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Michelle Le Beau

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Molecular Sequence Data

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Chromosomes, Human, Pair 5

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Publications

TOP 3
Jiang Yanwen; Lucas Isabelle; Young David J; Davis Elizabeth M; Karrison Theodore; Rest Joshua S; Le Beau Michelle M
Common fragile sites are characterized by histone hypoacetylation.
Qian Z; Mao L; Fernald A A; Yu H; Luo R; Jiang Y; Anastasi J; Valk P J; Delwel R; Le Beau M M
Enhanced expression of FHL2 leads to abnormal myelopoiesis in vivo.
Abdel-Wahab Omar; Mullally Ann; Hedvat Cyrus; Garcia-Manero Guillermo; Patel Jay; Wadleigh Martha; Malinge Sebastien; Yao JinJuan; Kilpivaara Outi; Bhat Rukhmi; Huberman Kety; Thomas Sabrena; Dolgalev Igor; Heguy Adriana; Paietta Elisabeth; Le Beau Michelle M; Beran Miloslav; Tallman Martin S; Ebert Benjamin L; Kantarjian Hagop M; Stone Richard M; Gilliland D Gary; Crispino John D; Levine Ross L
Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies.

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All Publications

2009: Jiang Yanwen; Lucas Isabelle; Young David J; Davis Elizabeth M; Karrison Theodore; Rest Joshua S; Le Beau Michelle M
Common fragile sites are characterized by histone hypoacetylation.
Human molecular genetics 2009;18(23):4501-12.
2009: Qian Z; Mao L; Fernald A A; Yu H; Luo R; Jiang Y; Anastasi J; Valk P J; Delwel R; Le Beau M M
Enhanced expression of FHL2 leads to abnormal myelopoiesis in vivo.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2009;23(9):1650-7.
2009: Abdel-Wahab Omar; Mullally Ann; Hedvat Cyrus; Garcia-Manero Guillermo; Patel Jay; Wadleigh Martha; Malinge Sebastien; Yao JinJuan; Kilpivaara Outi; Bhat Rukhmi; Huberman Kety; Thomas Sabrena; Dolgalev Igor; Heguy Adriana; Paietta Elisabeth; Le Beau Michelle M; Beran Miloslav; Tallman Martin S; Ebert Benjamin L; Kantarjian Hagop M; Stone Richard M; Gilliland D Gary; Crispino John D; Levine Ross L
Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies.
Blood 2009;114(1):144-7.
2009: Vardiman James W; Thiele Jüergen; Arber Daniel A; Brunning Richard D; Borowitz Michael J; Porwit Anna; Harris Nancy Lee; Le Beau Michelle M; Hellström-Lindberg Eva; Tefferi Ayalew; Bloomfield Clara D
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes.
Blood 2009;114(5):937-51.
2009: Knight Jeffrey A; Skol Andrew D; Shinde Abhijit; Hastings Darcie; Walgren Richard A; Shao Jin; Tennant Thelma R; Banerjee Mekhala; Allan James M; Le Beau Michelle M; Larson Richard A; Graubert Timothy A; Cox Nancy J; Onel Kenan
Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility.
Blood 2009;113(22):5575-82.
2008: Wong Jasmine C; Le Beau Michelle M; Shannon Kevin
Tumor suppressor gene inactivation in myeloid malignancies.
Best practice & research. Clinical haematology 2008;21(4):601-14.
2008: Li Zejuan; Lu Jun; Sun Miao; Mi Shuangli; Zhang Hao; Luo Roger T; Chen Ping; Wang Yungui; Yan Ming; Qian Zhijian; Neilly Mary Beth; Jin Jie; Zhang Yanming; Bohlander Stefan K; Zhang Dong-Er; Larson Richard A; Le Beau Michelle M; Thirman Michael J; Golub Todd R; Rowley Janet D; Chen Jianjun
Distinct microRNA expression profiles in acute myeloid leukemia with common translocations.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(40):15535-40.
2008: Qian Zhijian; Chen Lina; Fernald Anthony A; Williams Bart O; Le Beau Michelle M
A critical role for Apc in hematopoietic stem and progenitor cell survival.
The Journal of experimental medicine 2008;205(9):2163-75.
2008: Ellis Nathan A; Huo Dezheng; Yildiz Ozlem; Worrillow Lisa J; Banerjee Mekhala; Le Beau Michelle M; Larson Richard A; Allan James M; Onel Kenan
MDM2 SNP309 and TP53 Arg72Pro interact to alter therapy-related acute myeloid leukemia susceptibility.
Blood 2008;112(3):741-9.
2008: Mullighan Charles G; Miller Christopher B; Radtke Ina; Phillips Letha A; Dalton James; Ma Jing; White Deborah; Hughes Timothy P; Le Beau Michelle M; Pui Ching-Hon; Relling Mary V; Shurtleff Sheila A; Downing James R
BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros.
Nature 2008;453(7191):110-4.
2008: Shannon Kevin M; Le Beau Michelle M
Cancer: hay in a haystack.
Nature 2008;451(7176):252-3.
2008: Kirsammer Gina; Jilani Sarah; Liu Hui; Davis Elizabeth; Gurbuxani Sandeep; Le Beau Michelle M; Crispino John D
Highly penetrant myeloproliferative disease in the Ts65Dn mouse model of Down syndrome.
Blood 2008;111(2):767-75.
2007: Mi Shuangli; Lu Jun; Sun Miao; Li Zejuan; Zhang Hao; Neilly Mary Beth; Wang Yungui; Qian Zhijian; Jin Jie; Zhang Yanming; Bohlander Stefan K; Le Beau Michelle M; Larson Richard A; Golub Todd R; Rowley Janet D; Chen Jianjun
MicroRNA expression signatures accurately discriminate acute lymphoblastic leukemia from acute myeloid leukemia.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(50):19971-6.
2007: Lucas Isabelle; Palakodeti Aparna; Jiang Yanwen; Young David J; Jiang Nan; Fernald Anthony A; Le Beau Michelle M
High-throughput mapping of origins of replication in human cells.
EMBO reports 2007;8(8):770-7.
2007: Ostler K R; Davis E M; Payne S L; Gosalia B B; Expósito-Céspedes J; Le Beau M M; Godley L A
Cancer cells express aberrant DNMT3B transcripts encoding truncated proteins.
Oncogene 2007;26(38):5553-63.
2007: Joslin John M; Fernald Anthony A; Tennant Thelma R; Davis Elizabeth M; Kogan Scott C; Anastasi John; Crispino John D; Le Beau Michelle M
Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders.
Blood 2007;110(2):719-26.
2007: Boyapati Anita; Yan Ming; Peterson Luke F; Biggs Joseph R; Le Beau Michelle M; Zhang Dong-Er
A leukemia fusion protein attenuates the spindle checkpoint and promotes aneuploidy.
Blood 2007;109(9):3963-71.
2007: Olney Harold J; Le Beau Michelle M
Evaluation of recurring cytogenetic abnormalities in the treatment of myelodysplastic syndromes.
Leukemia research 2007;31(4):427-34.
2007: Markus Jan; Garin Matthew T; Bies Juraj; Galili Naomi; Raza Azra; Thirman Michael J; Le Beau Michelle M; Rowley Janet D; Liu P Paul; Wolff Linda
Methylation-independent silencing of the tumor suppressor INK4b (p15) by CBFbeta-SMMHC in acute myelogenous leukemia with inv(16).
Cancer research 2007;67(3):992-1000.
2007: Singh Zeba N; Huo Dezheng; Anastasi John; Smith Sonali M; Karrison Theodore; Le Beau Michelle M; Larson Richard A; Vardiman James W
Therapy-related myelodysplastic syndrome: morphologic subclassification may not be clinically relevant.
American journal of clinical pathology 2007;127(2):197-205.
2007: Lones Mark A; Heerema Nyla A; Le Beau Michelle M; Sposto Richard; Perkins Sherrie L; Kadin Marshall E; Kjeldsberg Carl R; Meadows Anna; Siegel Stuart; Buckley Jonathan; Abromowitch Minnie; Kersey John; Bergeron Sharon; Cairo Mitchell S; Sanger Warren G
Chromosome abnormalities in advanced stage lymphoblastic lymphoma of children and adolescents: a report from CCG-E08.
