| Year |
Citation |
Score |
| 2020 |
Stoddart A, Wang J, Fernald AA, Davis EM, Johnson CR, Hu C, Cheng JX, McNerney ME, Le Beau MM. Cytotoxic Therapy-Induced Effects on Both Hematopoietic and Marrow Stromal Cells Promotes Therapy-Related Myeloid Neoplasms. Blood Cancer Discovery. 1. PMID 32924016 DOI: 10.1158/2643-3230.bcd-19-0028 |
0.342 |
|
| 2016 |
Meyer SE, Qin T, Muench DE, Masuda K, Venkatasubramanian M, Orr E, Suarez L, Gore SD, Delwel R, Paietta E, Tallman MS, Fernandez H, Melnick A, Le Beau MM, Kogan S, et al. Dnmt3a haploinsufficiency transforms Flt3-ITD myeloproliferative disease into a rapid, spontaneous, and fully-penetrant acute myeloid leukemia. Cancer Discovery. PMID 27016502 DOI: 10.1158/2159-8290.Cd-16-0008 |
0.39 |
|
| 2016 |
Stoddart A, Qian Z, Fernald AA, Bergerson RJ, Wang J, Karrison T, Anastasi J, Bartom ET, Sarver AL, McNerney ME, Largaespada DA, Le Beau MM. Retroviral insertional mutagenesis identifies the del(5q) genes, CXXC5, TIFAB and ETF1, as well as the Wnt pathway, as potential targets in del(5q) myeloid neoplasms. Haematologica. PMID 26944478 DOI: 10.3324/Haematol.2015.139527 |
0.338 |
|
| 2015 |
Sundaravel S, Duggan R, Bhagat T, Ebenezer DL, Liu H, Yu Y, Bartenstein M, Unnikrishnan M, Karmakar S, Liu TC, Torregroza I, Quenon T, Anastasi J, McGraw KL, Pellagatti A, ... ... Le Beau MM, et al. Reduced DOCK4 expression leads to erythroid dysplasia in myelodysplastic syndromes. Proceedings of the National Academy of Sciences of the United States of America. 112: E6359-E6368. PMID 26578796 DOI: 10.1073/Pnas.1516394112 |
0.33 |
|
| 2015 |
Amabile G, Di Ruscio A, Müller F, Welner RS, Yang H, Ebralidze AK, Zhang H, Levantini E, Qi L, Martinelli G, Brummelkamp T, Le Beau MM, Figueroa ME, Bock C, Tenen DG. Dissecting the role of aberrant DNA methylation in human leukaemia. Nature Communications. 6: 7091. PMID 25997600 DOI: 10.1038/Ncomms8091 |
0.36 |
|
| 2014 |
Flach J, Bakker ST, Mohrin M, Conroy PC, Pietras EM, Reynaud D, Alvarez S, Diolaiti ME, Ugarte F, Forsberg EC, Le Beau MM, Stohr BA, Méndez J, Morrison CG, Passegué E. Replication stress is a potent driver of functional decline in ageing haematopoietic stem cells. Nature. 512: 198-202. PMID 25079315 DOI: 10.1038/Nature13619 |
0.344 |
|
| 2014 |
Young DJ, Stoddart A, Nakitandwe J, Chen SC, Qian Z, Downing JR, Le Beau MM. Knockdown of Hnrnpa0, a del(5q) gene, alters myeloid cell fate in murine cells through regulation of AU-rich transcripts. Haematologica. 99: 1032-40. PMID 24532040 DOI: 10.3324/haematol.2013.098657 |
0.315 |
|
| 2014 |
Stoddart A, Fernald AA, Wang J, Davis EM, Karrison T, Anastasi J, Le Beau MM. Haploinsufficiency of del(5q) genes, Egr1 and Apc, cooperate with Tp53 loss to induce acute myeloid leukemia in mice. Blood. 123: 1069-78. PMID 24381225 DOI: 10.1182/blood-2013-07-517953 |
0.391 |
|
| 2014 |
Dose M, Emmanuel AO, Chaumeil J, Zhang J, Sun T, Germar K, Aghajani K, Davis EM, Keerthivasan S, Bredemeyer AL, Sleckman BP, Rosen ST, Skok JA, Le Beau MM, Georgopoulos K, et al. β-Catenin induces T-cell transformation by promoting genomic instability. Proceedings of the National Academy of Sciences of the United States of America. 111: 391-6. PMID 24371308 DOI: 10.1073/Pnas.1315752111 |
0.348 |
|
| 2014 |
Stoddart A, Wang J, Fernald AA, Karrison T, Anastasi J, Le Beau MM. Cell intrinsic and extrinsic factors synergize in mice with haploinsufficiency for Tp53, and two human del(5q) genes, Egr1 and Apc. Blood. 123: 228-38. PMID 24264229 DOI: 10.1182/blood-2013-05-506568 |
0.344 |
|
| 2013 |
Vasanthakumar A, Lepore JB, Zegarek MH, Kocherginsky M, Singh M, Davis EM, Link PA, Anastasi J, Le Beau MM, Karpf AR, Godley LA. Dnmt3b is a haploinsufficient tumor suppressor gene in Myc-induced lymphomagenesis. Blood. 121: 2059-63. PMID 23315164 DOI: 10.1182/Blood-2012-04-421065 |
0.309 |
|
| 2013 |
McNerney ME, Brown CD, Wang X, Bartom ET, Karmakar S, Bandlamudi C, Yu S, Ko J, Sandall BP, Stricker T, Anastasi J, Grossman RL, Cunningham JM, Le Beau MM, White KP. CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia. Blood. 121: 975-83. PMID 23212519 DOI: 10.1182/Blood-2012-04-426965 |
0.434 |
|
| 2011 |
Godley LA, Cunningham J, Dolan ME, Huang RS, Gurbuxani S, McNerney ME, Larson RA, Leong H, Lussier Y, Onel K, Odenike O, Stock W, White KP, Le Beau MM. An integrated genomic approach to the assessment and treatment of acute myeloid leukemia. Seminars in Oncology. 38: 215-24. PMID 21421111 DOI: 10.1053/J.Seminoncol.2011.01.003 |
0.333 |
|
| 2011 |
Lubelsky Y, Sasaki T, Kuipers MA, Lucas I, Le Beau MM, Carignon S, Debatisse M, Prinz JA, Dennis JH, Gilbert DM. Pre-replication complex proteins assemble at regions of low nucleosome occupancy within the Chinese hamster dihydrofolate reductase initiation zone. Nucleic Acids Research. 39: 3141-55. PMID 21148149 DOI: 10.1093/Nar/Gkq1276 |
0.342 |
|
| 2010 |
Jones L, Wei G, Sevcikova S, Phan V, Jain S, Shieh A, Wong JC, Li M, Dubansky J, Maunakea ML, Ochoa R, Zhu G, Tennant TR, Shannon KM, Lowe SW, ... Le Beau MM, et al. Gain of MYC underlies recurrent trisomy of the MYC chromosome in acute promyelocytic leukemia. The Journal of Experimental Medicine. 207: 2581-94. PMID 21059853 DOI: 10.1084/Jem.20091071 |
0.388 |
|
| 2010 |
Mohrin M, Bourke E, Alexander D, Warr MR, Barry-Holson K, Le Beau MM, Morrison CG, Passegué E. Hematopoietic stem cell quiescence promotes error-prone DNA repair and mutagenesis. Cell Stem Cell. 7: 174-85. PMID 20619762 DOI: 10.1016/J.Stem.2010.06.014 |
0.304 |
|
| 2010 |
Shah MY, Vasanthakumar A, Barnes NY, Figueroa ME, Kamp A, Hendrick C, Ostler KR, Davis EM, Lin S, Anastasi J, Le Beau MM, Moskowitz IP, Melnick A, Pytel P, Godley LA. DNMT3B7, a truncated DNMT3B isoform expressed in human tumors, disrupts embryonic development and accelerates lymphomagenesis. Cancer Research. 70: 5840-50. PMID 20587527 DOI: 10.1158/0008-5472.CAN-10-0847 |
0.305 |
|
| 2010 |
Wong JC, Zhang Y, Lieuw KH, Tran MT, Forgo E, Weinfurtner K, Alzamora P, Kogan SC, Akagi K, Wolff L, Le Beau MM, Killeen N, Shannon K. Use of chromosome engineering to model a segmental deletion of chromosome band 7q22 found in myeloid malignancies. Blood. 115: 4524-32. PMID 20233966 DOI: 10.1182/Blood-2009-07-232504 |
0.367 |
|
| 2010 |
Wang J, Fernald AA, Anastasi J, Le Beau MM, Qian Z. Haploinsufficiency of Apc leads to ineffective hematopoiesis. Blood. 115: 3481-8. PMID 20065296 DOI: 10.1182/blood-2009-11-251835 |
0.365 |
|
| 2010 |
Qian Z, Joslin JM, Tennant TR, Reshmi SC, Young DJ, Stoddart A, Larson RA, Le Beau MM. Cytogenetic and genetic pathways in therapy-related acute myeloid leukemia. Chemico-Biological Interactions. 184: 50-7. PMID 19958752 DOI: 10.1016/J.Cbi.2009.11.025 |
