Artículos de revistas sobre el tema "Germline ETV6"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Germline ETV6".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.
Rampersaud, Evadnie, David S. Ziegler, Ilaria Iacobucci, Debbie Payne-Turner, Michelle L. Churchman, Kasmintan A. Schrader, Vijai Joseph et al. "Germline deletion of ETV6 in familial acute lymphoblastic leukemia". Blood Advances 3, n.º 7 (2 de abril de 2019): 1039–46. http://dx.doi.org/10.1182/bloodadvances.2018030635.
Texto completoMoriyama, Takaya, Monika Metzger, Gang Wu, Rina Nishii, Maoxiang Qian, Meenakshi Devidas, Wenjian Yang et al. "Germline Genetic Variation in ETV6 and Predisposition to Childhood Acute Lymphoblastic Leukemia". Blood 126, n.º 23 (3 de diciembre de 2015): 695. http://dx.doi.org/10.1182/blood.v126.23.695.695.
Texto completoJärviaho, Tekla, Benedicte Bang, Vasilios Zachariadis, Fulya Taylan, Jukka Moilanen, Merja Möttönen, C. I. Edvard Smith, Arja Harila-Saari, Riitta Niinimäki y Ann Nordgren. "Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting ETV6". Blood Advances 3, n.º 18 (13 de septiembre de 2019): 2722–31. http://dx.doi.org/10.1182/bloodadvances.2018028795.
Texto completoNishii, Rina, Rebekah Baskin, Takaya Moriyama, Keito Hoshitsuki, Monika L. Metzger, Gang Wu, Meenakshi Devidas et al. "Comprehensive Functional Characterization of Germline ETV6 Variants Associated with Inherited Predisposition to Acute Lymphoblastic Leukemia in Children". Blood 128, n.º 22 (2 de diciembre de 2016): 1085. http://dx.doi.org/10.1182/blood.v128.22.1085.1085.
Texto completoRio-Machin, Ana y Jude Fitzgibbon. "Germline ETV6 variants: not ALL created equally". Blood 137, n.º 3 (21 de enero de 2021): 288–89. http://dx.doi.org/10.1182/blood.2020008190.
Texto completoRomero, Diana. "ETV6 germline mutation — a risk for ALL". Nature Reviews Clinical Oncology 13, n.º 1 (17 de noviembre de 2015): 4. http://dx.doi.org/10.1038/nrclinonc.2015.211.
Texto completoJones, Courtney L., Gregory Kirkpatrick, Courtney Fleenor, Welsh Seth, Leila J. Noetzli, Susan Fosmire, Dmitry Baturin et al. "ETV6 Regulates Pax5 Expression in Early B Cell Development". Blood 128, n.º 22 (2 de diciembre de 2016): 2655. http://dx.doi.org/10.1182/blood.v128.22.2655.2655.
Texto completoKirkpatrick, Greg, Courtney Jones, Susan Fosmire, Christopher Porter y Jorge DiPaola. "2485". Journal of Clinical and Translational Science 1, S1 (septiembre de 2017): 65–66. http://dx.doi.org/10.1017/cts.2017.234.
Texto completoFeurstein, Simone y Lucy A. Godley. "Germline ETV6 mutations and predisposition to hematological malignancies". International Journal of Hematology 106, n.º 2 (29 de mayo de 2017): 189–95. http://dx.doi.org/10.1007/s12185-017-2259-4.
Texto completoBernardi, Simona, Mirko Farina, Camilla Zanaglio, Federica Cattina, Nicola Polverelli, Francesca Schieppati, Federica Re et al. "ETV6: A Candidate Gene for Predisposition to “Blend Pedigrees”? A Case Report from the NEXT-Famly Clinical Trial". Case Reports in Hematology 2020 (11 de enero de 2020): 1–7. http://dx.doi.org/10.1155/2020/2795656.
Texto completoBernardi, Simona, Camilla Zanaglio, Elif Dereli Eke, Federica Cattina, Mirko Farina, Stefania Masneri, Benedetta Rambaldi et al. "Identification of a Novel Mutation Predisposing to Familial AML and MDS Syndrome By a NGS Approach". Blood 132, Supplement 1 (29 de noviembre de 2018): 4387. http://dx.doi.org/10.1182/blood-2018-99-109927.
