg, 2009 .

Molecular evolution of human and rabbit beta-globin mRNAs.

S. Weissman, F. Kafatos, A. Efstratiadis, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Structure, Organization, and Expression of the Human Band 7.2b Gene, a Candidate Gene for Hereditary Hydrocytosis (*)

B. Forget, P. Gallagher, 1995, The Journal of Biological Chemistry.

USE OF GLOBIN cDNA AS A HYBRIDIZATION PROBE FOR GLOBIN mRNA *

D. Housman, A. Skoultchi, B. Forget, 1974, Annals of the New York Academy of Sciences.

Waldenström's macroglobulinemia with generalized amyloidosis.

B. Forget, H. Sheldon, J. W. Squires, 1966, Archives of internal medicine.

Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron.

F. Collins, S. Weissman, B. Forget, 1986, The EMBO journal.

Disorders of Hemoglobin

D. Weatherall, D. Higgs, M. Steinberg, 2009 .

A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation.

M. Arcasoy, B. Forget, K. Harris, 1999, Experimental hematology.

Production of mouse globin in heterokaryons of mouse erythroleukaemia cells and human fibroblasts.

A. Deisseroth, B. Alter, B. Forget, 1977, Journal of cell science.

Insertion of synthetic copies of human globin genes into bacterial plasmids.

J. T. Wilson, S. Weissman, L. Villa-komaroff, 1978, Nucleic acids research.

Short interspersed repetitive DNA elements in eucaryotes: Transposable DNA elements generated by reverse transcription of RNA pol III transcripts?

S. Weissman, P. Jagadeeswaran, B. Forget, 1981, Cell.

Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridization.

T. Shows, P. Watkins, B. Forget, 1990, Cytogenetics and cell genetics.

Erythropoietin mediates terminal granulocytic differentiation of committed myeloid cells with ectopic erythropoietin receptor expression

M. Arcasoy, B. Forget, N. Berliner, 2001, European journal of haematology.

Erythroid cell differentiation.

D. Housman, B. Forget, J. Glass, 1976, Hamatologie und Bluttransfusion.

Sequences of human repetitive DNA, non-alpha-globin genes, and major histocompatibility locus genes.

P. A. Biro, S. Weissman, C. Stoeckert, 1983, Cold Spring Harbor symposia on quantitative biology.

The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotes

V. Viprakasit, N. Akar, N. Al-Allawi, 2016, British journal of haematology.

Variability in the amount of β-globin mRNA in β 0 thalassemia

D. Housman, B. Forget, W. Prensky, 1978, Cell.

Synthesis of DNA complementary to separated human alpha and beta globin messenger RNAs.

D. Housman, B. Forget, E. Benz, 1975, Proceedings of the National Academy of Sciences of the United States of America.

The molecular genetics of the thalassemia syndromes.

B. Forget, E. Benz, 1975, Progress in hematology.

Defect in messenger RNA for human hemoglobin synthesis in beta thalassemia.

B. Forget, E. Benz, 1971, The Journal of clinical investigation.

Intranuclear defect in beta-globin mRNA accumulation due to a premature translation termination codon.

K. Takeshita, B. Forget, E. Benz, 1984, Blood.

Negative regulation of globin gene expression during megakaryocytic differentiation of a human erythroleukemic cell line

B. Forget, N. Lumelsky, 1991, Molecular and cellular biology.

RNA of low molecular weight in KB cells infected with adenovirus type 2.

S. Weissman, B. Forget, P. Reich, 1966, Journal of molecular biology.

Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

B. Forget, V. Schulz, P. Gallagher, 2014, Haematologica.

NUCLEOTIDE SEQUENCES OF HUMAN GLOBIN MESSENGER RNA *

S. Weissman, D. Baltimore, C. Marotta, 1974, Annals of the New York Academy of Sciences.

ANALYSIS OF β‐GLOBIN GENES IN β^ THALASSEMIA *

P. A. Biro, D. Tuan, B. Forget, 1980 .

Potentiation of human erythropoiesis in vitro by thyroid hormone

R. Hoffman, B. Forget, N. Dainiak, 1978, Nature.

The pathophysiology and molecular genetics of beta thalassemia.

