Weidong Ding

Pfizer (United States) — United States

Pharmacology, Toxicology and Pharmaceutics · Life Sciences

22h-index1.9kcitations50works5.12yr avg
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Research Topics

Bioactive Compounds and Antitumor Agents(8), Cyclization and Aryne Chemistry(7), Protein Structure and Dynamics(4), Microbial Natural Products and Biosynthesis(4), Synthesis and Biological Evaluation(4)

Publications50 total

Synergistic antitumor effects and mechanisms of KPT-330 combined with venetoclax in Acute Myeloid Leukemia
Blood·2025
CHN1 suppresses B-cell non-Hodgkin lymphoma progression via akt/mTOR pathway
Blood·2025
Efficacy and safety of venetoclax and azacitidine for acute myeloid leukemia in China: a real-world single-center study
BMC Cancer·2025· 2 citedOpen Access
Inhibiting peptidylarginine deiminases (PAD1-4) by targeting a Ca2+ dependent allosteric binding site
Nature Communications·2025· 8 citedOpen Access
Analysis of Trigger Mechanism of Pseudospark Switch with Different Trigger Modes
SSRN Electronic Journal·2025Open Access
Polatuzumab Vedotin Plus Anti-CD20 Monoclonal Antibody and Dexamethasone in Previously Untreated Very Old/Frail Patients with Diffuse Large B-Cell Lymphoma
Blood·2024· 1 cited
Efficacy and safety of bispecific antibodies vs. immune checkpoint blockade combination therapy in cancer: a real-world comparison
Molecular Cancer·2024· 30 citedOpen Access
Zanubrutinib Plus Rituximab in Older Unfit or Frail Previously Untreated Diffuse Large B-Cell Lymphoma: A Prospective Study Based on Comprehensive Geriatric Assessment
SSRN Electronic Journal·2024Open Access
Single-cell phenotypic profiling to identify a set of immune cell protein biomarkers for relapsed and refractory diffuse large B cell lymphoma: A single-center study
Journal of Leukocyte Biology·2022· 8 cited
DesA Prognostic Risk Model of LncRNAs in Patients With Acute Myeloid Leukaemia Based on TCGA Data
Frontiers in Bioengineering and Biotechnology·2022· 18 citedOpen Access
Natural Product Bis-Intercalator Depsipeptides as a New Class of Payloads for Antibody–Drug Conjugates
Bioconjugate Chemistry·2018· 21 cited
Delineating the role of cooperativity in the design of potent PROTACs for BTK
Proceedings of the National Academy of Sciences·2018· 409 citedOpen Access
Rational approach to highly potent and selective apoptosis signal-regulating kinase 1 (ASK1) inhibitors
European Journal of Medicinal Chemistry·2017· 24 citedOpen Access
Molecular characterization and expression profile of the estrogen receptor α gene during different reproductive phases in Monopterus albus
Scientific Reports·2016· 8 citedOpen Access
Selectively targeting an inactive conformation of interleukin-2-inducible T-cell kinase by allosteric inhibitors
Biochemical Journal·2014· 22 cited
Selectively targeting an inactive conformation of IL-2-induced T cell kinase by allosteric inhibitors.
2014· 2 cited
Molecular cloning of propiomelanocortin cDNA and multi-tissue mRNA expression in Parasilurus asotus
Journal of Fishery Sciences of China·2013
Homologous Rearranged DNA can Change Phenotype and Genotype of the Host by Transgenic Method and a QTL Related to Weight was Obtained from it
Advance Journal of Food Science and Technology·2013· 2 citedOpen Access
Characterization of a reductively-activated elimination pathway relevant to the biological chemistry of the kinamycins and lomaiviticins
Chemical Science·2011· 15 cited
Cloning and expression of anti-mullerian hormone partial gene and preparation of polyclonal antibody
JOURNAL OF FISHERIES OF CHINA·2010
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Frequent Co-authors

George A. Ellestad(20), Girija Krishnamurthy(10), Ann Aulabaugh(7), Alan G. Sutherland(6), Cynthia Hess Kenny(6), Lidia Mosyak(6), Valerie S. Bernan(5), Désirée H.H. Tsao(5), Thomas S. Rush(5), Elizabeth G. Dushin(5), Peter J. Petersen(5), Keiko Tabei(4), Lee D. Jennings(4), Leonard A. McDonald(4), William M. Maiese(4), Alexey Ruzin(4), Xiaoya Yun(4), Jeanne S. Chang(3), Michael Greenstein(3), Mohani N. Sukhdeo(3)