Texto completoKarastaneva, Anna, Karin Nebral, Axel Schlagenhauf, Marcel Baschin, Raghavendra Palankar, Herbert Juch, Ellen Heitzer et al. "Novel phenotypes observed in patients with ETV6-linked leukaemia/familial thrombocytopenia syndrome and a biallelic ARID5B risk allele as leukaemogenic cofactor". Journal of Medical Genetics 57, n.º 6 (8 de noviembre de 2019): 427–33. http://dx.doi.org/10.1136/jmedgenet-2019-106339.
Texto completoDirse, Vaidas, Rimvydas Norvilas, Egle Gineikiene, Rėda Matuzevičienė, Laimonas Griskevicius y Egle Preiksaitiene. "ETV6 and NOTCH1 germline variants in adult acute leukemia". Leukemia & Lymphoma 59, n.º 4 (4 de agosto de 2017): 1022–24. http://dx.doi.org/10.1080/10428194.2017.1359742.
Texto completoZhang, Michael Y., Jane E. Churpek, Siobán B. Keel, Tom Walsh, Ming K. Lee, Keith R. Loeb, Suleyman Gulsuner et al. "Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy". Nature Genetics 47, n.º 2 (12 de enero de 2015): 180–85. http://dx.doi.org/10.1038/ng.3177.
Texto completoGocho, Yoshihiro y Jun J. Yang. "Genetic defects in hematopoietic transcription factors and predisposition to acute lymphoblastic leukemia". Blood 134, n.º 10 (5 de septiembre de 2019): 793–97. http://dx.doi.org/10.1182/blood.2018852400.
Texto completoFisher, Marlie H., Greg Kirkpatrick, Courtney L. Jones, Brett M. Stevens, Michael Callaghan, Eric Pietras, Kenneth L. Jones, Christopher C. Porter y Jorge Di Paola. "Germline Mutations in ETV6 are Associated with In Vivo cytoplasmic Localization of ETV6 and Cause Transcriptional Dysregulation of Interferon Response Genes". Blood 134, Supplement_1 (13 de noviembre de 2019): 2316. http://dx.doi.org/10.1182/blood-2019-132032.
Texto completoDifilippo, Emma Catherine, Alejandro Ferrer, Laura Schultz-Rogers, Naseema Gangat, Shakila P. Khan, Aref Al-Kali, Abhishek A. Mangaonkar et al. "Spectrum of Hematological Malignancies in 130 Patients with Germline Predisposition Syndromes - Mayo Clinic Germline Predisposition Study". Blood 136, Supplement 1 (5 de noviembre de 2020): 34–35. http://dx.doi.org/10.1182/blood-2020-139050.
Texto completoHo, Thanh, Juliana Perez Botero, William J. Hogan, Saad S. Kenderian, Naseema Gangat, Ayalew Tefferi, Roshini S. Abraham et al. "Clinical Spectrum of Germline Mutations with Predisposition to Myeloid Neoplasms- 2016 World Health Organization Classification Update". Blood 128, n.º 22 (2 de diciembre de 2016): 300. http://dx.doi.org/10.1182/blood.v128.22.300.300.
Texto completoDi Paola, Jorge. "Novel Congenital Platelet Disorders". Blood 128, n.º 22 (2 de diciembre de 2016): SCI—39—SCI—39. http://dx.doi.org/10.1182/blood.v128.22.sci-39.sci-39.
Texto completoTopka, Sabine, Joseph Vijai, Michael F. Walsh, Lauren Jacobs, Ann Maria, Danylo Villano, Pragna Gaddam et al. "Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia". PLOS Genetics 11, n.º 6 (23 de junio de 2015): e1005262. http://dx.doi.org/10.1371/journal.pgen.1005262.
Texto completoFisher, Marlie H., Leila J. Noetzli, Michael Callaghan, Walter H. Kahr, Jesse W. Rowley y Jorge Di Paola. "Studying the Role of ETV6 in Megakaryopoiesis and Thrombopoiesis Using a Novel CRISPR-Cas9 Halotag Genome Editing Strategy". Blood 134, Supplement_1 (13 de noviembre de 2019): 2468. http://dx.doi.org/10.1182/blood-2019-131967.
Texto completorodriguez-Hernandez, Guillermo, Julia Hauer, Alberto Martín-Lorenzo, Daniel Schaefer, Christoph Bartenhagen, Idoia Garcia-Ramirez, Franziska Auer et al. "A New ETV6-RUNX1 In Vivo Model Produces a Phenocopy of the Human Pb-ALL". Blood 126, n.º 23 (3 de diciembre de 2015): 3658. http://dx.doi.org/10.1182/blood.v126.23.3658.3658.