0.744 |
|
| 2010 |
Palakodeti A, Lucas I, Jiang Y, Young DJ, Fernald AA, Karrison T, Le Beau MM. Impaired replication dynamics at the FRA3B common fragile site. Human Molecular Genetics. 19: 99-110. PMID 19815620 DOI: 10.1093/Hmg/Ddp470 |
0.699 |
|
| 2009 |
Jiang Y, Lucas I, Young DJ, Davis EM, Karrison T, Rest JS, Le Beau MM. Common fragile sites are characterized by histone hypoacetylation. Human Molecular Genetics. 18: 4501-12. PMID 19717471 DOI: 10.1093/Hmg/Ddp410 |
0.6 |
|
| 2008 |
Wong JC, Le Beau MM, Shannon K. Tumor suppressor gene inactivation in myeloid malignancies. Best Practice & Research. Clinical Haematology. 21: 601-14. PMID 19041599 DOI: 10.1016/J.Beha.2008.09.001 |
0.378 |
|
| 2008 |
Mullighan CG, Miller CB, Radtke I, Phillips LA, Dalton J, Ma J, White D, Hughes TP, Le Beau MM, Pui CH, Relling MV, Shurtleff SA, Downing JR. BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros. Nature. 453: 110-4. PMID 18408710 DOI: 10.1038/nature06866 |
0.347 |
|
| 2008 |
Kirsammer G, Jilani S, Liu H, Davis E, Gurbuxani S, Le Beau MM, Crispino JD. Highly penetrant myeloproliferative disease in the Ts65Dn mouse model of Down syndrome. Blood. 111: 767-75. PMID 17901249 DOI: 10.1182/Blood-2007-04-085670 |
0.324 |
|
| 2007 |
Lucas I, Palakodeti A, Jiang Y, Young DJ, Jiang N, Fernald AA, Le Beau MM. High-throughput mapping of origins of replication in human cells. Embo Reports. 8: 770-7. PMID 17668008 DOI: 10.1038/Sj.Embor.7401026 |
0.71 |
|
| 2007 |
Joslin JM, Fernald AA, Tennant TR, Davis EM, Kogan SC, Anastasi J, Crispino JD, Le Beau MM. Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders. Blood. 110: 719-26. PMID 17420284 DOI: 10.1182/Blood-2007-01-068809 |
0.756 |
|
| 2007 |
Boyapati A, Yan M, Peterson LF, Biggs JR, Le Beau MM, Zhang DE. A leukemia fusion protein attenuates the spindle checkpoint and promotes aneuploidy. Blood. 109: 3963-71. PMID 17197431 DOI: 10.1182/blood-2006-09-045583 |
0.365 |
|
| 2007 |
Lones MA, Heerema NA, Le Beau MM, Sposto R, Perkins SL, Kadin ME, Kjeldsberg CR, Meadows A, Siegel S, Buckley J, Abromowitch M, Kersey J, Bergeron S, Cairo MS, Sanger WG. Chromosome abnormalities in advanced stage lymphoblastic lymphoma of children and adolescents: a report from CCG-E08 Cancer Genetics and Cytogenetics. 172: 1-11. PMID 17175373 DOI: 10.1016/J.Cancergencyto.2006.07.011 |
0.349 |
|
| 2006 |
Lones MA, Heerema NA, Le Beau MM, Perkins SL, Kadin ME, Kjeldsberg CR, Sposto R, Meadows A, Siegel S, Buckley J, Finlay J, Abromowitch M, Cairo MS, Sanger WG. Complex secondary chromosome abnormalities in advanced stage anaplastic large cell lymphoma of children and adolescents: a report from CCG-E08. Cancer Genetics and Cytogenetics. 171: 89-96. PMID 17116485 DOI: 10.1016/J.Cancergencyto.2006.04.019 |
0.362 |
|
| 2006 |
Stephens K, Weaver M, Leppig KA, Maruyama K, Emanuel PD, Le Beau MM, Shannon KM. Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies. Blood. 108: 1684-9. PMID 16690971 DOI: 10.1182/Blood-2005-11-011486 |
0.4 |
|
| 2006 |
Djokic M, Le Beau MM, Swinnen LJ, Smith SM, Rubin CM, Anastasi J, Carlson KM. Post-transplant lymphoproliferative disorder subtypes correlate with different recurring chromosomal abnormalities. Genes, Chromosomes & Cancer. 45: 313-8. PMID 16283619 DOI: 10.1002/gcc.20287 |
0.314 |
|
| 2005 |
Larson RA, Le Beau MM. Therapy-related myeloid leukaemia: a model for leukemogenesis in humans. Chemico-Biological Interactions. 153: 187-95. PMID 15935816 DOI: 10.1016/j.cbi.2005.03.023 |
0.344 |
|
| 2005 |
Curtiss NP, Bonifas JM, Lauchle JO, Balkman JD, Kratz CP, Emerling BM, Green ED, Le Beau MM, Shannon KM. Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22. Genomics. 85: 600-7. PMID 15820312 DOI: 10.1016/J.Ygeno.2005.01.013 |
0.399 |
|
| 2005 |
Fischbach NA, Rozenfeld S, Shen W, Fong S, Chrobak D, Ginzinger D, Kogan SC, Radhakrishnan A, Le Beau MM, Largman C, Lawrence HJ. HOXB6 overexpression in murine bone marrow immortalizes a myelomonocytic precursor in vitro and causes hematopoietic stem cell expansion and acute myeloid leukemia in vivo. Blood. 105: 1456-66. PMID 15522959 DOI: 10.1182/blood-2004-04-1583 |
0.369 |
|
| 2004 |
Lones MA, Sanger WG, Le Beau MM, Heerema NA, Sposto R, Perkins SL, Buckley J, Kadin ME, Kjeldsberg CR, Meadows A, Siegel S, Finlay J, Bergeron S, Cairo MS. Chromosome abnormalities may correlate with prognosis in Burkitt/Burkitt-like lymphomas of children and adolescents: a report from Children's Cancer Group Study CCG-E08. Journal of Pediatric Hematology/Oncology. 26: 169-78. PMID 15125609 DOI: 10.1097/00043426-200403000-00006 |
0.348 |
|
| 2004 |
Palakodeti A, Han Y, Jiang Y, Le Beau MM. The role of late/slow replication of the FRA16D in common fragile site induction. Genes, Chromosomes & Cancer. 39: 71-6. PMID 14603443 DOI: 10.1002/Gcc.10290 |
0.695 |
|
| 2003 |
Le Beau MM, Davis EM, Patel B, Phan VT, Sohal J, Kogan SC. Recurring chromosomal abnormalities in leukemia in PML-RARA transgenic mice identify cooperating events and genetic pathways to acute promyelocytic leukemia. Blood. 102: 1072-4. PMID 12689927 DOI: 10.1182/Blood-2003-01-0155 |
0.303 |
|
| 2003 |
Lensch MW, Tischkowitz M, Christianson TA, Reifsteck CA, Speckhart SA, Jakobs PM, O'Dwyer ME, Olson SB, Le Beau MM, Hodgson SV, Mathew CG, Larson RA, Bagby GC. Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia. Blood. 102: 7-16. PMID 12637330 DOI: 10.1182/blood-2002-09-2781 |
0.352 |
|
| 2002 |
Emerling BM, Bonifas J, Kratz CP, Donovan S, Taylor BR, Green ED, Le Beau MM, Shannon KM. MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia. Oncogene. 21: 4849-54. PMID 12101424 DOI: 10.1038/Sj.Onc.1205615 |
0.376 |
|
| 2002 |
Le Beau MM, Bitts S, Davis EM, Kogan SC. Recurring chromosomal abnormalities in leukemia in PML-RARA transgenic mice parallel human acute promyelocytic leukemia. Blood. 99: 2985-91. PMID 11929790 DOI: 10.1182/blood.V99.8.2985 |
0.366 |
|
| 2002 |
Zhang Y, Strissel P, Strick R, Chen J, Nucifora G, Le Beau MM, Larson RA, Rowley JD. Genomic DNA breakpoints in AML1/RUNX1 and ETO cluster with topoisomerase II DNA cleavage and DNase I hypersensitive sites in t(8;21) leukemia. Proceedings of the National Academy of Sciences of the United States of America. 99: 3070-5. PMID 11867721 DOI: 10.1073/pnas.042702899 |
0.45 |
|
| 2002 |
Kratz CP, Emerling BM, Bonifas J, Wang W, Green ED, Le Beau MM, Shannon KM. Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor. Blood. 99: 372-4. PMID 11756194 DOI: 10.1182/Blood.V99.1.372 |
0.448 |
|
| 2001 |
