| Year |
Citation |
Score |
| 2016 |
Gallagher PG, Maksimova Y, Schulz VP, Forget BG. 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. Hemoglobin. 40: 361-364. PMID 27821015 DOI: 10.1080/03630269.2016.1214921 |
0.322 |
|
| 2016 |
Jiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Başak AN, Osorio L, ... ... Forget BG, et al. The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes. British Journal of Haematology. PMID 26771086 DOI: 10.1111/Bjh.13909 |
0.338 |
|
| 2014 |
Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH. Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia. Hemoglobin. 38: 381-4. PMID 25347256 DOI: 10.3109/03630269.2014.971960 |
0.318 |
|
| 2014 |
Yu H, Neale G, Zhang H, Lee HM, Ma Z, Zhou S, Forget BG, Sorrentino BP. Downregulation of Prdm16 mRNA is a specific antileukemic mechanism during HOXB4-mediated HSC expansion in vivo. Blood. 124: 1737-47. PMID 25082879 DOI: 10.1182/Blood-2013-10-534735 |
0.322 |
|
| 2014 |
Edward HL, Morrison T, Milton JN, Luo H, Davis L, Forget BG, Steinberg MH, Chui DHK. Analysis of (δβ)0 Thalassemia and HPFH Deletions Suggest a Hierarchy of Cis-Acting Elements Regulating Fetal Hemoglobin Gene Expression. Blood. 124: 54-54. DOI: 10.1182/Blood.V124.21.54.54 |
0.359 |
|
| 2014 |
Lezon-Geyda K, Maksimova Y, Schulz VP, Forget BG, Gallagher PG. Severe Alpha-Spectrin Linked Recessive Hereditary Spherocytosis Blood. 124: 4011-4011. DOI: 10.1182/Blood.V124.21.4011.4011 |
0.395 |
|
| 2014 |
Jiang Z, Huang S, Luo HY, Akar N, Basak A, Al-Allawi N, Unal S, Gumruk F, Davis L, Morrison T, Campbell A, Gallagher PG, Forget BG, Steinberg MH, Chui DH. Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β0-Thalassemia Mutation Blood. 124: 2690-2690. DOI: 10.1182/Blood.V124.21.2690.2690 |
0.373 |
|
| 2013 |
Luo H, Al-Allawi N, Unal S, Gumruk F, Osorio-Almeida L, Davis L, Morrison T, Campbell AD, Steinberg MH, Gallagher PG, Forget BG, Chui DHK. Patients Homozygous For Codon 8 (–AA) Frame-Shift β0-Thalassemia Mutation With Markedly Increased HbF Blood. 122: 3455-3455. DOI: 10.1182/Blood.V122.21.3455.3455 |
0.414 |
|
| 2013 |
Tasha M, Luo H, Davis L, Theberge R, McComb ME, Costello CE, Boudreaux J, Han Z, Steinberg MH, Forget BG, Chui DH. Neonatal Hemolytic Anemia and (δβ)0-Thalassemia Caused By Novel Deletions Involving The β-Globin Gene Cluster Blood. 122: 3452-3452. DOI: 10.1182/Blood.V122.21.3452.3452 |
0.429 |
|
| 2012 |
Bogardus HH, Maksimova YD, Forget BG, Gallagher PG. A de novo band 3 mutation in hereditary spherocytosis. Pediatric Blood & Cancer. 58: 1004. PMID 22170767 DOI: 10.1002/Pbc.23400 |
0.305 |
|
| 2012 |
Campbell A, Luo H, Benson K, Davis L, Gallagher PG, Steinberg MH, Fraser P, Forget BG, Chui DHK. Severe Impairment of γ-Globin Gene Silencing in an Asymptomatic Adult Patient Homozygous for the Codon 8 (–AA) Frame-Shift β 0 -Thalassemia Mutation Blood. 120: 1022-1022. DOI: 10.1182/Blood.V120.21.1022.1022 |
0.434 |
|
| 2011 |
Forget BG. Progress in understanding the hemoglobin switch. The New England Journal of Medicine. 365: 852-4. PMID 21879905 DOI: 10.1056/Nejme1106969 |
0.374 |
|
| 2011 |
Bogardus H, Schulz VP, Maksimova Y, Miller BA, Forget BG, Gallagher PG. Transfusion-Dependent Alpha-Spectrin Deficient Hemolytic Anemia Due to Maternal Uniparental Disomy Blood. 118: 1030-1030. DOI: 10.1182/Blood.V118.21.1030.1030 |
0.421 |
|
| 2010 |
Lee HM, Zhang H, Schulz V, Tuck DP, Forget BG. Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells. Blood. 116: 720-30. PMID 20404135 DOI: 10.1182/Blood-2009-11-253872 |
