Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A
Auer F, Rüschendorf F, Gombert M, Husemann P, Ginzel S, Izraeli S, Harit M, Weintraub M, Weinstein OY, Lerer I, Stepensky P, et al. (2014)
Leukemia 28(5): 1136-1138.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
Autor*in
Auer, F.;
Rüschendorf, F.;
Gombert, Michael;
Husemann, PeterUniBi;
Ginzel, Sebastian;
Izraeli, S.;
Harit, M.;
Weintraub, M.;
Weinstein, O. Y.;
Lerer, I.;
Stepensky, P.;
Borkhardt, Arndt
Alle
Alle
Einrichtung
Erscheinungsjahr
2014
Zeitschriftentitel
Leukemia
Band
28
Ausgabe
5
Seite(n)
1136-1138
ISSN
0887-6924
eISSN
1476-5551
Page URI
https://pub.uni-bielefeld.de/record/2677865
Zitieren
Auer F, Rüschendorf F, Gombert M, et al. Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A. Leukemia. 2014;28(5):1136-1138.
Auer, F., Rüschendorf, F., Gombert, M., Husemann, P., Ginzel, S., Izraeli, S., Harit, M., et al. (2014). Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A. Leukemia, 28(5), 1136-1138. doi:10.1038/leu.2013.363
Auer, F., Rüschendorf, F., Gombert, Michael, Husemann, Peter, Ginzel, Sebastian, Izraeli, S., Harit, M., et al. 2014. “Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A”. Leukemia 28 (5): 1136-1138.
Auer, F., Rüschendorf, F., Gombert, M., Husemann, P., Ginzel, S., Izraeli, S., Harit, M., Weintraub, M., Weinstein, O. Y., Lerer, I., et al. (2014). Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A. Leukemia 28, 1136-1138.
Auer, F., et al., 2014. Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A. Leukemia, 28(5), p 1136-1138.
F. Auer, et al., “Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A”, Leukemia, vol. 28, 2014, pp. 1136-1138.
Auer, F., Rüschendorf, F., Gombert, M., Husemann, P., Ginzel, S., Izraeli, S., Harit, M., Weintraub, M., Weinstein, O.Y., Lerer, I., Stepensky, P., Borkhardt, A., Hauer, J.: Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A. Leukemia. 28, 1136-1138 (2014).
Auer, F., Rüschendorf, F., Gombert, Michael, Husemann, Peter, Ginzel, Sebastian, Izraeli, S., Harit, M., Weintraub, M., Weinstein, O. Y., Lerer, I., Stepensky, P., Borkhardt, Arndt, and Hauer, J. “Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A”. Leukemia 28.5 (2014): 1136-1138.
18 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
Next-Generation Sequencing in Acute Lymphoblastic Leukemia.
Coccaro N, Anelli L, Zagaria A, Specchia G, Albano F., Int J Mol Sci 20(12), 2019
PMID: 31208040
Coccaro N, Anelli L, Zagaria A, Specchia G, Albano F., Int J Mol Sci 20(12), 2019
PMID: 31208040
Epigenetic Priming in Childhood Acute Lymphoblastic Leukemia.
Raboso-Gallego J, Casado-García A, Isidro-Hernández M, Vicente-Dueñas C., Front Cell Dev Biol 7(), 2019
PMID: 31380372
Raboso-Gallego J, Casado-García A, Isidro-Hernández M, Vicente-Dueñas C., Front Cell Dev Biol 7(), 2019
PMID: 31380372
Primary Immunodeficiency and Cancer Predisposition Revisited: Embedding Two Closely Related Concepts Into an Integrative Conceptual Framework.
Haas OA., Front Immunol 9(), 2018
PMID: 30809233
Haas OA., Front Immunol 9(), 2018
PMID: 30809233
Germline Genetic IKZF1 Variation and Predisposition to Childhood Acute Lymphoblastic Leukemia.