Cancer genetics and cytogenetics 2007;172(1):1-11.
2006: Lones Mark A; Heerema Nyla A; Le Beau Michelle M; Perkins Sherrie L; Kadin Marshall E; Kjeldsberg Carl R; Sposto Richard; Meadows Anna; Siegel Stuart; Buckley Jonathan; Finlay Jonathan; Abromowitch Minnie; Cairo Mitchell S; Sanger Warren G
Complex secondary chromosome abnormalities in advanced stage anaplastic large cell lymphoma of children and adolescents: a report from CCG-E08.
Cancer genetics and cytogenetics 2006;171(2):89-96.
2006: Stephens Karen; Weaver Molly; Leppig Kathleen A; Maruyama Kyoko; Emanuel Peter D; Le Beau Michelle M; Shannon Kevin M
Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies.
Blood 2006;108(5):1684-9.
2006: Chan Iris T; Kutok Jeffery L; Williams Ifor R; Cohen Sarah; Moore Sandra; Shigematsu Hirokazu; Ley Timothy J; Akashi Koichi; Le Beau Michelle M; Gilliland D Gary
Oncogenic K-ras cooperates with PML-RAR alpha to induce an acute promyelocytic leukemia-like disease.
Blood 2006;108(5):1708-15.
2006: Djokic Miroslav; Le Beau Michelle M; Swinnen Lode J; Smith Sonali M; Rubin Charles M; Anastasi John; Carlson Katrin M
Post-transplant lymphoproliferative disorder subtypes correlate with different recurring chromosomal abnormalities.
Genes, chromosomes & cancer 2006;45(3):313-8.
2006: Sternsdorf Thomas; Phan Vernon T; Maunakea Mei Lin; Ocampo Corinne B; Sohal Jastinder; Silletto Angela; Galimi Francesco; Le Beau Michelle M; Evans Ronald M; Kogan Scott C
Forced retinoic acid receptor alpha homodimers prime mice for APL-like leukemia.
Cancer cell 2006;9(2):81-94.
2006: Kuo Ya-Huei; Landrette Sean F; Heilman Susan A; Perrat Paola N; Garrett Lisa; Liu Pu P; Le Beau Michelle M; Kogan Scott C; Castilla Lucio H
Cbf beta-SMMHC induces distinct abnormal myeloid progenitors able to develop acute myeloid leukemia.
Cancer cell 2006;9(1):57-68.
2005: Luo Hui; Li Qing; O'Neal Julie; Kreisel Friederike; Le Beau Michelle M; Tomasson Michael H
c-Myc rapidly induces acute myeloid leukemia in mice without evidence of lymphoma-associated antiapoptotic mutations.
Blood 2005;106(7):2452-61.
2005: Larson Richard A; Le Beau Michelle M
Therapy-related myeloid leukaemia: a model for leukemogenesis in humans.
Chemico-biological interactions 2005;153-154():187-95.
2005: Curtiss Nicole P; Bonifas Jeannette M; Lauchle Jennifer O; Balkman Jason D; Kratz Christian P; Emerling Brooke M; Green Eric D; Le Beau Michelle M; Shannon Kevin M
Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22.
Genomics 2005;85(5):600-7.
2005: Kebriaei P; Kline J; Stock W; Kasza K; Le Beau M M; Larson R A; van Besien K
Impact of disease burden at time of allogeneic stem cell transplantation in adults with acute myeloid leukemia and myelodysplastic syndromes.
Bone marrow transplantation 2005;35(10):965-70.
2005: Li Xiaxin; Le Beau Michelle M; Ciccone Samantha; Yang Feng-Chun; Freie Brian; Chen Shi; Yuan Jin; Hong Ping; Orazi Attilio; Haneline Laura S; Clapp D Wade
Ex vivo culture of Fancc-/- stem/progenitor cells predisposes cells to undergo apoptosis, and surviving stem/progenitor cells display cytogenetic abnormalities and an increased risk of malignancy.
Blood 2005;105(9):3465-71.
2005: Fischbach Neal A; Rozenfeld Sofia; Shen Weifang; Fong Stephen; Chrobak Daniel; Ginzinger David; Kogan Scott C; Radhakrishnan Archana; Le Beau Michelle M; Largman Corey; Lawrence H Jeffrey
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 2005;105(4):1456-66.
2004: Farag Sherif S; Ruppert Amy S; Mrózek Krzysztof; Carroll Andrew J; Pettenati Mark J; Le Beau Michelle M; Peterson Bercedis L; Powell Bayard L; Ozer Howard; Silver Richard T; Larson Richard A; Bloomfield Clara D;
Prognostic significance of additional cytogenetic abnormalities in newly diagnosed patients with Philadelphia chromosome-positive chronic myelogenous leukemia treated with interferon-alpha: a Cancer and Leukemia Group B study.
International journal of oncology 2004;25(1):143-51.
2004: Rosenbauer Frank; Wagner Katharina; Kutok Jeffery L; Iwasaki Hiromi; Le Beau Michelle M; Okuno Yutaka; Akashi Koichi; Fiering Steven; Tenen Daniel G
Acute myeloid leukemia induced by graded reduction of a lineage-specific transcription factor, PU.1.
Nature genetics 2004;36(6):624-30.
2004: Le Doan T; Kong Namie; Zhu Yuan; Lauchle Jennifer O; Aiyigari Abigail; Braun Benjamin S; Wang Endi; Kogan Scott C; Le Beau Michelle M; Parada Luis; Shannon Kevin M
Somatic inactivation of Nf1 in hematopoietic cells results in a progressive myeloproliferative disorder.
Blood 2004;103(11):4243-50.
2004: Kebriaei Partow; Winter Jane N; Laport Ginna G; Le Beau Michelle M; Dewald Gordon; Larson Richard A
Multiple unrelated clonal abnormalities in host bone marrow cells after allogeneic stem cell transplantation.
Leukemia research 2004;28(5):537-40.
2004: Lones Mark A; Sanger Warren G; Le Beau Michelle M; Heerema Nyla A; Sposto Richard; Perkins Sherrie L; Buckley Jonathan; Kadin Marshall E; Kjeldsberg Carl R; Meadows Anna; Siegel Stuart; Finlay Jonathan; Bergeron Sharon; Cairo Mitchell S;
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 : official journal of the American Society of Pediatric Hematology/Oncology 2004;26(3):169-78.
2004: Side Lucy E; Curtiss Nicole P; Teel Kathryn; Kratz Christian; Wang Pauline W; Larson Richard A; Le Beau Michelle M; Shannon Kevin M
RAS, FLT3, and TP53 mutations in therapy-related myeloid malignancies with abnormalities of chromosomes 5 and 7.
Genes, chromosomes & cancer 2004;39(3):217-23.
2004: Loh Mignon L; Vattikuti Shashaank; Schubbert Suzanne; Reynolds Melissa G; Carlson Elaine; Lieuw Kenneth H; Cheng Jennifer W; Lee Connie M; Stokoe David; Bonifas Jeannette M; Curtiss Nicole P; Gotlib Jason; Meshinchi Soheil; Le Beau Michelle M; Emanuel Peter D; Shannon Kevin M
Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis.
Blood 2004;103(6):2325-31.
2004: Braun Benjamin S; Tuveson David A; Kong Namie; Le Doan T; Kogan Scott C; Rozmus Jacob; Le Beau Michelle M; Jacks Tyler E; Shannon Kevin M
Somatic activation of oncogenic Kras in hematopoietic cells initiates a rapidly fatal myeloproliferative disorder.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(2):597-602.
2004: Palakodeti Aparna; Han Yu; Jiang Yanwen; Le Beau Michelle M
The role of late/slow replication of the FRA16D in common fragile site induction.
Genes, chromosomes & cancer 2004;39(1):71-6.
2003: Ranger Ann M; Zha Jiping; Harada Hisashi; Datta Sandeep Robert; Danial Nika N; Gilmore Andrew P; Kutok Jeffery L; Le Beau Michelle M; Greenberg Michael E; Korsmeyer Stanley J
Bad-deficient mice develop diffuse large B cell lymphoma.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(16):9324-9.