0.358 |
|
| 2008 |
Tolpinrud W, Maksimova YD, Forget BG, Gallagher PG. Nonsense mutations of the alpha-spectrin gene in hereditary pyropoikilocytosis. Haematologica. 93: 1752-4. PMID 18815189 DOI: 10.3324/Haematol.13639 |
0.361 |
|
| 2008 |
Sangerman J, Maksimova Y, Edelman EJ, Morrow JS, Forget BG, Gallagher PG. Ankyrin-linked hereditary spherocytosis in an African-American kindred. American Journal of Hematology. 83: 789-94. PMID 18704959 DOI: 10.1002/Ajh.21254 |
0.418 |
|
| 2008 |
Zhang H, Chen W, Rogulina S, Lee HM, Forget BG. Acute Myeloid Leukemia in Mice Associated with Retrovirally-Mediated Overexpression of HOXB4 Blood. 112: 4484-4484. DOI: 10.1182/Blood.V112.11.4484.4484 |
0.33 |
|
| 2008 |
Gallagher PG, Ferreira JDS, Costa FF, Saad STO, Forget BG. A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis: Short Report British Journal of Haematology. 111: 1190-1193. DOI: 10.1111/J.1365-2141.2000.02441.X |
0.374 |
|
| 2007 |
Zhang HZ, Rogulina S, Chen W, Degar BA, Forget BG. Effects of the Homeodomain Gene Pitx2 on Self-Renewal of Hematopoietic Stem Cells. Blood. 110: 95-95. DOI: 10.1182/Blood.V110.11.95.95 |
0.327 |
|
| 2007 |
Tolpinrud W, Gaetani M, Maksimova Y, Mootien S, Harper S, Forget BG, Speicher DW, Gallagher PG. Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia. Blood. 110: 1706-1706. DOI: 10.1182/Blood.V110.11.1706.1706 |
0.362 |
|
| 2006 |
Zhang HZ, Degar BA, Rogoulina S, Resor C, Booth CJ, Sinning J, Gage PJ, Forget BG. Hematopoiesis following disruption of the Pitx2 homeodomain gene. Experimental Hematology. 34: 167-78. PMID 16459185 DOI: 10.1016/J.Exphem.2005.11.002 |
0.345 |
|
| 2006 |
Kieusseian A, Chagraoui J, Kerdudo C, Mangeot PE, Gage PJ, Navarro N, Izac B, Uzan G, Forget BG, Dubart-Kupperschmitt A. Expression of Pitx2 in stromal cells is required for normal hematopoiesis. Blood. 107: 492-500. PMID 16195330 DOI: 10.1182/Blood-2005-02-0529 |
0.305 |
|
| 2005 |
Costa DB, Lozovatsky L, Gallagher PG, Forget BG. A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred. Blood. 106: 4367-9. PMID 16150946 DOI: 10.1182/Blood-2005-05-1813 |
0.402 |
|
| 2005 |
Wang L, Arcasoy MO, Watowich SS, Forget BG. Cytokine signals through STAT3 promote expression of granulocyte secondary granule proteins in 32D cells. Experimental Hematology. 33: 308-17. PMID 15730854 DOI: 10.1016/J.Exphem.2004.11.014 |
0.31 |
|
| 2004 |
Gallagher PG, Zhang Z, Morrow JS, Forget BG. 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. 84: 229-34. PMID 14661034 DOI: 10.1038/Labinvest.3700029 |
0.35 |
|
| 2004 |
Costa DB, Gallagher PG, Forget BG. A Position +5 Intronic Mutation in the α-Spectrin Gene Is Associated with Marked Deficiency of α-Spectrin Production in the First Reported Cases of Hereditary Pyropoikilocytosis. Blood. 104: 576-576. DOI: 10.1182/Blood.V104.11.576.576 |
0.428 |
|
| 2004 |
Lee HM, Zhang H, Forget BG. Identifying Downstream Targets of HOXB4 Using the EML Primitive Hematopoietic Progenitor Cell Line. Blood. 104: 4150-4150. DOI: 10.1182/Blood.V104.11.4150.4150 |
0.341 |
|
| 2003 |
Lambert JF, Liu M, Colvin GA, Dooner M, McAuliffe CI, Becker PS, Forget BG, Weissman SM, Quesenberry PJ. Marrow stem cells shift gene expression and engraftment phenotype with cell cycle transit. The Journal of Experimental Medicine. 197: 1563-72. PMID 12782718 DOI: 10.1084/Jem.20030031 |
0.326 |
|
| 2002 |
Arcasoy MO, Karayal AF, Segal HM, Sinning JG, Forget BG. A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis. Blood. 99: 3066-9. PMID 11929803 DOI: 10.1182/Blood.V99.8.3066 |
