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Author Details
Full Name
Oliver Hantschel
Affiliation
Institute of Physiological Chemistry, University of Marburg 35032 Marburg Germany .
ORCID
Career Start Year
2003
Papers
72
H Index
33
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35975004
Synthesis of the l- and d-SH2 domain of the leukaemia oncogene Bcr-Abl.
RSC Chem Biol
2022
34110462
Crizotinib acts as ABL1 inhibitor combining ATP-binding with allosteric inhibition and is active against native BCR-ABL1 and its resistance and compound mutants BCR-ABL1<sup>T315I</sup> and BCR-ABL1<sup>T315I-E255K</sup>.
Ann Hematol
2021
33623882
Precision Medicine in Hematology 2021: Definitions, Tools, Perspectives, and Open Questions.
Hemasphere
2021
34155202
Tuning SAS-6 architecture with monobodies impairs distinct steps of centriole assembly.
Nat Commun
2021
32353124
CDK6 degradation hits Ph+ ALL hard.
Blood
2020
32807795
Selective inhibition of STAT3 signaling using monobodies targeting the coiled-coil and N-terminal domains.
Nat Commun
2020
32385234
Btk SH2-kinase interface is critical for allosteric kinase activation and its targeting inhibits B-cell neoplasms.
Nat Commun
2020
32145686
Monobodies as enabling tools for structural and mechanistic biology.
Curr Opin Struct Biol
2020
30991025
γ-Catenin-Dependent Signals Maintain BCR-ABL1<sup>+</sup> B Cell Acute Lymphoblastic Leukemia.
Cancer Cell
2019
31339688
Rapid Screen for Tyrosine Kinase Inhibitor Resistance Mutations and Substrate Specificity.
ACS Chem Biol
2019
31025848
Targeted Protein Degradation through Cytosolic Delivery of Monobody Binders Using Bacterial Toxins.
ACS Chem Biol
2019
30962580
The phosphatase UBASH3B/Sts-1 is a negative regulator of Bcr-Abl kinase activity and leukemogenesis.
Leukemia
2019
29319304
ATP Site Ligands Determine the Assembly State of the Abelson Kinase Regulatory Core via the Activation Loop Conformation.
J Am Chem Soc
2018
29249144
BioSITe: A Method for Direct Detection and Quantitation of Site-Specific Biotinylation.
J Proteome Res
2018
28983061
BCR-ABL1 compound mutants display differential and dose-dependent responses to ponatinib.
Haematologica
2018
27573554
NDEL1-PDGFRB fusion gene in a myeloid malignancy with eosinophilia associated with resistance to tyrosine kinase inhibitors.
Leukemia
2017
28111465
Differential signaling networks of Bcr-Abl p210 and p190 kinases in leukemia cells defined by functional proteomics.
Leukemia
2017
28347651
Selective Targeting of SH2 Domain-Phosphotyrosine Interactions of Src Family Tyrosine Kinases with Monobodies.
J Mol Biol
2017
29185244
Monobodies as possible next-generation protein therapeutics - a perspective.
Swiss Med Wkly
2017
29108223
Bcr-Abl: one kinase, two isoforms, two diseases.
Oncotarget
2017
28985346
Single-molecule kinetic analysis of HP1-chromatin binding reveals a dynamic network of histone modification and DNA interactions.
Nucleic Acids Res
2017
29235475
Structural and functional dissection of the DH and PH domains of oncogenic Bcr-Abl tyrosine kinase.
Nat Commun
2017
28970898
Kinase-templated abiotic reaction.
Chem Sci
2017
28652245
Unpaired Extracellular Cysteine Mutations of CSF3R Mediate Gain or Loss of Function.
Cancer Res
2017
27916124
Alkaline phosphatase-fused repebody as a new format of immuno-reagent for an immunoassay.
Anal Chim Acta
2017
26864341
Normal ABL1 is a tumor suppressor and therapeutic target in human and mouse leukemias expressing oncogenic ABL1 kinases.
Blood
2016
26677978
Identification and Characterization of Tyrosine Kinase Nonreceptor 2 Mutations in Leukemia through Integration of Kinase Inhibitor Screening and Genomic Analysis.
Cancer Res
2016
27682200
HRD Motif as the Central Hub of the Signaling Network for Activation Loop Autophosphorylation in Abl Kinase.
J Chem Theory Comput
2016
26912659
Allosteric Inhibition of Bcr-Abl Kinase by High Affinity Monobody Inhibitors Directed to the Src Homology 2 (SH2)-Kinase Interface.
J Biol Chem
2016
27052766
2016 International Symposium on Chemical Biology of the NCCR Chemical Biology Campus Biotech, Geneva 13-15.1.2016.
Chimia (Aarau)
2016
25531586
Unexpected off-targets and paradoxical pathway activation by kinase inhibitors.
ACS Chem Biol
2015
26039345
Kinase Regulation in Mycobacterium tuberculosis: Variations on a Theme.
Structure
2015
25721043
Targeting BCR-ABL and JAK2 in Ph+ ALL.
Blood
2015
25779001
Crystal structure of an SH2-kinase construct of c-Abl and effect of the SH2 domain on kinase activity.
Biochem J
2015
23872305
NUP214-ABL1-mediated cell proliferation in T-cell acute lymphoblastic leukemia is dependent on the LCK kinase and various interacting proteins.
Haematologica
2014
25399951
The SH2 domain of Abl kinases regulates kinase autophosphorylation by controlling activation loop accessibility.
Nat Commun
2014
24412932
c-Abl phosphorylates α-synuclein and regulates its degradation: implication for α-synuclein clearance and contribution to the pathogenesis of Parkinson's disease.
Hum Mol Genet
2014
23823659
Specificity and mechanism-of-action of the JAK2 tyrosine kinase inhibitors ruxolitinib and SAR302503 (TG101348).
Leukemia
2014
23277196
Mechanisms of resistance to BCR-ABL and other kinase inhibitors.
Biochim Biophys Acta
2013
23980151
Dissection of the BCR-ABL signaling network using highly specific monobody inhibitors to the SHP2 SH2 domains.
Proc Natl Acad Sci U S A
2013
21903413
Nilotinib as frontline and second-line therapy in chronic myeloid leukemia: open questions.
Crit Rev Oncol Hematol
2012
23226581
Structure, regulation, signaling, and targeting of abl kinases in cancer.
Genes Cancer
2012
23002203
The growing arsenal of ATP-competitive and allosteric inhibitors of BCR-ABL.
Cancer Res
2012
22975324
Mig6 is a sensor of EGF receptor inactivation that directly activates c-Abl to induce apoptosis during epithelial homeostasis.
Dev Cell
2012
23148230
Cell biology: a key driver of therapeutic innovation.
J Cell Biol
2012
22298820
Allosteric BCR-ABL inhibitors in Philadelphia chromosome-positive acute lymphoblastic leukemia: novel opportunities for drug combinations to overcome resistance.
Haematologica
2012
22286129
BCR-ABL uncouples canonical JAK2-STAT5 signaling in chronic myeloid leukemia.
Nat Chem Biol
2012
22000011
Targeting the SH2-kinase interface in Bcr-Abl inhibits leukemogenesis.
Cell
2011
22084171
Targeting allosteric regulatory modules in oncoproteins: "drugging the undruggable".
Oncotarget
2011
19890374
A comprehensive target selectivity survey of the BCR-ABL kinase inhibitor INNO-406 by kinase profiling and chemical proteomics in chronic myeloid leukemia cells.
Leukemia
2010
1 - 50 of 72
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