2003: Le Beau Michelle M; Davis Elizabeth M; Patel Bhumi; Phan Vernon T; Sohal Jastinder; Kogan Scott C
Recurring chromosomal abnormalities in leukemia in PML-RARA transgenic mice identify cooperating events and genetic pathways to acute promyelocytic leukemia.
Blood 2003;102(3):1072-4.
2003: Phan Vernon T; Shultz David B; Truong Bao-Tran H; Blake Timothy J; Brown Anna L; Gonda Thomas J; Le Beau Michelle M; Kogan Scott C
Cooperation of cytokine signaling with chimeric transcription factors in leukemogenesis: PML-retinoic acid receptor alpha blocks growth factor-mediated differentiation.
Molecular and cellular biology 2003;23(13):4573-85.
2003: Lensch M William; Tischkowitz Marc; Christianson Tracy A; Reifsteck Carol A; Speckhart S Ashley; Jakobs Petra M; O'Dwyer Michael E; Olson Susan B; Le Beau Michelle M; Hodgson Shirley V; Mathew Christopher G; Larson Richard A; Bagby Grover C
Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia.
Blood 2003;102(1):7-16.
2003: Smith Sonali M; Le Beau Michelle M; Huo Dezheng; Karrison Theodore; Sobecks Ronald M; Anastasi John; Vardiman James W; Rowley Janet D; Larson Richard A
Clinical-cytogenetic associations in 306 patients with therapy-related myelodysplasia and myeloid leukemia: the University of Chicago series.
Blood 2003;102(1):43-52.
2003: Sohal Jastinder; Phan Vernon T; Chan Philip V; Davis Elizabeth M; Patel Bhumi; Kelly Louise M; Abrams Tinya J; O'Farrell Anne Marie; Gilliland D Gary; Le Beau Michelle M; Kogan Scott C
A model of APL with FLT3 mutation is responsive to retinoic acid and a receptor tyrosine kinase inhibitor, SU11657.
Blood 2003;101(8):3188-97.
2003: Fair Keri; Le Beau Michelle M
Characterization of translocations in human cancer.
Methods in molecular biology (Clifton, N.J.) 2003;222():327-37.
2002: Qian Zhijian; Fernald Anthony A; Godley Lucy A; Larson Richard A; Le Beau Michelle M
Expression profiling of CD34+ hematopoietic stem/ progenitor cells reveals distinct subtypes of therapy-related acute myeloid leukemia.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(23):14925-30.
2002: Gozzetti Alessandro; Davis Elizabeth M; Espinosa Rafael; Fernald Anthony A; Anastasi John; Le Beau Michelle M
Identification of novel cryptic translocations involving IGH in B-cell non-Hodgkin's lymphomas.
Cancer research 2002;62(19):5523-7.
2002: Bender Carla F; Sikes Michael L; Sullivan Ruth; Huye Leslie Erskine; Le Beau Michelle M; Roth David B; Mirzoeva Olga K; Oltz Eugene M; Petrini John H J
Cancer predisposition and hematopoietic failure in Rad50(S/S) mice.
Genes & development 2002;16(17):2237-51.
2002: Wechsler Joshua; Greene Marianne; McDevitt Michael A; Anastasi John; Karp Judith E; Le Beau Michelle M; Crispino John D
Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome.
Nature genetics 2002;32(1):148-52.
2002: Emerling Brooke M; Bonifas Jeannette; Kratz Christian P; Donovan Shane; Taylor Brigit R; Green Eric D; Le Beau Michelle M; Shannon Kevin M
MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia.
Oncogene 2002;21(31):4849-54.
2002: Corbin Shantel; Neilly Mary E; Espinosa Rafael; Davis Elizabeth M; McKeithan Timothy W; Le Beau Michelle M
Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.
Cancer research 2002;62(12):3477-84.
2002: Sato Yuko; Izumi Tohru; Kanamori Hirakazu; Davis Elizabeth M; Miura Yasusada; Larson Richard A; Le Beau Michelle M; Ozawa Keiya; Rowley Janet D
t(1;3)(p36;p21) is a recurring therapy-related translocation.
Genes, chromosomes & cancer 2002;34(2):186-92.
2002: Abe Mark K; Saelzler Matthew P; Espinosa Rafael; Kahle Kristopher T; Hershenson Marc B; Le Beau Michelle M; Rosner Marsha Rich
ERK8, a new member of the mitogen-activated protein kinase family.
The Journal of biological chemistry 2002;277(19):16733-43.
2002: Kosak Steven T; Skok Jane A; Medina Kay L; Riblet Roy; Le Beau Michelle M; Fisher Amanda G; Singh Harinder
Subnuclear compartmentalization of immunoglobulin loci during lymphocyte development.
Science (New York, N.Y.) 2002;296(5565):158-62.
2002: Le Beau Michelle M; Bitts Sheila; Davis Elizabeth M; Kogan Scott C
Recurring chromosomal abnormalities in leukemia in PML-RARA transgenic mice parallel human acute promyelocytic leukemia.
Blood 2002;99(8):2985-91.
2002: Zhang Yanming; Strissel Pamela; Strick Reiner; Chen Jianjun; Nucifora Giuseppina; Le Beau Michelle M; Larson Richard A; Rowley Janet D
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 2002;99(5):3070-5.
2002: Kratz Christian P; Emerling Brooke M; Bonifas Jeannette; Wang Winfred; Green Eric D; Le Beau Michelle M; Shannon Kevin M
Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor.
Blood 2002;99(1):372-4.
2001: Kratz C P; Emerling B M; Donovan S; Laig-Webster M; Taylor B R; Thompson P; Jensen S; Banerjee A; Bonifas J; Makalowski W; Green E D; Le Beau M M; Shannon K M
Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies.
Genomics 2001;77(3):171-80.
2001: Olney H J; Le Beau M M
The cytogenetics of myelodysplastic syndromes.
Best practice & research. Clinical haematology 2001;14(3):479-95.
2001: Sanchez-Izquierdo D; Siebert R; Harder L; Marugan I; Gozzetti A; Price H P; Gesk S; Hernandez-Rivas J M; Benet I; Solé F; Sonoki T; Le Beau M M; Schlegelberger B; Dyer M J; Garcia-Conde J; Martinez-Climent J A
Detection of translocations affecting the BCL6 locus in B cell non-Hodgkin's lymphoma by interphase fluorescence in situ hybridization.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(9):1475-84.
2001: Sato Y; Kobayashi H; Suto Y; Olney H J; Davis E M; Super H G; Espinosa R; Le Beau M M; Rowley J D
Chromosomal instability in chromosome band 12p13: multiple breaks leading to complex rearrangements including cytogenetically undetectable sub-clones.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(8):1193-202.
2001: Lai F; Godley L A; Joslin J; Fernald A A; Liu J; Espinosa R; Zhao N; Pamintuan L; Till B G; Larson R A; Qian Z; Le Beau M M
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 2001;71(2):235-45.
2001: Stoffel A; Le Beau M M
The API2/MALT1 fusion product may lead to germinal center B cell lymphomas by suppression of apoptosis.
Human heredity 2001;51(1-2):1-7.
2000: Lai F; Godley L A; Fernald A A; Orelli B J; Pamintuan L; Zhao N; Le Beau M M
cDNA cloning and genomic structure of three genes localized to human chromosome band 5q31 encoding potential nuclear proteins.
Genomics 2000;70(1):123-30.
2000: Gozzetti A; Le Beau M M
Fluorescence in situ hybridization: uses and limitations.
Seminars in hematology 2000;37(4):320-33.
2000: Wang P W; Eisenbart J D; Espinosa R; Davis E M; Larson R A; Le Beau M M
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 2000;67(1):28-39.
2000: Lai F; Orelli B J; Till B G; Godley L A; Fernald A A; Pamintuan L; Le Beau M M
Molecular characterization of KLHL3, a human homologue of the Drosophila kelch gene.
Genomics 2000;66(1):65-75.