B. Forget, 1993, The Mount Sinai journal of medicine, New York.

Gamma-beta thalassemia: a cause of hemolytic disease of the newborn.

Y. Kan, D. Nathan, B. Forget, 1972, The New England journal of medicine.

Analyses of linked beta-globin genes suggest that nondeletion forms of hereditary persistence of fetal hemoglobin are bona fide switching mutants.

B. Forget, F. Gillespie, J. Metherall, 1988, American journal of human genetics.

Abnormally spliced messenger RNA in erythroid cells from patients with β + thalassemia and monkey cells expressing a cloned β +-thalassemic gene

S. Weissman, Y. Fukumaki, P. Ghosh, 1982, Cell.

Defective processing of beta mRNA in different forms of beta +-thalassemia.

B. Forget, E. Benz, A. Scarpa, 1982, Transactions of the Association of American Physicians.

Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population

F. Collins, S. Weissman, H. Kazazian, 1984 .

Expression of the Affected Aγ Globin Gene Associated with Greek Nondeletion Hereditary Persistence of Fetal Hemoglobin

C. Stoeckert, B. Forget, M. Sherman, 1987 .

Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

S. Hayette, B. Forget, J. Delaunay, 1997, American journal of hematology.

Idiopathic thrombocytopenic purpura occurring in a subject previously splenectomized for traumatic splenic rupture. Role of splenosis in the pathogenesis of thrombocytopenia.

B. Forget, T. Duffy, E. Mazur, 1978, The American journal of medicine.

Molecular studies of genetic disorders affecting the expression of the human beta-globin gene: a model system for the analysis of inborn errors of metabolism.

B. Forget, 1982, Recent progress in hormone research.

Nucleotide sequence of the coding portion of human alpha globin messenger RNA.

J. T. Wilson, S. Weissman, B. Forget, 1980, The Journal of biological chemistry.

Sequences Downstream of the Erythroid Promoter Are Required for High Level Expression of the Human α-Spectrin Gene*

D. Bodine, B. Forget, P. Gallagher, 2004, Journal of Biological Chemistry.

Nucleotide sequences of human globin messenger RNA.

S. Weissman, D. Baltimore, I. Verma, 1980, Proceedings of the National Academy of Sciences of the United States of America.

A low molecular weight ribonucleic acid synthesized by Escherichia coli in the presence of chloramphenicol: characterization and relation to normally synthesized 5 s ribonucleic acid.

B. Forget, B. Jordan, R. Monier, 1971, Journal of molecular biology.

Resistance of E. coli ribosomal 5S RNA to degradation by ribonuclease in reconstituted ribosomal particles.

B. Forget, M. Reynier, 1970, Biochemical and biophysical research communications.

A naturally occurring 43 s ribosomal precursor particle in Escherichia coli: nature and ribonucleic acid composition.

B. Forget, F. Varricchio, 1970, Journal of molecular biology.

5S RNA Synthesized by Escherichia coli in Presence of Chloramphenicol: Different 5'-Terminal Sequences

B. Forget, B. Jordan, 1970, Science.

Prenatal Diagnosis of Homozygous α-Thalassemia

Y. Kan, B. Forget, M. Mahoney, 1979 .

Prenatal Diagnosis of Classic Hemophilia

J. Hobbins, I. Merkatz, B. Forget, 1979, Thrombosis and Haemostasis.

Downstream targets of HOXB 4 in a cell line model of primitive hematopoietic progenitor cells

D. Tuck, B. Forget, V. Schulz, 2010 .

Cloning of a Portion of the Chromosomal Gene and cDNA for Human β-Fodrin, the Nonerythroid Form of β-Spectrin

R. Eddy, T. Shows, Jan-Gowth Chang, 1993 .

The distal cytoplasmic domain of the erythropoietin receptor induces granulocytic differentiation in 32D cells.

M. Arcasoy, B. Forget, X. Hu, 1998, Blood.

Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene.

