PubMed

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

Lee H, Park J, Forget BG, Gaines P.

Regen Med. 2009 Sep;4(5):759-69.PMID: 19761400 [PubMed - in process]Related articles

Nonsense mutations of the alpha-spectrin gene in hereditary pyropoikilocytosis.

Tolpinrud W, Maksimova YD, Forget BG, Gallagher PG.

Haematologica. 2008 Nov;93(11):1752-4. Epub 2008 Sep 24. No abstract available. PMID: 18815189 [PubMed - indexed for MEDLINE]Related articlesFree article

Ankyrin-linked hereditary spherocytosis in an African-American kindred.

Sangerman J, Maksimova Y, Edelman EJ, Morrow JS, Forget BG, Gallagher PG.

Am J Hematol. 2008 Oct;83(10):789-94.PMID: 18704959 [PubMed - indexed for MEDLINE]Related articles

De novo and acquired forms of alpha thalassemia.

Forget BG.

Curr Hematol Rep. 2006 Mar;5(1):11-4. Review.PMID: 16537041 [PubMed - indexed for MEDLINE]Related articles

Hematopoiesis following disruption of the Pitx2 homeodomain gene.

Zhang HZ, Degar BA, Rogoulina S, Resor C, Booth CJ, Sinning J, Gage PJ, Forget BG.

Exp Hematol. 2006 Feb;34(2):167-78.PMID: 16459185 [PubMed - indexed for MEDLINE]Related articles

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

Kieusseian A, Chagraoui J, Kerdudo C, Mangeot PE, Gage PJ, Navarro N, Izac B, Uzan G, Forget BG, Dubart-Kupperschmitt A.

Blood. 2006 Jan 15;107(2):492-500. Epub 2005 Sep 29.PMID: 16195330 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Costa DB, Lozovatsky L, Gallagher PG, Forget BG.

Blood. 2005 Dec 15;106(13):4367-9. Epub 2005 Sep 8.PMID: 16150946 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Wang L, Arcasoy MO, Watowich SS, Forget BG.

Exp Hematol. 2005 Mar;33(3):308-17.PMID: 15730854 [PubMed - indexed for MEDLINE]Related articlesFree article

Sequences downstream of the erythroid promoter are required for high level expression of the human alpha-spectrin gene.

Wong EY, Lin J, Forget BG, Bodine DM, Gallagher PG.

J Biol Chem. 2004 Dec 31;279(53):55024-33. Epub 2004 Sep 27.PMID: 15456760 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Gallagher PG, Zhang Z, Morrow JS, Forget BG.

Lab Invest. 2004 Feb;84(2):229-34.PMID: 14661034 [PubMed - indexed for MEDLINE]Related articlesFree article

Marrow stem cells shift gene expression and engraftment phenotype with cell cycle transit.

Lambert JF, Liu M, Colvin GA, Dooner M, McAuliffe CI, Becker PS, Forget BG, Weissman SM, Quesenberry PJ.

J Exp Med. 2003 Jun 2;197(11):1563-72.PMID: 12782718 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Arcasoy MO, Karayal AF, Segal HM, Sinning JG, Forget BG.

Blood. 2002 Apr 15;99(8):3066-9.PMID: 11929803 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Arcasoy MO, Maun NA, Perez L, Forget BG, Berliner N.

Eur J Haematol. 2001 Aug;67(2):77-87.PMID: 11722594 [PubMed - indexed for MEDLINE]Related articles

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

Degar BA, Baskaran N, Hulspas R, Quesenberry PJ, Weissman SM, Forget BG.

Exp Hematol. 2001 Jul;29(7):894-902.PMID: 11438212 [PubMed - indexed for MEDLINE]Related articles

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

Gallagher PG, Ferreira JD, Costa FF, Saad ST, Forget BG.

Br J Haematol. 2000 Dec;111(4):1190-3.PMID: 11167760 [PubMed - indexed for MEDLINE]Related articles

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

Gallagher PG, Romana M, Tse WT, Lux SE, Forget BG.

Blood. 2000 Aug 1;96(3):1136-43.PMID: 10910934 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Dooner GJ, Barker JE, Gallagher PG, Debatis ME, Brown AH, Forget BG, Becker PS.

