Roland Berger
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Roland Berger's Degrees
- PhD Molecular Biology University of California, Berkeley
- Doctorate Medicine Stanford University
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(Suggest an Edit or Addition)Roland Berger's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera (2005) (2656)
- All-trans retinoic acid as a differentiation therapy for acute promyelocytic leukemia. I. Clinical results. (1990) (1257)
- NB4, a maturation inducible cell line with t(15;17) marker isolated from a human acute promyelocytic leukemia (M3). (1991) (924)
- A TEL-JAK2 fusion protein with constitutive kinase activity in human leukemia. (1997) (837)
- A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. (2005) (718)
- The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. (1995) (570)
- NB 4 , a Maturation Inducible Cell Line With t ( 15 ; 17 ) Marker Isolated From a Human Acute Promyelocytic Leukemia ( M 3 ) (507)
- High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. (1995) (461)
- Structure, localization and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute promyelocytic leukemia (APL): structural similarities with a new family of oncoproteins. (1992) (444)
- Identification of BTG2, an antiproliferative p53–dependent component of the DNA damage cellular response pathway (1996) (418)
- The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia. (2005) (377)
- Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party. Groupe Français de Cytogénétique Hématologique, Groupe de Français d'Hematologie Cellulaire, UK Cancer Cytogenetics Group and BIOMED 1 European Community-Concerted Action "Mole (2000) (333)
- Chromosomal abnormalities identify high-risk and low-risk patients with acute lymphoblastic leukemia. (1986) (293)
- A unique clonal JAK 2 mutation leading to constitutive signalling causes polycythaemia (2005) (269)
- Correlation between immunoglobulin light chain expression and variant translocation in Burkitt's lymphoma (1982) (260)
- A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia (2001) (259)
- The signal transducer and activator of transcription STAT5b gene is a new partner of retinoic acid receptor alpha in acute promyelocytic-like leukaemia. (1999) (259)
- Essential thrombocythemias. Clinical evolutionary and biological data (1986) (244)
- Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites. (1984) (242)
- t( 12;21): A new recurrent translocation in acute lymphoblastic leukemia (1994) (239)
- AF6q21, a novel partner of the MLL gene in t(6;11)(q21;q23), defines a forkhead transcriptional factor subfamily. (1997) (228)
- Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia (2001) (228)
- Molecular basis of IIq23 rearrangements in hematopoietic malignant proliferations (1995) (227)
- Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia. (1993) (226)
- P53 gene mutations in acute myeloid leukemia with 17p monosomy. (1991) (208)
- Identification of driver and passenger mutations of FLT3 by high-throughput DNA sequence analysis and functional assessment of candidate alleles. (2007) (203)
- The BCMA gene, preferentially expressed during B lymphoid maturation, is bidirectionally transcribed. (1994) (197)
- A novel class of zinc finger/leucine zipper genes identified from the molecular cloning of the t(10;11) translocation in acute leukemia. (1995) (189)
- The clinical significance of karyotype in acute myelogenous leukemia. (1989) (181)
- Chromosomal localization of the human proto-oncogene c-ets (1984) (181)
- Cytogenetic studies on 519 consecutive de novo acute nonlymphocytic leukemias. (1987) (169)
- Fusion of Huntingtin Interacting Protein 1 to Platelet-Derived Growth Factor β Receptor (PDGFβR) in Chronic Myelomonocytic Leukemia With t(5;7)(q33;q11.2) (1998) (163)
- Subacute and chronic myelomonocytic leukemia in children (juvenile CML). Clinical and hematologic observations, and identification of prognostic factors (1984) (159)
- A new gene, BCM, on chromosome 16 is fused to the interleukin 2 gene by a t(4;16)(q26;p13) translocation in a malignant T cell lymphoma. (1992) (153)
- Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells. (2000) (149)
- Treatment of first relapse in acute promyelocytic leukaemia with all-trans retinoic acid (1990) (146)
- The characterization of murine BCMA gene defines it as a new member of the tumor necrosis factor receptor superfamily. (1998) (146)
- Cytogenetic studies on African Burkitt's lymphoma cell lines: t(8;14), t(2;8) and t(8;22) translocations. (1981) (145)
- Immortalization of human adult normal prostatic epithelial cells by liposomes containing large T-SV40 gene. (1991) (145)
- Long-term survival in acute myelogenous leukemia: a second follow-up of the Fourth International Workshop on Chromosomes in Leukemia. (1994) (141)
- Leucine-zipper dimerization motif encoded by the AF17 gene fused to ALL-1 (MLL) in acute leukemia. (1994) (140)
- Bone Marrow Transplantation in Fanconi Anaemia (1980) (139)
- Novel activating JAK2 mutation in a patient with Down syndrome and B-cell precursor acute lymphoblastic leukemia. (2007) (138)
- Mutations in the p53 gene in myelodysplastic syndromes. (1991) (135)
- HOX11L2 expression defines a clinical subtype of pediatric T-ALL associated with poor prognosis. (2002) (135)
- A new type of p16INK4/MTS1 gene transcript expressed in B-cell malignancies. (1995) (134)
- Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogénétique Hématologique (GFCH). (2002) (134)
- The t(10;11) translocation in acute myeloid leukemia (M5) consistently fuses the leucine zipper motif of AF10 onto the HRX gene. (1995) (130)
- Chromosomal abnormalities and their clinical significance in acute lymphoblastic leukemia. Third International Workshop on Chromosomes in Leukemia. (1983) (130)
- Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5' part of the tal-1 gene. (1991) (129)
- Mutations of the P53 gene in acute myeloid leukaemia (1992) (129)
- RETINOIC ACID THERAPY FOR PROMYELOCYTIC LEUKAEMIA (1989) (128)
- Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T‐cell leukemias (1990) (125)
- A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q23. (1995) (123)
- The TEL gene products: nuclear phosphoproteins with DNA binding properties (1997) (121)
- NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique (2006) (117)