Texto completoJunk, Stefanie V., Norman Klein, Sabine Schreek, Martin Zimmermann, Anja Möricke, Kirsten Bleckmann, Gunnar Cario, Martin Schrappe, Christian P. Kratz y Martin Stanulla. "TP53, ETV6 and RUNX1 Germline Variants in Patients Developing Secondary Neoplasms after Treatment for Childhood Acute Lymphoblastic Leukemia". Blood 130, Suppl_1 (7 de diciembre de 2017): 884. http://dx.doi.org/10.1182/blood.v130.suppl_1.884.884.
Texto completoEllinghaus, E., M. Stanulla, G. Richter, D. Ellinghaus, G. te Kronnie, G. Cario, G. Cazzaniga et al. "Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia". Leukemia 26, n.º 5 (11 de noviembre de 2011): 902–9. http://dx.doi.org/10.1038/leu.2011.302.
Texto completoMaierhofer, Anna, Constance Baer, Christian Pohlkamp, Manja Meggendorfer, Wolfgang Kern, Claudia Haferlach y Torsten Haferlach. "Putative Germline Variants in the Predisposition Genes DDX41, ETV6 and GATA2 investigated in 1,228 Patients with Sporadic AML or MDS". Blood 136, Supplement 1 (5 de noviembre de 2020): 17–18. http://dx.doi.org/10.1182/blood-2020-140742.
Texto completoBaskin, Rebekah, Rina Nishii, Javad Nadaf, Katherine Verbist, Paige Tedrick, Keito Hoshitsuki, Maoxiang Qian et al. "Functional analysis of germline ETV6 variants associated with familial thrombocytopenia and acute lymphoblastic leukemia". Experimental Hematology 53 (septiembre de 2017): S126—S127. http://dx.doi.org/10.1016/j.exphem.2017.06.320.
Texto completode Smith, Adam J., Geneviève Lavoie, Kyle M. Walsh, Sumeet Aujla, Erica Evans, Helen M. Hansen, Ivan Smirnov et al. "Germline GAB2 Mutations in Childhood Acute Lymphoblastic Leukemia". Blood 132, Supplement 1 (29 de noviembre de 2018): 388. http://dx.doi.org/10.1182/blood-2018-99-119235.
Texto completoOkpanyi, Vera, Christoph Bartenhagen, Michael Gombert, Vera Binder, Hans-Ulrich Klein, Silja Roettgers, Jochen Harbott, Martin Dugas y Arndt Borkhardt. "Global Identification of Genomic Structural Variants In Childhood ETV6/RUNX1 (TEL/AML1) Acute Lymphoblastic Leukemias by Mate-Pair Massively Parallel Sequencing." Blood 116, n.º 21 (19 de noviembre de 2010): 3364. http://dx.doi.org/10.1182/blood.v116.21.3364.3364.
Texto completoMoriyama, Takaya, Monika L. Metzger, Gang Wu, Rina Nishii, Maoxiang Qian, Meenakshi Devidas, Wenjian Yang et al. "Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study". Lancet Oncology 16, n.º 16 (diciembre de 2015): 1659–66. http://dx.doi.org/10.1016/s1470-2045(15)00369-1.
Texto completoNoetzli, Leila, Richard W. Lo, Alisa B. Lee-Sherick, Michael Callaghan, Patrizia Noris, Anna Savoia, Madhvi Rajpurkar et al. "Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia". Nature Genetics 47, n.º 5 (25 de marzo de 2015): 535–38. http://dx.doi.org/10.1038/ng.3253.
Texto completoDuployez, Nicolas, Wadih Abou Chahla, Sophie Lejeune, Alice Marceau-Renaut, Guillaume Letizia, Thomas Boyer, Sandrine Geffroy et al. "Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia". European Journal of Haematology 100, n.º 1 (9 de noviembre de 2017): 104–7. http://dx.doi.org/10.1111/ejh.12981.
Texto completoPoggi, Marjorie, Matthias Canault, Marie Favier, Ernest Turro, Paul Saultier, Dorsaf Ghalloussi, Veronique Baccini et al. "Germline variants in ETV6 underlie reduced platelet formation, platelet dysfunction and increased levels of circulating CD34 + progenitors". Haematologica 102, n.º 2 (23 de septiembre de 2016): 282–94. http://dx.doi.org/10.3324/haematol.2016.147694.
