M. Weidner

发表

FLT3 and CDK4/6 inhibitors: Signaling mechanisms and tumor burden in subcutaneous and orthotopic mouse models of acute myeloid leukemia

Yu-Nien Sun, Cheng-Pang Hsu, Yaping Zhang, 2014, Journal of Pharmacokinetics and Pharmacodynamics.

Synthesis and structure-activity relationship of trisubstituted thiazoles as Cdc7 kinase inhibitors.

Guomin Yao, M. Bartberger, J. Bailis, 2014, European journal of medicinal chemistry.

Discovery of AMG 925, a FLT3 and CDK4 dual kinase inhibitor with preferential affinity for the activated state of FLT3.

K. Pattabiraman, Zhulun Wang, C. Quéva, 2014, Journal of medicinal chemistry.

Determination of the DNA crosslinking sequence specificity of reductively activated mitomycin C at single-nucleotide resolution: deoxyguanosine residues at CpG are crosslinked preferentially

M. Weidner, P. B. Hopkins, J. Millard, 1990 .

Small Molecule Therapeutics Preclinical Evaluation of AMG 925 , a FLT 3 / CDK 4 Dual Kinase Inhibitor for Treating Acute Myeloid Leukemia

A. Kamb, Ji Ma, J. Medina, 2014 .

Sequence preferences of DNA interstrand cross-linking agents: dG-to-dG cross-linking at 5'-CG by structurally simplified analogues of mitomycin C.

S. Sigurdsson, M. Weidner, P. B. Hopkins, 1990, Biochemistry.

Sequence preferences of DNA interstrand cross-linking agents: Importance of minimal DNA structural reorganization in the cross-linking reactions of mechlorethamine, cisplatin and mitomycin C

S. Sigurdsson, M. Weidner, J. J. Kirchner, 1991 .

Determination at single nucleotide resolution of the sequence specificity of DNA interstrand crosslinking agents in DNA fragments

M. Weidner, P. B. Hopkins, J. Millard, 1989 .

Preclinical Evaluation of AMG 925, a FLT3/CDK4 Dual Kinase Inhibitor for Treating Acute Myeloid Leukemia

Alexander Kamb, John Eksterowicz, C. Quéva, 2014, Molecular Cancer Therapeutics.

Hydroxyl radical footprinting.

J. Hayes, B. Dombroski, T. Tullius, 1991, Methods in enzymology.

SLC46A3 Is Required to Transport Catabolites of Noncleavable Antibody Maytansine Conjugates from the Lysosome to the Cytoplasm.

D. Rock, Brooke M. Rock, W. Fanslow, 2015, Cancer research.

FLT3 and CDK4/6 inhibitors: Signaling mechanisms and tumor burden in subcutaneous and orthotopic mouse models of acute myeloid leukemia

Yu‐Nien Sun, Cheng-Pang Hsu, Yilong Zhang, 2014, Journal of Pharmacokinetics and Pharmacodynamics.

Proteolytic artifacts in SDS-PAGE analysis of selected periodontal pathogens.

D. Grenier, M. Weidner, D. Mayrand, 1996, Oral microbiology and immunology.

Sequence preferences of DNA interstrand crosslinking agents: quantitation of interstrand crosslink locations in DNA duplex fragments containing multiple crosslinkable sites.

M. Weidner, J. J. Kirchner, P. B. Hopkins, 1991, Nucleic acids research.

Discovery of AMG 925, a FLT3 and CDK4 dual kinase inhibitor with preferential affinity for the activated state of FLT3.

K. Pattabiraman, Zhulun Wang, C. Quéva, 2014, Journal of medicinal chemistry.