2000: Lai F; Fernald A A; Zhao N; Le Beau M M
cDNA cloning, expression pattern, genomic structure and chromosomal location of RAB6KIFL, a human kinesin-like gene.
Gene 2000;248(1-2):117-25.
2000: Carlson K M; Vignon C; Bohlander S; Martinez-Climent J A; Le Beau M M; Rowley J D
Identification and molecular characterization of CALM/AF10fusion products in T cell acute lymphoblastic leukemia and acute myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(1):100-4.
2000: Korthäuer U; Nagel W; Davis E M; Le Beau M M; Menon R S; Mitchell E O; Kozak C A; Kolanus W; Bluestone J A
Anergic T lymphocytes selectively express an integrin regulatory protein of the cytohesin family.
Journal of immunology (Baltimore, Md. : 1950) 2000;164(1):308-18.
1999: Godley L A; Lai F; Liu J; Zhao N; Le Beau M M
TTID: A novel gene at 5q31 encoding a protein with titin-like features.
Genomics 1999;60(2):226-33.
1999: Wang P W; Eisenbart J D; Cordes S P; Barsh G S; Stoffel M; Le Beau M M
Human KRML (MAFB): cDNA cloning, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias.
Genomics 1999;59(3):275-81.
1999: Larson R A; Wang Y; Banerjee M; Wiemels J; Hartford C; Le Beau M M; Smith M T
Prevalence of the inactivating 609C-->T polymorphism in the NAD(P)H:quinone oxidoreductase (NQO1) gene in patients with primary and therapy-related myeloid leukemia.
Blood 1999;94(2):803-7.
1999: Sobecks R M; Le Beau M M; Anastasi J; Williams S F
Myelodysplasia and acute leukemia following high-dose chemotherapy and autologous bone marrow or peripheral blood stem cell transplantation.
Bone marrow transplantation 1999;23(11):1161-5.
1999: Wetzler M; Dodge R K; Mrózek K; Carroll A J; Tantravahi R; Block A W; Pettenati M J; Le Beau M M; Frankel S R; Stewart C C; Szatrowski T P; Schiffer C A; Larson R A; Bloomfield C D
Prospective karyotype analysis in adult acute lymphoblastic leukemia: the cancer and leukemia Group B experience.
Blood 1999;93(11):3983-93.
1999: Mahgoub N; Taylor B R; Le Beau M M; Gratiot M; Carlson K M; Atwater S K; Jacks T; Shannon K M
Myeloid malignancies induced by alkylating agents in Nf1 mice.
Blood 1999;93(11):3617-23.
1999: Stoffel A; Rao P H; Louie D C; Krauter K; Liebowitz D N; Koeppen H; Le Beau M M; Chaganti R S
Chromosome 18 breakpoint in t(11;18)(q21;q21) translocation associated with MALT lymphoma is proximal to BCL2 and distal to DCC.
Genes, chromosomes & cancer 1999;24(2):156-9.
1998: Zhao N; Lai F; Fernald A A; Eisenbart J D; Espinosa R; Wang P W; Le Beau M M
Human CDC23: cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias.
Genomics 1998;53(2):184-90.
1998: Roulston D; Espinosa R; Nucifora G; Larson R A; Le Beau M M; Rowley J D
CBFA2(AML1) translocations with novel partner chromosomes in myeloid leukemias: association with prior therapy.
Blood 1998;92(8):2879-85.
1998: Chen M; She H; Davis E M; Spicer C M; Kim L; Ren R; Le Beau M M; Li W
Identification of Nck family genes, chromosomal localization, expression, and signaling specificity.
The Journal of biological chemistry 1998;273(39):25171-8.
1998: Ong S T; Le Beau M M
Chromosomal abnormalities and molecular genetics of non-Hodgkin's lymphoma.
Seminars in oncology 1998;25(4):447-60.
1998: Luu H H; Zagaja G P; Dubauskas Z; Chen S L; Smith R C; Watabe K; Ichikawa Y; Ichikawa T; Davis E M; Le Beau M M; Rinker-Schaeffer C W
Identification of a novel metastasis-suppressor region on human chromosome 12.
Cancer research 1998;58(16):3561-5.
1998: Furuta H; Horikawa Y; Iwasaki N; Hara M; Sussel L; Le Beau M M; Davis E M; Ogata M; Iwamoto Y; German M S; Bell G I
Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese.
Diabetes 1998;47(8):1356-8.
1998: Allen R J; Smith S D; Moldwin R L; Lu M M; Giordano L; Vignon C; Suto Y; Harden A; Tomek R; Veldman T; Ried T; Larson R A; Le Beau M M; Rowley J D; Zeleznik-Le N
Establishment and characterization of a megakaryoblast cell line with amplification of MLL.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1998;12(7):1119-27.
1998: Carney J P; Maser R S; Olivares H; Davis E M; Le Beau M; Yates J R; Hays L; Morgan W F; Petrini J H
The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response.
Cell 1998;93(3):477-86.
1998: Le Beau M M; Drabkin H; Glover T W; Gemmill R; Rassool F V; McKeithan T W; Smith D I
An FHIT tumor suppressor gene?
Genes, chromosomes & cancer 1998;21(4):281-9.
1998: Le Beau M M; Rassool F V; Neilly M E; Espinosa R; Glover T W; Smith D I; McKeithan T W
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 1998;7(4):755-61.
1998: Wang P W; Iannantuoni K; Davis E M; Espinosa R; Stoffel M; Le Beau M M
Refinement of the commonly deleted segment in myeloid leukemias with a del(20q).
Genes, chromosomes & cancer 1998;21(2):75-81.
1997: Sato Y; Bohlander S K; Kobayashi H; Reshmi S; Suto Y; Davis E M; Espinosa R; Hoopes R; Montgomery K T; Kucherlapati R S; Le Beau M M; Rowley J D
Heterogeneity in the breakpoints in balanced rearrangements involving band 12p13 in hematologic malignancies identified by fluorescence in situ hybridization: TEL (ETV6 ) is involved in only one half.
Blood 1997;90(12):4886-93.
1997: Wang P; Spielberger R T; Thangavelu M; Zhao N; Davis E M; Iannantuoni K; Larson R A; Le Beau M M
dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53.
Genes, chromosomes & cancer 1997;20(3):282-91.
1997: Ong S T; Fong K M; Bader S A; Minna J D; Le Beau M M; McKeithan T W; Rassool F V
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 1997;20(1):16-23.
1997: Sato Y; Bohlander S K; Kobayashi H; Suto Y; Davis E M; Espinosa R; Le Beau M M; Rowley J D
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 1997;97(2):157-60.
1997: Zhao N; Stoffel A; Wang P W; Eisenbart J D; Espinosa R; Larson R A; Le Beau M M
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 1997;94(13):6948-53.
1997: Levi-Setti R; Chabala J M; Gavrilov K; Espinosa R; Le Beau M M
Imaging of BrdU-labeled human metaphase chromosomes with a high resolution scanning ion microprobe.
Microscopy research and technique 1997;36(4):301-12.
1997: Stock W; Westbrook C A; Peterson B; Arthur D C; Szatrowski T P; Silver R T; Sher D A; Wu D; Le Beau M M; Schiffer C A; Bloomfield C D
Value of molecular monitoring during the treatment of chronic myeloid leukemia: a Cancer and Leukemia Group B study.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 1997;15(1):26-36.
1997: Espinosa R; Le Beau M M
Gene mapping by FISH.
Methods in molecular biology (Clifton, N.J.) 1997;68():53-76.
1996: Yamagata K; Oda N; Kaisaki P J; Menzel S; Furuta H; Vaxillaire M; Southam L; Cox R D; Lathrop G M; Boriraj V V; Chen X; Cox N J; Oda Y; Yano H; Le Beau M M; Yamada S; Nishigori H; Takeda J; Fajans S S; Hattersley A T; Iwasaki N; Hansen T; Pedersen O; Polonsky K S; Bell G I
Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)
Nature 1996;384(6608):455-8.
1996: Chutkow W A; Simon M C; Le Beau M M; Burant C F
Cloning, tissue expression, and chromosomal localization of SUR2, the putative drug-binding subunit of cardiac, skeletal muscle, and vascular KATP channels.