M. Arcasoy, B. Forget, B. Degar, 1997, Blood.

Genomic organization of the human erythropoietin receptor gene.

L. Penny, B. Forget, 1991, Genomics.

A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin

S. Weissman, P. Jagadeeswaran, B. Forget, 1982, Nature.

Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin

D. Tuan, B. Forget, J. K. Deriel, 1980, Nature.

Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin

S. Weissman, C. Stoeckert, B. Forget, 1987, Molecular and cellular biology.

Oligonucleotides produced by digestion of KB cell ribosomal 5 S ribonucleic acid with specific nucleases.

S. Weissman, B. Forget, 1968, The Journal of biological chemistry.

Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site.

B. Forget, P. Gallagher, J. Morrow, 2004, Laboratory investigation; a journal of technical methods and pathology.

A structurally abnormal erythropoietin receptor gene in a human erythroleukemia cell line.

T. Kitamura, L. Penny, B. Forget, 1992, Experimental hematology.

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

F. Costa, B. Forget, P. Gallagher, 1991 .

Globin Chain Electrophoresis for Prenatal Diagnosis of β Thalassemia

B. Alter, B. Forget, E. Coupal, 1981 .

Genetic basis of the polymorphisms of the αI domain of spectrin

B. Forget, P. Gallagher, M. Romana, 1997 .

Hemin control of heme biosynthesis and catabolism in a human leukemia cell line.

R. Hoffman, B. Forget, M. Murnane, 1980, Blood.

Studies of globin chain synthesis and globin mRNA content in a patient homozygous for hemoglobin Lepore.

D. Housman, B. Forget, E. Benz, 1978, Hemoglobin.

β-Globin mRNA in Ferrara β0-thalassaemia

B. Forget, D. Hillman, 1977, Nature.

The aminoacyl-tRNA population of human reticulocytes.

D. Hatfield, B. Forget, F. Varricchio, 1982, The Journal of biological chemistry.

Nucleotide sequence of 3' untranslated portion of human alpha globin mRNA.

J. T. Wilson, S. Weissman, C. Marotta, 1977, Nucleic acids research.

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

S. Weissman, J. Starck, R. Sarkar, 1994 .

Expression of Human Globin Genes in Transgenic Mice Carrying the β‐Globin Gene Cluster with a Mutation Causing Gγβ+ Hereditary Persistence of Fetal Hemoglobin a

S. Weissman, Minoru Tanaka, B. Forget, 1990 .

PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES: THE NEW ENGLAND APPROACH *

S. Orkin, B. Alter, D. Nathan, 1980, Annals of the New York Academy of Sciences.

Hemin control of heme biosynthesis and catabolism in a human leukemia cell line

R. Hoffman, B. Forget, M. Murnane, 1980 .

Reverse transcription and direct amplification of cellular RNA transcripts by Taq polymerase.

B. Forget, W. Tse, 1990, Gene.

δβ Thalassemia and Hereditary Persistence of Fetal Hemoglobin

B. Forget, J. Bollekens, 1991 .

Classification of the disorders of hemoglobin.

H. Bunn, B. Forget, P. Sodani, 2013, Cold Spring Harbor perspectives in medicine.

Hemoglobin synthesis in human BFU-E and CFU-E-derived erythroid colonies

D. Housman, B. Forget, D. Nathan, 1979 .

Hemoglobin synthesis in human BFU-E and CFU-E-derived erythroid colonies.

D. Housman, B. Forget, D. Nathan, 1979, Blood.

Clinical and molecular correlations in the sickle/β+‐thalassemia syndrome

B. Forget, G. Atweh, 1987 .

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

F. Collins, G. Stamatoyannopoulos, M. Bender, 1986, Blood.

Molecular Basis of Hereditary Persistence of Fetal Hemoglobin

B. Forget, 1998, Annals of the New York Academy of Sciences.

A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin

F. Collins, S. Weissman, B. Forget, 1985, Nature.

Embryonic-fetal erythroid characteristics of a human leukemic cell line.