0.38 |
|
| 2001 |
Degar BA, Baskaran N, Hulspas R, Quesenberry PJ, Weissman SM, Forget BG. The homeodomain gene Pitx2 is expressed in primitive hematopoietic stem/progenitor cells but not in their differentiated progeny. Experimental Hematology. 29: 894-902. PMID 11438212 DOI: 10.1016/S0301-472X(01)00661-0 |
0.319 |
|
| 2001 |
Arcasoy MO, Maun NA, Perez L, Forget BG, Berliner N. Erythropoietin mediates terminal granulocytic differentiation of committed myeloid cells with ectopic erythropoietin receptor expression. European Journal of Haematology. 67: 77-87. DOI: 10.1034/J.1600-0609.2001.T01-1-00491.X |
0.323 |
|
| 2000 |
Gallagher PG, Ferreira JDS, Costa FF, Saad STO, Forget BG. A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis British Journal of Haematology. 111: 1190-1193. PMID 11167760 DOI: 10.1046/J.1365-2141.2000.02441.X |
0.391 |
|
| 2000 |
Dooner GJ, Barker JE, Gallagher PG, Debatis ME, Brown AH, Forget BG, Becker PS. Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro. Experimental Hematology. 28: 765-74. PMID 10907638 DOI: 10.1016/S0301-472X(00)00185-5 |
0.35 |
|
| 2000 |
Gallagher PG, Romana M, Tse WT, Lux SE, Forget BG. The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter. Blood. 96: 1136-1143. DOI: 10.1182/Blood.V96.3.1136.015K48_1136_1143 |
0.416 |
|
| 1999 |
Feingold EA, Penny LA, Nienhuis AW, Forget BG. An olfactory receptor gene is located in the extended human beta-globin gene cluster and is expressed in erythroid cells. Genomics. 61: 15-23. PMID 10512676 DOI: 10.1006/Geno.1999.5935 |
0.413 |
|
| 1999 |
Arcasoy MO, Harris KW, Forget BG. A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation Experimental Hematology. 27: 63-74. PMID 9923445 DOI: 10.1016/S0301-472X(98)00003-4 |
0.357 |
|
| 1998 |
Gallagher PG, Forget BG. Hematologically Important Mutations: Spectrin and Ankyrin Variants in Hereditary Spherocytosis Blood Cells Molecules and Diseases. 24: 539-543. PMID 9887280 DOI: 10.1006/Bcmd.1998.0217 |
0.321 |
|
| 1998 |
Sabatino DE, Cline AP, Gallagher PG, Garrett LJ, Stamatoyannopoulos G, Forget BG, Bodine DM. Substitution of the human β-spectrin promoter for the human (A)γ- globin promoter prevents silencing of a linked human β-globin gene in transgenic mice Molecular and Cellular Biology. 18: 6634-6640. PMID 9774678 DOI: 10.1128/Mcb.18.11.6634 |
0.398 |
|
| 1998 |
Forget BG. Molecular Basis of Hereditary Persistence of Fetal Hemoglobin Annals of the New York Academy of Sciences. 850: 38-44. PMID 9668525 DOI: 10.1111/J.1749-6632.1998.Tb10460.X |
0.431 |
|
| 1998 |
Gallagher PG, Forget BG. An Alternate Promoter Directs Expression of a Truncated, Muscle-specific Isoform of the Human Ankyrin 1 Gene Journal of Biological Chemistry. 273: 1339-1348. PMID 9430667 DOI: 10.1074/Jbc.273.3.1339 |
0.335 |
|
| 1997 |
Gallagher PG, Forget BG. Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis. Blood Cells Molecules and Diseases. 23: 417-421. PMID 9446757 DOI: 10.1006/Bcmd.1997.0160 |
0.31 |
|
| 1997 |
Gallagher PG, Romana M, Wong C, Forget BG. Genetic basis of the polymorphisms of the αI domain of spectrin American Journal of Hematology. 56: 107-111. PMID 9326352 DOI: 10.1002/(Sici)1096-8652(199710)56:2<107::Aid-Ajh6>3.0.Co;2-2 |
0.338 |
|
| 1997 |
Gallagher PG, Tse WT, Scarpa AL, Lux SE, Forget BG. Structure and Organization of the Human Ankyrin-1 Gene BASIS FOR COMPLEXITY OF PRE-mRNA PROCESSING Journal of Biological Chemistry. 272: 19220-19228. PMID 9235914 DOI: 10.1074/Jbc.272.31.19220 |
