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Frontiers in Oncology|July 8, 2014
Strategies of dose escalation in the treatment of locally advanced non-small cell lung cancer: image guidance and beyondAlexander Chi, Nam Phong Nguyen, James S Welsh, et al.
Cells|November 2, 2019
The Oncogene AF1Q is Associated with WNT and STAT Signaling and Offers a Novel Independent Prognostic Marker in Patients with Resectable Esophageal CancerElisabeth S Gruber, Georg Oberhuber, Peter Birner, et al.
Leukemia & Lymphoma|October 6, 2007
Antiangiogenic activity of thalidomide in combination with fludarabine, carboplatin, and topotecan for high-risk acute myelogenous leukemiaPaul Barr, Pingfu Fu, Hillard Lazarus, et al.
Cells|December 29, 2020
Erratum: Gruber, E.S.; et al. The Oncogene AF1Q is Associated with WNT and STAT Signaling and Offers a Novel Independent Prognostic Marker in Patients with Resectable Esophageal Cancer. <i>Cells</i> 2019, <i>8</i>, 1357Elisabeth S Gruber, Georg Oberhuber, Peter Birner, et al.
Blood|March 22, 2007
Abnormal hematopoiesis in Gab2 mutant miceYi Zhang, Ernesto Diaz-Flores, Geqiang Li, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 30, 2013
Sibling donor and recipient immune modulation with atorvastatin for the prophylaxis of acute graft-versus-host diseaseMehdi Hamadani, Laura F Gibson, Scot C Remick, et al.
Cancer Research|June 4, 2008
Identification of 6-benzylthioinosine as a myeloid leukemia differentiation-inducing compoundDavid N Wald, Hanna M Vermaat, Shaolei Zang, et al.
British Journal of Haematology|April 19, 2011
MIR29B regulates expression of MLLT11 (AF1Q), an MLL fusion partner, and low MIR29B expression associates with adverse cytogenetics and poor overall survival in AMLYin Xiong, Zejuan Li, Min Ji, et al.
Oncotarget|January 20, 2018
Targeting T-cell malignancies using anti-CD4 CAR NK-92 cellsKevin G Pinz, Elizabeth Yakaboski, Alexander Jares, et al.
Genes & Diseases|July 3, 2025
Corrigendum to "Monogenic deficiency in murine intestinal Cdc42 leads to mucosal inflammation that induces crypt dysplasia" [Genes & Dis 11 (2024) 413-429]Dongsheng Zhang, Wenjuan Tang, Haitao Niu, et al.
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