Kratz CP, Emerling BM, Donovan S, Laig-Webster M, Taylor BR, Thompson P, Jensen S, Banerjee A, Bonifas J, Makalowski W, Green ED, Le Beau MM, Shannon KM. Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies. Genomics. 77: 171-80. PMID 11597142 DOI: 10.1006/Geno.2001.6636 |
0.457 |
|
| 2001 |
Lai F, Godley LA, Joslin J, Fernald AA, Liu J, Espinosa R, Zhao N, Pamintuan L, Till BG, Larson RA, Qian Z, Le Beau MM. Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q). Genomics. 71: 235-45. PMID 11161817 DOI: 10.1006/Geno.2000.6414 |
0.752 |
|
| 2001 |
Stoffel A, Le Beau MM. The API2/MALT1 fusion product may lead to germinal center B cell lymphomas by suppression of apoptosis. Human Heredity. 51: 1-7. PMID 11096264 DOI: 10.1159/000022952 |
0.366 |
|
| 2001 |
Gozzetti A, Le Beau MM. Fluorescence in situ hybridization: uses and limitations. Seminars in Hematology. 37: 320-33. PMID 11071355 DOI: 10.1016/S0037-1963(00)90013-1 |
0.321 |
|
| 2001 |
Wang PW, Eisenbart JD, Espinosa R, Davis EM, Larson RA, Le Beau MM. Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map. Genomics. 67: 28-39. PMID 10945467 DOI: 10.1006/geno.2000.6215 |
0.463 |
|
| 2000 |
Lai F, Godley LA, Fernald AA, Orelli BJ, Pamintuan L, Zhao N, Le Beau MM. cDNA cloning and genomic structure of three genes localized to human chromosome band 5q31 encoding potential nuclear proteins. Genomics. 70: 123-30. PMID 11087669 DOI: 10.1006/Geno.2000.6345 |
0.382 |
|
| 2000 |
Lai F, Orelli BJ, Till BG, Godley LA, Fernald AA, Pamintuan L, Le Beau MM. Molecular characterization of KLHL3, a human homologue of the Drosophila kelch gene. Genomics. 66: 65-75. PMID 10843806 DOI: 10.1006/Geno.2000.6181 |
0.411 |
|
| 2000 |
Shuster MI, Han L, Le Beau MM, Davis E, Sawicki M, Lese CM, Park NH, Colicelli J, Gollin SM. A consistent pattern of RIN1 rearrangements in oral squamous cell carcinoma cell lines supports a breakage-fusion-bridge cycle model for 11q13 amplification. Genes, Chromosomes & Cancer. 28: 153-63. PMID 10825000 DOI: 10.1002/(Sici)1098-2264(200006)28:2<153::Aid-Gcc4>3.0.Co;2-9 |
0.441 |
|
| 2000 |
Lai F, Fernald AA, Zhao N, Le Beau MM. cDNA cloning, expression pattern, genomic structure and chromosomal location of RAB6KIFL, a human kinesin-like gene. Gene. 248: 117-25. PMID 10806357 DOI: 10.1016/S0378-1119(00)00135-9 |
0.387 |
|
| 1999 |
Godley LA, Lai F, Liu J, Zhao N, Le Beau MM. TTID: A novel gene at 5q31 encoding a protein with titin-like features. Genomics. 60: 226-33. PMID 10486214 DOI: 10.1006/Geno.1999.5912 |
0.342 |
|
| 1999 |
Wang PW, Eisenbart JD, Cordes SP, Barsh GS, Stoffel M, Le Beau MM. Human KRML (MAFB): cDNA cloning, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias. Genomics. 59: 275-81. PMID 10444328 DOI: 10.1006/Geno.1999.5884 |
0.444 |
|
| 1999 |
Stoffel A, Rao PH, Louie DC, Krauter K, Liebowitz DN, Koeppen H, Le Beau MM, Chaganti RSK. Chromosome 18 breakpoint in t(11;18)(q21;q21) translocation associated with MALT lymphoma is proximal to BCL2 and distal to DCC Genes Chromosomes and Cancer. 24: 156-159. PMID 9885983 DOI: 10.1002/(Sici)1098-2264(199902)24:2<156::Aid-Gcc9>3.0.Co;2-X |
0.415 |
|
| 1998 |
Zhao N, Lai F, Fernald AA, Eisenbart JD, Espinosa R, Wang PW, Le Beau MM. Human CDC23: cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias. Genomics. 53: 184-90. PMID 9790767 DOI: 10.1006/geno.1998.5473 |
0.428 |
|
| 1998 |
Chen M, She H, Davis EM, Spicer CM, Kim L, Ren R, Le Beau MM, Li W. Identification of Nck family genes, chromosomal localization, expression, and signaling specificity. The Journal of Biological Chemistry. 273: 25171-8. PMID 9737977 DOI: 10.1074/Jbc.273.39.25171 |
0.31 |
|
| 1998 |
Dissing M, Le Beau MM, Pedersen-Bjergaard J. Inversion of chromosome 16 and uncommon rearrangements of the CBFB and MYH11 genes in therapy-related acute myeloid leukemia: rare events related to DNA-topoisomerase II inhibitors? Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 16: 1890-6. PMID 9586906 DOI: 10.1200/jco.1998.16.5.1890 |
0.364 |
|
| 1998 |
Le Beau MM, Drabkin H, Glover TW, Gemmill R, Rassool FV, McKeithan TW, Smith DI. An FHIT tumor suppressor gene? Genes, Chromosomes & Cancer. 21: 281-9. PMID 9559339 DOI: 10.1002/(SICI)1098-2264(199804)21:4<281::AID-GCC1>3.0.CO;2-V |
0.301 |
|
| 1998 |
Le Beau MM, Rassool FV, Neilly ME, Espinosa R, Glover TW, Smith DI, McKeithan TW. Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction. Human Molecular Genetics. 7: 755-61. PMID 9499431 DOI: 10.1093/hmg/7.4.755 |
0.483 |
|
| 1998 |
Wang PW, Iannantuoni K, Davis EM, Espinosa R, Stoffel M, Le Beau MM. Refinement of the commonly deleted segment in myeloid leukemias with a del(20q). Genes, Chromosomes & Cancer. 21: 75-81. PMID 9491317 DOI: 10.1002/(Sici)1098-2264(199802)21:2<75::Aid-Gcc1>3.0.Co;2-4 |
0.423 |
|
| 1998 |
Wang P, Spielberger RT, Thangavelu M, Zhao N, Davis EM, Iannantuoni K, Larson RA, Le Beau MM. dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53. Genes, Chromosomes & Cancer. 20: 282-91. PMID 9365836 DOI: 10.1002/(SICI)1098-2264(199711)20:3<282::AID-GCC9>3.0.CO;2-Z |
0.302 |
|
| 1998 |
Roulston D, Espinosa R, Nucifora G, Larson RA, Le Beau MM, Rowley JD. CBFA2(AML1) Translocations With Novel Partner Chromosomes in Myeloid Leukemias: Association With Prior Therapy Blood. 92: 2879-2885. DOI: 10.1182/blood.v92.8.2879 |
0.451 |
|
| 1997 |
Ong ST, Fong KM, Bader SA, Minna JD, Le Beau MM, McKeithan TW, Rassool FV. Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines. Genes, Chromosomes & Cancer. 20: 16-23. PMID 9290949 DOI: 10.1002/(SICI)1098-2264(199709)20:1<16::AID-GCC3>3.0.CO;2-C |
0.387 |
|
| 1997 |
Sato Y, Bohlander SK, Kobayashi H, Suto Y, Davis EM, Espinosa R, Le Beau MM, Rowley JD. Identification of pericentric inversion 12, inv(12)(p13.1q11), by fluorescence in situ hybridization in a patient with acute myeloid leukemia (AML-M6). Cancer Genetics and Cytogenetics. 97: 157-60. PMID 9283600 DOI: 10.1016/S0165-4608(96)00335-4 |
0.321 |
|
| 1997 |
Zhao N, Stoffel A, Wang PW, Eisenbart JD, Espinosa R, Larson RA, Le Beau MM. Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map. Proceedings of the National Academy of Sciences of the United States of America. 94: 6948-53. PMID 9192672 DOI: 10.1073/pnas.94.13.6948 |
0.442 |
|
| 1997 |
Levi-Setti R, Chabala JM, Gavrilov K, Espinosa R, Le Beau MM. Imaging of BrdU-labeled human metaphase chromosomes with a high resolution scanning ion microprobe. Microscopy Research and Technique. 36: 301-12. PMID 9140930 DOI: 10.1002/(Sici)1097-0029(19970215)36:4<301::Aid-Jemt8>3.0.Co;2-O |
0.372 |
|
| 1997 |
Janßen U, Davis EM, Le Beau MM, Stoffel W. Human mitochondrial enoyl-CoA hydratase gene (ECHS1): Structural organization and assignment to chromosome 10q26.2-q26.3 Genomics. 40: 470-475. PMID 9073515 DOI: 10.1006/Geno.1996.4597 |