Diabetes 1996;45(10):1439-45.
1996: Le Beau M M; Espinosa R; Davis E M; Eisenbart J D; Larson R A; Green E D
Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases.
Blood 1996;88(6):1930-5.
1996: Furuta H; Nishi S; Le Beau M M; Fernald A A; Yano H; Bell G I
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 1996;36(1):206-9.
1996: Rassool F V; Le Beau M M; Shen M L; Neilly M E; Espinosa R; Ong S T; Boldog F; Drabkin H; McCarroll R; McKeithan T W
Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.
Genomics 1996;35(1):109-17.
1996: Levi-Setti R; Chabala J M; Gavrilov K; Espinosa R; Le Beau M M
Advances in high resolution SIMS studies of BrdU-labelled human metaphase chromosomes.
Cellular and molecular biology (Noisy-le-Grand, France) 1996;42(3):301-24.
1996: Anastasi J; Feng J; Dickstein J I; Le Beau M M; Rubin C M; Larson R A; Rowley J D; Vardiman J W
Lineage involvement by BCR/ABL in Ph+ lymphoblastic leukemias: chronic myelogenous leukemia presenting in lymphoid blast vs Ph+ acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(5):795-802.
1996: Stoffel M; Le Beau M M; Espinosa R; Bohlander S F; Le Paslier D; Cohen D; Xiang K S; Cox N J; Fajans S S; Bell G I
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 1996;93(9):3937-41.
1996: Olopade O I; Roulston D; Baker T; Narvid S; Le Beau M M; Freireich E J; Larson R A; Golomb H M
Familial myeloid leukemia associated with loss of the long arm of chromosome 5.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(4):669-74.
1995: Martinez-Climent J A; Espinosa R; Thirman M J; Le Beau M M; Rowley J D
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 : official journal of the American Society of Pediatric Hematology/Oncology 1995;17(4):277-83.
1995: Takeda J; Espinosa R; Eng S; Le Beau M M; Bell G I
Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library.
Genomics 1995;29(1):276-81.
1995: Dreyling M H; Bohlander S K; Le Beau M M; Olopade O I
Refined mapping of genomic rearrangements involving the short arm of chromosome 9 in acute lymphoblastic leukemias and other hematologic malignancies.
Blood 1995;86(5):1931-8.
1995: Dreyling M H; Kobayashi H; Olopade O I; Le Beau M M; Rowley J D; Bohlander S K
Detection of 9p deletions in leukemia cell lines by interphase fluorescence in situ hybridization with YAC-derived probes.
Cancer genetics and cytogenetics 1995;83(1):46-55.
1995: Martinez-Climent J A; Thirman M J; Espinosa R; Le Beau M M; Rowley J D
Detection of 11q23/MLL rearrangements in infant leukemias with fluorescence in situ hybridization and molecular analysis.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(8):1299-304.
1995: Sato Y; Suto Y; Pietenpol J; Golub T R; Gilliland D G; Davis E M; Le Beau M M; Roberts J M; Vogelstein B; Rowley J D
TEL and KIP1 define the smallest region of deletions on 12p13 in hematopoietic malignancies.
Blood 1995;86(4):1525-33.
1995: Stoffel M; Fernald A A; Le Beau M M; Bell G I
Assignment of the gastric inhibitory polypeptide receptor gene (GIPR) to chromosome bands 19q13.2-q13.3 by fluorescence in situ hybridization.
Genomics 1995;28(3):607-9.
1995: Olopade O I; Pomykala H M; Hagos F; Sveen L W; Espinosa R; Dreyling M H; Gursky S; Stadler W M; Le Beau M M; Bohlander S K
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 1995;92(14):6489-93.
1995: Stoffel M; Stein R; Wright C V; Espinosa R; Le Beau M M; Bell G I
Localization of human homeodomain transcription factor insulin promoter factor 1 (IPF1) to chromosome band 13q12.1.
Genomics 1995;28(1):125-6.
1995: el-Maghrabi M R; Lange A J; Jiang W; Yamagata K; Stoffel M; Takeda J; Fernald A A; Le Beau M M; Bell G I; 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 1995;27(3):520-5.
1995: Tsaur M L; Menzel S; Lai F P; Espinosa R; Concannon P; Spielman R S; Hanis C L; Cox N J; Le Beau M M; German M S
Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM.
Diabetes 1995;44(5):592-6.
1995: Anastasi J; Feng J; Le Beau M M; Larson R A; Rowley J D; Vardiman J W
The relationship between secondary chromosomal abnormalities and blast transformation in chronic myelogenous leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(4):628-33.
1995: Takeda J; Fernald A A; Yamagata K; Le Beau M M; Bell G I
Localization of human somatostatin receptor 5 gene (SSTR5) to chromosome band 16p13.3 by fluorescence in situ hybridization.
Genomics 1995;26(3):638-9.
1995: Joventino L P; Stock W; Lane N J; Daly K M; Mick R; Le Beau M M; Larson R A
Certain HLA antigens are associated with specific morphologic and cytogenetic subsets of acute myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(3):433-9.
1995: Le Beau M M; Song C; Davis E M; Hiipakka R A; Kokontis J M; Liao S
Assignment of the human ubiquitous receptor gene (UNR) to 19q13.3 using fluorescence in situ hybridization.
Genomics 1995;26(1):166-8.
1995: Martinez-Climent J A; Lane N J; Rubin C M; Morgan E; Johnstone H S; Mick R; Murphy S B; Vardiman J W; Larson R A; Le Beau M M
Clinical and prognostic significance of chromosomal abnormalities in childhood acute myeloid leukemia de novo.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(1):95-101.
1995: Rassool F V; Neilly M E; McGuire K L; McKeithan T W; Le Beau M M
Localization of the Chinese hamster MHC locus to chromosome 1q17-->q18 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1995;71(1):62-3.
1995: Jones E M; Fernald A; Bell G I; Le Beau M M
Assignment of SLC6A9 to human chromosome band 1p33 by in situ hybridization.
Cytogenetics and cell genetics 1995;71(3):211.
1994: Kobayashi H; Montgomery K T; Bohlander S K; Adra C N; Lim B L; Kucherlapati R S; Donis-Keller H; Holt M S; Le Beau M M; Rowley J D
Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.
Blood 1994;84(10):3473-82.
1994: Espinosa R; Funahashi T; Hadjiagapiou C; Le Beau M M; Davidson N O
Assignment of the gene encoding the human apolipoprotein B mRNA editing enzyme (APOBEC1) to chromosome 12p13.1.
Genomics 1994;24(2):414-5.
1994: German M S; Wang J; Fernald A A; Espinosa R; Le Beau M M; Bell G I
Localization of the genes encoding two transcription factors, LMX1 and CDX3, regulating insulin gene expression to human chromosomes 1 and 13.
Genomics 1994;24(2):403-4.
1994: Stoffel M; Espinosa R; Trabb J B; Le Beau M M; Bell G I
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 1994;23(3):697-9.
1994: Downie P A; Vogelzang N J; Moldwin R L; Le Beau M M; Anastasi J; Allen R J; Myers S E; Larson R A; Smith S D
Establishment of a leukemia cell line with i(12p) from a patient with a mediastinal germ cell tumor and acute lymphoblastic leukemia.
Cancer research 1994;54(18):4999-5004.
1994: Jones E M; Menzel S; Espinosa R; Le Beau M M; Bell G I; 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 1994;23(2):490-1.
1994: Yano H; Philipson L H; Kugler J L; Tokuyama Y; Davis E M; Le Beau M M; Nelson D J; Bell G I; Takeda J
Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA.
Molecular pharmacology 1994;45(5):854-60.
1994: Stoffel M; Espinosa R; Powell K L; Philipson L H; Le Beau M M; Bell G I
Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.
Genomics 1994;21(1):254-6.
1994: Menzel S; Stoffel M; Espinosa R; Fernald A A; Le Beau M M; Bell G I
Localization of the glucagon receptor gene to human chromosome band 17q25.
Genomics 1994;20(2):327-8.
1994: Yasuda K; Espinosa R; Takeda J; Le Beau M M; Bell G I
Localization of the kappa opioid receptor gene to human chromosome band 8q11.2.