0.379 |
|
| 1997 |
Arcasoy MO, Romana M, Fabry ME, Skarpidi E, Nagel RL, Forget BG. 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. 17: 2076-2089. PMID 9121456 DOI: 10.1128/Mcb.17.4.2076 |
0.418 |
|
| 1997 |
Morlé L, Bozon M, Alloisio N, Vallier A, Hayette S, Pascal O, Monier D, Philippe N, Forget BG, Delaunay J. Ankyrin Bugey: a de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis. American Journal of Hematology. 54: 242-8. PMID 9067504 DOI: 10.1002/(Sici)1096-8652(199703)54:3<242::Aid-Ajh11>3.0.Co;2-F |
0.383 |
|
| 1997 |
Tse WT, Gallagher PG, Jenkins PB, Wang Y, Benoit L, Speicher D, Winkelmann JC, Agre P, Forget BG, Marchesi SL. Amino-acid substitution in α-spectrin commonly coinherited with nondominant hereditary spherocytosis American Journal of Hematology. 54: 233-241. PMID 9067503 DOI: 10.1002/(Sici)1096-8652(199703)54:3<233::Aid-Ajh10>3.0.Co;2-E |
0.336 |
|
| 1997 |
Gallagher PG, Petruzzi MJ, Weed SA, Zhang Z, Marchesi SL, Mohandas N, Morrow JS, Forget BG. Mutation of a highly conserved residue of βI spectrin associated with fatal and near-fatal neonatal hemolytic anemia Journal of Clinical Investigation. 99: 267-277. PMID 9005995 DOI: 10.1172/Jci119155 |
0.356 |
|
| 1997 |
Gallagher PG, Forget BG. An alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin-1 gene (ANK-1). • 654 Pediatric Research. 41: 111-111. DOI: 10.1203/00006450-199704001-00674 |
0.33 |
|
| 1997 |
Arcasoy MO, Degar BA, Harris KW, Forget BG. Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene. Blood. 89: 4628-4635. DOI: 10.1182/Blood.V89.12.4628 |
0.424 |
|
| 1996 |
Gallagher PG, Forget BG. Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosis. Blood Cells Molecules and Diseases. 22: 254-258. PMID 9075575 DOI: 10.1006/Bcmd.1996.0105 |
0.321 |
|
| 1996 |
Glele-Kakai C, Garbarz M, Lecomte M, Leborgne S, Galand C, Bournier O, Devaux I, Gautero H, Zohoun I, Gallagher PG, Forget BG, Dhermy D. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin. British Journal of Haematology. 95: 57-66. PMID 8857939 DOI: 10.1046/J.1365-2141.1996.D01-1869.X |
0.358 |
|
| 1996 |
Eber SW, Gonzalez JM, Lux ML, Scarpa AL, Tse WT, Dornwell M, Herbers J, Kugler W, Ozcan R, Pekrun A, Gallagher PG, Schroter W, Forget BG, Lux SE. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nature Genetics. 13: 214-218. PMID 8640229 DOI: 10.1038/Ng0696-214 |
0.357 |
|
| 1996 |
Jenkins PB, Abou-Alfa GK, Dhermy D, Bursaux E, Féo C, Scarpa AL, Lux SE, Garbarz M, Forget BG, Gallagher PG. A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis. Journal of Clinical Investigation. 97: 373-380. PMID 8567957 DOI: 10.1172/Jci118425 |
0.38 |
|
| 1995 |
Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL, Mohandas N, Forget BG. Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte β-spectrin gene Journal of Clinical Investigation. 95: 1174-1182. PMID 7883966 DOI: 10.1172/Jci117766 |
0.365 |
|
| 1995 |
Gallagher PG, Forget BG. Structure, Organization, and Expression of the Human Band 7.2b Gene, a Candidate Gene for Hereditary Hydrocytosis Journal of Biological Chemistry. 270: 26358-26363. PMID 7592848 DOI: 10.1074/Jbc.270.44.26358 |
0.395 |
|
| 1994 |
Gallagher PG, Upender M, Ward DC, Forget BG. The gene for human erythrocyte membrane protein band 7.2 (EPB72) maps to 9q33-q34 centromeric to the Philadelphia chromosome translocation breakpoint region. Genomics. 18: 167-9. PMID 8276411 DOI: 10.1006/Geno.1993.1449 |
0.359 |
|
| 1994 |