0.423 |
|
| 1997 |
Broccoli D, Chong L, Oelmann S, Fernald AA, Marziliano N, van Steensel B, Kipling D, Le Beau MM, de Lange T. Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domains. Human Molecular Genetics. 6: 69-76. PMID 9002672 DOI: 10.1093/Hmg/6.1.69 |
0.336 |
|
| 1996 |
Furuta H, Nishi S, Le Beau MM, Fernald AA, Yano H, Bell GI. Sequence of human hexokinase III cDNA and assignment of the human hexokinase III gene (HK3) to chromosome band 5q35.2 by fluorescence in situ hybridization. Genomics. 36: 206-9. PMID 8812439 DOI: 10.1006/Geno.1996.0448 |
0.317 |
|
| 1996 |
Rassool FV, Le Beau MM, Shen ML, Neilly ME, Espinosa R, Ong ST, Boldog F, Drabkin H, McCarroll R, McKeithan TW. Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2 Genomics. 35: 109-117. PMID 8661111 DOI: 10.1006/geno.1996.0329 |
0.412 |
|
| 1996 |
Bosio A, Binczek E, Le Beau MM, Fernald AA, Stoffel W. The human gene CGT encoding the UDP-galactose ceramide galactosyl transferase (cerebroside synthase): cloning, characterization, and assignment to human chromosome 4, band q26. Genomics. 34: 69-75. PMID 8661025 DOI: 10.1006/Geno.1996.0242 |
0.367 |
|
| 1996 |
Stoffel M, Le Beau MM, Espinosa R, Bohlander SF, Le Paslier D, Cohen D, Xiang KS, Cox NJ, Fajans SS, Bell GI. A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene. Proceedings of the National Academy of Sciences of the United States of America. 93: 3937-41. PMID 8632993 DOI: 10.1073/Pnas.93.9.3937 |
0.451 |
|
| 1996 |
Takeda J, Espinosa R, Eng S, Le Beau MM, Bell GI. Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library. Genomics. 29: 276-81. PMID 8530086 DOI: 10.1006/Geno.1995.1245 |
0.33 |
|
| 1995 |
Stoffel M, Espinosa R, Trabb JB, Le Beau MM, Bell GI. Human type I pituitary adenylate cyclase activating polypeptide receptor (ADCYAP1R): localization to chromosome band 7p14 and integration into the cytogenetic, physical, and genetic map of chromosome 7. Genomics. 23: 697-9. PMID 7851900 DOI: 10.1006/Geno.1994.1560 |
0.435 |
|
| 1995 |
Le Beau MM, Song C, Davis EM, Hiipakka RA, Kokontis JM, Liao S. Assignment of the human ubiquitous receptor gene (UNR) to 19q13.3 using fluorescence in situ hybridization. Genomics. 26: 166-8. PMID 7782080 DOI: 10.1016/0888-7543(95)80100-Z |
0.382 |
|
| 1995 |
Dreyling MH, Kobayashi H, Olopade OI, Le Beau MM, Rowley JD, Bohlander SK. Detection of 9p deletions in leukemia cell lines by interphase fluorescence in situ hybridization with YAC-derived probes. Cancer Genetics and Cytogenetics. 83: 46-55. PMID 7656204 DOI: 10.1016/S0165-4608(95)00026-7 |
0.32 |
|
| 1995 |
Rassool FV, Neilly ME, McGuire KL, McKeithan TW, Le Beau MM. Localization of the chinese hamster MHC locus to chromosome 1q17→q18 by fluorescence in situ hybridization Cytogenetic and Genome Research. 71: 62-63. PMID 7606930 DOI: 10.1159/000134064 |
0.4 |
|
| 1995 |
Olopade OI, Pomykala HM, Hagos F, Sveen LW, Espinosa R, Dreyling MH, Gursky S, Stadler WM, Le Beau MM, Bohlander SK. Construction of a 2.8-megabase yeast artificial chromosome contig and cloning of the human methylthioadenosine phosphorylase gene from the tumor suppressor region on 9p21. Proceedings of the National Academy of Sciences of the United States of America. 92: 6489-93. PMID 7604019 DOI: 10.1073/Pnas.92.14.6489 |
0.384 |
|
| 1995 |
Martinez-Climent JA, Espinosa R, Thirman MJ, Le Beau MM, Rowley JD. Abnormalities of chromosome band 11q23 and the MLL gene in pediatric myelomonocytic and monoblastic leukemias. Identification of the t(9;11) as an indicator of long survival. Journal of Pediatric Hematology/Oncology. 17: 277-83. PMID 7583381 DOI: 10.1097/00043426-199511000-00001 |
0.332 |
|
| 1995 |
el-Maghrabi MR, Lange AJ, Jiang W, Yamagata K, Stoffel M, Takeda J, Fernald AA, Le Beau MM, Bell GI, Baker L. Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency. Genomics. 27: 520-5. PMID 7558035 DOI: 10.1006/Geno.1995.1085 |
0.333 |
|
| 1995 |
Dreyling M, Bohlander S, Le Beau M, Olopade O. Refined mapping of genomic rearrangements involving the short arm of chromosome 9 in acute lymphoblastic leukemias and other hematologic malignancies Blood. 86: 1931-1938. DOI: 10.1182/Blood.V86.5.1931.Bloodjournal8651931 |
0.392 |
|
| 1995 |
Sato Y, Suto Y, Pietenpol J, Golub T, Gilliland D, Davis E, Le Beau M, Roberts J, Vogelstein B, Rowley J. TEL and KIP1 define the smallest region of deletions on 12p13 in hematopoietic malignancies Blood. 86: 1525-1533. DOI: 10.1182/Blood.V86.4.1525.Bloodjournal8641525 |
0.371 |
|
| 1994 |
Bohlander SK, Espinosa R, Fernald AA, Rowley JD, Le Beau MM, DÃaz MO. Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization. Cytogenetics and Cell Genetics. 65: 108-10. PMID 8404060 |
0.325 |
|
| 1994 |
Yasuda K, Espinosa R, Takeda J, Le Beau MM, Bell GI. Localization of the kappa opioid receptor gene to human chromosome band 8q11.2. Genomics. 19: 596-7. PMID 8188308 DOI: 10.1006/Geno.1994.1117 |
0.421 |
|
| 1994 |
Le Beau MM, Carver LA, Espinosa R, Schmidt JV, Bradfield CA. Chromosomal localization of the human AHR locus encoding the structural gene for the Ah receptor to 7p21-->p15. Cytogenetics and Cell Genetics. 66: 172-6. PMID 8125016 DOI: 10.1159/000133694 |
0.359 |
|
| 1994 |
Stoffel M, Espinosa R, Powell KL, Philipson LH, Le Beau MM, Bell GI. Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): Localization to chromosome 2 and identification of a simple tandem repeat polymorphism Genomics. 21: 254-256. PMID 8088798 DOI: 10.1006/Geno.1994.1253 |
0.409 |
|
| 1994 |
Menzel S, Stoffel M, Espinosa R, Fernald AA, Le Beau MM, Bell GI. Localization of the glucagon receptor gene to human chromosome band 17q25. Genomics. 20: 327-8. PMID 8020989 DOI: 10.1006/Geno.1994.1179 |
0.449 |
|
| 1994 |
Jones EM, Menzel S, Espinosa R, Le Beau MM, Bell GI, Takeda J. Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism. Genomics. 23: 490-1. PMID 7835902 DOI: 10.1006/Geno.1994.1529 |
0.443 |
|
| 1994 |
German MS, Wang J, Fernald AA, Espinosa R, Le Beau MM, Bell GI. Localization of the genes encoding two transcription factors, LMX1 and CDX3, regulating insulin gene expression to human chromosomes 1 and 13. Genomics. 24: 403-4. PMID 7698771 DOI: 10.1006/geno.1994.1639 |
0.302 |
|
| 1994 |
Kobayashi H, Montgomery K, Bohlander S, Adra C, Lim B, Kucherlapati R, Donis-Keller H, Holt M, Le Beau M, Rowley J. Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases Blood. 84: 3473-3482. DOI: 10.1182/blood.v84.10.3473.3473 |
0.41 |
|
| 1993 |
Le Beau MM, Espinosa R, Neuman WL, Stock W, Roulston D, Larson RA, Keinanen M, Westbrook CA. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases. Proceedings of the National Academy of Sciences of the United States of America. 90: 5484-8. PMID 8516290 DOI: 10.1073/Pnas.90.12.5484 |