Texto completoVarghese, Anna M., Isha Singh, Rituraj Singh, Siddharth Kunte, Joanne F. Chou, Marinela Capanu, Winston Wong et al. "Early-Onset Pancreas Cancer: Clinical Descriptors, Genomics, and Outcomes". JNCI: Journal of the National Cancer Institute 113, n.º 9 (23 de marzo de 2021): 1194–202. http://dx.doi.org/10.1093/jnci/djab038.
Texto completoBaskin-Doerfler, Rebekah, Mackenzie Bloom, Ninad Oak, Katherine Verbist, Paige Tedrick, Rachel Bassett, Rina Nishii et al. "ASSESSING THE IMPACT OF A B-ALL-ASSOCIATED GERMLINE ETV6 VARIANT ON MURINE HEMATOPOIESIS AND STEM CELL FUNCTION". Experimental Hematology 76 (agosto de 2019): S58. http://dx.doi.org/10.1016/j.exphem.2019.06.328.
Texto completoKansal, Rina. "Germline Predisposition to Myeloid Neoplasms in Inherited Bone Marrow Failure Syndromes, Inherited Thrombocytopenias, Myelodysplastic Syndromes and Acute Myeloid Leukemia: Diagnosis and Progression to Malignancy". Journal of Hematology Research 8 (2 de junio de 2021): 11–38. http://dx.doi.org/10.12974/2312-5411.2021.08.3.
Texto completoTrevino, Lisa R., Wenjian Yang, Stephen Hunger, William L. Carroll, Meenakshi Devidas, Cheryl L. Willman, James Downing, William E. Evans, Ching-Hon Pui y Mary V. Relling. "Children with t(12;21)/TEL-AML1-Positive Acute Lymphoblastic Leukemia Exhibit a Distinct Germline Genomic Signature." Blood 110, n.º 11 (16 de noviembre de 2007): 760. http://dx.doi.org/10.1182/blood.v110.11.760.760.
Texto completoKirály, Péter Attila, Krisztián Kállay, Dóra Marosvári, Gábor Benyó, Anita Szőke, Judit Csomor y Csaba Bödör. "Familiáris myelodysplasiás szindróma és akut myeloid leukaemia klinikai és genetikai háttere". Orvosi Hetilap 157, n.º 8 (febrero de 2016): 283–89. http://dx.doi.org/10.1556/650.2016.30375.
Texto completoYoshino, Hiroshi, Yohei Nishiyama, Hiroshi Kamma, Tomohiro Chiba, Masachika Fujiwara, Takehiro Karaho, Yasunao Kogashiwa et al. "Functional characterization of a germline ETV6 variant associated with inherited thrombocytopenia, acute lymphoblastic leukemia, and salivary gland carcinoma in childhood". International Journal of Hematology 112, n.º 2 (4 de mayo de 2020): 217–22. http://dx.doi.org/10.1007/s12185-020-02885-y.
Texto completoMedford, Arielle J., Lauren Oshry, Baris Boyraz, Lesli Kiedrowski, Sofia Menshikova, Anna Butusova, Charles S. Dai et al. "TRK inhibitor in a patient with metastatic triple-negative breast cancer and NTRK fusions identified via cell-free DNA analysis". Therapeutic Advances in Medical Oncology 15 (enero de 2023): 175883592311528. http://dx.doi.org/10.1177/17588359231152844.
Texto completoMullighan, Charles G., Xiaoping Su, Jing Ma, Wenjian Yang, Mary V. Relling, William L. Carroll, Gregory Reaman et al. "Genome-Wide Profiling of High-Risk Pediatric Acute Lymphoblastic Leukemia (ALL): The ALL Pilot Project for the Therapeutically Applicable Research To Generate Effective Treatments (TARGET) Initiative." Blood 110, n.º 11 (16 de noviembre de 2007): 229. http://dx.doi.org/10.1182/blood.v110.11.229.229.
Texto completoBraunstein, Evan M., Ruijuan Li, Nara Sobreira, Christopher Gocke, Robert A. Brodsky, David Valle y Linzhao Cheng. "A Germline Mutation in ERBB3 Predisposes to Inherited Erythroid Myelodysplasia/Erythroleukemia". Blood 126, n.º 23 (3 de diciembre de 2015): 4105. http://dx.doi.org/10.1182/blood.v126.23.4105.4105.