- Localization of the human luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chromosome 2p21. (1990) (115)
- Long‐term survival of patients with acute myeloid leukemia (1997) (111)
- A novel gene, AF-1p, fused to HRX in t(1;11)(p32;q23), is not related to AF-4, AF-9 nor ENL. (1994) (110)
- Acute monocytic leukemia chromosome studies. (1982) (109)
- Simultaneous localization of cosmids and chromosome R-banding by fluorescence microscopy: application to regional mapping of human chromosome 11. (1990) (108)
- Cytogenetic studies on acute monocytic leukemia. (1980) (106)
- t(8;14) Translocation in a Burkitt's Type of Lymphoblastic Leukaemia (L3) (1979) (101)
- Cloning of a new member of the insulin gene superfamily (INSL4) expressed in human placenta. (1995) (100)
- In Vitro Effect of Cyclophosphamide Metabolites on Chromosomes of Fanconi Anaemia Patients (1980) (100)
- High-throughput sequence analysis of the tyrosine kinome in acute myeloid leukemia. (2007) (99)
- Cytogenetic studies on Burkitt's lymphoma-leukemia. (1982) (99)
- Therapy-related acute promyelocytic leukemia: a report on 16 cases. (1992) (98)
- Cytogenetic Studies in Acute Promyelocytic Leukemia: A Survey of Secondary Chromosomal Abnormalities (1991) (98)
- Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21). (1996) (97)
- Fusion of Huntingtin interacting protein 1 to platelet-derived growth factor beta receptor (PDGFbetaR) in chronic myelomonocytic leukemia with t(5;7)(q33;q11.2). (1998) (96)
- Prognostic significance of chromosomal abnormalities in acute nonlymphocytic leukemia: a study of 343 patients. (1987) (95)
- A retinoid acid 'resistant' t(15;17) acute promyelocytic leukemia cell line: isolation, morphological, immunological, and molecular features. (1992) (93)
- Isolation of chromosome 21–specific yeast artificial chromosomes from a total human genome library (1992) (93)
- The t(1;12)(q21;p13) translocation of human acute myeloblastic leukemia results in a TEL-ARNT fusion. (2000) (92)
- The chromosomal localization of the human follicle-stimulating hormone receptor gene (FSHR) on 2p21-p16 is similar to that of the luteinizing hormone receptor gene. (1993) (92)
- Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites. (1985) (90)
- Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphoma. (1996) (90)
- t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH) (2003) (89)
- Evi-1 expression in leukemic patients with rearrangements of the 3q25-q28 chromosomal region. (1992) (89)
- Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia. (1992) (89)
- Detection of minimal residual disease in acute myelomonocytic leukemia with abnormal marrow eosinophils by nested polymerase chain reaction with allele specific amplification. (1994) (80)
- t(15;17) in a promyelocytic form of chronic myeloid leukemia blastic crisis. (1983) (80)
- Phenotype of early erythroblastic leukemias. (1986) (80)
- The t(6;11)(q27;q23) translocation in acute leukemia: a laboratory and clinical study of 30 cases (1998) (79)
- Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia. (2006) (77)
- Philadelphia chromosome positive blood B lymphocytes in chronic myelocytic leukemia. (1981) (76)
- Assignment of the human thyroid stimulating hormone receptor (TSHR) gene to chromosome 14q31. (1990) (75)
- Acute lymphoblastic leukemia and chromosome 21. (1997) (73)
- M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: a report of 59 cases by the Groupe Français d'Hématologie Cellulaire (GFHC) and the Groupe Français de Cytogénétique Hématologique (GFCH). (2003) (73)
- Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases. (1992) (71)
- Cytogenetic studies of 103 patients with acute myelogenous leukemia in relapse. (1989) (70)
- Cytologic characterization and significance of normal karyotypes in t(8;21) acute myeloblastic leukemia (1982) (70)
- Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia (2001) (69)
- The t(10;11)(p12;q23) translocation in acute leukaemia: a cytogenetic and clinical study of 20 patients (1998) (68)
- [Acute promyelocytic leukemia: retrospective study of 119 patients treated with daunorubicin]. (1984) (68)
- Ph1+bcr- acute leukemias: implication of Alu sequences in a chromosomal translocation occurring in the new cluster region within the BCR gene. (1989) (66)
- Various types of rearrangements target TLX3 locus in T‐cell acute lymphoblastic leukemia (2004) (63)
- Chromosome studies in polycythemia vera patients. (1984) (63)
- The JAK 2 V 617 F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia , but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia (2005) (62)
- Philadelphia-positive acute leukemia: lineage promiscuity and inconsistently rearranged breakpoint cluster region. (1988) (62)
- Recurrence of OTT–MAL fusion in t(1;22) of infant AML‐M7 (2002) (62)
- Localization of the human progesterone receptor gene to chromosome 11q22–q23 (1987) (60)
- A third tal-1 promoter is specifically used in human T cell leukemias (1992) (58)
- Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia (2003) (58)
- Trisomy 4: an entity within acute nonlymphocytic leukemia. (1987) (57)
- A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY (1992) (57)
- Cytological types of mitoses and chromosome abnormalities in acute leukemia. (1983) (57)
- Breakpoint clusters of the PML gene in acute promyelocytic leukemia: Primary structure of the reciprocal products of the PML‐RARA gene in a patient with t(15;17) (1993) (56)
- Structural alterations of the BCR and ABL genes in Ph1 positive acute leukemias with rearrangements in the BCR gene first intron: further evidence implicating Alu sequences in the chromosome translocation. (1989) (54)
- Abnormalities of the short arm of chromosome 12 in acute nonlymphocytic leukemia and dysmyelopoietic syndrome. (1986) (54)
- HOX11L2/TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32). (2006) (54)
- Interphase cytogenetics by fluorescent in situ hybridization (FISH) for characterization of monosomy-7-associated myeloid disorders. (1993) (54)
- Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders: rearrangements of DNA satellite II and new recurrent translocations (1999) (53)
- Molecular rearrangements of the MYL gene in acute promyelocytic leukemia (APL, M3) define a breakpoint cluster region as well as some molecular variants. (1992) (53)