0.429 |
|
| 1993 |
Sturrock AB, Espinosa R, Hoidal JR, Le Beau MM. Localization of the gene encoding proteinase-3 (the Wegener's granulomatosis autoantigen) to human chromosome band 19p13.3. Cytogenetics and Cell Genetics. 64: 33-4. PMID 8508676 DOI: 10.1159/000133555 |
0.364 |
|
| 1993 |
Baron BW, Nucifora G, McCabe N, Espinosa R, Le Beau MM, McKeithan TW. Identification of the gene associated with the recurring chromosomal translocations t(3;14)(q27;q32) and t(3;22)(q27;q11) in B-cell lymphomas. Proceedings of the National Academy of Sciences of the United States of America. 90: 5262-6. PMID 8506375 DOI: 10.1073/pnas.90.11.5262 |
0.468 |
|
| 1993 |
Stoffel M, Xiang KS, Espinosa R, Cox NJ, Le Beau MM, Bell GI. cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young. Human Molecular Genetics. 2: 1-4. PMID 8490617 DOI: 10.1093/Hmg/2.1.1 |
0.392 |
|
| 1993 |
Yamada Y, Stoffel M, Espinosa R, Xiang KS, Seino M, Seino S, Le Beau MM, Bell GI. Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms. Genomics. 15: 449-52. PMID 8449518 DOI: 10.1006/Geno.1993.1088 |
0.435 |
|
| 1993 |
Kobayashi H, Espinosa R, Thirman MJ, Gill HJ, Fernald AA, Diaz MO, Le Beau MM, Rowley JD. Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization. Blood. 82: 547-51. PMID 8329710 |
0.355 |
|
| 1993 |
Yasuda K, Espinosa R, Davis EM, Le Beau MM, Bell GI. Human somatostatin receptor genes: Localization of SSTR5 to human chromosome 20p11.2 Genomics. 17: 785-786. PMID 8244401 DOI: 10.1006/Geno.1993.1410 |
0.328 |
|
| 1993 |
Neuman WL, Westbrook CA, Dixon M, Espinosa R, Patel YD, Nakamura Y, Weiffenbach B, Le Beau MM. Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization. Cytogenetics and Cell Genetics. 62: 207-10. PMID 8095009 DOI: 10.1159/000133477 |
0.314 |
|
| 1993 |
Kobayashi H, Espinosa R, Thirman MJ, Fernald AA, Shannon K, Diaz MO, Le Beau MM, Rowley JD. Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization. Genes, Chromosomes & Cancer. 7: 204-8. PMID 7692945 DOI: 10.1002/Gcc.2870070404 |
0.365 |
|
| 1993 |
Sanford JP, Sait SNJ, Pan L, Nowak NJ, Gill HJ, Le Beau MM, Diaz MO, Zabel B, Shows TB. Characterization of two 11q23.3-11q24 deletions and mapping of associated anonymous DNA markers Genes Chromosomes and Cancer. 7: 67-73. PMID 7687455 DOI: 10.1002/gcc.2870070202 |
0.464 |
|
| 1993 |
Kobayashi H, Espinosa R, Fernald AA, Begy C, Diaz MO, Le Beau MM, Rowley JD. Analysis of deletions of the long arm of chromosome 11 in hematologic malignancies with fluorescence in situ hybridization. Genes, Chromosomes & Cancer. 8: 246-52. PMID 7512368 DOI: 10.1002/gcc.2870080407 |
0.412 |
|
| 1993 |
Super H, McCabe N, Thirman M, Larson R, Le Beau M, Pedersen-Bjergaard J, Philip P, Diaz M, Rowley J. Rearrangements of the MLL gene in therapy-related acute myeloid leukemia in patients previously treated with agents targeting DNA- topoisomerase II Blood. 82: 3705-3711. DOI: 10.1182/blood.v82.12.3705.3705 |
0.367 |
|
| 1993 |
Anastasi J, Feng J, Le Beau M, Larson R, Rowley J, Vardiman J. Cytogenetic clonality in myelodysplastic syndromes studied with fluorescence in situ hybridization: lineage, response to growth factor therapy, and clone expansion Blood. 81: 1580-1585. DOI: 10.1182/blood.v81.6.1580.bloodjournal8161580 |
0.319 |
|
| 1992 |
Rubin CM, Le Beau MM, Mick R, Bitter MA, Nachman J, Rudinsky R, Appel HJ, Morgan E, Suarez CR, Schumacher HR. Impact of chromosomal translocations on prognosis in childhood acute lymphoblastic leukemia. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 9: 2183-92. PMID 1960559 DOI: 10.1200/JCO.1991.9.12.2183 |
0.325 |
|
| 1992 |
Xia Y, Brown L, Yang CY, Tsan JT, Siciliano MJ, Espinosa R, Le Beau MM, Baer RJ. TAL2, a helix-loop-helix gene activated by the (7;9)(q34;q32) translocation in human T-cell leukemia. Proceedings of the National Academy of Sciences of the United States of America. 88: 11416-20. PMID 1763056 DOI: 10.1073/pnas.88.24.11416 |
0.365 |
|
| 1992 |
Espinosa R, Lemons RS, Perlman RK, Kuo WL, Rosner MR, Le Beau MM. Localization of the gene encoding insulin-degrading enzyme to human chromosome 10, bands q23----q25. Cytogenetics and Cell Genetics. 57: 184-6. PMID 1743072 DOI: 10.1159/000133142 |
0.395 |
|
| 1992 |
Thangavelu M, Neuman WL, Espinosa R, Nakamura Y, Westbrook CA, Le Beau MM. A physical and genetic linkage map of the distal long arm of human chromosome 5. Cytogenetics and Cell Genetics. 59: 27-30. PMID 1733669 DOI: 10.1159/000133193 |
0.371 |
|
| 1992 |
Davey FR, Lawrence D, MacCallum J, Varney J, Hutchison R, Wurster-Hill D, Schiffer C, Sobol RE, Ciminelli N, Le Beau M, Bloomfield CD. Morphologic characteristics of acute lymphoblastic leukemie (ALL) with abnormalities of chromosome 8, band q24 American Journal of Hematology. 40: 183-191. PMID 1609772 DOI: 10.1002/ajh.2830400306 |
0.303 |
|
| 1992 |
Brown L, Espinosa R, Le Beau MM, Siciliano MJ, Baer R. HEN1 and HEN2: a subgroup of basic helix-loop-helix genes that are coexpressed in a human neuroblastoma. Proceedings of the National Academy of Sciences of the United States of America. 89: 8492-6. PMID 1528853 DOI: 10.1073/pnas.89.18.8492 |
0.323 |
|
| 1992 |
Levi-Setti R, Le Beau M. Cytogenetic applications of high resolution secondary ion imaging microanalysis: detection and mapping of tracer isotopes in human chromosomes. Biology of the Cell. 74: 51-8. PMID 1511248 DOI: 10.1016/0248-4900(92)90008-O |
0.301 |
|
| 1992 |
Bohlander SK, Espinosa R, Le Beau MM, Rowley JD, Díaz MO. A method for the rapid sequence-independent amplification of microdissected chromosomal material. Genomics. 13: 1322-4. PMID 1505965 DOI: 10.1016/0888-7543(92)90057-Y |
0.412 |
|
| 1992 |
Yeldandi AV, Patel YD, Liao M, Kao FT, Rao MS, Reddy JK, Le Beau MM. Localization of the human urate oxidase gene (UOX) to 1p22. Cytogenetics and Cell Genetics. 61: 121-2. PMID 1395718 DOI: 10.1159/000133386 |
0.327 |
|
| 1992 |
Neuman WL, Le Beau MM, Farber RA, Lindgren V, Westbrook CA. Somatic cell hybrid mapping of human chromosome band 5q31: a region important to hematopoiesis. Cytogenetics and Cell Genetics. 61: 103-6. PMID 1395713 DOI: 10.1159/000133381 |
0.426 |
|
| 1992 |
Olopade OI, Bohlander SK, Pomykala H, Maltepe E, Van Melle E, Le Beau MM, Diaz MO. Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia Genomics. 14: 437-443. PMID 1385305 DOI: 10.1016/S0888-7543(05)80238-1 |
0.351 |
|
| 1992 |
Onodera N, McCabe NR, Nachman JB, Johnson FL, Le Beau MM, Rowley JD, Rubin CM. Hyperdiploidy arising from near-haploidy in childhood acute lymphoblastic leukemia. Genes, Chromosomes & Cancer. 4: 331-6. PMID 1377941 DOI: 10.1002/gcc.2870040410 |