Amin KM, Scarpa AL, Winkelmann JC, Curtis PJ, Forget BG. The exon-intron organization of the human erythroid beta-spectrin gene. Genomics. 18: 118-25. PMID 8276395 DOI: 10.1006/Geno.1993.1434 |
0.415 |
|
| 1994 |
Upender M, Gallagher PG, Moon RT, Ward DC, Forget BG. Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridization. Cytogenetics and Cell Genetics. 66: 39-41. PMID 8275706 DOI: 10.1159/000133660 |
0.315 |
|
| 1994 |
Gallagher PG, Lecomte M, Galand C, Wang Y, Tse WT, Forget BG. Location and PCR‐based detection of three polymorphisms of the human erythrocyte β‐spectrin gene (SPTB) British Journal of Haematology. 88: 413-414. PMID 7803294 DOI: 10.1111/J.1365-2141.1994.Tb05043.X |
0.371 |
|
| 1994 |
Starck J, Sarkar R, Romana M, Bhargava A, Scarpa AL, Tanaka M, Chamberlain JW, Weissman SM, Forget BG. Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region Blood. 84: 1656-1665. DOI: 10.1182/Blood.V84.5.1656.Bloodjournal8451656 |
0.359 |
|
| 1993 |
Chang JG, Scarpa A, Eddy RL, Byers MG, Harris AS, Morrow JS, Watkins P, Shows TB, Forget BG. Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin. Genomics. 17: 287-93. PMID 8406479 DOI: 10.1006/Geno.1993.1323 |
0.383 |
|
| 1993 |
Forget BG. YAC transgenes: bigger is probably better. Proceedings of the National Academy of Sciences of the United States of America. 90: 7909-7911. PMID 8367441 DOI: 10.1073/Pnas.90.17.7909 |
0.359 |
|
| 1993 |
Becker PS, Tse WT, Lux SE, Forget BG. Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1. Journal of Clinical Investigation. 92: 612-616. PMID 8102379 DOI: 10.1172/Jci116628 |
0.389 |
|
| 1993 |
Jenkins PB, Gallagher PG, Forget BG. Analysis of a Pst I polymorphism of the human erythrocyte band 3 gene (EPB3) British Journal of Haematology. 85: 816-818. PMID 7918052 DOI: 10.1111/J.1365-2141.1993.Tb03232.X |
0.363 |
|
| 1993 |
Gallagher P, Roberts W, Benoit L, Speicher D, Marchesi S, Forget B. Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion Blood. 82: 2210-2215. DOI: 10.1182/Blood.V82.7.2210.2210 |
0.343 |
|
| 1992 |
Gallagher P, Tse W, Forget B. Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene [letter] Blood. 80: 1856-1857. DOI: 10.1182/Blood.V80.7.1856.1856 |
0.336 |
|
| 1991 |
Garbarz M, Tse WT, Gallagher PG, Picat C, Lecomte MC, Galibert F, Dhermy D, Forget BG. 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. Journal of Clinical Investigation. 88: 76-81. PMID 2056132 DOI: 10.1172/Jci115307 |
0.418 |
|
| 1991 |
Lumelsky NL, Forget BG. Negative regulation of globin gene expression during megakaryocytic differentiation of a human erythroleukemic cell line. Molecular and Cellular Biology. 11: 3528-3536. PMID 2046667 DOI: 10.1128/Mcb.11.7.3528 |
0.408 |
|
| 1991 |
Tse WT, Menninger JC, Yang-Feng TL, Francke U, Sahr KE, Lux SE, Ward DC, Forget BG. Isolation and chromosomal localization of a novel nonerythroid ankyrin gene. Genomics. 10: 858-66. PMID 1833308 DOI: 10.1016/0888-7543(91)90173-C |
0.386 |
|
| 1991 |
Kotula L, Laury-Kleintop LD, Showe L, Sahr K, Linnenbach AJ, Forget B, Curtis PJ. The exon-intron organization of the human erythrocyte α-spectrin gene Genomics. 9: 131-140. PMID 1672285 DOI: 10.1016/0888-7543(91)90230-C |
0.426 |
|
| 1991 |
Penny LA, Forget BG. Genomic organization of the human erythropoietin receptor gene Genomics. 11: 974-980. PMID 1664413 DOI: 10.1016/0888-7543(91)90022-7 |
0.38 |
|
| 1991 |
Tse WT, Gallagher PG, Pothier B, Costa FF, Scarpa A, Delaunay J, Forget BG. An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216) Blood. 78: 517-523. DOI: 10.1182/Blood.V80.8.2115.Bloodjournal8082115 |