R. Hoffman, E. Snyder, B. Forget, 1980, Proceedings of the National Academy of Sciences of the United States of America.

The thalassemias: molecular mechanisms of human genetic disease.

R. Spritz, B. Forget, 1983, American journal of human genetics.

RNA polymerase III transcriptional units are interspersed among human non-alpha-globin genes.

P. A. Biro, James T. Elder, S. Weissman, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Base substitution in an intervening sequence of a beta+-thalassemic human globin gene.

P. A. Biro, James T. Elder, S. Weissman, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Hemoglobin Indianapolis (,8112[G14] Arginine) AN UNSTABLE /3-CHAIN VARIANT PRODUCING THE PHENOTYPE OF SEVERE /3-THALASSEMIA

M. Steinberg, B. Forget, L. Boxer, 2022 .

Imbalanced globin chain synthesis in cultured erythroid progenitor cells from thalassemic bone marrow and peripheral blood.

R. Hoffman, B. Forget, V. Floyd, 1981, Blood.

Substitution of the Human β-Spectrin Promoter for the Human Aγ-Globin Promoter Prevents Silencing of a Linked Human β-Globin Gene in Transgenic Mice

G. Stamatoyannopoulos, D. Bodine, B. Forget, 1998, Molecular and Cellular Biology.

Globin messenger RNA in hemoglobin H disease.

P. Swerdlow, B. Forget, E. Benz, 1973, Blood.

Quantitative deficiency of chain-specific globin messenger ribonucleic acids in the thalassemia syndromes.

D. Housman, A. Skoultchi, B. Forget, 1973, Proceedings of the National Academy of Sciences of the United States of America.

β Globin messenger RNA content of bone marrow erythroblasts in heterozygous β‐thalassemia

B. Forget, E. Benz, J. Pritchard, 1984 .

Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.

S. Weissman, E. Feingold, B. Forget, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Restriction endonuclease mapping of the human γ globin gene loci

P. A. Biro, H. Lazarus, D. Tuan, 1979 .

Human beta-globin messenger RNA. I. Nucleotide sequences derived from complementary RNA.

S. Weissman, C. Marotta, B. Forget, 1977, The Journal of biological chemistry.

Massive splenic infarction in an adolescent with hemoglobin S‐HPFH

B. Forget, D. Chui, Hong‐yuan Luo, 2013, Pediatric blood & cancer.

Ankyrin‐linked hereditary spherocytosis in an African–American kindred

J. Sangerman, B. Forget, P. Gallagher, 2008, American journal of hematology.

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

C. Stolle, L. Penny, B. Forget, 1990, Blood.

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.

E. Feingold, B. Forget, EA Feingold, 1989, Blood.

Nucleotide Sequence of KB Cell 5S RNA

S. Weissman, B. Forget, 1967, Science.

The homeodomain gene Pitx2 is expressed in primitive hematopoietic stem/progenitor cells but not in their differentiated progeny.

S. Weissman, P. Quesenberry, N. Baskaran, 2001, Experimental hematology.

An olfactory receptor gene is located in the extended human beta-globin gene cluster and is expressed in erythroid cells.

E. Feingold, A. Nienhuis, L. Penny, 1999, Genomics.

A conserved gene 3' to the HPFH-1 deletion breakpoint may have an effect on fetal globin gene expression in HPFH-1.

L. Penny, B. Forget, 1989, Progress in clinical and biological research.

The nucleotide sequence of ribosomal 5 S ribonucleic acid from KB cells.

S. Weissman, B. Forget, 1969, The Journal of biological chemistry.

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

L. Deaven, L. Penny, B. Forget, 1990, Blood.

The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter.

B. Forget, P. Gallagher, S. Lux, 2000, Blood.

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8

F. Collins, D. Ward, U. Francke, 1990, Nature.

Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype

B. Forget, V. Schulz, P. Gallagher, 2016, Hemoglobin.

Nucleotide sequence of human beta globin messenger RNA.

B. Forget, 1977, Hemoglobin.

Isolation and chromosomal localization of a novel nonerythroid ankyrin gene.