0.413 |
|
| 1992 |
Park JK, Le Beau MM, Shows TB, Rowley JD, Diaz MO. A complex genetic rearrangement in a t(10;14)(q24;q11) associated with T- cell acute lymphoblastic leukemia Genes Chromosomes and Cancer. 4: 32-40. PMID 1377007 |
0.413 |
|
| 1992 |
Paietta E, Van Ness B, Le Beau MM, Bennett J, Cassileth P, Wiernik PH. Translocation (2;9)(p12;p23) in a case of acute leukemia with t(4;11)(q21;q23). Lack of rearrangement of the kappa and interferon gene loci. Cancer Genetics and Cytogenetics. 60: 82-5. PMID 1375531 DOI: 10.1016/0165-4608(92)90238-4 |
0.336 |
|
| 1992 |
Dixon MJ, Dixon J, Raskova D, Le Beau MM, Williamson R, Klinger K, Landes GM. Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2. Human Molecular Genetics. 1: 249-53. PMID 1303194 DOI: 10.1093/hmg/1.4.249 |
0.376 |
|
| 1992 |
Larson R, Le Beau M, Ratain M, Rowley J. Balanced translocations involving chromosome bands 11q23 and 21q22 in therapy-related leukemia [letter] Blood. 79: 1892-1893. DOI: 10.1182/blood.v79.7.1892.1892 |
0.325 |
|
| 1992 |
Neuman W, Rubin C, Rios R, Larson R, Le Beau M, Rowley J, Vardiman J, Schwartz J, Farber R. Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders Blood. 79: 1501-1510. DOI: 10.1182/blood.v79.6.1501.1501 |
0.429 |
|
| 1991 |
Mikol DD, Alexakos MJ, Bayley CA, Lemons RS, Le Beau MM, Stefansson K. Structure and chromosomal localization of the gene for the oligodendrocyte-myelin glycoprotein. The Journal of Cell Biology. 111: 2673-9. PMID 2277079 DOI: 10.1083/jcb.111.6.2673 |
0.389 |
|
| 1991 |
Le Beau MM, Geurts van Kessel AH. Report of the committee on the genetic constitution of chromosome 18. Cytogenetics and Cell Genetics. 55: 216-7. PMID 2073836 DOI: 10.1159/000133014 |
0.317 |
|
| 1991 |
Rubin CM, Le Beau MM. Cytogenetic abnormalities in childhood acute lymphoblastic leukemia. The American Journal of Pediatric Hematology/Oncology. 13: 202-16. PMID 2069231 DOI: 10.1097/00043426-199122000-00017 |
0.304 |
|
| 1991 |
Gao J, Erickson P, Gardiner K, Le Beau MM, Diaz MO, Patterson D, Rowley JD, Drabkin HA. Isolation of a yeast artificial chromosome spanning the 8;21 translocation breakpoint t(8;21)(q22;q22.3) in acute myelogenous leukemia Proceedings of the National Academy of Sciences of the United States of America. 88: 4882-4886. PMID 2052570 DOI: 10.1073/Pnas.88.11.4882 |
0.487 |
|
| 1991 |
Mancuso DJ, Tuley EA, Westfield LA, Lester-Mancuso TL, Le Beau MM, Sorace JM, Sadler JE. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction. Biochemistry. 30: 253-69. PMID 1988024 DOI: 10.1021/bi00215a036 |
0.312 |
|
| 1991 |
Westbrook CA, Neuman WL, Hewitt J, Kidd KK, Le Beau MM, Williamson R. Report of the chromosome 5 workshop. Genomics. 10: 1105-9. PMID 1916818 DOI: 10.1016/0888-7543(91)90211-V |
0.345 |
|
| 1991 |
Lorenzana AN, Rubin CM, Le Beau MM, Nachman J, Connolly P, Subramanian U, Johnson FL, McKeithan TW. Immunoglobulin gene rearrangements in acute lymphoblastic leukemia with the 9;11 translocation. Genes, Chromosomes & Cancer. 3: 74-7. PMID 1906342 DOI: 10.1002/gcc.2870030113 |
0.333 |
|
| 1991 |
Rassool FV, McKeithan TW, Neilly ME, van Melle E, Espinosa R, Le Beau MM. Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites. Proceedings of the National Academy of Sciences of the United States of America. 88: 6657-61. PMID 1862089 DOI: 10.1073/pnas.88.15.6657 |
0.447 |
|
| 1991 |
Rosenberg M, Fuchs E, Le Beau MM, Eddy RL, Shows TB. Three epidermal and one simple epithelial type II keratin genes map to human chromosome 12. Cytogenetics and Cell Genetics. 57: 33-8. PMID 1713141 DOI: 10.1159/000133109 |
0.392 |
|
| 1991 |
Burnett RC, David JC, Harden AM, Le Beau MM, Rowley JD, Diaz MO. The LCK gene is involved in the t(1;7)(p34;q34) in the T-cell acute lymphoblastic leukemia derived cell line, HSB-2. Genes, Chromosomes & Cancer. 3: 461-7. PMID 1663780 DOI: 10.1002/gcc.2870030608 |
0.458 |
|
| 1991 |
Anastasi J, Vardiman J, Rudinsky R, Patel M, Nachman J, Rubin C, Le Beau M. Direct correlation of cytogenetic findings with cell morphology using in situ hybridization: an analysis of suspicious cells in bone marrow specimens of two patients completing therapy for acute lymphoblastic leukemia Blood. 77: 2456-2462. DOI: 10.1182/blood.v77.11.2456.2456 |
0.324 |
|
| 1990 |
Lemons RS, Espinosa R, Rebentisch M, McCormick F, Ladner M, Le Beau MM. Chromosomal localization of the gene encoding GTPase-activating protein (RASA) to human chromosome 5, bands q13-q15. Genomics. 6: 383-5. PMID 2307479 DOI: 10.1016/0888-7543(90)90581-E |
0.381 |
|
| 1990 |
Chada S, Le Beau MM, Casey L, Newburger PE. Isolation and chromosomal localization of the human glutathione peroxidase gene Genomics. 6: 268-271. PMID 2307470 DOI: 10.1016/0888-7543(90)90566-D |
0.423 |
|
| 1990 |
Chandrasekharappa SC, Rebelsky MS, Firak TA, Le Beau MM, Westbrook CA. A long-range restriction map of the interleukin-4 and interleukin-5 linkage group on chromosome 5. Genomics. 6: 94-9. PMID 2303264 DOI: 10.1016/0888-7543(90)90452-Z |
0.395 |
|
| 1990 |
Diaz MO, Rubin CM, Harden A, Ziemin S, Larson RA, Le Beau MM, Rowley JD. Deletions of interferon genes in acute lymphoblastic leukemia. The New England Journal of Medicine. 322: 77-82. PMID 2294436 DOI: 10.1056/NEJM199001113220202 |
0.359 |
|
| 1990 |
Ohno H, Furukawa T, Fukuhara S, Zong SQ, Kamesaki H, Shows TB, Le Beau MM, McKeithan TW, Kawakami T, Honjo T. Molecular analysis of a chromosomal translocation, t(9;14)(p13;q32), in a diffuse large-cell lymphoma cell line expressing the Ki-1 antigen. Proceedings of the National Academy of Sciences of the United States of America. 87: 628-32. PMID 2153959 DOI: 10.1073/Pnas.87.2.628 |
0.436 |
|
| 1990 |
Becker MA, Heidler SA, Bell GI, Seino S, Le Beau MM, Westbrook CA, Neuman W, Shapiro LJ, Mohandas TK, Roessler BJ. Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes. Genomics. 8: 555-61. PMID 1962753 DOI: 10.1016/0888-7543(90)90043-T |
0.434 |
|
| 1990 |
Watson ML, Kingsmore SF, Johnston GI, Siegelman MH, Le Beau MM, Lemons RS, Bora NS, Howard TA, Weissman IL, McEver RP. Genomic organization of the selectin family of leukocyte adhesion molecules on human and mouse chromosome 1. The Journal of Experimental Medicine. 172: 263-72. PMID 1694218 DOI: 10.1084/jem.172.1.263 |
0.423 |
|
| 1990 |
Gulcher JR, Alexakos MJ, Le Beau MM, Lemons RS, Stefansson K. Chromosomal localization of the human hexabrachion (tenascin) gene and evidence for recent reduplication within the gene. Genomics. 6: 616-22. PMID 1692804 DOI: 10.1016/0888-7543(90)90495-G |
0.394 |
|
| 1990 |