- The most frequent t(14;19)(q32;q13)-positive B-cell malignancy corresponds to an aggressive subgroup of atypical chronic lymphocytic leukemia (2008) (53)
- Nitrogen mustard-induced chromosome breakage: A tool for Fanconi's anemia diagnosis (1980) (52)
- Characterization of in vitro culture of HIV-negative Kaposi’s sarcoma-derived cells. In vitro responses to alfa interferon (1997) (50)
- Unique balanced chromosome abnormalities in treatment‐related myelodysplastic syndromes and acute myeloid leukemia: Report from an International Workshop † (2002) (48)
- Leukemia : Official Journal of the Leukemia Society of America, Leukemia Research Fund, U.K (2008) (48)
- Chromosomal abnormalities identify high-risk and low-risk patients with acute lymphoblastic leukemia (1986) (46)
- Fanconi anemia. Chromosome breakage and cell cycle studies. (1993) (46)
- Translocation t(5;12)(q31‐q33;p12‐p13): a non‐random translocation associated with a myeloid disorder with eosinophilia (1994) (46)
- Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12. (1991) (45)
- Infrequent mutations in the P53 gene in primary human T-cell acute lymphoblastic leukemia. (1991) (45)
- Analysis of TEL proteins in human leukemias (1998) (43)
- Establishment of a human T-cell hybrid line with suppressive activity (1981) (43)
- Role of granulocyte‐macrophage colony‐stimulating factor, Interleukin‐3 and Interleukin‐5 in the eosinophilia associated with T cell lymphoma (1993) (42)
- C-banding studies in various blood disorders (1979) (42)
- Molecular cloning of a DNA fragment from human chromosome 14(14q11) involved in T‐cell malignancies. (1985) (42)
- Philadelphia-positive acute leukemia. Cytogenetic and molecular aspects. (1990) (42)
- The TEL-Jak2 oncoprotein induces Socs1 expression and altered cytokine response in Ba/F3 cells (2001) (42)
- Transforming potential of the T‐cell acute lymphoblastic leukemia‐associated homeobox genes HOXA13, TLX1, and TLX3 (2006) (41)
- Molecular mechanisms of a t(8;14)(q24;q11) translocation juxtaposing c-myc and TcR-alpha genes in a T-cell leukaemia: involvement of a V alpha internal heptamer. (1988) (41)
- BCL2 gene activation and protein expression in follicular lymphoma: a report on 64 cases. (1993) (41)
- Chromosomal localization of the human D3 dopamine receptor gene (1991) (41)
- In situ hybridization to interphase nuclei in acute leukemia (1993) (41)
- Chromosome abnormalities in bone marrow of Fanconi anemia patients. (1993) (41)
- Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRβ-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique Hématologique (2007) (40)
- Y chromosome loss in leukemias (1979) (40)
- Differences between blastic chronic myeloid leukemia and Ph-positive acute leukemia. (1993) (39)
- C-banding studies in acute nonlymphocytic leukemia. (1982) (39)
- Cytogenetic studies on acute nonlymphocytic leukemias following polycythemia vera. (1984) (39)
- Cytogenetics of T-cell malignant lymphoma. Report of 17 cases and review of the chromosomal breakpoints. (1988) (37)
- Characterization of a novel ETS gene, TELB, encoding a protein structurally and functionally related to TEL (2000) (37)
- Cytogenetic study of 75 erythroleukemias. (2005) (37)
- Faconi anemia and bone marrow clonal chromosome abnormalities. (1996) (37)
- Direct hybridization of sorted human chromosomes: localization of the Y chromosome on the flow karyotype. (1983) (36)
- Molecular cloning of a 5' segment of the genomic phl gene defines a new breakpoint cluster region (bcr2) in Philadelphia-positive acute leukemias. (1988) (36)
- Cytologic characterization and significance of normal karyotypes in t(8;21) acute myeloblastic leukemia. (1982) (36)
- Somatic segregation and Fanconi anemia (1977) (36)
- Monosomy-7 in childhood hemopoietic disorders. (1990) (36)
- C-band heteromorphism in breast cancer patients. (1985) (36)
- Cytogenetic study of 130 childhood acute nonlymphocytic leukemias. (1990) (35)
- Loss of the NPM1 gene in myeloid disorders with chromosome 5 rearrangements (2006) (35)
- Secondary acute myeloblastic leukemia with t(16;21) (q24;q22). involving the AML1 gene. (1996) (35)
- Partial duplication of HRX in acute leukemia with trisomy 11. (1995) (34)
- Inactivation of the P16INK4/MTS1 gene by a chromosome translocation t(9;14)(p21-22;q11) in an acute lymphoblastic leukemia of B-cell type. (1996) (34)
- Centric and pericentric chromosome rearrangements in hematopoietic malignancies (1999) (34)
- A t(8;14)(q24;q11) translocation in a T‐cell leukemia (L1‐all) with c‐myc and TcR‐alpha chain locus rearrangements (1986) (33)
- Localization of the chromosome 15 breakpoints and expression of multiple PML-RAR alpha transcripts in acute promyelocytic leukemia: a study of 28 Chinese patients. (1993) (33)
- MLL-AF1q fusion resulting from t(1;11) in acute leukemia (1999) (33)
- Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias. (1994) (33)
- NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance (2005) (33)
- Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique Hématologique. (2006) (33)
- Hunting 11q23 deletions with fluorescence in situ hybridization (FISH). (1994) (33)
- Chromosome mapping of the human RAS-related RAP1A, RAP1B, and RAP2 genes to chromosomes 1p12----p13, 12q14, and 13q34, respectively. (1990) (32)
- Variant translocation in a non endemic case of Burkitt's lymphoma: t (8;22) in an Epstein--Barr virus negative tumour and in a derived cell line. (1981) (32)
- Molecular analysis of a t(9;14)(p11;q32) translocation occurring in a case of human alpha heavy chain disease. (1989) (32)
- Cytogenetics of Burkitt's lymphoma-leukaemia: a review. (1985) (32)
- Secondary nonrandom chromosomal abnormalities of band 13q34 in burkitt lymphoma‐leukemia (1989) (32)
- Cytogenetic studies of Burkitt lymphoma-leukemia in patients with acquired immunodeficiency syndrome. (1988) (31)
- Malignant lymphomas with band 8q24 chromosome abnormality: a morphologic continuum extending from Burkitt's to immunoblastic lymphoma (1984) (31)
- Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia (1995) (31)
- Cytogenetic studies of 44 T-cell acute lymphoblastic leukemias. (1990) (31)
- Genomic organization of the human ERM (ETV5) gene, a PEA3 group member of ETS transcription factors. (1996) (30)
- Jumping translocations. (2007) (30)
- AML1-MTG16 fusion gene in therapy-related acute leukemia with t(16;21)(q24;q22); two new cases (2000) (30)
