Joaquin Arribas

researcher

Joaquin Arribas is …
instance of (P31):
humanQ5

External links are
P496ORCID iD0000-0002-0504-0664
P1053ResearcherIDM-4482-2014
P1153Scopus author ID7103041117

P69educated atAutonomous University of MadridQ788091
P108employerAutonomous University of BarcelonaQ43452
Autonomous University of MadridQ788091
Memorial Sloan Kettering Cancer CenterQ1808012
Vall d'Hebron Hospital UniversitariQ3826080
Catalan Institution for Research and Advanced StudiesQ5051216
Carlos III Health InstituteQ5918335
Hospital del MarQ9004969
Frederick National Laboratory for Cancer ResearchQ28405614
Vall d'Hebron Institute of OncologyQ81933223
P106occupationresearcherQ1650915

Reverse relations

author (P50)
Q54508329A dominant-negative N-terminal fragment of HER2 frequently expressed in breast cancers.
Q37550854ADAM17 as a therapeutic target in multiple diseases.
Q53776259Cancer Therapeutic Resistance: Progress and Perspectives (April 7-8, 2016 - Barcelona, Spain).
Q37199267Cancer network activity associated with therapeutic response and synergism
Q92859268Chromosome 12p Amplification in Triple-Negative/BRCA1-Mutated Breast Cancer Associates with Emergence of Docetaxel Resistance and Carboplatin Sensitivity
Q35625995Clinical benefit of lapatinib-based therapy in patients with human epidermal growth factor receptor 2-positive breast tumors coexpressing the truncated p95HER2 receptor.
Q45341269Clinical response to a lapatinib-based therapy for a Li-Fraumeni syndrome patient with a novel HER2V659E mutation.
Q91046381Clinicopathological and Molecular Characterization of Metastatic Gastrointestinal Stromal Tumors with Prolonged Benefit to Frontline Imatinib
Q50145710Coamplification of miR-4728 protects HER2-amplified breast cancers from targeted therapy.
Q40505812Combined epidermal growth factor receptor targeting with the tyrosine kinase inhibitor gefitinib (ZD1839) and the monoclonal antibody cetuximab (IMC-C225): superiority over single-agent receptor targeting.
Q39216531Constitutive HER2 signaling promotes breast cancer metastasis through cellular senescence.
Q40087664Defective cyclin B1 induction in trastuzumab-emtansine (T-DM1) acquired resistance in HER2-positive breast cancer.
Q42486287Ectodomain shedding of the hypoxia-induced carbonic anhydrase IX is a metalloprotease-dependent process regulated by TACE/ADAM17.
Q38875168Effect of cellular senescence on the growth of HER2-positive breast cancers.
Q34736064Effect of p95HER2/611CTF on the response to trastuzumab and chemotherapy.
Q90796782Elevated WBP2 Expression in HER2-positive Breast Cancers Correlates with Sensitivity to Trastuzumab-based Neoadjuvant Therapy: A Retrospective and Multicentric Study
Q56999346Enhancing the Biological Relevance of Secretome-Based Proteomics by Linking Tumor Cell Proliferation and Protein Secretion
Q40144433Expression of p95HER2, a truncated form of the HER2 receptor, and response to anti-HER2 therapies in breast cancer.
Q91087787Extracellular HMGA1 Promotes Tumor Invasion and Metastasis in Triple-Negative Breast Cancer
Q112699608GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells
Q37636623Gasdermin B expression predicts poor clinical outcome in HER2-positive breast cancer
Q90710806Genetic alterations in the PI3K/AKT pathway and baseline AKT activity define AKT inhibitor sensitivity in breast cancer patient-derived xenografts
Q37777538HER2 Fragmentation and Breast Cancer Stratification
Q64069811HER2 and p95HER2 differentially regulate miRNA expression in MCF-7 breast cancer cells and downregulate MYB proteins through miR-221/222 and miR-503
Q41735415High HER2 expression correlates with response to the combination of lapatinib and trastuzumab.
Q37142882High HER2 protein levels correlate with increased survival in breast cancer patients treated with anti-HER2 therapy.
Q46681137Ibrutinib exerts potent antifibrotic and antitumor activities in mouse models of pancreatic adenocarcinoma.
Q39095733Interrogating open issues in cancer precision medicine with patient-derived xenografts.
Q92965702LOXL2-mediated H3K4 oxidation reduces chromatin accessibility in triple-negative breast cancer cells
Q92947583MEN1309/OBT076, a First-In-Class Antibody-Drug Conjugate Targeting CD205 in Solid Tumors
Q48190414MSK1 regulates luminal cell differentiation and metastatic dormancy in ER+ breast cancer
Q81738842Matrix metalloproteases and tumor invasion
Q37708733Modeling anti-IL-6 therapy using breast cancer patient-derived xenografts.
Q72111433Modulation of the Multicatalytic Proteinase Complex by Lipids, Interconversion and Proteolytic Processing
Q58702635Multicenter Phase II Study of Lurbinectedin in BRCA-Mutated and Unselected Metastatic Advanced Breast Cancer and Biomarker Assessment Substudy
Q41956426N-terminal cleavage of proTGFalpha occurs at the cell surface by a TACE-independent activity.
Q27851451NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations.
Q47130450Oncogenic p95HER2/611CTF primes human breast epithelial cells for metabolic stress-induced down-regulation of FLIP and activation of TRAIL-R/Caspase-8-dependent apoptosis.
Q63979688PTBP1-Mediated Alternative Splicing Regulates the Inflammatory Secretome and the Pro-tumorigenic Effects of Senescent Cells
Q48328230Pancreatic cancer heterogeneity and response to Mek inhibition
Q35663687Patterns of HER2 Gene Amplification and Response to Anti-HER2 Therapies
Q38965541Poly (ADP-ribose) polymerase inhibition enhances trastuzumab antitumour activity in HER2 overexpressing breast cancer.
Q94552637Preclinical activity of PI3K inhibitor Copanlisib in Gastrointestinal Stromal Tumor
Q53822191Publisher Correction: MSK1 regulates luminal cell differentiation and metastatic dormancy in ER+ breast cancer.
Q52596087RAD51 foci as a functional biomarker of homologous recombination repair and PARP inhibitor resistance in germline BRCA mutated breast cancer.
Q51814356Recycling of cell surface pro-transforming growth factor-{alpha} regulates epidermal growth factor receptor activation.
Q50902443Resistance to the Antibody-Drug Conjugate T-DM1 Is Based in a Reduction in Lysosomal Proteolytic Activity.
Q35939308Role of ADAM17 in the non-cell autonomous effects of oncogene-induced senescence.
Q54976637Silencing of adaptor protein SH3BP2 reduces KIT/PDGFRA receptors expression and impairs gastrointestinal stromal tumors growth.
Q57809682TGFβ-activated USP27X deubiquitinase regulates cell migration and chemoresistance via stabilization of Snail1
Q92717496TRAIL receptor activation overcomes resistance to trastuzumab in HER2 positive breast cancer cells
Q38899794Targeting the EGF/HER Ligand-Receptor System in Cancer.
Q33593917The cleavage of semaphorin 3C induced by ADAMTS1 promotes cell migration
Q57837760The protease MT1-MMP drives a combinatorial proteolytic program in activated endothelial cells
Q91409346Therapeutic targeting of HER2-CB2R heteromers in HER2-positive breast cancer
Q52286403Treating cancer's kinase 'addiction'.
Q58000899Who will benefit from treatment against EGFR?
Q57042030p95HER2-T cell bispecific antibody for breast cancer treatment

Search more.