Rubin C, Larson R, Anastasi J, Winter J, Thangavelu M, Vardiman J, Rowley J, Le Beau M. t(3;21)(q26;q22): a recurring chromosomal abnormality in therapy- related myelodysplastic syndrome and acute myeloid leukemia Blood. 76: 2594-2598. DOI: 10.1182/blood.v76.12.2594.2594 |
0.31 |
|
| 1989 |
Testa JR, Parsa NZ, Le Beau MM, Vande Woude GF. Localization of the proto-oncogene MOS to 8q11-q12 by in situ chromosomal hybridization. Genomics. 3: 44-7. PMID 3220476 DOI: 10.1016/0888-7543(88)90157-7 |
0.386 |
|
| 1989 |
Thangavelu M, Bitter MA, Larson RA, Davis EM, Rowley JD, Le Beau MM. Der(5)t(5;7)(q11.2;p11.2): a new recurring abnormality in malignant myeloid disorders. Cancer Genetics and Cytogenetics. 37: 1-8. PMID 2917326 DOI: 10.1016/0165-4608(89)90067-8 |
0.368 |
|
| 1989 |
Le Beau MM, Ryan D, Pericak-Vance MA. Report of the committee on the genetic constitution of chromosomes 18 and 19. Cytogenetics and Cell Genetics. 51: 338-57. PMID 2676376 DOI: 10.1159/000132798 |
0.317 |
|
| 1989 |
Rubin CM, Le Beau MM. Chromosomal abnormalities in myeloid hematologic malignancies. Current Topics in Microbiology and Immunology. 149: 25-34. PMID 2659280 DOI: 10.1007/978-3-642-74623-9_2 |
0.35 |
|
| 1989 |
Park JK, McKeithan TW, Le Beau MM, Bitter MA, Frankli n WA, Rowley JD, Diaz MO. An (8;14)(q24;q11) translocation involving the T-cell receptor α-chain gene and the MYC oncogene 3' region in a B-cell lymphoma Genes Chromosomes and Cancer. 1: 15-22. PMID 2535034 |
0.431 |
|
| 1989 |
Hooberman AL, Carrino JJ, Leibowitz D, Rowley JD, Le Beau MM, Arlin ZA, Westbrook CA. Unexpected heterogeneity of BCR-ABL fusion mRNA detected by polymerase chain reaction in Philadelphia chromosome-positive acute lymphoblastic leukemia. Proceedings of the National Academy of Sciences of the United States of America. 86: 4259-63. PMID 2498881 DOI: 10.1073/Pnas.86.11.4259 |
0.346 |
|
| 1989 |
Thangavelu M, Le Beau MM. Chromosomal Abnormalities in Hodgkin’s Disease Hematology/Oncology Clinics of North America. 3: 221-236. DOI: 10.1016/S0889-8588(18)30552-5 |
0.309 |
|
| 1988 |
Harris BN, Davis EM, Le Beau MM, Bitter MA, Kaminer LS, Morgan E, Rowley JD. Variant translocations (9;11): identification of the critical genetic rearrangement. Cancer Genetics and Cytogenetics. 30: 171-5. PMID 3422044 DOI: 10.1016/0165-4608(88)90108-2 |
0.369 |
|
| 1988 |
Martin AO, Northrup H, Ledbetter DH, Trask B, van den Engh G, Le Beau MM, Beaudet AL, Gray JW, Sekhon G, Krassikoff N. Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis. American Journal of Medical Genetics. 31: 643-54. PMID 3228143 DOI: 10.1002/Ajmg.1320310320 |
0.338 |
|
| 1988 |
Davidson MK, Le Beau MM, Eddy RL, Shows TB, DiPietro LA, Kingzette M, Hanly WC. Genetic mapping of the human polymeric immunoglobulin receptor gene to chromosome region 1q31----q41. Cytogenetics and Cell Genetics. 48: 107-11. PMID 3197448 DOI: 10.1159/000132601 |
0.426 |
|
| 1988 |
Hattori K, Angel P, Le Beau MM, Karin M. Structure and chromosomal localization of the functional intronless human JUN protooncogene. Proceedings of the National Academy of Sciences of the United States of America. 85: 9148-52. PMID 3194415 DOI: 10.1073/pnas.85.23.9148 |
0.366 |
|
| 1988 |
Anastasi J, Pettenati MJ, Le Beau MM, Kwaan HC, Weil SC. Acute lymphoblastic leukemia in a patient with longstanding polycythemia vera: Cytogenetic analysis reveals two distinct abnormal clones American Journal of Hematology. 29: 33-37. PMID 3177367 DOI: 10.1002/ajh.2830290108 |
0.317 |
|
| 1988 |
Joseph LJ, Le Beau MM, Jamieson GA, Acharya S, Shows TB, Rowley JD, Sukhatme VP. Molecular cloning, sequencing, and mapping of EGR2, a human early growth response gene encoding a protein with "zinc-binding finger" structure. Proceedings of the National Academy of Sciences of the United States of America. 85: 7164-8. PMID 3140236 DOI: 10.1073/pnas.85.19.7164 |
0.307 |
|
| 1988 |
Diaz MO, Ziemin S, Le Beau MM, Pitha P, Smith SD, Chilcote RR, Rowley JD. Homozygous deletion of the α- and β1-interferon genes in human leukemia and derived cell lines Proceedings of the National Academy of Sciences of the United States of America. 85: 5259-5263. PMID 3134658 DOI: 10.1073/pnas.85.14.5259 |
0.386 |
|
| 1988 |
Weil SC, Rosner GL, Reid MS, Chisholm RL, Lemons RS, Swanson MS, Carrino JJ, Diaz MO, Le Beau MM. Translocation and rearrangement of myeloperoxidase gene in acute promyelocytic leukemia. Science (New York, N.Y.). 240: 790-2. PMID 2896388 DOI: 10.1126/Science.2896388 |
0.456 |
|
| 1988 |
Farber RA, Phalen T, Neuman WL, Le Beau MM, Wasmuth JJ, Dobbs M. An anonymous DNA segment pTP5E (D5S70) maps to the long arm of chromosome 5 and identifies a Taq I polymorphism. Nucleic Acids Research. 16: 2360. PMID 2895914 DOI: 10.1093/Nar/16.5.2360 |
0.425 |
|
| 1988 |
Westbrook C, Rubin C, Carrino J, Le Beau M, Bernards A, Rowley J. Long-range mapping of the Philadelphia chromosome by pulsed-field gel electrophoresis Blood. 71: 697-702. DOI: 10.1182/Blood.V71.3.697.697 |
0.454 |
|
| 1987 |
Le Beau MM, Epstein ND, O'Brien SJ, Nienhuis AW, Yang YC, Clark SC, Rowley JD. The interleukin 3 gene is located on human chromosome 5 and is deleted in myeloid leukemias with a deletion of 5q Proceedings of the National Academy of Sciences of the United States of America. 84: 5913-5917. PMID 3497400 DOI: 10.1073/Pnas.84.16.5913 |
0.409 |
|
| 1987 |
Pettenati MJ, Le Beau MM, Lemons RS, Shima EA, Kawasaki ES, Larson RA, Sherr CJ, Diaz MO, Rowley JD. Assignment of CSF-1 to 5q33.1: evidence for clustering of genes regulating hematopoiesis and for their involvement in the deletion of the long arm of chromosome 5 in myeloid disorders. Proceedings of the National Academy of Sciences of the United States of America. 84: 2970-4. PMID 3495006 DOI: 10.1073/pnas.84.9.2970 |
0.422 |
|
| 1987 |
Rubin CM, Larson RA, Bitter MA, Carrino JJ, Le Beau MM, Diaz MO, Rowley JD. Association of a chromosomal 3;21 translocation with the blast phase of chronic myelogenous leukemia Blood. 70: 1338-1342. PMID 3478099 |
0.344 |
|
| 1987 |
Westbrook CA, Rubin CM, Le Beau MM, Kaminer LS, Smith SD, Rowley JD, Diaz MO. Molecular analysis of TCRB and ABL in a t(7;9)-containing cell line (SUP-T3) from a human T-cell leukemia. Proceedings of the National Academy of Sciences of the United States of America. 84: 251-5. PMID 3025859 DOI: 10.1073/Pnas.84.1.251 |
0.411 |
|
| 1987 |
Lublin DM, Lemons RS, Le Beau MM, Holers VM, Tykocinski ML, Medof ME, Atkinson JP. The gene encoding decay-accelerating factor (DAF) is located in the complement-regulatory locus on the long arm of chromosome 1 Journal of Experimental Medicine. 165: 1731-1736. PMID 2438369 DOI: 10.1084/jem.165.6.1731 |
0.376 |
|
| 1987 |
