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An Mb1-Cre-driven oncogenic Kras mutation results in a mouse model of T-acute lymphoblastic leukemia/lymphoma with short latency and high penetrance.

作者信息

Junco Jacob J, Chen Taylor, Rashid Raushan, Terrell Maci, Gant Vincent U, Miller Matthew, Rau Rachel, Lacorazza H Daniel, Rabin Karen R

机构信息

Texas Children's Cancer Center, Department of Pediatrics, Baylor College of Medicine (BCM), Houston, TX, USA.

Department of Pathology & Immunology, BCM, Houston, TX, USA.

出版信息

Leukemia. 2021 Jun;35(6):1777-1781. doi: 10.1038/s41375-020-01036-w. Epub 2020 Sep 11.

Abstract
摘要

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本文引用的文献

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RAS: Striking at the Core of the Oncogenic Circuitry.
Front Oncol. 2019 Sep 24;9:965. doi: 10.3389/fonc.2019.00965. eCollection 2019.
2
Drugging an undruggable pocket on KRAS.
Proc Natl Acad Sci U S A. 2019 Aug 6;116(32):15823-15829. doi: 10.1073/pnas.1904529116. Epub 2019 Jul 22.
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Lmo2 expression defines tumor cell identity during T-cell leukemogenesis.
EMBO J. 2018 Jul 13;37(14). doi: 10.15252/embj.201798783. Epub 2018 Jun 7.
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Constitutive Ras signaling and inactivation cooperate during the development of B-ALL in mice.
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High selective pressure for Notch1 mutations that induce Myc in T-cell acute lymphoblastic leukemia.
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Mutational landscape, clonal evolution patterns, and role of RAS mutations in relapsed acute lymphoblastic leukemia.
Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):11306-11311. doi: 10.1073/pnas.1608420113. Epub 2016 Sep 21.
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The earliest thymic T cell progenitors sustain B cell and myeloid lineage potential.
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