D. Ward, U. Francke, T. Yang-Feng, 1991, Genomics.

Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.

B. Forget, P. Gallagher, 1998, Blood cells, molecules & diseases.

The exon-intron organization of the human erythroid beta-spectrin gene.

B. Forget, J. Winkelmann, P. Curtis, 1993, Genomics.

Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.

B. Forget, S. Lux, W. Tse, 1993, The Journal of clinical investigation.

Amino‐acid substitution in α‐spectrin commonly coinherited with nondominant hereditary spherocytosis

D. Speicher, P. Agre, B. Forget, 1997, American journal of hematology.

Spectrin genes in health and disease.

B. Forget, P. Gallagher, 1993, Seminars in hematology.

Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis.

B. Forget, P. Gallagher, 1997, Blood cells, molecules & diseases.

Spectrin St Louis and the alpha LELY allele.

B. Forget, P. Gallagher, 1994, Blood.

Hematopoiesis following disruption of the Pitx2 homeodomain gene.

B. Forget, C. Booth, P. Gage, 2006, Experimental hematology.

Downregulation of Prdm16 mRNA is a specific antileukemic mechanism during HOXB4-mediated HSC expansion in vivo.

G. Neale, B. Sorrentino, B. Forget, 2014, Blood.

HEMATOPOIESIS AND STEM CELLS Downregulation of Prdm 16 mRNA is a speci fi c antileukemic mechanism during HOXB 4-mediated HSC expansion in vivo

G. Neale, B. Sorrentino, B. Forget, 2014 .

Molecular lesions in thalassemia

B. Forget, 1978 .

Absence of functional messenger RNA activity for beta globin chain synthesis in beta 0-thalassemia.

P. Swerdlow, B. Forget, E. Benz, 1975, Blood.

Hemolytic anemias: congenital and acquired.

B. Forget, 1980, Hospital practice.

Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro.

M. Debatis, B. Forget, P. Gallagher, 2000, Experimental hematology.

A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis.

M. Arcasoy, B. Forget, J. Sinning, 2002, Blood.

Hemoglobinopathies Pluripotent Stem Cells in Research and Treatment

H. Bunn, B. Forget, 2013 .

Familial polycythemia due to truncations of the erythropoietin receptor.

M. Arcasoy, B. Forget, B. A. Dègan, 2000, Transactions of the American Clinical and Climatological Association.

Induction of erythropoietic colonies in a human chronic myelogenous leukemia cell line.

R. Hoffman, E. Benz, B. Forget, 1979, Blood.

Evidence that expression of SpαI/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous α-spectrin allele

F. Morlé, B. Forget, J. Delaunay, 1990, Human Genetics.

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

L. Valentino, B. Forget, P. Gallagher, 1991, Blood.

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.

F. Galibert, B. Forget, P. Gallagher, 1991, The Journal of clinical investigation.

The exon-intron organization of the human erythrocyte α-spectrin gene

L. Showe, B. Forget, A. Linnenbach, 1991 .

A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis

F. Costa, B. Forget, S. Saad, 2000, British journal of haematology.

Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.

S. Weed, N. Mohandas, B. Forget, 1997, The Journal of clinical investigation.

The thalassemia syndromes: models for the molecular analysis of human disease.

B. Forget, E. Benz, 1982, Annual review of medicine.

Absence of messenger RNA for beta globin chain in beta(0) thalassaemia.

D. Housman, A. Skoultchi, C. Baglioni, 1974, Nature.

Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.

N. Mohandas, B. Forget, P. Gallagher, 1995, The Journal of clinical investigation.

G'YP+ Hereditary persistence of fetal hemoglobin: Cosmid cloning and identification of a specific mutation 5' to the Gy gene

F. Collins, S. Weissman, C. Stoeckert, 1999 .

Structural features of the DNA flanking the human non-alpha globin genes: implications in the control of fetal hemoglobin switching.

P. A. Biro, S. Weissman, P. Jagadeeswaran, 1981, Transactions of the Association of American Physicians.

A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain.