Churchman ML, Qian M, Te Kronnie G, Zhang R, Yang W, Zhang H, Lana T, Tedrick P, Baskin R, Verbist K, Peters JL, Devidas M, Larsen E, Moore IM, Gu Z, Qu C, Yoshihara H, Porter SN, Pruett-Miller SM, Wu G, Raetz E, Martin PL, Bowman WP, Winick N, Mardis E, Fulton R, Stanulla M, Evans WE, Relling MV, Pui CH, Hunger SP, Loh ML, Handgretinger R, Nichols KE, Yang JJ, Mullighan CG., Cancer Cell 33(5), 2018
PMID: 29681510
Churchman ML, Qian M, Te Kronnie G, Zhang R, Yang W, Zhang H, Lana T, Tedrick P, Baskin R, Verbist K, Peters JL, Devidas M, Larsen E, Moore IM, Gu Z, Qu C, Yoshihara H, Porter SN, Pruett-Miller SM, Wu G, Raetz E, Martin PL, Bowman WP, Winick N, Mardis E, Fulton R, Stanulla M, Evans WE, Relling MV, Pui CH, Hunger SP, Loh ML, Handgretinger R, Nichols KE, Yang JJ, Mullighan CG., Cancer Cell 33(5), 2018
PMID: 29681510
Activating PAX gene family paralogs to complement PAX5 leukemia driver mutations.
Hart MR, Anderson DJ, Porter CC, Neff T, Levin M, Horwitz MS., PLoS Genet 14(9), 2018
PMID: 30216339
Hart MR, Anderson DJ, Porter CC, Neff T, Levin M, Horwitz MS., PLoS Genet 14(9), 2018
PMID: 30216339
Germline activating TYK2 mutations in pediatric patients with two primary acute lymphoblastic leukemia occurrences.
Waanders E, Scheijen B, Jongmans MC, Venselaar H, van Reijmersdal SV, van Dijk AH, Pastorczak A, Weren RD, van der Schoot CE, van de Vorst M, Sonneveld E, Hoogerbrugge N, van der Velden VH, Gruhn B, Hoogerbrugge PM, van Dongen JJ, Geurts van Kessel A, van Leeuwen FN, Kuiper RP., Leukemia 31(4), 2017
PMID: 27733777
Waanders E, Scheijen B, Jongmans MC, Venselaar H, van Reijmersdal SV, van Dijk AH, Pastorczak A, Weren RD, van der Schoot CE, van de Vorst M, Sonneveld E, Hoogerbrugge N, van der Velden VH, Gruhn B, Hoogerbrugge PM, van Dongen JJ, Geurts van Kessel A, van Leeuwen FN, Kuiper RP., Leukemia 31(4), 2017
PMID: 27733777
Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.
Ripperger T, Bielack SS, Borkhardt A, Brecht IB, Burkhardt B, Calaminus G, Debatin KM, Deubzer H, Dirksen U, Eckert C, Eggert A, Erlacher M, Fleischhack G, Frühwald MC, Gnekow A, Goehring G, Graf N, Hanenberg H, Hauer J, Hero B, Hettmer S, von Hoff K, Horstmann M, Hoyer J, Illig T, Kaatsch P, Kappler R, Kerl K, Klingebiel T, Kontny U, Kordes U, Körholz D, Koscielniak E, Kramm CM, Kuhlen M, Kulozik AE, Lamottke B, Leuschner I, Lohmann DR, Meinhardt A, Metzler M, Meyer LH, Moser O, Nathrath M, Niemeyer CM, Nustede R, Pajtler KW, Paret C, Rasche M, Reinhardt D, Rieß O, Russo A, Rutkowski S, Schlegelberger B, Schneider D, Schneppenheim R, Schrappe M, Schroeder C, von Schweinitz D, Simon T, Sparber-Sauer M, Spix C, Stanulla M, Steinemann D, Strahm B, Temming P, Thomay K, von Bueren AO, Vorwerk P, Witt O, Wlodarski M, Wössmann W, Zenker M, Zimmermann S, Pfister SM, Kratz CP., Am J Med Genet A 173(4), 2017
PMID: 28168833
Ripperger T, Bielack SS, Borkhardt A, Brecht IB, Burkhardt B, Calaminus G, Debatin KM, Deubzer H, Dirksen U, Eckert C, Eggert A, Erlacher M, Fleischhack G, Frühwald MC, Gnekow A, Goehring G, Graf N, Hanenberg H, Hauer J, Hero B, Hettmer S, von Hoff K, Horstmann M, Hoyer J, Illig T, Kaatsch P, Kappler R, Kerl K, Klingebiel T, Kontny U, Kordes U, Körholz D, Koscielniak E, Kramm CM, Kuhlen M, Kulozik AE, Lamottke B, Leuschner I, Lohmann DR, Meinhardt A, Metzler M, Meyer LH, Moser O, Nathrath M, Niemeyer CM, Nustede R, Pajtler KW, Paret C, Rasche M, Reinhardt D, Rieß O, Russo A, Rutkowski S, Schlegelberger B, Schneider D, Schneppenheim R, Schrappe M, Schroeder C, von Schweinitz D, Simon T, Sparber-Sauer M, Spix C, Stanulla M, Steinemann D, Strahm B, Temming P, Thomay K, von Bueren AO, Vorwerk P, Witt O, Wlodarski M, Wössmann W, Zenker M, Zimmermann S, Pfister SM, Kratz CP., Am J Med Genet A 173(4), 2017
PMID: 28168833
A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.
