Daniel Zingg

8PUBLICATIONS
94CO-AUTHORS
Molecular targetsHaematological tumours
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Publications (8)

|Dec 29, 2025
C-Terminal Truncation and Fusion Partner Determine Oncogenicity of FGFR3.

Julia Yemelyanenko, Jinhyuk Bhin, Eline van der Burg

|Oct 27, 2025
PI3Kα Inhibitor and Degrader Inavolisib Can Co-opt FGFR2 to Enhance Responses in Patients with PIK3CA-Mutated Solid Tumors and in Preclinical Models.

Dejan Juric, Kyung Song, Radia M Johnson

|Jun 24, 2025
The C-Terminal Kinase Domain-Binding and Suppression Motif Prevents Constitutive Activation of FGFR2.

Daniel Zingg, Chi-Chuan Lin, Julia Yemelyanenko

|Aug 29, 2023
MYC is a clinically significant driver of mTOR inhibitor resistance in breast cancer.

Jinhyuk Bhin, Julia Yemelyanenko, Xue Chao

|Sep 01, 2022
Publisher Correction: Truncated FGFR2 is a clinically actionable oncogene in multiple cancers.

Daniel Zingg, Jinhyuk Bhin, Julia Yemelyanenko

|Aug 10, 2022
Truncated FGFR2 is a clinically actionable oncogene in multiple cancers.

Daniel Zingg, Jinhyuk Bhin, Julia Yemelyanenko

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