Genomics 1994;19(3):596-7.
1994: Bohlander S K; Espinosa R; Fernald A A; Rowley J D; Le Beau M M; Díaz M O
Sequence-independent amplification and labeling of yeast artificial chromosomes for fluorescence in situ hybridization.
Cytogenetics and cell genetics 1994;65(1-2):108-10.
1994: Le Beau M M; Carver L A; Espinosa R; Schmidt J V; Bradfield C A
Chromosomal localization of the human AHR locus encoding the structural gene for the Ah receptor to 7p21-->p15.
Cytogenetics and cell genetics 1994;66(3):172-6.
1994: Westbrook C A; Le Beau M M; Neuman W L; Keinanen M; Yamaoka L H; Speer M C; Espinosa R; Nakamura Y; Williamson R; Mullan M
Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain.
Cytogenetics and cell genetics 1994;67(2):86-93.
1993: Lehto M; Xiang K; Stoffel M; Espinosa R; Groop L C; Le Beau M M; Bell G I
Human hexokinase II: localization of the polymorphic gene to chromosome 2.
Diabetologia 1993;36(12):1299-302.
1993: Super H J; McCabe N R; Thirman M J; Larson R A; Le Beau M M; Pedersen-Bjergaard J; Philip P; Diaz M O; Rowley J D
Rearrangements of the MLL gene in therapy-related acute myeloid leukemia in patients previously treated with agents targeting DNA-topoisomerase II.
Blood 1993;82(12):3705-11.
1993: Roulston D; Espinosa R; Stoffel M; Bell G I; Le Beau M M
Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.
Blood 1993;82(11):3424-9.
1993: Kobayashi H; Espinosa R; Fernald A A; Begy C; Diaz M O; Le Beau M M; Rowley J D
Analysis of deletions of the long arm of chromosome 11 in hematologic malignancies with fluorescence in situ hybridization.
Genes, chromosomes & cancer 1993;8(4):246-52.
1993: Yasuda K; Espinosa R; Davis E M; Le Beau M M; Bell G I
Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2.
Genomics 1993;17(3):785-6.
1993: Stoffel M; Espinosa R; Le Beau M M; Bell G I
Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6.
Diabetes 1993;42(8):1215-8.
1993: Kobayashi H; Espinosa R; Thirman M J; Fernald A A; Shannon K; Diaz M O; Le Beau M M; Rowley J D
Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization.
Genes, chromosomes & cancer 1993;7(4):204-8.
1993: Lorenzana A N; McCabe N R; Goodell W R; Zhang L Q; Miley D; Le Beau M M; Goldman S; Smith S D
Characterization of a CD34+ cell line established from a child with large cell cutaneous lymphoma.
Cancer 1993;72(3):931-7.
1993: Kobayashi H; Espinosa R; Thirman M J; Gill H J; Fernald A A; Diaz M O; Le Beau M M; Rowley J D
Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization.
Blood 1993;82(2):547-51.
1993: Le Beau M M; Espinosa R; Neuman W L; Stock W; Roulston D; Larson R A; Keinanen M; Westbrook C A
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 1993;90(12):5484-8.
1993: Baron B W; Nucifora G; McCabe N; Espinosa R; Le Beau M M; McKeithan T W
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 1993;90(11):5262-6.
1993: Kobayashi H; Espinosa R; Thirman M J; Davis E M; Diaz M O; Le Beau M M; Rowley J D
Variability of 11q23 rearrangements in hematopoietic cell lines identified with fluorescence in situ hybridization.
Blood 1993;81(11):3027-33.
1993: Sanford J P; Sait S N; Pan L; Nowak N J; Gill H J; Le Beau M M; Diaz M O; Zabel B; Shows T B
Characterization of two 11q23.3-11q24 deletions and mapping of associated anonymous DNA markers.
Genes, chromosomes & cancer 1993;7(2):67-73.
1993: Stoffel M; Espinosa R; Keller S R; Lienhard G E; Le Beau M M; Bell G I
Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism.
Diabetologia 1993;36(4):335-7.
1993: Spielberger R T; Dickstein J I; Le Beau M M; Larson R A; Daly K M; Vardiman J W; Golomb H M
Acute myeloid leukaemia following interferon-alfa treatment of hairy cell leukaemia.
British journal of haematology 1993;83(3):519-20.
1993: Anastasi J; Feng J; Le Beau M M; Larson R A; Rowley J D; Vardiman J W
Cytogenetic clonality in myelodysplastic syndromes studied with fluorescence in situ hybridization: lineage, response to growth factor therapy, and clone expansion.
Blood 1993;81(6):1580-5.
1993: Lehto M; Stoffel M; Groop L; Espinosa R; Le Beau M M; Bell G I
Assignment of the gene encoding glycogen synthase (GYS) to human chromosome 19, band q13.3.
Genomics 1993;15(2):460-1.
1993: Yamada Y; Stoffel M; Espinosa R; Xiang K S; Seino M; Seino S; Le Beau M M; Bell G I
Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms.
Genomics 1993;15(2):449-52.
1993: Stoffel M; Xiang K S; Espinosa R; Cox N J; Le Beau M M; Bell G I
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 1993;2(1):1-4.
1993: Le Beau M M; Overhauser J; Straub R E; Silverman G; Gilliam T C; Ott J; O'Connell P; Francke U; Geurts van Kessel A
Report of the first international workshop on human chromosome 18 mapping.
Cytogenetics and cell genetics 1993;63(2):78-96.
1993: Neuman W L; Westbrook C A; Dixon M; Espinosa R; Patel Y D; Nakamura Y; Weiffenbach B; Le Beau M M
Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1993;62(4):207-10.
1992: Olopade O I; Thangavelu M; Larson R A; Mick R; Kowal-Vern A; Schumacher H R; Le Beau M M; Vardiman J W; Rowley J D
Clinical, morphologic, and cytogenetic characteristics of 26 patients with acute erythroblastic leukemia.
Blood 1992;80(11):2873-82.
1992: Gradishar W J; Le Beau M M; O'Laughlin R; Vardiman J W; Larson R A
Clinical and cytogenetic responses to granulocyte-macrophage colony-stimulating factor in therapy-related myelodysplasia.
Blood 1992;80(10):2463-70.
1992: White D M; Mikol D D; Espinosa R; Weimer B; Le Beau M M; Stefansson K
Structure and chromosomal localization of the human gene for a brain form of prostaglandin D2 synthase.
The Journal of biological chemistry 1992;267(32):23202-8.
1992: Le Beau M M; Ito C; Cogswell P; Espinosa R; Fernald A A; Baldwin A S
Chromosomal localization of the genes encoding the p50/p105 subunits of NF-kappa B (NFKB2) and the I kappa B/MAD-3 (NFKBI) inhibitor of NF-kappa B to 4q24 and 14q13, respectively.
Genomics 1992;14(2):529-31.
1992: Olopade O I; Bohlander S K; Pomykala H; Maltepe E; Van Melle E; Le Beau M M; Diaz M O
Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia.
Genomics 1992;14(2):437-43.
1992: Thangavelu M; Snyder L; Anastasi J; Le Beau M M; Kirven M; Picchio G; Mosier D E; Rowley J D
Cytogenetic characterization of B-cell lymphomas from severe combined immunodeficiency disease mice given injections of lymphocytes from Epstein-Barr virus-positive donors.
Cancer research 1992;52(17):4678-81.
1992: Bohlander S K; Espinosa R; Le Beau M M; Rowley J D; Díaz M O
A method for the rapid sequence-independent amplification of microdissected chromosomal material.
Genomics 1992;13(4):1322-4.
1992: Seino S; Yamada Y; Espinosa R; Le Beau M M; Bell G I
Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3.
Genomics 1992;13(4):1375-7.
1992: Onodera N; McCabe N R; Nachman J B; Johnson F L; Le Beau M M; Rowley J D; Rubin C M
Hyperdiploidy arising from near-haploidy in childhood acute lymphoblastic leukemia.
Genes, chromosomes & cancer 1992;4(4):331-6.
1992: Rassool F V; Le Beau M M; Neilly M E; van Melle E; Espinosa R; McKeithan T W
Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA.