Scollon S, Anglin AK, Thomas M, Turner JT, Wolfe Schneider K., J Genet Couns 26(3), 2017
PMID: 28357779
Scollon S, Anglin AK, Thomas M, Turner JT, Wolfe Schneider K., J Genet Couns 26(3), 2017
PMID: 28357779
B lymphoblastic leukemia/lymphoma: new insights into genetics, molecular aberrations, subclassification and targeted therapy.
Zhang X, Rastogi P, Shah B, Zhang L., Oncotarget 8(39), 2017
PMID: 29029550
Zhang X, Rastogi P, Shah B, Zhang L., Oncotarget 8(39), 2017
PMID: 29029550
Intragenic amplification of PAX5: a novel subgroup in B-cell precursor acute lymphoblastic leukemia?
Schwab C, Nebral K, Chilton L, Leschi C, Waanders E, Boer JM, Žaliová M, Sutton R, Öfverholm II, Ohki K, Yamashita Y, Groeneveld-Krentz S, Froňková E, Bakkus M, Tchinda J, Barbosa TDC, Fazio G, Mlynarski W, Pastorczak A, Cazzaniga G, Pombo-de-Oliveira MS, Trka J, Kirschner-Schwabe R, Imamura T, Barbany G, Stanulla M, Attarbaschi A, Panzer-Grümayer R, Kuiper RP, den Boer ML, Cavé H, Moorman AV, Harrison CJ, Strehl S., Blood Adv 1(19), 2017
PMID: 29296789
Schwab C, Nebral K, Chilton L, Leschi C, Waanders E, Boer JM, Žaliová M, Sutton R, Öfverholm II, Ohki K, Yamashita Y, Groeneveld-Krentz S, Froňková E, Bakkus M, Tchinda J, Barbosa TDC, Fazio G, Mlynarski W, Pastorczak A, Cazzaniga G, Pombo-de-Oliveira MS, Trka J, Kirschner-Schwabe R, Imamura T, Barbany G, Stanulla M, Attarbaschi A, Panzer-Grümayer R, Kuiper RP, den Boer ML, Cavé H, Moorman AV, Harrison CJ, Strehl S., Blood Adv 1(19), 2017
PMID: 29296789
Modeling the process of childhood ETV6-RUNX1 B-cell leukemias.
Rodríguez-Hernández G, Schäfer D, Gavilán A, Vicente-Dueñas C, Hauer J, Borkhardt A, Sánchez-García I., Oncotarget 8(60), 2017
PMID: 29254279
Rodríguez-Hernández G, Schäfer D, Gavilán A, Vicente-Dueñas C, Hauer J, Borkhardt A, Sánchez-García I., Oncotarget 8(60), 2017
PMID: 29254279
Treatment-related toxicities in children with acute lymphoblastic leukaemia predisposition syndromes.
Schmiegelow K., Eur J Med Genet 59(12), 2016
PMID: 26876989
Schmiegelow K., Eur J Med Genet 59(12), 2016
PMID: 26876989
Genetic predisposition to leukemia and other hematologic malignancies.
Feurstein S, Drazer MW, Godley LA., Semin Oncol 43(5), 2016
PMID: 27899193
Feurstein S, Drazer MW, Godley LA., Semin Oncol 43(5), 2016
PMID: 27899193
Germ line mutations associated with leukemias.
Porter CC., Hematology Am Soc Hematol Educ Program 2016(1), 2016
PMID: 27913495
Porter CC., Hematology Am Soc Hematol Educ Program 2016(1), 2016
PMID: 27913495
Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.