F. Costa, B. Forget, P. Gallagher, 1991, The Journal of biological chemistry.

Synthesis of DNA Complementary to Sepa

B. Forget, R. Mccaffrey, 2016 .

Pathogenesis of the thalassemia syndromes.

B. Forget, E. Benz, 1980, Pathobiology annual.

Complete nucleotide sequence of the human δ-globin gene

S. Weissman, R. Spritz, B. Forget, 1980, Cell.

STRUCTURES IN INTERGENIC DNA OF NON-ALPHA GLOBIN GENES OF MAN

P. A. Biro, S. Weissman, R. Spritz, 1981 .

Human beta-globin messenger RNA. III. Nucleotide sequences derived from complementary DNA.

S. Weissman, C. Marotta, B. Forget, 1977, The Journal of biological chemistry.

STRUCTURE OF THE HUMAN GLOBIN GENES

S. Weissman, R. Spritz, P. Choudary, 1979 .

Abnormally spliced messenger RNA in erythroid cells from patients with beta+ thalassemia and monkey cells expressing a cloned beta+-thalassemic gene.

S. Weissman, Y. Fukumaki, B. Forget, 1982, Cell.

Cloning and Nucleotide Sequence Analysis of Human Embryonic ζ-Globin cDNA

B. Forget, M. Cohen-Solal, J. K. Deriel, 1982 .

Substitution of the Human b-Spectrin Promoter for the Human A g-Globin Promoter Prevents Silencing of a Linked Human b-Globin Gene in Transgenic Mice

G. Stamatoyannopoulos, D. Bodine, B. Forget, 1998 .

Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An Unstable Hemoglobin Variant Causing Severe Hemolytic Anemia

M. Steinberg, B. Forget, D. Chui, 2014, Hemoglobin.

Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells.

D. Tuck, B. Forget, V. Schulz, 2010, Blood.

Nucleotide sequences of the 3'-terminal untranslated region of messenger RNA for human beta globin chain.

S. Weissman, C. Marotta, B. Forget, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Polyadenylation of a human mitochondrial ribosomal RNA transcript detected by molecular cloning.

K. Takeshita, S. Baserga, S. Malcolm, 1985, Gene.

Structure and Organization of the Human Ankyrin-1 Gene

B. Forget, P. Gallagher, S. Lux, 1997, The Journal of Biological Chemistry.

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

D. Speicher, B. Forget, P. Gallagher, 1993 .

Cotransfer of circular and linear prokaryotic and eukaryotic DNA sequences into mouse cells.

R. Kucherlapati, D. Tuan, A. Skoultchi, 1980, Proceedings of the National Academy of Sciences of the United States of America.

HETEROGENEITY OF MESSENGER RNA DEFECTS IN THE THALASSEMIA SYNDROMES

J. Kantor, B. Forget, E. Benz, 1980, Annals of the New York Academy of Sciences.

Marrow Stem Cells Shift Gene Expression and Engraftment Phenotype with Cell Cycle Transit

S. Weissman, P. Quesenberry, M. Dooner, 2003, The Journal of experimental medicine.

Hereditary Pyropoikilocytosis and Elliptocytosis in a White French Family (Arg to His) at Position 22 of the Spectrin a1 Domain With the Spectrin Variant Related to a CGT to CAT Codon Change

F. Galibert, B. Forget, I. Devaux, 2016 .

Analysis of a Pst I polymorphism of the human erythrocyte band 3 gene (EPB3)

B. Forget, P. Gallagher, P. B. Jenkins, 1993, British Journal of Haematology.

Low Molecular Weight RNA Components from KB Cells

B. Forget, S. Weissman, 1967, Nature.

A de novo band 3 mutation in hereditary spherocytosis

B. Forget, P. Gallagher, Y. Maksimova, 2012, Pediatric blood & cancer.

5 S RNA and the assembly of bacterial ribosomes.

B. Forget, B. Jordan, J. Feunteun, 1969, Cold Spring Harbor symposia on quantitative biology.

Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.

D. Speicher, B. Forget, P. Gallagher, 1996, American journal of human genetics.

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

L. Denoroy, B. Forget, C. Féo, 1992, Blood.

Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton.