Texto completoBloom, Mackenzie, Rebekah Baskin-Doerfler, Ninad Oak, Patrick Ozark, Katherine Verbist, Alexa Stroh, Chunliang Li, Rina Nishii, Jun Yang y Kim Nichols. "3049 – THROMBOCYTOPENIA 5-ASSOCIATED GERMLINE ETV6 VARIANT IMPAIRS THE HEMATOPOIETIC STEM AND PROGENITOR CELL STRESS RESPONSE AND INDUCES AN INFLAMMATORY GENE SIGNATURE". Experimental Hematology 100 (agosto de 2021): S66. http://dx.doi.org/10.1016/j.exphem.2021.12.268.
Texto completoJunk, Stefanie V., Norman Klein, Sabine Schreek, Martin Zimmermann, Anja Möricke, Kirsten Bleckmann, Julia Alten et al. "TP53, ETV6 and RUNX1 germline variants in a case series of patients developing secondary neoplasms after treatment for childhood acute lymphoblastic leukemia". Haematologica 104, n.º 9 (9 de julio de 2019): e402-e405. http://dx.doi.org/10.3324/haematol.2018.205849.
Texto completoKwok, Brian, Renee Mohrmann, Kim Janatpour, Yin Xu, Matthew McGinniss, Aine Yung, Hong Drum et al. "Next-Generation Sequencing Of ASXL1, TP53, RUNX1, EZH2, and ETV6 Identifies a Significant Proportion Of Lower-Risk Myelodysplastic Syndromes With Poor Prognostic Indicators". Blood 122, n.º 21 (15 de noviembre de 2013): 1552. http://dx.doi.org/10.1182/blood.v122.21.1552.1552.
Texto completoVoshtina, Ensi, Arun K. Singavi, Amanda Jacquart, Lyndsey Runaas, Ehab L. Atallah, Laura C. Michaelis y Sameem Abedin. "Systematic Screening for Familial Leukemia Based on Somatic Genomic Profiling Results". Blood 132, Supplement 1 (29 de noviembre de 2018): 2253. http://dx.doi.org/10.1182/blood-2018-99-117020.
Texto completoTrottier, Amy M., Ira L. Kraft, Lawrence J. Druhan, Amanda Lance, Belinda R. Avalos y Lucy A. Godley. "New Germline Syndrome Discovery: Heterozygous CSF3R Mutations May Predispose to Myeloid and Lymphoid Malignancies". Blood 134, Supplement_1 (13 de noviembre de 2019): 2543. http://dx.doi.org/10.1182/blood-2019-129492.
Texto completoQian, Maoxiang, Heng Xu, Virginia Perez-Andreu, Kathryn G. Roberts, Hui Zhang, Wenjian Yang, Shouyue Zhang et al. "Novel susceptibility variants at the ERG locus for childhood acute lymphoblastic leukemia in Hispanics". Blood 133, n.º 7 (14 de febrero de 2019): 724–29. http://dx.doi.org/10.1182/blood-2018-07-862946.
Texto completoWu, Hsin-Ta, Ekaterina Kalashnikova, Samay Mehta, Raheleh Salari, Himanshu Sethi, Bernhard Zimmermann, Paul R. Billings y Alexey Aleshin. "Characterization of clonal hematopoiesis of indeterminate potential mutations from germline whole exome sequencing data." Journal of Clinical Oncology 38, n.º 15_suppl (20 de mayo de 2020): 1525. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.1525.
Texto completode Smith, Adam J., Kyle M. Walsh, Ivan Smirnov, Sumeet Aujla, Erica Sanders, Hansen M. Helen, Catherine Metayer y Joseph L. Wiemels. "Somatic and Germline Mutational Heterogeneity in High Hyperdiploid Acute Lymphoblastic Leukemia". Blood 128, n.º 22 (2 de diciembre de 2016): 1727. http://dx.doi.org/10.1182/blood.v128.22.1727.1727.
Texto completoHosono, Naoko, Hasan Rehman, Bartlomiej Przychodzen, Ines Gomez-Segui, Kathryn M. Guinta, Kenichi Yoshida, Satoru Miyano et al. "Various Germline Congenital Disorder Genes Are Somatically Mutated in Myeloid Malignancies". Blood 120, n.º 21 (16 de noviembre de 2012): 1405. http://dx.doi.org/10.1182/blood.v120.21.1405.1405.
Texto completo