Zhang MY, Churpek JE, Keel SB, Walsh T, Lee MK, Loeb KR, Gulsuner S, Pritchard CC, Sanchez-Bonilla M, Delrow JJ, Basom RS, Forouhar M, Gyurkocza B, Schwartz BS, Neistadt B, Marquez R, Mariani CJ, Coats SA, Hofmann I, Lindsley RC, Williams DA, Abkowitz JL, Horwitz MS, King MC, Godley LA, Shimamura A., Nat Genet 47(2), 2015
PMID: 25581430
Zhang MY, Churpek JE, Keel SB, Walsh T, Lee MK, Loeb KR, Gulsuner S, Pritchard CC, Sanchez-Bonilla M, Delrow JJ, Basom RS, Forouhar M, Gyurkocza B, Schwartz BS, Neistadt B, Marquez R, Mariani CJ, Coats SA, Hofmann I, Lindsley RC, Williams DA, Abkowitz JL, Horwitz MS, King MC, Godley LA, Shimamura A., Nat Genet 47(2), 2015
PMID: 25581430
Molecular basis and clinical significance of genetic aberrations in B-cell precursor acute lymphoblastic leukemia.
Ghazavi F, Lammens T, Van Roy N, Poppe B, Speleman F, Benoit Y, Van Vlierberghe P, De Moerloose B., Exp Hematol 43(8), 2015
PMID: 26101161
Ghazavi F, Lammens T, Van Roy N, Poppe B, Speleman F, Benoit Y, Van Vlierberghe P, De Moerloose B., Exp Hematol 43(8), 2015
PMID: 26101161
Infection causes childhood leukemia.
Hauer J, Martín-Lorenzo A, Sánchez-García I., Aging (Albany NY) 7(9), 2015
PMID: 26412458
Hauer J, Martín-Lorenzo A, Sánchez-García I., Aging (Albany NY) 7(9), 2015
PMID: 26412458
Genetically engineered mouse models of human B-cell precursor leukemias.
Hauer J, Borkhardt A, Sánchez-García I, Cobaleda C., Cell Cycle 13(18), 2014
PMID: 25486471
Hauer J, Borkhardt A, Sánchez-García I, Cobaleda C., Cell Cycle 13(18), 2014
PMID: 25486471
6 References
Daten bereitgestellt von Europe PubMed Central.
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia.
Shah S, Schrader KA, Waanders E, Timms AE, Vijai J, Miething C, Wechsler J, Yang J, Hayes J, Klein RJ, Zhang J, Wei L, Wu G, Rusch M, Nagahawatte P, Ma J, Chen SC, Song G, Cheng J, Meyers P, Bhojwani D, Jhanwar S, Maslak P, Fleisher M, Littman J, Offit L, Rau-Murthy R, Fleischut MH, Corines M, Murali R, Gao X, Manschreck C, Kitzing T, Murty VV, Raimondi S, Kuiper RP, Simons A, Schiffman JD, Onel K, Plon SE, Wheeler D, Ritter D, Ziegler DS, Tucker K, Sutton R, Chenevix-Trench G, Li J, Huntsman DG, Hansford S, Senz J, Walsh T, Lee M, Hahn CN, Roberts K, King MC, Lo SM, Levine RL, Viale A, Socci ND, Nathanson KL, Scott HS, Daly M, Lipkin SM, Lowe SW, Downing JR, Altshuler D, Sandlund JT, Horwitz MS, Mullighan CG, Offit K., Nat. Genet. 45(10), 2013
PMID: 24013638
Shah S, Schrader KA, Waanders E, Timms AE, Vijai J, Miething C, Wechsler J, Yang J, Hayes J, Klein RJ, Zhang J, Wei L, Wu G, Rusch M, Nagahawatte P, Ma J, Chen SC, Song G, Cheng J, Meyers P, Bhojwani D, Jhanwar S, Maslak P, Fleisher M, Littman J, Offit L, Rau-Murthy R, Fleischut MH, Corines M, Murali R, Gao X, Manschreck C, Kitzing T, Murty VV, Raimondi S, Kuiper RP, Simons A, Schiffman JD, Onel K, Plon SE, Wheeler D, Ritter D, Ziegler DS, Tucker K, Sutton R, Chenevix-Trench G, Li J, Huntsman DG, Hansford S, Senz J, Walsh T, Lee M, Hahn CN, Roberts K, King MC, Lo SM, Levine RL, Viale A, Socci ND, Nathanson KL, Scott HS, Daly M, Lipkin SM, Lowe SW, Downing JR, Altshuler D, Sandlund JT, Horwitz MS, Mullighan CG, Offit K., Nat. Genet. 45(10), 2013
PMID: 24013638
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.