- Leukaemic non‐Hodgkin's lymphomas with hyperdiploid cells and t(ll;14)(ql3;q32): a subtype of mantle cell lymphoma? (1995) (30)
- A cluster of expressed zinc finger protein genes in the pericentromeric region of human chromosome 10. (1992) (30)
- Chromosome studies in plasma cell leukemia and multiple myeloma in transformation (1992) (30)
- Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation. (1991) (30)
- Effects of granulocyte-macrophage colony-stimulating factor and erythropoietin on leukemic erythroid colony formation in human early erythroblastic leukemias. (1987) (30)
- Molecular cytogenetics of childhood acute myelogenous leukaemias (1997) (29)
- A new translocation in Burkitt's tumor cells (2004) (29)
- Trisomy 6 as the sole chromosome abnormality in myeloid disorders. (1994) (29)
- AML-1 gene rearrangement and AML-1-ETO gene expression as molecular markers of acute myeloblastic leukemia with t(8;21). (1994) (29)
- Cytogenetic studies on acute myelomonocytic leukaemia (M4) with eosinophilia. (1985) (29)
- Ph1-positive, bcr-negative acute leukemias: clustering of breakpoints on chromosome 22 in the 3' end of the BCR gene first intron. (1989) (29)
- Molecular cytogenetics of t(12;21) (p13;q22). (1996) (28)
- The human type II collagen gene (COL2A1) assigned to 12q14.3 (1986) (28)
- Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity: a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH) (2008) (27)
- Chromosomal localization of two human zinc finger protein genes, ZNF24 (KOX17) and ZNF29 (KOX26), to 18q12 and 17p13-p12, respectively. (1991) (26)
- Retinoic acids in the treatment of acute promyelocytic leukemia. (1990) (26)
- Establishment of a human acute promyelocytic leukemia-ascites model in SCID mice. (1996) (26)
- Chromosome abnormalities of the short arm of chromosome 12 in hematopoietic malignancies: a report including three novel translocations involving the TEL/ETV6 gene (1997) (26)
- A Simple Method for Prenatal Diagnosis of Trisomy 21 on Uncultured Amniocytes (1993) (26)
- Cytogenetic abnormalities in thyroid adenomas. (1991) (26)
- JEM-1, a novel gene encoding a leucine-zipper nuclear factor upregulated during retinoid-induced maturation of NB4 promyelocytic leukaemia (1997) (26)
- Cytogenetic studies in four cases of alpha chain disease. (1986) (25)
- Cytogenetic studies of Sézary cells. (1987) (25)
- C-band pattern in lymphocytes of patients with soft tissue sarcomas. (1983) (25)
- Promyelocytic blast crisis of chronic myelocytic leukemia with both t(9;22) and t(15;17) in M3 cells (1984) (25)
- Origin of the high constitutive level of progesterone receptor in T47-D breast cancer cells (1991) (25)
- Cytogenetic studies on Burkitt's lymphoma cell lines. (1983) (25)
- Complex chromosomal abnormalities in acute nonlymphocytic leukemia. (1986) (24)
- Chromosomal localization of the human histamine H1-receptor gene (1994) (24)
- A translocation (7;10)(q35;q21) in a differentiated papillary carcinoma of the thyroid. (1989) (24)
- Flow cytometry isolation and improved visualization of sorted mouse chromosomes. Purification of chromosomes X and ISO-1 from cell lines with Robertsonian translocations. (1984) (24)
- Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome-acute myeloid leukemia actually differ? (2007) (23)
- A simple diagnostic test for Fanconi anemia by flow cytometry. (1991) (23)
- Mapping of a human fibrillar collagen gene, pro α1(XI) (COL11A1), to the p21 region of chromosome 1 (1988) (23)
- Molecular analysis of a variant 18;22 translocation in a case of lymphocytic lymphoma (1993) (23)
- Chromosome painting in acute monocytic leukemia (1993) (23)
- Localization of a new type of X-linked liver glycogenosis to the chromosomal region Xp22 containing the liver alpha-subunit of phosphorylase kinase (PHKA2). (1994) (22)
- Detection of single-copy genes by nonisotopic in situ hybridization on human chromosomes (1989) (22)
- T cell-derived blast crisis in chronic myelocytic leukemia. (1987) (22)
- Cytogenetic studies on 19 papillary thyroid carcinomas (1992) (22)
- Sister chromatid exchanges induced by nitrogen mustard in Fanconi's anemia. Application to the detection of heterozygotes and interpretation of the results (1980) (21)
- New localizations of VH sequences by in situ hybridization with biotinylated probes (1990) (21)
- Minimal residual disease (MRD) in remission t(8;21) AML and in vivo differentiation detected by FISH and CD34+ cell sorting (2001) (21)
- A novel real-time RT-PCR assay for quantification of OTT-MAL fusion transcript reliable for diagnosis of t(1;22) and minimal residual disease (MRD) detection (2003) (21)
- Interstitial telomere repeats in translocations of hematopoietic disorders (2000) (21)
- The human genes for the α and γ subunits of the mast cell receptor for immunoglobulin E are located on human chromosome band 1823 (2005) (21)
- Rapid and early determination of sex using trophoblast biopsy specimens and Y chromosome specific DNA probes. (1984) (21)
- Deregulation of cyclin D2 by juxtaposition with T‐cell receptor alpha/delta locus in t(12;14)(p13;q11)‐positive childhood T‐cell acute lymphoblastic leukemia (2006) (20)
- Malignant and reactive erythroblasts in erythroleukemia (M6). (1983) (20)
- The chromosomes in hematology. (1981) (20)
- Production of erythropoietin by cloned malignant murine erythroid cells. (1985) (19)
- Cytogenetic studies in patients with Richter's syndrome. (1994) (19)
- [Fanconi's anemia. Incidence of its development into leukemia]. (1983) (19)
- The human homolog of the myeloproliferative virus maps to chromosome band 1p34 (1989) (19)
- The gene for the type II (p75) tumor necrosis factor receptor (TNF-RII) is localized on band 1p36.2–p36.3 (1991) (19)
- CALM-AF10 fusion gene in leukemias: simple and inversion-associated translocation (10;11). (2000) (19)
- Cytogenetic studies on acute nonlymphocytic leukemia in relapse. (1988) (18)
- 14q- in two hairy cell leukemia patients. (1985) (18)
- SPLENECTOMY AND BONE MARROW TRANSPLANTATION IN CHRONIC GRANULOCYTIC LEUKAEMIA (1983) (18)
- Chromosome microdissection in leukemia: A powerful tool for the analysis of complex chromosomal rearrangements (1996) (18)
- Diagnosis of Fanconi's anemia by flow cytometry. (1990) (18)
- Burkitt's lymphoma occurring 6 years after Hodgkin's disease. (1980) (18)