Exp Hematol. 2000 Jul;28(7):765-74.PMID: 10907638 [PubMed - indexed for MEDLINE]Related articles

Familial polycythemia due to truncations of the erythropoietin receptor.

Forget BG, Degan BA, Arcasoy MO.

Trans Am Clin Climatol Assoc. 2000;111:38-44; discussion 44-5.PMID: 10881330 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Feingold EA, Penny LA, Nienhuis AW, Forget BG.

Genomics. 1999 Oct 1;61(1):15-23.PMID: 10512676 [PubMed - indexed for MEDLINE]Related articles

A human beta-spectrin gene promoter directs high level expression in erythroid but not muscle or neural cells.

Gallagher PG, Sabatino DE, Romana M, Cline AP, Garrett LJ, Bodine DM, Forget BG.

J Biol Chem. 1999 Mar 5;274(10):6062-73.PMID: 10037687 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Arcasoy MO, Harris KW, Forget BG.

Exp Hematol. 1999 Jan;27(1):63-74.PMID: 9923445 [PubMed - indexed for MEDLINE]Related articles

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

Gallagher PG, Forget BG.

Blood Cells Mol Dis. 1998 Dec;24(4):539-43. Review. No abstract available. PMID: 9887280 [PubMed - indexed for MEDLINE]Related articles

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.

Sabatino DE, Cline AP, Gallagher PG, Garrett LJ, Stamatoyannopoulos G, Forget BG, Bodine DM.

Mol Cell Biol. 1998 Nov;18(11):6634-40.PMID: 9774678 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Harris KW, Hu XJ, Schultz S, Arcasoy MO, Forget BG, Clare N.

Blood. 1998 Aug 15;92(4):1219-24.PMID: 9694710 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular basis of hereditary persistence of fetal hemoglobin.

Forget BG.

Ann N Y Acad Sci. 1998 Jun 30;850:38-44. Review.PMID: 9668525 [PubMed - indexed for MEDLINE]Related articles

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

Gallagher PG, Forget BG.

Blood Cells Mol Dis. 1997 Dec;23(3):417-21. Review. No abstract available. PMID: 9446757 [PubMed - indexed for MEDLINE]Related articles

An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 gene.

Gallagher PG, Forget BG.

J Biol Chem. 1998 Jan 16;273(3):1339-48.PMID: 9430667 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Gallagher PG, Romana M, Wong C, Forget BG.

Am J Hematol. 1997 Oct;56(2):107-11.PMID: 9326352 [PubMed - indexed for MEDLINE]Related articles

Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing.

Gallagher PG, Tse WT, Scarpa AL, Lux SE, Forget BG.

J Biol Chem. 1997 Aug 1;272(31):19220-8.PMID: 9235914 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Arcasoy MO, Degar BA, Harris KW, Forget BG.

Blood. 1997 Jun 15;89(12):4628-35.PMID: 9192789 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Arcasoy MO, Romana M, Fabry ME, Skarpidi E, Nagel RL, Forget BG.

Mol Cell Biol. 1997 Apr;17(4):2076-89.PMID: 9121456 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Morlé L, Bozon M, Alloisio N, Vallier A, Hayette S, Pascal O, Monier D, Philippe N, Forget BG, Delaunay J.

Am J Hematol. 1997 Mar;54(3):242-8.PMID: 9067504 [PubMed - indexed for MEDLINE]Related articles

Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosis.

Tse WT, Gallagher PG, Jenkins PB, Wang Y, Benoit L, Speicher D, Winkelmann JC, Agre P, Forget BG, Marchesi SL.

Am J Hematol. 1997 Mar;54(3):233-41.PMID: 9067503 [PubMed - indexed for MEDLINE]Related articles

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

Gallagher PG, Petruzzi MJ, Weed SA, Zhang Z, Marchesi SL, Mohandas N, Morrow JS, Forget BG.

J Clin Invest. 1997 Jan 15;99(2):267-77.PMID: 9005995 [PubMed - indexed for MEDLINE]Related articlesFree article

Pitfalls of genetic testing.

Bunn HF, Stossel TP, Forget BG, Stamatoyannopoulos G, Weatherall DJ.