Chilcote R, Le Beau M, Dampier C, Pergament E, Verlinsky Y, Mohandas N, Frischer H, Rowley J. Association of red cell spherocytosis with deletion of the short arm of chromosome 8 Blood. 69: 156-159. DOI: 10.1182/blood.V69.1.156.bloodjournal691156 |
0.408 |
|
| 1986 |
Le Beau MM, Albain KS, Larson RA, Vardiman JW, Davis EM, Blough RR, Golomb HM, Rowley JD. Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 4: 325-45. PMID 3950675 DOI: 10.1200/JCO.1986.4.3.325 |
0.38 |
|
| 1986 |
Le Beau MM, McKeithan TW, Shima EA, Goldman-Leikin RE, Chan SJ, Bell GI, Rowley JD, Diaz MO. T-cell receptor α-chain gene is split in a human T-cell leukemia cell line with a t(11;14)(p15;q11) Proceedings of the National Academy of Sciences of the United States of America. 83: 9744-9748. PMID 3540949 DOI: 10.1073/Pnas.83.24.9744 |
0.382 |
|
| 1986 |
McKeithan TW, Shima EA, Le Beau MM, Minowada J, Rowley JD, Diaz MO. Molecular cloning of the breakpoint junction of a human chromosomal 8;14 translocation involving the T-cell receptor α-chain gene and sequences on the 3' side of MYC Proceedings of the National Academy of Sciences of the United States of America. 83: 6636-6640. PMID 3529089 DOI: 10.1073/pnas.83.17.6636 |
0.393 |
|
| 1986 |
Shima EA, Le Beau MM, McKeithan TW, Minowada J, Showe LC, Mak TW, Minden MD, Rowley JD, Diaz MO. Gene encoding the alpha chain of the T-cell receptor is moved immediately downstream of c-myc in a chromosomal 8;14 translocation in a cell line from a human T-cell leukemia. Proceedings of the National Academy of Sciences of the United States of America. 83: 3439-43. PMID 3517860 DOI: 10.1073/Pnas.83.10.3439 |
0.393 |
|
| 1986 |
Le Beau MM, Rowley JD. Chromosomal abnormalities in leukemia and lymphoma: clinical and biological significance. Advances in Human Genetics. 15: 1-54. PMID 3513482 DOI: 10.1007/978-1-4615-8356-1_1 |
0.316 |
|
| 1986 |
Le Beau MM, Pettenati MJ, Lemons RS, Diaz MO, Westbrook CA, Larson RA, Sherr CJ, Rowley JD. Assignment of the GM-CSF, CSF-1, and FMS genes to human chromosome 5 provides evidence for linkage of a family of genes regulating hematopoiesis and for their involvement in the deletion (5q) in myeloid disorders. Cold Spring Harbor Symposia On Quantitative Biology. 51: 899-909. PMID 3495397 DOI: 10.1101/Sqb.1986.051.01.103 |
0.364 |
|
| 1986 |
Le Beau MM, Westbrook CA, Diaz MO, Larson RA, Rowley JD, Gasson JC, Golde DW, Sherr CJ. Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders. Science (New York, N.Y.). 231: 984-7. PMID 3484837 DOI: 10.1126/Science.3484837 |
0.415 |
|
| 1986 |
Le Beau MM, Rowley JD, Ferro MT, San Román C. Constitutional t(15;17): clarification of the chromosomal breakpoints. Cancer Genetics and Cytogenetics. 20: 175-7. PMID 3455857 DOI: 10.1016/0165-4608(86)90124-X |
0.326 |
|
| 1986 |
Diaz MO, Le Beau MM, Pitha P, Rowley JD. Interferon and c-ets-1 genes in the translocation (9;11)(p22;q23) in human acute monoytic leukemia Science. 231: 265-267. PMID 3455787 |
0.443 |
|
| 1986 |
Le Beau MM, Rowley JD, Sacchi N, Watson DK, Papas TS, Diaz MO. Hu-ets-2 is translocated to chromosome 8 in the t(8;21) in acute myelogenous leukemia Cancer Genetics and Cytogenetics. 23: 269-274. PMID 3021321 DOI: 10.1016/0165-4608(86)90189-5 |
0.422 |
|
| 1986 |
Look AT, Peiper SC, Rebentisch MB, Ashmun RA, Roussel MF, Lemons RS, Le Beau MM, Rubin CM, Sherr CJ. Molecular cloning, expression, and chromosomal localization of the gene encoding a human myeloid membrane antigen (gp150) Journal of Clinical Investigation. 78: 914-921. PMID 2428842 DOI: 10.1172/JCI112680 |
0.428 |
|
| 1986 |
Larson R, Williams S, Le Beau M, Bitter M, Vardiman J, Rowley J. Acute myelomonocytic leukemia with abnormal eosinophils and inv(16) or t(16;16) has a favorable prognosis Blood. 68: 1242-1249. DOI: 10.1182/blood.V68.6.1242.bloodjournal6861242 |
0.313 |
|
| 1986 |
Le Beau M. Chromosomal fragile sites and cancer-specific rearrangements Blood. 67: 849-858. DOI: 10.1182/blood.v67.4.849.849 |
0.307 |
|
| 1985 |
Diaz MO, Le Beau MM, Harden A, Rowley JD. Trisomy 8 in human hematologic neoplasia and the c-myc and c-mos oncogenes. Leukemia Research. 9: 1437-42. PMID 4079453 DOI: 10.1016/0145-2126(85)90033-5 |
0.302 |
|
| 1985 |
Westbrook CA, Le Beau MM, Diaz MO, Groffen J, Rowley JD. Chromosomal localization and characterization of c-abl in the t(6;9) of acute nonlymphocytic leukemia. Proceedings of the National Academy of Sciences of the United States of America. 82: 8742-6. PMID 3866248 DOI: 10.1073/Pnas.82.24.8742 |
0.392 |
|
| 1985 |
Diaz MO, Le Beau MM, Rowley JD, Drabkin HA, Patterson D. The role of the c-mos gene in the 8;21 translocation in human acute myeloblastic leukemia Science. 229: 767-769. PMID 3860954 DOI: 10.1126/science.3860954 |
0.4 |
|
| 1985 |
Le Beau MM, Bitter MA, Kaneko Y, Ueshima Y, Rowley JD. Insertion (10;11)(p11;q23q24) in two cases of acute monocytic leukemia. Leukemia Research. 9: 605-11. PMID 3859710 DOI: 10.1016/0145-2126(85)90140-7 |
0.336 |
|
| 1985 |
Suarez CR, Le Beau MM, Silberman S, Fresco R, Rowley JD. Acute megakaryoblastic leukemia in Down's syndrome: report of a case and review of cytogenetic findings. Medical and Pediatric Oncology. 13: 225-31. PMID 3159953 DOI: 10.1002/mpo.2950130413 |
0.344 |
|
| 1985 |
Drabkin HA, Diaz M, Bradley CM, Le Beau MM, Rowley JD, Patterson D. Isolation and analysis of the 21q+ chromosome in the acute myelogenous leukemia 8;21 translocation: Evidence that c-mos is not translocated Proceedings of the National Academy of Sciences of the United States of America. 82: 464-468. PMID 2982159 DOI: 10.1073/pnas.82.2.464 |
0.455 |
|
| 1985 |
Le Beau MM, Westbrook CA, Diaz MO, Rowley JD. c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders. Proceedings of the National Academy of Sciences of the United States of America. 82: 6692-6. PMID 2413444 DOI: 10.1073/Pnas.82.19.6692 |
0.433 |
|
| 1985 |
Bitter M, Neilly M, Le Beau M, Pearson M, Rowley J. Rearrangements of chromosome 3 involving bands 3q21 and 3q26 are associated with normal or elevated platelet counts in acute nonlymphocytic leukemia Blood. 66: 1362-1370. DOI: 10.1182/blood.v66.6.1362.1362 |
0.319 |
|
| 1983 |
Albain KS, Le Beau MM, Vardiman JW, Golomb HM, Rowley JD. Development of dysmyelopoietic syndrome in a hairy cell leukemia patient treated with chlorambucil: cytogenetic and morphologic evaluation. Cancer Genetics and Cytogenetics. 8: 107-15. PMID 6825062 DOI: 10.1016/0165-4608(83)90042-0 |
0.398 |
|
| 1983 |
Le Beau MM, Larson RA, Bitter MA, Vardiman JW, Golomb HM, Rowley JD. Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological association. The New England Journal of Medicine. 309: 630-6. PMID 6577285 DOI: 10.1056/NEJM198309153091103 |
0.304 |
|
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