- Abnormalities of the short arm of chromosome 12 in T cell prolymphocytic leukemia (1998) (17)
- A case of chronic neutrophilic leukemia with deletion (11)(q23). (1999) (17)
- HOX 11 L 2 / TLX 3 is transcriptionally activated through T-cell regulatory elements downstream of BCL 11 B as a result of the t ( 5 ; 14 ) ( q 35 ; q 32 ) (2006) (17)
- Characterization of translocation t(1;14)(p32;q11) in a T and in a B acute leukemia. (1993) (17)
- Presence of three recurrent chromosomal reaarrangements, t(2;3)(p12;q37), del(8)(q24), and t(14;18), in an acute lymphoblastic leukemia. (1996) (16)
- The human genes for the alpha and gamma subunits of the mast cell receptor for immunoglobulin E are located on human chromosome band 1q23. (1990) (16)
- HOX 11 L 2 expression defines a clinical subtype of pediatric TALL associated with poor prognosis (2002) (16)
- Translocation t(10;11) involving the MLL gene in acute myeloid leukemia. Importance of fluorescence in situ hybridization (FISH) analysis. (1996) (16)
- Chromosomal rearrangement on chromosome 11q14-q21 in T cell acute lymphoblastic leukemia. (1989) (16)
- Chromosomal studies of leukemic and preleukemic Fanconii's anemia patients: examples of acquired 'chromosomal amplification.'. (1980) (16)
- A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia (1997) (15)
- In situ hybridization ascertains the presence of a translocation t(6;11) in an acute monocytic leukemia (1990) (15)
- Cytogenetic characterization of a new human papillary thyroid carcinoma permanent cell line (GLAG-66). (1993) (15)
- Constitutional C-band pattern in patients with adenomatosis of the colon and rectum. (1985) (15)
- D21S418E identifies a cAMP-regulated gene located on chromosome 21q22.3 that is expressed in placental syncytiotrophoblast and choriocarcinoma cells. (1993) (15)
- Malignant myeloblastic transformation of murine long‐term bone marrow cultures by F‐MuLV: In vitro reproduction of a long‐term leukemogenesis, and investigation of preleukemic events (1983) (15)
- Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22. (1991) (14)
- Differences in human C-band pattern between two European populations. (2008) (14)
- Clonal chromosome abnormalities in Fanconi anemia. (1996) (14)
- Inversion‐associated translocations in acute myelomonocytic leukemia with eosinophilia (1995) (14)
- Translocation t(3;22)(q27;q11) in non-Hodgkin's malignant lymphoma: chromosome painting and molecular studies. (1993) (14)
- Cytogenetic study of a European Burkitt's lymphoma cell line. (1979) (14)
- Constitutive heterochromatin C-band polymorphism in prostatic cancer. (1991) (13)
- P 53 Gene Mutations in Acute Myeloid Leukemia With 17 p Monosomy (2003) (13)
- t(14;18) AND BCL‐2 GENE REARRANGEMENT IN A B‐CHRONIC LYMPHOCYTIC LEUKAEMIA (1992) (13)
- Chromosomal studies of leukemic and preleukemic Fanconi's anemia patients (1980) (13)
- The 5-HT2B receptor gene maps to 2q36.3-2q37.1. (1996) (13)
- Karyotype and cell phenotypes in primary acute leukemias. (1981) (13)
- The 11q23 breakpoint in acute leukemia with t(11;19)(q23;p13) is distal to those of t(4;11), t(6;11) and t(9;11) (1992) (13)
- Alterations of the putative tumor suppressor gene p16/MTS1 in human hematological malignancies. (1994) (13)
- Localization of the villin gene on human chromosome 2q35-q36 and on mouse chromosome 1 (1988) (13)
- Partial trisomy 6p (1979) (13)
- Cytogenetic study of 130 childhood acute nonlymphocytic leukemias. (1988) (12)
- Chromosomal localization of the human V3 pituitary vasopressin receptor gene (AVPR3) to 1q32. (1995) (12)
- Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia. (2004) (12)
- Distinct MLL gene rearrangements associated with successive acute monocytic and lymphoblastic leukemias in the same patient. (1994) (12)
- BCL2 complex rearrangement in follicular lymphoma: translocation mbr/JH and deletion in the vcr region of the same BCL2 allele. (1993) (12)
- Tumor‐associated karyotypic lesions coselected with in vitro macrophage differentiation (1992) (11)
- 100 Cytogenetic abnormalities in thyroid tumors (1989) (11)
- Cytogenetic studies on patients with medullary carcinoma of the thyroid. (1987) (11)
- Bone marrow transplantation for Fanconi anemia. (1984) (11)
- Nodular lymphocyte predominance Hodgkin's disease featuring blood atypical polyclonal B‐cell lymphocytosis (1993) (11)
- A new case of translocation t(6;11)(q21;q23) in a therapy‐related acute myeloid leukemia resulting in an MLL–AF6q21 fusion (1998) (11)
- Molecular analysis of T-cell receptor transcripts in a human T-cell leukemia bearing a t(1;14) and an inv(7); cell surface expression of a TCR-beta chain in the absence of alpha chain. (1993) (11)
- The gene for the type 1 tumor necrosis factor receptor (TNF-R1) is localized on band 12p13 (1991) (11)
- Trisomy 14: a recurring cytogenetic abnormality associated with myeloid disorders. (1995) (11)
- Childhood B-cell acute lymphoblastic leukemia with FAB-L1 morphology and a t(9;11) translocation involving the MLL gene. (1996) (11)
- Non-randomness in complex translocations of chronic myeloid leukaemia. (2009) (10)
- Bone marrow graft of a Fanconi's anemia patient. Cytogenetic study (1980) (10)
- 5q- anomaly in acute lymphoblastic leukemia. (1992) (10)
- Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23–6q24 (1989) (10)
- Rearrangements of 11q (1984) (10)
- Whole arm translocation t(17;18): a non-random abnormality of myeloid cell proliferation. (1993) (10)
- [Acute myeloblastic leukemia with involvement of the basophilic cell line and anomalies of the short arm of chromosome 12 (12p)]. (1985) (10)
- Transcriptional activation of the cardiac homeobox gene CSX1/NKX2-5 in a B-cell chronic lymphoproliferative disorder (2008) (10)
- Two Burkitt's lymphomas with chromosome 6 long arm deletions. (1985) (10)
- Molecular analysis of chromosomal breakpoints in three examples of chromosomal translocation involving the TEL gene (1999) (10)
- Selection of cells with different chromosomal localizations of the amplified c-myc gene during in vivo and in vitro growth of the breast carcinoma cell line SW 613-S (2004) (10)
- An interstitial 11q23 deletion proven to be a rearrangement interrupting the MLL gene in an infant with acute myeloblastic leukemia. (1996) (10)
- Cryptic translocations involving chromosome 20 in polycythemia vera. (2004) (10)