0.391 |
|
| 1991 |
Floyd PB, Gallagher PG, Valentino LA, Davis M, Marchesi SL, Forget BG. 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. 78: 1364-1372. DOI: 10.1182/Blood.V78.5.1364.Bloodjournal7851364 |
0.368 |
|
| 1991 |
Bollekens JA, Forget BG. δβ Thalassemia and Hereditary Persistence of Fetal Hemoglobin Hematology-Oncology Clinics of North America. 5: 399-422. DOI: 10.1016/S0889-8588(18)30422-2 |
0.373 |
|
| 1990 |
Tanaka M, Nolan JA, Bhargava AK, Rood K, Collins FS, Weissman SM, Forget BG, Chamberlain JW. 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. 612: 167-78. PMID 2291546 DOI: 10.1111/J.1749-6632.1990.Tb24303.X |
0.432 |
|
| 1990 |
Fukushima Y, Byers MG, Watkins PC, Winkelmann JC, Forget BG, Shows TB. Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridization. Cytogenetics and Cell Genetics. 53: 232-3. PMID 2209094 DOI: 10.1159/000132939 |
0.351 |
|
| 1990 |
Lux SE, Tse WT, Menninger JC, John KM, Harris P, Shalev O, Chilcote RR, Marchesi SL, Watkins PC, Bennett V, McIntosh S, Collins FS, Francke U, Ward DC, Forget BG. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 Nature. 345: 736-739. PMID 2141669 DOI: 10.1038/345736A0 |
0.37 |
|
| 1990 |
Tse WT, Lecomte MC, Costa FF, Garbarz M, Feo C, Boivin P, Dhermy D, Forget BG. Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association. Journal of Clinical Investigation. 86: 909-916. PMID 1975598 DOI: 10.1172/Jci114792 |
0.383 |
|
| 1989 |
Sahr KE, Tobe T, Scarpa A, Laughinghouse K, Marchesi SL, Agre P, Linnenbach AJ, Marchesi VT, Forget BG. Sequence and exon-intron organization of the DNA encoding the αI domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis Journal of Clinical Investigation. 84: 1243-1252. PMID 2794061 DOI: 10.1172/Jci114291 |
0.404 |
|
| 1989 |
Feingold E, Forget B. 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. 74: 2178-2186. DOI: 10.1182/Blood.V74.6.2178.Bloodjournal7462178 |
0.448 |
|
| 1988 |
Winkelmann J, Leto T, Watkins P, Eddy R, Shows T, Linnenbach A, Sahr K, Kathuria N, Marchesi V, Forget B. Molecular cloning of the cDNA for human erythrocyte beta-spectrin Blood. 72: 328-334. DOI: 10.1182/Blood.V72.1.328.328 |
0.385 |
|
| 1987 |
Atweh GF, Forget BG. Clinical and molecular correlations in the sickle/β+-thalassemia syndrome American Journal of Hematology. 24: 31-36. PMID 3799593 DOI: 10.1002/Ajh.2830240105 |
0.375 |
|
| 1987 |
Stoeckert CJ, Metherall JE, Yamakawa M, Eisenstadt JM, Weissman SM, Forget BG. Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobin Molecular and Cellular Biology. 7: 2999-3003. PMID 2444873 DOI: 10.1128/Mcb.7.8.2999 |
0.407 |
|
| 1986 |
Linnenbach AJ, Speicher DW, Marchesi VT, Forget BG. Cloning of a portion of the chromosomal gene for human erythrocyte alpha-spectrin by using a synthetic gene fragment. Proceedings of the National Academy of Sciences of the United States of America. 83: 2397-2401. PMID 3458204 DOI: 10.1073/Pnas.83.8.2397 |
0.365 |
|
| 1985 |
Baserga SJ, Linnenbach AJ, Malcolm S, Ghosh P, Malcolm AD, Takeshita K, Forget BG, Benz EJ. Polyadenylation of a human mitochondrial ribosomal RNA transcript detected by molecular cloning. Gene. 35: 305-12. PMID 4043734 DOI: 10.1016/0378-1119(85)90009-5 |
0.333 |
|
| 1985 |
Atweh GF, Anagnou NP, Shearin J, Forget BG, Kaufman RE. Beta-thalassemia resulting from a single nucleotide substitution in an acceptor splice site. Nucleic Acids Research. 13: 777-90. PMID 2987809 DOI: 10.1093/Nar/13.3.777 |
0.418 |
|
| 1985 |