American journal of human genetics 1992;50(6):1243-51.
1992: Anastasi J; Le Beau M M; Vardiman J W; Fernald A A; Larson R A; Rowley J D
Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescence in situ hybridization to interphase cells: a simple and sensitive method.
Blood 1992;79(7):1796-801.
1992: Wagner A J; Le Beau M M; Diaz M O; Hay N
Expression, regulation, and chromosomal localization of the Max gene.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(7):3111-5.
1992: Neuman W L; Rubin C M; Rios R B; Larson R A; Le Beau M M; Rowley J D; Vardiman J W; Schwartz J L; Farber R A
Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders.
Blood 1992;79(6):1501-10.
1992: Park J K; Le Beau M M; Shows T B; Rowley J D; Diaz M O
A complex genetic rearrangement in a t(10;14)(q24;q11) associated with T-cell acute lymphoblastic leukemia.
Genes, chromosomes & cancer 1992;4(1):32-40.
1992: Thangavelu M; Neuman W L; Espinosa R; Nakamura Y; Westbrook C A; Le Beau M M
A physical and genetic linkage map of the distal long arm of human chromosome 5.
Cytogenetics and cell genetics 1992;59(1):27-30.
1992: Stock W; Chandrasekharappa S C; Neuman W L; Le Beau M M; Brownstein B H; Westbrook C A
Characterization of yeast artificial chromosomes containing interleukin genes on human chromosome 5.
Cytogenetics and cell genetics 1992;61(4):263-5.
1992: Le Beau M M
Deletions of chromosome 5 in malignant myeloid disorders.
Cancer surveys 1992;15():143-59.
1992: Yeldandi A V; Patel Y D; Liao M; Kao F T; Rao M S; Reddy J K; Le Beau M M
Localization of the human urate oxidase gene (UOX) to 1p22.
Cytogenetics and cell genetics 1992;61(2):121-2.
1992: Neuman W L; Le Beau M M; Farber R A; Lindgren V; Westbrook C A
Somatic cell hybrid mapping of human chromosome band 5q31: a region important to hematopoiesis.
Cytogenetics and cell genetics 1992;61(2):103-6.
1991: Rubin C M; Le Beau M M; Mick R; Bitter M A; Nachman J; Rudinsky R; Appel H J; Morgan E; Suarez C R; Schumacher H R
Impact of chromosomal translocations on prognosis in childhood acute lymphoblastic leukemia.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 1991;9(12):2183-92.
1991: Burnett R C; David J C; Harden A M; Le Beau M M; Rowley J D; Diaz M O
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 1991;3(6):461-7.
1991: O'Bryan J P; Frye R A; Cogswell P C; Neubauer A; Kitch B; Prokop C; Espinosa R; Le Beau M M; Earp H S; Liu E T
axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinase.
Molecular and cellular biology 1991;11(10):5016-31.
1991: Westbrook C A; Neuman W L; Hewitt J; Kidd K K; Le Beau M M; Williamson R
Report of the chromosome 5 workshop.
Genomics 1991;10(4):1105-9.
1991: Rassool F V; McKeithan T W; Neilly M E; van Melle E; Espinosa R; Le Beau M M
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 1991;88(15):6657-61.
1991: Anastasi J; Vardiman J W; Rudinsky R; Patel M; Nachman J; Rubin C M; Le Beau M 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 1991;77(11):2456-62.
1991: Patwardhan S; Gashler A; Siegel M G; Chang L C; Joseph L J; Shows T B; Le Beau M M; Sukhatme V P
EGR3, a novel member of the Egr family of genes encoding immediate-early transcription factors.
Oncogene 1991;6(6):917-28.
1991: Li Y S; Le Beau M M; Mick R; Rowley J D
The proportion of abnormal karyotypes in acute leukemia samples related to method of preparation.
Cancer genetics and cytogenetics 1991;52(1):93-100.
1991: Anastasi J; Thangavelu M; Vardiman J W; Hooberman A L; Bian M L; Larson R A; Le Beau M M
Interphase cytogenetic analysis detects minimal residual disease in a case of acute lymphoblastic leukemia and resolves the question of origin of relapse after allogeneic bone marrow transplantation.
Blood 1991;77(5):1087-91.
1991: Larson R A; Lukin C L; Daly K M; Mick R; Gore S; Le Beau M M
Circulating immune complexes correlate with remission duration in acute myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(2):131-7.
1991: Lorenzana A N; Rubin C M; Le Beau M M; Nachman J; Connolly P; Subramanian U; Johnson F L; McKeithan T W
Immunoglobulin gene rearrangements in acute lymphoblastic leukemia with the 9;11 translocation.
Genes, chromosomes & cancer 1991;3(1):74-7.
1991: Rubin C M; Le Beau M M
Cytogenetic abnormalities in childhood acute lymphoblastic leukemia.
The American journal of pediatric hematology/oncology 1991;13(2):202-16.
1991: Espinosa R; Lemons R S; Perlman R K; Kuo W L; Rosner M R; Le Beau M M
Localization of the gene encoding insulin-degrading enzyme to human chromosome 10, bands q23----q25.
Cytogenetics and cell genetics 1991;57(4):184-6.
1991: Rosenberg M; Fuchs E; Le Beau M M; Eddy R L; Shows T B
Three epidermal and one simple epithelial type II keratin genes map to human chromosome 12.
Cytogenetics and cell genetics 1991;57(1):33-8.
1990: Mikol D D; Alexakos M J; Bayley C A; Lemons R S; Le Beau M M; Stefansson K
Structure and chromosomal localization of the gene for the oligodendrocyte-myelin glycoprotein.
The Journal of cell biology 1990;111(6 Pt 1):2673-9.
1990: Rubin C M; Larson R A; Anastasi J; Winter J N; Thangavelu M; Vardiman J W; Rowley J D; Le Beau M M
t(3;21)(q26;q22): a recurring chromosomal abnormality in therapy-related myelodysplastic syndrome and acute myeloid leukemia.
Blood 1990;76(12):2594-8.
1990: Becker M A; Heidler S A; Bell G I; Seino S; Le Beau M M; Westbrook C A; Neuman W; Shapiro L J; Mohandas T K; Roessler B J
Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes.
Genomics 1990;8(3):555-61.
1990: Thangavelu M; Olopade O; Beckman E; Vardiman J W; Larson R A; McKeithan T W; Le Beau M M; Rowley J D
Clinical, morphologic, and cytogenetic characteristics of patients with lymphoid malignancies characterized by both t(14;18)(q32;q21) and t(8;14)(q24;q32) or t(8;22)(q24;q11).
Genes, chromosomes & cancer 1990;2(2):147-58.
1990: Bitter M A; Franklin W A; Larson R A; McKeithan T W; Rubin C M; Le Beau M M; Stephens J K; Vardiman J W
Morphology in Ki-1(CD30)-positive non-Hodgkin's lymphoma is correlated with clinical features and the presence of a unique chromosomal abnormality, t(2;5)(p23;q35).
The American journal of surgical pathology 1990;14(4):305-16.
1990: Gulcher J R; Alexakos M J; Le Beau M M; Lemons R S; Stefansson K
Chromosomal localization of the human hexabrachion (tenascin) gene and evidence for recent reduplication within the gene.
Genomics 1990;6(4):616-22.
1990: Le Beau M M
Chromosomal abnormalities in non-Hodgkin's lymphomas.
Seminars in oncology 1990;17(1):20-9.
1990: Chandrasekharappa S C; Rebelsky M S; Firak T A; Le Beau M M; Westbrook C A
A long-range restriction map of the interleukin-4 and interleukin-5 linkage group on chromosome 5.
Genomics 1990;6(1):94-9.
1990: Anastasi J; Le Beau M M; Vardiman J W; Westbrook C A
Detection of numerical chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe.
The American journal of pathology 1990;136(1):131-9.
1990: Diaz M O; Rubin C M; Harden A; Ziemin S; Larson R A; Le Beau M M; Rowley J D
Deletions of interferon genes in acute lymphoblastic leukemia.
The New England journal of medicine 1990;322(2):77-82.