- Cytogenetic Studies in Fanconi Anemia: Induced Chromosomal Breakage and Cytogenetics of Leukemia (1989) (9)
- International System for Cytogenetic Nomenclature (ISCN) — guidelines on cancer cytogenetics (1990) (9)
- NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia. (2008) (9)
- The genes for MHC class II regulatory factors RFX1 and RFX2 are located on the short arm of chromosome 19. (1992) (9)
- Chromosome rearrangements in acquired malignant diseases. (1982) (9)
- Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1. (1988) (9)
- Hemizygous deletion of the 3' end of the RB1 gene in a case of Philadelphia positive-acute lymphoblastic leukemia. (1991) (9)
- Chromosome mapping of the human ras-related rab3A gene to 19p13.2. (1989) (9)
- A novel translocation, t(9;11)(q33;q23) involving the HRX gene in an acute monocytic leukemia. (1993) (8)
- Chromosome 16 inversion-associated translocation: two new cases. (1999) (8)
- Regional assignment of red cell acid phosphatase locus to band 2p25 (1979) (8)
- Rearrangements of the RARA and PML genes in a cytogenetic variant of acute promyelocytic leukemia (1993) (8)
- Uneven frequencies of secondary chromosomal abnormalities in acute myeloid leukemias with t(8;21), t(15;17), and inv(16). (2000) (8)
- FISH analysis of translocations involving the short arm of chromosome 9 in lymphoid malignancies (1997) (8)
- Translocation t(11;11)(q13;q23) and HRX gene rearrangement associated with therapy-related leukemia in a child previously treated with VP16. (1994) (8)
- Jumping translocations (2007) (8)
- Identical abnormality of the short arm of chromosome 18 in two Philadelphia-positive chronic myelocytic leukemia patients with erythroblastic transformation, resulting in duplication of BCR-ABL1 fusion. (2002) (7)
- Two human genes encoding zinc finger proteins, ZNF12 (KOX 3) and ZNF 26 (KOX 20), map to chromosomes 7p22-p21 and 12q24.33, respectively (1991) (7)
- Chromosomal deletions in non-Hodgkin's malignant lymphomas. (1990) (7)
- The ras-related ral gene maps to chromosome 7p15-22 (1988) (7)
- Non-Hodgkin’s lymphomas and myeloid disorders: deletions associated with t(2;5) and t(3;5) detected by FISH (1998) (7)
- A simple device to obtain high local concentrations of material sorted by flow cytometry for biochemical or morphological analysis. (1984) (7)
- Abnormalities of chromosome 18 in myelodysplastic syndromes and secondary leukemia. (1992) (7)
- The gene for the α2 chain of the human fibrillar collagen type XI (COL11A2) assigned to the short arm of chromosome 6 (1990) (7)
- Ring chromosome 8 and translocation t(8;21) in a patient with acute myeloblastic leukemia. (2002) (6)
- [Translocation t(1; 14) and rearrangement of the gene for the alpha chain of the T-cell receptor in acute T-lymphoblastic leukemia]. (1986) (6)
- A novel translocation, t(9;21)(q13;q22) rearranging the RUNX1 gene in acute myelomonocytic leukemia. (2002) (6)
- Translocation (2;3)(p22;q28) is associated with myeloid disorders. (1995) (6)
- 22q- and 8q- in a non-Burkitt lymphoma. (1983) (6)
- Localization of the human gene encoding heterogeneous nuclear RNA ribonucleoprotein G (hnRNP-G) to chromosome 6p12 (1992) (6)
- [Translocations t(2;8) and t(8;22) in continuous cell lines of African Burkitt's lymphoma]. (1980) (6)
- Acute megakaryocytic leukaemia with acquired polysomy 21 and translocation t(1;21). (2000) (6)
- Loss of chromosome 22 in patients with refractory anemia with excess of blasts (RAEB) in transformation and acute leukemia after RAEB. (1992) (6)
- Molecular analysis of 12 patients with the t(8;2l) translocation and M2 acute myelogenous leukemia (1992) (6)
- MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literature. (2008) (6)
- Human and mouse Krüppel-like (MOK2) orthologue genes encode two different zinc finger proteins (1995) (6)
- Is trisomy 4 a secondary chromosomal abnormality in acute myeloblastic leukemia? (1995) (6)
- Karyotypes and cell phenotypes in acute leukemia following other diseases. (1981) (6)
- New variant translocation in acute myelomonocytic leukemia with bone marrow eosinophilia. (1992) (6)
- Loss of the TEL/ETV6 gene by a second translocation in ALL patients with t(12;21). (1999) (6)
- Partial deletion of the long arm of chromosome 5: a fluorescence in situ hybridization study using band-specific painting probes generated by chromosome microdissection. (1996) (5)
- [Monoblastic (M5a) form of relapse in acute myeloblastic (M2) leukemia with t(8;21)]. (1986) (5)
- Lack of mutations in the P53 gene exons 5 to 8 in ataxia-telangiectasia. (1993) (5)
- Relapse as acute monoblastic leukemia (AML-M5) of t(6;9) acute myeloblastic leukemia (AML-M2). (1992) (5)
- t(8;21) prior to acute leukemia. (1993) (5)
- Duplication of band 12q24 in acute myeloblastic leukemia. (1999) (5)
- Chromosome assignment of four RAS-related RAB genes (1991) (5)
- C-band polymorphism in non-Hodgkin lymphoma. (2008) (5)
- Precise Localization of a Gene Responsible for Ataxia-Telangiectasia on Chromosome 11q (1993) (5)
- Burkitt-type acute leukemia in a patient with B-prolymphocytic leukemia: evidence for a common origin. (2005) (4)
- Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19 (1993) (4)
- Location and function of critical genes in leukemogenesis inferred from cytogenetic abnormalities in hematologic malignancies. (2000) (4)
- [Association of acrocentric chromosomes in blood diseases]. (1970) (4)
- Are cells with trisomy 10 always malignant in hematopoietic disorders? (1999) (4)
- [Abscence of chromosomes abnormalities and acute leukemia : relationships with normal bone marrow cells]. (1980) (4)
- cDNA sequence, genomic organization and mapping of PDE6D, the human gene encoding the delta subunit of the cGMP phosphodiesterase of retinal rod cells to chromosome 2q36. (1997) (4)
- B-cell acute lymphoblastic leukemia with tandem t(14;14)(q11;q32). (2001) (4)
- Cytogenetic evaluation of bone marrow involvement in Burkitt's lymphoma. (1988) (4)
- Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation (2008) (4)
- Are most secondary acute lymphoblastic leukemias mixed acute leukemias? (1989) (4)
- A simple method for improving the reproductibility of the R-banding technique (2004) (4)
- Chromosomal localization of amplified c-myc in a human colon adenocarcinoma cell line with a biotinylated probe. (1988) (4)
- Acute megakaryoblastic leukemia and loss of the RUNX1 gene. (2006) (4)
- Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia. (2008) (4)
- Cytogenetic Studies of 32 Malignant Lymphomas (1985) (4)
- [T (15;17) translocation in acute promyelocytic and acute nonpromyelocytic leukemia (author's transl)]. (1979) (4)
- Interleukin-2 receptor beta chain locus rearrangement in a T-cell acute lymphoblastic leukemia. (2007) (4)
- [Rearrangement of the c-myc proto-oncogene locus in a cell line of T-lymphoblastic origin]. (1985) (4)
- Chromosomal abnormalities in T-cell malignant lymphoma. (1991) (4)
- Translocation t(3;5)(q24;q32) in two acute nonlymphocytic leukemias. (1987) (4)
- Expression of the MN1–TEL fusion protein in the human UCSD/AML1 leukemic cell line (2004) (4)
- Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA2) to chromosome 2p22-p23. (1996) (4)
- [Effect of chlormethin chlorhydrate on the chromosomes in Fanconi's anemia: application to diagnosis and detection of heterozygotes]. (1980) (3)
- Molecular cytogenetics of acute lymphoblastic leukemia. (1991) (3)
- Partial deletion of chromosome 2 in non-Hodgkin lymphoma. (1991) (3)
- Lack of mutations in the TP53 tumor suppressor gene exons 5 to 8 in Fanconi's anemia. (1991) (3)
- A YAC contig in 6p23 based on sequence tagged sites. (1994) (3)
- A New Congenital Dysmegakaryopoietic Thrombocytopenia ( Paris-Trousseau ) Associated With Giant Platelet &-Granules and Chromosome 11 Deletion at l lq 23 (2002) (3)
- Two human leukemic T cell lines with a t(8;14)(q24;q11) translocation (KE-37R and SKW3 cells) may have a common origin. (1988) (3)
- Deletion of (7p13p14) in non-Hodgkin's lymphoma. (1990) (3)
- [Acute monocytic leukemia with chromosome 11 anomalies]. (1979) (3)
- [Is there a functional equivalence between abnormalities of the long arm of chromosome 1 and the presence of Epstein-Barr virus in continuous lines of Burkitt's lymphoma?]. (1984) (3)
- [Cellular senescence and survival of T lymphocytes]. (1995) (3)
- [Human cytogenetics. From 1956 to 2006]. (2007) (3)
- Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA. (1998) (3)
- Chromosome studies of in vitro senescent lymphocytes: nonrandom trisomy 2. (2002) (3)
- HAEMOPOIETIC RECOVERY FROM Ph1 POSITIVE CHRONIC GRANULOCYTIC LEUKAEMIA (1987) (3)
- Common sequence in chromosome translocations affecting B‐ and T‐cell malignancies: A novel recombination site? (1993) (3)
- Specific in vitro amplified probe detects the E2A gene rearrangement in the t(1;19) acute lymphoblastic leukemia. (1990) (3)
- [Induced leukemias. Cytogenetical and cytological aspects. Comparison with primitive leukemias (author's transl)]. (1981) (3)
- [A recurrent mutation of the JAK2 gene in chronic myeloproliferative disorders]. (2006) (3)
- [Chromosomal abnormalities and Waldenström macroglobulinemia]. (2008) (3)
- Dual localization of the human gene encoding hnRNP I/PTB protein to chromosomes 19p13.3 and 14q23 (1996) (3)
- Acute Myeloid Leukemia in Children Less Than Two Years Old: Clinical, Cytologic and Cytogenetic Correlations Comparison with other age categories. A clinical survey of 39 cases. (1991) (2)
- An EcoRI restriction fragment length polymorphism (RFLP) in the human c-erb A locus (2004) (2)
- Cytogenetic studies of 32 malignant lymphomas with special emphasis to variation of chromosomal abnormalities and significance of normal mitoses (1985) (2)
- A comment on the paper: Reciprocal translocation and the Philadelphia chromosome By Jessie L. Watt and Brenda M. Page, Hum. Genet. 42, 163–170 (1978) (1978) (2)
- Translocation t(8;21)(q22;q22): cytogenetics and molecular biology. (1994) (2)
- [Molecular basis of the t(1;22)(p13;q13) specific for human acute megakaryoblastic leukemia]. (2003) (2)
- No abnormal C-band polymorphism in lung cancer patients. (2008) (2)
- The proteinase 3 (PRTN3) gene is localized on 19p13.3 and is distal to the E2A gene. (1995) (2)
- Loss of genetic material from the short arm of chromosome 12 is a frequent secondary abnormality in non-Hodgkin's lymphoma. (1991) (2)
- Chromosomal localization of two KOX zinc finger genes on chromosome bands 7q21-q22. (1995) (2)
- a human acute promyelocytic leukemia (M3) NB4, a maturation inducible cell line with t(15;17) marker isolated from (2011) (2)
- Cytogenetics of acute leukemia. (1992) (2)
- Fluorescence in situ hybridization on metaphase chromosomes with biotinylated probes. In situ hybridization, biotin labeling, cosmids, gene mapping, oncogene amplification. (1990) (2)
- Localization of actin-related sequences by in situ hybridization to R-banded human chromosomes (2004) (2)
- Acquired trisomy 2 is not systematically associated with tumors. (2004) (2)
- Non-radioactive in situ hybridization to metaphase and interphase nuclei of malignant cells (1993) (2)
- [Isoprinosine and human chromosomes (author's transl)]. (1980) (2)
- [Translocation t(8;14) in acute lymphoblastic leukaemia, Burkitt type (author's transl)]. (1979) (2)
- C-BAND HETEROMORPHOSM IN BREAST CANCER PATIENTS (1985) (2)
- [Prognostic value of chromosome anomalies in acute non-lymphoblastic leukemias]. (1983) (2)
- A new Ph1+, bcr cell line derived from a patient with ALL-L1 gained autonomy in culture concomitant to CD23 expression. (1990) (2)
- Studies of BCR rearrangements in Philadelphia-positive acute leukemia. (1991) (2)
- C6) Mutations of the P53 gene in myelodysplastic syndromes (MDS). A report on 152 cases (1991) (2)
- Some recent aspects of the molecular biology of human lymphoma. (1993) (2)
- Relapse as acute monocytic leukaemia of acute lymphoblastic leukaemia with t(4;11). (1992) (1)
- Transcriptional Activation of the Cardiac Homeobox Gene CSX1/NKX2-5 in a B-Cell Chronic Lymphoproliferative Disorder. (2004) (1)
- ACUTE LYMPHOBLASTIC LEUKEMIA (ALL) WITH TEL-AML1 FUSION RNA. CLINICAL AND BIOLOGICAL FEATURES IN 17 CHILDREN TREATED WITH A UNIQUE PROTOCOL. 140 (1997) (1)
- [Acute myelomonocytic leukemia with abnormal eosinophils]. (2020) (1)
- [Mosaicism t(9;22) / t(1;9;22) resulting in Philadelphia chromosome (author's transl)]. (1981) (1)
- Rearrangement of the E2A gene in the t (1;19) acute lymphoblastic leukemia. (1991) (1)
- [Translocation t (8; 21) and acute granulocytic leukemia: interpretation of normal mitoses]. (1981) (1)
- Centromeric, pericentromeric and heterochromatin abnormalities in chromosomal rearrangements of human leukemia (2000) (1)
- [Children born of leukemic parents. Apropos of 23 children]. (1982) (1)