Collins FS, Metherall JE, Yamakawa M, Pan J, Weissman SM, Forget BG. A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin Nature. 313: 325-326. PMID 2578620 DOI: 10.1038/313325A0 |
0.454 |
|
| 1985 |
Feingold EA, Collins FS, Metherall JE, Stoeckert CJ, Weissman SM, Forget BG. 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. 445: 159-69. PMID 2409868 DOI: 10.1111/J.1749-6632.1985.Tb17185.X |
0.367 |
|
| 1984 |
Benz EJ, Pritchard J, Hillman D, Glass J, Forget BG. Beta globin messenger RNA content of bone marrow erythroblasts in heterozygous beta-thalassemia. American Journal of Hematology. 16: 33-45. PMID 6695907 DOI: 10.1002/Ajh.2830160105 |
0.325 |
|
| 1983 |
Tuan D, Feingold E, Newman M, Weissman SM, Forget BG. Different 3' end points of deletions causing δβ-thalassemia and hereditary persistence of fetal hemoglobin: Implications for the control of γ-globin gene expression in man Proceedings of the National Academy of Sciences of the United States of America. 80: 6937-6941. PMID 6196781 DOI: 10.1073/Pnas.80.22.6937 |
0.444 |
|
| 1982 |
Fukumaki Y, Ghosh PK, Benz EJ, Reddy VB, Lebowitz P, Forget BG, Weissman SM. Abnormally spliced messenger RNA in erythroid cells from patients with β+ thalassemia and monkey cells expressing a cloned β+-thalassemic gene Cell. 28: 585-593. PMID 6280877 DOI: 10.1016/0092-8674(82)90213-6 |
0.38 |
|
| 1982 |
Forget BG. 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. Recent Progress in Hormone Research. 38: 257-277. PMID 6181542 DOI: 10.1016/B978-0-12-571138-8.50012-3 |
0.347 |
|
| 1982 |
Jagadeeswaran P, Tuan D, Forget BG, Weissman SM. A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin Nature. 296: 469-470. PMID 6174873 DOI: 10.1038/296469A0 |
0.442 |
|
| 1980 |
Tuan D, Forget BG. Physicochemical measurement of the base composition of mRNA-related sequences of the human α and β globin genes Molecular Biology Reports. 6: 179-183. PMID 7442665 DOI: 10.1007/Bf00775413 |
0.368 |
|
| 1980 |
Spritz RA, DeRiel JK, Forget BG, Weissman SM. Complete nucleotide sequence of the human δ-globin gene Cell. 21: 639-646. PMID 7438204 DOI: 10.1016/0092-8674(80)90427-4 |
0.421 |
|
| 1980 |
Cavallesco C, Forget BG, deRiel JK, Wilson LB, Wilson JT, Weissman SM. Nucleotide sequence of human G gamma globin messenger RNA. Gene. 12: 215-21. PMID 7250702 DOI: 10.1016/0378-1119(80)90103-1 |
0.353 |
|
| 1980 |
Efstratiadis A, Posakony JW, Maniatis T, Lawn RM, O'Connell C, Spritz RA, DeRiel JK, Forget BG, Weissman SM, Slightom JL, Blechl AE, Smithies O, Baralle FE, Shoulders CC, Proudfoot NJ. The structure and evolution of the human beta-globin gene family. Cell. 21: 653-68. PMID 6985477 DOI: 10.1016/0092-8674(80)90429-8 |
0.425 |
|
| 1980 |
Benz EJ, Murnane MJ, Tonkonow BL, Berman BW, Mazur EM, Cavallesco C, Jenko T, Snyder EL, Forget BG, Hoffman R. Embryonic-fetal erythroid characteristics of a human leukemic cell line. Proceedings of the National Academy of Sciences of the United States of America. 77: 3509-13. PMID 6932034 DOI: 10.1073/Pnas.77.6.3509 |
0.302 |
|
| 1980 |
Tuan D, Biro PA, Riel JKD, Forget BG. ANALYSIS OF β‐GLOBIN GENES IN β^ THALASSEMIA Annals of the New York Academy of Sciences. 344: 12-30. PMID 6930862 DOI: 10.1111/J.1749-6632.1980.Tb33645.X |
0.344 |
|
| 1980 |
Tuan D, Murnane MJ, deRiel JL, Forget BG. Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin. Nature. 285: 335-7. PMID 6154897 DOI: 10.1038/285335A0 |
0.428 |
|
| 1980 |
