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Blood Cancer Journal|May 2, 2022
Hypomethylating agent and venetoclax with FLT3 inhibitor "triplet" therapy in older/unfit patients with FLT3 mutated AMLMusa Yilmaz, Hagop Kantarjian, Nicholas J Short, et al.
Kidney360|April 4, 2022
Abnormalities in Cardiac Structure and Function among Individuals with CKD: The COMBINE TrialAnn A Wang, Xuan Cai, Anand Srivastava, et al.
Bioorganic & Medicinal Chemistry Letters|November 12, 2010
Synthesis and biological evaluations of P4-benzoxaborole-substituted macrocyclic inhibitors of HCV NS3 proteaseCharles Z Ding, Yong-Kang Zhang, Xianfeng Li, et al.
JAMA Dermatology|March 16, 2017
Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Standard Reporting and Evaluation Guidelines: Results of a National Institutes of Health Working GroupEmanual Maverakis, Elizabeth A Wang, Kanade Shinkai, et al.
Nature Genetics|December 8, 1998
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairmentJ H Xia, C Y Liu, B S Tang, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 14, 2023
Triple-Negative Primary Myelofibrosis: A Bone Marrow Pathology Group StudyYahya A Al-Ghamdi, Jonathan Lake, Adam Bagg, et al.
European Journal of Endocrinology|September 15, 2021
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3James Nolan, Purdey J Campbell, Suzanne J Brown, et al.
IJTLD Open|May 27, 2024
Characteristics of TPT initiation and completion among people living with HIVL Gunde, A Wang, D Payne, et al.
American Journal of Hematology|April 10, 2019
DDX41 mutations in myeloid neoplasms are associated with male gender, TP53 mutations and high-risk diseaseAndrés E Quesada, Mark J Routbort, Courtney D DiNardo, et al.
Molecular Cancer Therapeutics|November 17, 2017
Characterization of SGN-CD123A, A Potent CD123-Directed Antibody-Drug Conjugate for Acute Myeloid LeukemiaFu Li, May Kung Sutherland, Changpu Yu, et al.
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