- [Cytogenetic studies in four cases of Fanconi's anemia (author's transl)]. (1975) (1)
- Fluorescence in situ hybridization and cytogenetics of hemopoietic malignancies: new developments. (1993) (1)
- Cytogenetic study of myeloid and erythroid colonies in chronic myeloid leukaemia with stable Ph1 mosaicism (1987) (1)
- A cryptic chromosome 19 abnormality in a patient with Ph-positive acute lymphoblastic leukemia. (2006) (1)
- [Abnormal localization of proto-oncogene c-ets 1 in acute leukemia with translocation t(1: 11)(q21: q23)]. (1986) (1)
- 103. The retinoic acid receptor alpha (RARA) gene is fused with a transcription unit on chromosome 11q in an Acute promyelocytic leukemia (APL) patient with variant t(11;17) translocation (1992) (1)
- [Myelomonocytoid leukemia, abnormal cellular clone with a marker chromosome, evolution with a possible cure]. (1978) (1)
- Homozygosity for 8pter→q22 in acute myeloblastic leukemia with t(8;21)(q22;q22) (1989) (1)
- [Correlation between variant translocation and the expression of immunoglobulin light chains in Burkitt-type lymphomas and leukemias]. (1981) (1)
- Cytogenetics of secondary acute non-lymphocytic leukemia. (1987) (1)
- INVOLVEMENT OF THE TEL GENE IN HUMAN LEUKEMOGENESIS. 42 (1997) (0)
- [Search for tumor suppressor genes: chromosome deletions and loss of heterozygote property in human tumors]. (1993) (0)
- [Anomalous incidence of chromosome 1 gh+ in chronic myeloid leukemia]. (1977) (0)
- [What is the use of cryopreserved tissue and cell banks? A geneticist's view point]. (1998) (0)
- Cytogenetics of acute nonlymphocytic leukemia in relapse. (1989) (0)
- [Karyotype analysis of testicular tumors]. (1970) (0)
- Cytogenetic abnormalities in 13 papillary thyroid carcinomas (1991) (0)
- gene consistently fuses the leucine zipper motif of AF10 onto the HRX The t(10;11) translocation in acute myeloid leukemia (M5) (2011) (0)
- Complex chromosome abnormality mimicking t(8;21)in an acute myeloblastic leukemia. (2001) (0)
- Contents Vol. 119, 2007 (2008) (0)
- Regional MappingoftheBattenDisease Locus(CLN3)to HumanChromosome16p12 (1991) (0)
- Cytogenetics acquisitions in malignant lymphomas. (1989) (0)
- [Cytogenetics and acute non-lymphoblastic leukemias. Value of short-term cultures]. (1983) (0)
- [A method of molecular hybridization identification of chromosomes purified with a cell sorter]. (1982) (0)
- A simple method for R-banding combined with in situ hybridization (2004) (0)
- associated with poor prognosis HOX11L2 expression defines a clinical subtype of pediatric T-ALL (2013) (0)
- Recent advances in fluorescence in situ hybridization (FISH) in hematology. (1995) (0)
- Report of 38 patients with hyperdiploid karyotype in acute myeloid leukemia: A groupe francais de cytogenetique hematologique study (2007) (0)
- Eleventh International Chromosome Conference (2004) (0)
- Three-way translocation involving band 6q21 in an acute lymphoblastic leukemia. (2007) (0)
- [Stereotyped chromosome abnormalities in human leukemia and lymphoma]. (1983) (0)
- [The value of chromosome anomalies in the prognosis of acute non-lymphoblastic leukemia in children]. (1988) (0)
- Double trisomy 8 and 21 in acute myelocytic leukemias, one with rearrangement of the RUNX1 gene. (2003) (0)
- [Promiscuous genes and chromosomal rearrangements of hematopoietic malignancies]. (1999) (0)
- BCL11B elements downstream of is transcriptionally activated through T-cell regulatory TLX3 / HOX11L2 (2013) (0)
- 5q- anomaly preceding acute myeloblastic leukemia with 53 chromosomes without chromosome 5 abnormality. (1993) (0)
- Gene by a Chromosome Translocation t ( 9 ; 14 ) ( p 21 †” 22 ; qll ) in an Acute Lymphoblastic Leukemia of B-Cell Type 1 (2006) (0)
- The t(14;19)(q32;q13) Translocation in B Lymphoproliferative Disorders: A Continuum from Chronic Lymphocytic Leukemia (CLL) to Marginal Zone Lymphoma (MZL)?. (2006) (0)
- Cytogenetic studies of 19 cases of thyroid papillary carcinomas (1992) (0)
- [Rearrangement of the proto-oncogene c-myc in fresh cells from Burkitt's leukemia (L3)]. (1985) (0)
- Microdissection and microcloning of human banded chromosomes. (1990) (0)
- Chromosomal abnormalities in malignant lymphoid cell proliferations: recent advances (1987) (0)
- Gène MLL (HRX, ALL-1, mixed-lineage leukemia) (1998) (0)
- Brief Novel activating JAK2 mutation in a patient with Down syndrome and B-cell precursor acute lymphoblastic leukemia (2007) (0)
- [Burkitt-type lymphoma following Hodgkin's disease]. (1980) (0)
- [A new variety of acute non-promyelocytic leukemia with t(15;17)]. (1979) (0)
- Translocation t(11;11)(p15;p15) in a case of acute lymphoblastic leukemia. (1988) (0)
- Chromosome rearrangements in acquired malignant diseases. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping. (1982) (0)
- [Thrombocythemia with Philadelphia chromosome. Secondary appearance of chronic myeloid leukemia]. (1983) (0)
- Human and Mouse Kriippel-Like ( MOK 2 ) Orthologue Genes Encode Two Different Zinc Finger Proteins (0)
- A new congenital thrombocytopenia associated with giant platelet alpha-granules, dysmegakaryopoiesis and chromosome 11 deletion at 11q23 Paris-Trousseau Thrombocytopenia (1993) (0)
- promyelocytic leukemia. I. Clinical results (see comments) All-trans retinoic acid as a differentiation therapy for acute (2011) (0)
- Dorian Gray mice exposed (1993) (0)
- Short communication NUP98eNSD1 fusion by insertion in acute myeloblastic leukemia (2008) (0)
- Cytogenetic characterization of a new permanent cell line (glag-66) from a human papillary thyroid carcinoma (1992) (0)
- Cytogénétique Hématologique (GFCH) d'Hématologie Cellulaire (GFHC) and the Groupe Français de gene mutations: a report of 59 cases by the Groupe Français M0 AML, clinical and biologic features of the disease, includingAML1 (2013) (0)
- Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nuclei (2004) (0)
- Brief report M0 AML, clinical and biologic features of the disease, including AML1 gene mutations: a report of 59 cases by the Groupe Franc¸ais d’He´matologie Cellulaire (GFHC) and the Groupe Franc¸ais de Cytoge´ne´tique He´matologique (GFCH) (2003) (0)
- Discrepancy between G and R bands (1981) (0)
- acute lymphoblastic The JAK 2 V 617 F activating mutation occurs in chronic myelomonocytic (2005) (0)
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