Zobrazeno 1 - 10 of 15 pro vyhledávání: '"Anne R. M. von Bergh"'
1
High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9
Autor: Ina Hainmann, H. Berna Beverloo, Jules P.P. Meijerink, Anne R. M. von Bergh, Gudmar Lönnerholm, Laura J. C. M. van Zutven, Ellen van Drunen, Elisabeth R. van Wering, Rob Pieters
Publikováno v: Genes Chromosomes & Cancer, 45, 731-739. Wiley-Liss Inc.
The t(7;12)(q36;p13) is a recurrent translocation involving the ETV6/TEL gene (12p13) and a heterogeneous breakpoint at 7q36. A fusion transcript between HLXB9 and ETV6 in AML with t(7;12) is occasionally found. To study the incidence of t(7;12) in i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a38526596cd9991e324aeda7bd14fdb0
https://doi.org/10.1002/gcc.20335
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2
Decreased PARP and procaspase-2 protein levels are associated with cellular drug resistance in childhood acute lymphoblastic leukemia
Autor: Monique L. den Boer, Anne R. M. von Bergh, Rob Pieters, H. Berna Beverloo, Karin M. Kazemier, G. E. Janka-Schaub, Amy Holleman
Publikováno v: Blood, 106(5), 1817-1823. American Society of Hematology
Drug resistance in childhood acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML) is associated with impaired ability to induce apoptosis. To elucidate causes of apoptotic defects, we studied the protein expression of Apaf-1, procaspas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6502732fab4542698952186b965fe3a
https://doi.org/10.1182/blood-2004-11-4296
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3
Identification of a novel RAS GTPase-activating protein (RASGAP) gene at 9q34 as anMLL fusion partner in a patient with de novo acute myeloid leukemia
Autor: Shama L. van Zelderen-Bhola, Pauline M. Wijers, J.H. Frederik Falkenburg, Philip M. Kluin, Anne R. M. von Bergh, Arjan J. Groot, Ed Schuuring
Publikováno v: GENES CHROMOSOMES & CANCER, 39(4), 324-334. Wiley
Genes Chromosomes and Cancer, 39(4), 324-334
Von Bergh, A R M, Wijers, P M, Groot, A J, Van Zelderen-Bhola, S, Falkenburg, J H F, Kluin, P M & Schuuring, E 2004, ' Identification of a Novel RAS GTPpase-Activating Protein (RASGAP) Gene at 9q34 as an MLL Fusion Partner in a Patient with De Novo Acute Leukemia ', Genes Chromosomes and Cancer, vol. 39, no. 4, pp. 324-334 . https://doi.org/10.1002/gcc.20004
The t(9;11) has been described in patients with acute myeloid leukemia (AML), and two genes [AF9 (at 9p21) and FBP17 (at 9q34)] have been cloned as fusion partners of the MLL gene. From an AML-M5 with a t(9;11)(q34;q23), we identified a novel MLL fus
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64371de6fc51d94ee266dc2d5460af34
https://doi.org/10.1002/gcc.20004
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4
Interstitial 11q Deletion Derived From a Maternal ins(4;11)(p14;q24-2q25): A Patient Report and Review
Autor: Cokkie H. Wouters, Linda J.A. Corel, Gido Huijbregts, Diane Van Opstal, Pino J. Poddighe, Carolien C.M. Van Nieuwland, Anne R. M. von Bergh, Dick Tibboel, Laura J. C. M. van Zutven, Yolande van Bever
Publikováno v: American Journal of Medical Genetics Part A, 149A(7), 1468-1475. Wiley-Liss Inc.
We present a family with multiple cytogenetic abnormalities, identified through a girl with several dysmorphic features and cardiac problems, suspected for Jacobsen syndrome. Cytogenetic analysis showed a 46,XX,del(11)(qter) karyotype, which was conf
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::448394459519c3284505dbfbdbb232dc
https://pure.eur.nl/en/publications/560088e0-eb79-4cab-ac70-0140b7c4bca5
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5
Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants
Autor: Anne R. M. von Bergh, Oskar A. Haas, Rolf Marschalek, Helmut H. Schmidt, Sabine Strehl, Ulrich Jäger, Claus Meyer, Margit König, Ivan F. Loncarevic, Björn Schneider, Steven D.P. Moore, Jochen Harbott, Marie Jarosova
Publikováno v: Genes, chromosomescancer. 45(11)
The majority of translocations that involve the long arms of chromosomes 11 and 17 in acute myeloid leukemia appear identical on the cytogenetic level. Nevertheless, they are diverse on the molecular level. At present, two genes are known in 11q23 an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc9de7387bd8cf84e8ee451becea2824
https://pubmed.ncbi.nlm.nih.gov/16897742
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6
Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene
Autor: Emine Önen, Georgine E. de Greef, Massimo Negrini, Anne R. M. von Bergh, Ellen van Drunen, Angelo Veronese, Sandra C. J. M. Velthuizen, H. Berna Beverloo, Marry M. van den Heuvel-Eibrink, Laura J. C. M. van Zutven, Cristina Mecucci
Publikováno v: Genes Chromosomes & Cancer, 45(5), 437-446. Wiley-Liss Inc.
Chromosome rearrangements are found in many acute leukemias. As a result, genes at the breakpoints can be disrupted, forming fusion genes. One of the genes involved in several chromosome aberrations in hematological malignancies is NUP98 (11p15). As
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c5bf858ea92dd426d80fe115229ad68
http://hdl.handle.net/11391/154061
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9
LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia
Autor: Margreet H. van Weel, Ed Schuuring, Paul Rombout, H. Berna Beverloo, Elisabeth R. van Wering, Rosalyn Slater, Anne R. M. von Bergh, Philip M. Kluin, G. C. Beverstock
Publikováno v: GENES CHROMOSOMES & CANCER, 35(1), 92-96. Wiley
Genes Chromosomes & Cancer, 35, 92-96. Wiley-Liss Inc.
Infant acute lymphoblastic leukemia (ALL) with MLL gene rearrangements is characterized by a proB phenotype and a poor clinical outcome. We analyzed an infant proB ALL with t(2; 11)(p 15;p 14) and an MLL rearrangement on Southern blot analysis, Rapid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e4ed07929f3df9d6a0e606437212492
https://research.rug.nl/en/publications/32409865-a609-4c87-8468-319b56710901
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10
A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias
Autor: Anne R. M. von Bergh, Ronald A. van Soest, Ed Schuuring, Hilde Vranckx, Toon Smetsers, Anne Hagemeijer, Philip M. Kluin, Shama L. van Zelderen-Bhola, Michel Stul, B Emanuel
Publikováno v: Genes Chromosomes and Cancer, 28(1), 14-22
Genes, Chromosomes & Cancer, 28, 1, pp. 14-22
Genes, Chromosomes & Cancer, 28, 14-22
Von Bergh, A, Emanuel, B, Van Zelderen-Bhola, S, Smetsers, T, Van Soest, R, Stul, M, Vranckx, H, Schuuring, E, Hagemeijer, A & Kluin, P 2000, ' A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias ', Genes Chromosomes and Cancer, vol. 28, no. 1, pp. 14-22 . https://doi.org/10.1002/(SICI)1098-2264(200005)28:1<14::AID-GCC2>3.0.CO;2-X
Reciprocal translocations involving the MLL gene on chromosome band 11q23 have been observed in both acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). In AML, identification of MLL breakpoints is an important prognostic factor. Bre
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::987685f4d75877c1012c91a19622f208
https://research.vumc.nl/en/publications/b9714784-d40d-4353-a6e5-41e89e450a24
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