1990: Le Beau M M
Cytogenetic and molecular analysis of the deletions of chromosome 5 in myeloid disorders.
Progress in clinical and biological research 1990;352():277-85.
1990: Le Beau M M
Chromosomal abnormalities in hematologic malignant diseases.
Progress in clinical and biological research 1990;340B():325-35.
1989: Le Beau M M; Bitter M A; Larson R A; Doane L A; Ellis E D; Franklin W A; Rubin C M; Kadin M E; Vardiman J W
The t(2;5)(p23;q35): a recurring chromosomal abnormality in Ki-1-positive anaplastic large cell lymphoma.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(12):866-70.
1989: Espinosa R; Sadler J E; Le Beau M M
Regional localization of the human thrombomodulin gene to 20p12-cen.
Genomics 1989;5(3):649-50.
1989: Park J K; McKeithan T W; Le Beau M M; Bitter M A; Franklin W A; Rowley J D; Diaz M O
An (8;14)(q24;q11) translocation involving the T-cell receptor alpha-chain gene and the MYC oncogene 3' region in a B-cell lymphoma.
Genes, chromosomes & cancer 1989;1(1):15-22.
1989: Thangavelu M; Le Beau M M
Chromosomal abnormalities in Hodgkin's disease.
Hematology/oncology clinics of North America 1989;3(2):221-36.
1989: Hooberman A L; Carrino J J; Leibowitz D; Rowley J D; Le Beau M M; Arlin Z A; Westbrook C A
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 1989;86(11):4259-63.
1989: Olopade O L; Anastasi J; Thangavelu M; Le Beau M M; Golomb H M
Cytogenetic abnormalities in a secondary lymphoma complicating cardiac transplantation.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(4):303-4.
1989: Schwartz J L; Karrison T; Le Beau M M; Larson R A; Sagher D; Strauss B; Rowley J D; Weichselbaum R R
Chromosomal sensitivity of lymphocytes from individuals with therapy-related acute nonlymphocytic leukemia.
Mutation research 1989;216(2):119-26.
1989: Le Beau M M; Lemons R S; Espinosa R; Larson R A; Arai N; Rowley J D
Interleukin-4 and interleukin-5 map to human chromosome 5 in a region encoding growth factors and receptors and are deleted in myeloid leukemias with a del(5q).
Blood 1989;73(3):647-50.
1989: Thangavelu M; Bitter M A; Larson R A; Davis E M; Rowley J D; Le Beau M M
Der(5)t(5;7)(q11.2;p11.2): a new recurring abnormality in malignant myeloid disorders.
Cancer genetics and cytogenetics 1989;37(1):1-8.
1989: Rowley J D; Le Beau M M
Cytogenetic and molecular analysis of therapy-related leukemia.
Annals of the New York Academy of Sciences 1989;567():130-40.
1988: Li Y S; Anastasi J; Larson R A; Le Beau M M; Vardiman J W; Rowley J D
A recurring chromosome rearrangement, dic(16;22), in acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1988;35(2):143-50.
1988: Larson R A; Wernli M; Le Beau M M; Daly K M; Pape L H; Rowley J D; Vardiman J W
Short remission durations in therapy-related leukemia despite cytogenetic complete responses to high-dose cytarabine.
Blood 1988;72(4):1333-9.
1988: Joseph L J; Le Beau M M; Jamieson G A; Acharya S; Shows T B; Rowley J D; Sukhatme V P
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 1988;85(19):7164-8.
1988: Anastasi J; Pettenati M J; Le Beau M M; Kwaan H C; Weil S C
Acute lymphoblastic leukemia in a patient with longstanding polycythemia vera: cytogenetic analysis reveals two distinct abnormal clones.
American journal of hematology 1988;29(1):33-7.
1988: Diaz M O; Ziemin S; Le Beau M M; Pitha P; Smith S D; Chilcote R R; Rowley J D
Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell lines.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(14):5259-63.
1988: Shepard K V; Larson R; Le Beau M M; Leichman L; Levin B
Acute leukemia occurring after radiotherapy and chemotherapy with a nitrosourea, PCNU.
Investigational new drugs 1988;6(2):121-4.
1988: Weil S C; Rosner G L; Reid M S; Chisholm R L; Lemons R S; Swanson M S; Carrino J J; Diaz M O; Le Beau M M
Translocation and rearrangement of myeloperoxidase gene in acute promyelocytic leukemia.
Science (New York, N.Y.) 1988;240(4853):790-2.
1988: Westbrook C A; Rubin C M; Carrino J J; Le Beau M M; Bernards A; Rowley J D
Long-range mapping of the Philadelphia chromosome by pulsed-field gel electrophoresis.
Blood 1988;71(3):697-702.
1988: Le Beau M M
Chromosomal fragile sites and cancer-specific breakpoints--a moderating viewpoint.
Cancer genetics and cytogenetics 1988;31(1):55-61.
1988: Farber R A; Phalen T; Neuman W L; Le Beau M M; Wasmuth J J; 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 1988;16(5):2360.
1988: Samuels B L; Larson R A; Le Beau M M; Daly K M; Bitter M A; Vardiman J W; Barker C M; Rowley J D; Golomb H M
Specific chromosomal abnormalities in acute nonlymphocytic leukemia correlate with drug susceptibility in vivo.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(2):79-83.
1988: Rosenberg M; RayChaudhury A; Shows T B; Le Beau M M; Fuchs E
A group of type I keratin genes on human chromosome 17: characterization and expression.
Molecular and cellular biology 1988;8(2):722-36.
1988: Harris B N; Davis E M; Le Beau M M; Bitter M A; Kaminer L S; Morgan E; Rowley J D
Variant translocations (9;11): identification of the critical genetic rearrangement.
Cancer genetics and cytogenetics 1988;30(1):171-5.
1987: Le Beau M M; Lemons R S; Carrino J J; Pettenati M J; Souza L M; Diaz M O; Rowley J D
Chromosomal localization of the human G-CSF gene to 17q11 proximal to the breakpoint of the t(15;17) in acute promyelocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1987;1(12):795-9.
1987: Rubin C M; Larson R A; Bitter M A; Carrino J J; Le Beau M M; Diaz M O; Rowley J D
Association of a chromosomal 3;21 translocation with the blast phase of chronic myelogenous leukemia.
Blood 1987;70(5):1338-42.
1987: Ratain M J; Kaminer L S; Bitran J D; Larson R A; Le Beau M M; Skosey C; Purl S; Hoffman P C; Wade J; Vardiman J W
Acute nonlymphocytic leukemia following etoposide and cisplatin combination chemotherapy for advanced non-small-cell carcinoma of the lung.
Blood 1987;70(5):1412-7.
1987: Bitter M A; Nachman J; Jones N; Franklin W A; Le Beau M M; Vardiman J W
Nonlymphoblastic T-cell lymphoma in children.
Cancer 1987;59(12):2099-103.
1987: Pettenati M J; Le Beau M M; Lemons R S; Shima E A; Kawasaki E S; Larson R A; Sherr C J; Diaz M O; Rowley J D
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 1987;84(9):2970-4.
1987: Westbrook C A; Rubin C M; Le Beau M M; Kaminer L S; Smith S D; Rowley J D; Diaz M O
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 1987;84(1):251-5.
1986: Le Beau M M; McKeithan T W; Shima E A; Goldman-Leikin R E; Chan S J; Bell G I; Rowley J D; Diaz M O
T-cell receptor alpha-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 1986;83(24):9744-8.
1986: McKeithan T W; Shima E A; Le Beau M M; Minowada J; Rowley J D; Diaz M O
Molecular cloning of the breakpoint junction of a human chromosomal 8;14 translocation involving the T-cell receptor alpha-chain gene and sequences on the 3' side of MYC.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(17):6636-40.
1986: Shima E A; Le Beau M M; McKeithan T W; Minowada J; Showe L C; Mak T W; Minden M D; Rowley J D; Diaz M O
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 1986;83(10):3439-43.
1986: Le Beau M M; Pettenati M J; Lemons R S; Diaz M O; Westbrook C A; Larson R A; Sherr C J; Rowley J D
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 1986;51 Pt 2():899-909.

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