N Engl J Med. 1996 Oct 17;335(16):1236; author reply 1236-7. No abstract available. PMID: 8999325 [PubMed - indexed for MEDLINE]Related articles

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

Glele-Kakai C, Garbarz M, Lecomte MC, Leborgne S, Galand C, Bournier O, Devaux I, Gautero H, Zohoun I, Gallagher PG, Forget BG, Dhermy D.

Br J Haematol. 1996 Oct;95(1):57-66.PMID: 8857939 [PubMed - indexed for MEDLINE]Related articles

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

Gallagher PG, Kotula L, Wang Y, Marchesi SL, Curtis PJ, Speicher DW, Forget BG.

Am J Hum Genet. 1996 Aug;59(2):351-9.PMID: 8755921 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Eber SW, Gonzalez JM, Lux ML, Scarpa AL, Tse WT, Dornwell M, Herbers J, Kugler W, Ozcan R, Pekrun A, Gallagher PG, Schröter W, Forget BG, Lux SE.

Nat Genet. 1996 Jun;13(2):214-8.PMID: 8640229 [PubMed - indexed for MEDLINE]Related articles

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.

Jenkins PB, Abou-Alfa GK, Dhermy D, Bursaux E, Féo C, Scarpa AL, Lux SE, Garbarz M, Forget BG, Gallagher PG.

J Clin Invest. 1996 Jan 15;97(2):373-80.PMID: 8567957 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Gallagher PG, Forget BG.

Blood Cells Mol Dis. 1996;22(3):254-8. No abstract available. PMID: 9075575 [PubMed - indexed for MEDLINE]Related articles

Structure, organization, and expression of the human band 7.2b gene, a candidate gene for hereditary hydrocytosis.

Gallagher PG, Forget BG.

J Biol Chem. 1995 Nov 3;270(44):26358-63.PMID: 7592848 [PubMed - indexed for MEDLINE]Related articlesFree article

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

Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL, Mohandas N, Forget BG.

J Clin Invest. 1995 Mar;95(3):1174-82.PMID: 7883966 [PubMed - indexed for MEDLINE]Related articlesFree article

Beta II-spectrin (fodrin) and beta I epsilon 2-spectrin (muscle) contain NH2- and COOH-terminal membrane association domains (MAD1 and MAD2).

Lombardo CR, Weed SA, Kennedy SP, Forget BG, Morrow JS.

J Biol Chem. 1994 Nov 18;269(46):29212-9.PMID: 7961888 [PubMed - indexed for MEDLINE]Related articlesFree article

Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB).

Gallagher PG, Lecomte MC, Galand C, Wang YP, Tse WT, Forget BG.

Br J Haematol. 1994 Oct;88(2):413-4.PMID: 7803294 [PubMed - indexed for MEDLINE]Related articles

Spectrin St Louis and the alpha LELY allele.

Gallagher PG, Forget BG.

Blood. 1994 Sep 1;84(5):1686-7. No abstract available. PMID: 8068958 [PubMed - indexed for MEDLINE]Related articlesFree article

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

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

Blood. 1994 Sep 1;84(5):1656-65.PMID: 7520781 [PubMed - indexed for MEDLINE]Related articlesFree article

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

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

Blood. 1994 Jun 15;83(12):3727-37.PMID: 7515719 [PubMed - indexed for MEDLINE]Related articlesFree article

A partial structural repeat forms the heterodimer self-association site of all beta-spectrins.

Kennedy SP, Weed SA, Forget BG, Morrow JS.

J Biol Chem. 1994 Apr 15;269(15):11400-8.PMID: 8157672 [PubMed - indexed for MEDLINE]Related articlesFree article

Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridization.

Upender M, Gallagher PG, Moon RT, Ward DC, Forget BG.

Cytogenet Cell Genet. 1994;66(1):39-41.PMID: 8275706 [PubMed - indexed for MEDLINE]Related articles

Analysis of a PstI polymorphism of the human erythrocyte band 3 gene (EPB3).

Jenkins PB, Gallagher PG, Forget BG.

Br J Haematol. 1993 Dec;85(4):816-8.PMID: 7918052 [PubMed - indexed for MEDLINE]Related articles