Duncan C, Biro PA, Choudary PV, Elder JT, Wang RR, Forget BG, de Riel JK, Weissman SM. RNA polymerase III transcriptional units are interspersed among human non-alpha-globin genes. Proceedings of the National Academy of Sciences of the United States of America. 76: 5095-9. PMID 388428 DOI: 10.1073/Pnas.76.10.5095 |
0.418 |
|
| 1979 |
Tuan D, Biro PA, deRiel JK, Lazarus H, Forget BG. Restriction endonuclease mapping of the human γ globin gene loci Nucleic Acids Research. 6: 2519-2544. PMID 461196 DOI: 10.1093/Nar/6.7.2519 |
0.413 |
|
| 1978 |
Forget BG, Cavallesco C, Benz EJ, McClure PD, Hillman DG, Krieger H, Clarke B, Housman D. Studies of globin chain synthesis and globin mRNA content in a patient homozygous for hemoglobin Lepore. Hemoglobin. 2: 117-28. PMID 640850 DOI: 10.3109/03630267809074779 |
0.35 |
|
| 1978 |
Forget BG. Molecular lesions in thalassemia Trends in Biochemical Sciences. 3: 86-90. DOI: 10.1016/S0968-0004(78)80005-X |
0.393 |
|
| 1977 |
Wilson JT, deRiel JK, Forget BG, Marotta CA, Weissman SM. Nucleotide sequence of 3' untranslated portion of human alpha globin mRNA. Nucleic Acids Research. 4: 2353-68. PMID 909779 DOI: 10.1093/Nar/4.7.2353 |
0.369 |
|
| 1977 |
Wilson JT, Forget BG, Wilson LB, Weissman SM. Human globin messenger RNA: importance of cloning for structural analysis. Science (New York, N.Y.). 196: 200-2. PMID 847468 DOI: 10.1126/Science.847468 |
0.334 |
|
| 1977 |
Cheung SW, Tishler PV, Atkins L, Sengupta SK, Modest EJ, Forget BG. Gene mapping by fluorescent in situ hybridization. Cell Biology International Reports. 1: 255-62. PMID 564744 DOI: 10.1016/0309-1651(77)90050-9 |
0.342 |
|
| 1977 |
Forget BG. Nucleotide sequence of human beta globin messenger RNA. Hemoglobin. 1: 879-881. PMID 342458 DOI: 10.3109/03630267709003915 |
0.34 |
|
| 1977 |
Kafatos FC, Efstratiadis A, Forget BG, Weissman SM. Molecular evolution of human and rabbit beta-globin mRNAs. Proceedings of the National Academy of Sciences of the United States of America. 74: 5618-22. PMID 271989 DOI: 10.1073/Pnas.74.12.5618 |
0.38 |
|
| 1976 |
Forget BG, Marotta CA, Weissman SM, Cohen-Solal M. Nucleotide sequences of the 3'-terminal untranslated region of messenger RNA for human beta globin chain. Proceedings of the National Academy of Sciences of the United States of America. 72: 3614-8. PMID 1059150 DOI: 10.1073/Pnas.72.9.3614 |
0.373 |
|
| 1975 |
Forget BG, Housman D, Benz EJ, McCaffrey RP. Synthesis of DNA complementary to separated human alpha and beta globin messenger RNAs. Proceedings of the National Academy of Sciences of the United States of America. 72: 984-8. PMID 48254 DOI: 10.1073/Pnas.72.3.984 |
0.307 |
|
| 1974 |
Marotta CA, Forget BG, Weissman SM, Verma IM, McCaffrey RP, Baltimore D. Nucleotide sequences of human globin messenger RNA. Proceedings of the National Academy of Sciences of the United States of America. 71: 2300-4. PMID 4135409 DOI: 10.1073/Pnas.71.6.2300 |
0.352 |
|
| 1972 |
Benz EJ, Forget BG. Defect in messenger RNA for human hemoglobin synthesis in beta thalassemia. The Journal of Clinical Investigation. 50: 2755-60. PMID 5129324 DOI: 10.1172/Jci106778 |
0.343 |
|
| 1972 |
Kan YW, Forget BG, Nathan DG. Gamma-Beta Thalassemia: A Cause of Hemolytic Disease of the Newborn The New England Journal of Medicine. 286: 129-134. PMID 5061687 DOI: 10.1056/Nejm197201202860304 |
0.313 |
|
| 1968 |
Forget BG, Weissman SM. Nucleotide sequence of KB cell 5S RNA. Science (New York, N.Y.). 158: 1695-9. PMID 6059650 DOI: 10.1126/Science.158.3809.1695 |
0.301 |
|
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