B. Forget, P. Gallagher, W. Tse, 1990, Seminars in perinatology.

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.

P. Agre, V. Marchesi, B. Forget, 1989, The Journal of clinical investigation.

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.

F. Morlé, B. Forget, K. Sahr, 1989, Blood.

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

F. Costa, B. Forget, P. Gallagher, 1991, Blood.

A Human β-Spectrin Gene Promoter Directs High Level Expression in Erythroid but Not Muscle or Neural Cells*

D. Bodine, B. Forget, D. Sabatino, 1999, The Journal of Biological Chemistry.

Cloning of a portion of the chromosomal gene for human erythrocyte alpha-spectrin by using a synthetic gene fragment.

D. Speicher, V. Marchesi, B. Forget, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Genetic basis of the polymorphisms of the alphaI domain of spectrin.

B. Forget, P. Gallagher, C. Wong, 1997, American journal of hematology/oncology.

Two Elliptocytogenic ai 174 Variants of the Spectrin al domain Spectrin Culoz ( GGT-RGTT ; al 40 Gly-oVal ) and Spectrin Lyon ( CTT-- ' TTT ; al 43 Leu-* Phe )

J. Starck, B. Forget, R. Rudigoz, 2022 .

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.

F. Morlé, B. Forget, J. Delaunay, 1990, Human genetics.

Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the αβ spectrin self-association binding site

B. Forget, P. Gallagher, J. Morrow, 2004, Laboratory Investigation.

Location and PCR‐based detection of three polymorphisms of the human erythrocyte β‐spectrin gene (SPTB)

B. Forget, P. Gallagher, M. Lecomte, 1994, British journal of haematology.

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

D. Speicher, B. Forget, P. Gallagher, 1993, Blood.

Molecular pathology of the thalassemias.

D. Nathan, B. Forget, 1976, Advances in internal medicine.

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

B. Forget, P. Gallagher, W. Tse, 1992 .

Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene.

B. Forget, P. Gallagher, W. Tse, 1992, Blood.

INTERVENING SEQUENCE MUTATION IN A CLONED HUMAN β + -THALASSEMIC GLOBIN GENE

P. A. Biro, S. Weissman, R. Spritz, 1981 .

Molecular cloning of the cDNA for human erythrocyte beta-spectrin.

R. Eddy, V. Marchesi, P. Watkins, 1988, Blood.

Erythroid and nonerythroid spectrins.

B. Forget, J. Winkelmann, B. Forget, 1993, Blood.

Ankyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrin

B. Forget, J. Morrow, J S Morrow, 1991, The Journal of cell biology.

Nucleotide sequence analysis of coding and noncoding regions of human beta-globin mRNA.

S. Weissman, C. Marotta, B. Forget, 1976, Progress in nucleic acid research and molecular biology.

New amber mutation in a beta-thalassemic gene with nonmeasurable levels of mutant messenger RNA in vivo.

H. Kazazian, B. Forget, H. Kazazian, 1988, The Journal of clinical investigation.

A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.

A. Baruchel, B. Forget, S. Ballas, 1992, The Journal of clinical investigation.

Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.

F. Costa, B. Forget, C. Féo, 1990, The Journal of clinical investigation.

Pitfalls of genetic testing.

G. Stamatoyannopoulos, T. Stossel, B. Forget, 1996, The New England journal of medicine.

The molecular basis of thalassemia.

B. Forget, Forget Bg, 1974, CRC critical reviews in biochemistry.

Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrin.

B. Forget, P. Gallagher, S. Lux, 1992, Transactions of the Association of American Physicians.

Disorders of Hemoglobin: THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS

D. Weatherall, D. Higgs, M. Steinberg, 2009 .

Disorders of Hemoglobin: The Normal Structure and Regulation of Human Globin Gene Clusters

R. Hardison, B. Forget, 2009 .

Ankyrin binds to the 15th repetitive unit of erythroid and nonerythroid beta-spectrin

B. Forget, J. Morrow, S. L. Warren, 1991, The Journal of cell biology.