Sherborne AL, Hosking FJ, Prasad RB, Kumar R, Koehler R, Vijayakrishnan J, Papaemmanuil E, Bartram CR, Stanulla M, Schrappe M, Gast A, Dobbins SE, Ma Y, Sheridan E, Taylor M, Kinsey SE, Lightfoot T, Roman E, Irving JA, Allan JM, Moorman AV, Harrison CJ, Tomlinson IP, Richards S, Zimmermann M, Szalai C, Semsei AF, Erdelyi DJ, Krajinovic M, Sinnett D, Healy J, Gonzalez Neira A, Kawamata N, Ogawa S, Koeffler HP, Hemminki K, Greaves M, Houlston RS., Nat. Genet. 42(6), 2010
PMID: 20453839
Sherborne AL, Hosking FJ, Prasad RB, Kumar R, Koehler R, Vijayakrishnan J, Papaemmanuil E, Bartram CR, Stanulla M, Schrappe M, Gast A, Dobbins SE, Ma Y, Sheridan E, Taylor M, Kinsey SE, Lightfoot T, Roman E, Irving JA, Allan JM, Moorman AV, Harrison CJ, Tomlinson IP, Richards S, Zimmermann M, Szalai C, Semsei AF, Erdelyi DJ, Krajinovic M, Sinnett D, Healy J, Gonzalez Neira A, Kawamata N, Ogawa S, Koeffler HP, Hemminki K, Greaves M, Houlston RS., Nat. Genet. 42(6), 2010
PMID: 20453839
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.
Papaemmanuil E, Hosking FJ, Vijayakrishnan J, Price A, Olver B, Sheridan E, Kinsey SE, Lightfoot T, Roman E, Irving JA, Allan JM, Tomlinson IP, Taylor M, Greaves M, Houlston RS., Nat. Genet. 41(9), 2009
PMID: 19684604
Papaemmanuil E, Hosking FJ, Vijayakrishnan J, Price A, Olver B, Sheridan E, Kinsey SE, Lightfoot T, Roman E, Irving JA, Allan JM, Tomlinson IP, Taylor M, Greaves M, Houlston RS., Nat. Genet. 41(9), 2009
PMID: 19684604
Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood.
Prasad RB, Hosking FJ, Vijayakrishnan J, Papaemmanuil E, Koehler R, Greaves M, Sheridan E, Gast A, Kinsey SE, Lightfoot T, Roman E, Taylor M, Pritchard-Jones K, Stanulla M, Schrappe M, Bartram CR, Houlston RS, Kumar R, Hemminki K., Blood 115(9), 2009
PMID: 20042726
Prasad RB, Hosking FJ, Vijayakrishnan J, Papaemmanuil E, Koehler R, Greaves M, Sheridan E, Gast A, Kinsey SE, Lightfoot T, Roman E, Taylor M, Pritchard-Jones K, Stanulla M, Schrappe M, Bartram CR, Houlston RS, Kumar R, Hemminki K., Blood 115(9), 2009
PMID: 20042726
Germline genomic variants associated with childhood acute lymphoblastic leukemia.
Trevino LR, Yang W, French D, Hunger SP, Carroll WL, Devidas M, Willman C, Neale G, Downing J, Raimondi SC, Pui CH, Evans WE, Relling MV., Nat. Genet. 41(9), 2009
PMID: 19684603
Trevino LR, Yang W, French D, Hunger SP, Carroll WL, Devidas M, Willman C, Neale G, Downing J, Raimondi SC, Pui CH, Evans WE, Relling MV., Nat. Genet. 41(9), 2009
PMID: 19684603
Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia.
Chen C, Bartenhagen C, Gombert M, Okpanyi V, Binder V, Rottgers S, Bradtke J, Teigler-Schlegel A, Harbott J, Ginzel S, Thiele R, Fischer U, Dugas M, Hu J, Borkhardt A., Genes Chromosomes Cancer 52(6), 2013
PMID: 23508829
Chen C, Bartenhagen C, Gombert M, Okpanyi V, Binder V, Rottgers S, Bradtke J, Teigler-Schlegel A, Harbott J, Ginzel S, Thiele R, Fischer U, Dugas M, Hu J, Borkhardt A., Genes Chromosomes Cancer 52(6), 2013
PMID: 23508829
Export
Markieren/ Markierung löschen
Markierte Publikationen
Web of Science
Dieser Datensatz im Web of Science®Quellen
PMID: 24287434
PubMed | Europe PMC
Suchen in
Google Scholar