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Pre-Clinical Rationale for Amcenestrant Combinations in HER2+/ER+ Breast Cancer
Amira F. Mahdi
, Niall Ashfield
, John Crown
, Denis M. Collins
Health Research Institute
Limerick Digital Cancer Research Centre
School of Medicine
Dublin City University
University College Dublin
Research output
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Dive into the research topics of 'Pre-Clinical Rationale for Amcenestrant Combinations in HER2+/ER+ Breast Cancer'. Together they form a unique fingerprint.
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Pharmacology, Toxicology and Pharmaceutical Science
Estrogen Receptor
100%
Estrogen Receptor Positive Breast Cancer
100%
Trastuzumab
100%
Protein Tyrosine Kinase Inhibitor
100%
Receptor
33%
Breast Cancer
33%
Western Blot
33%
Lapatinib
33%
IC50
33%
Combination Drug
33%
Acid Phosphatase
33%
Caspase 3
33%
Trastuzumab Emtansine
33%
Tucatinib
33%
Neratinib
33%
Biochemistry, Genetics and Molecular Biology
Estrogen Receptor
100%
Tyrosine Kinase Inhibitor
50%
Trastuzumab
50%
Programmed Cell Death
33%
Signal Transduction
16%
IC50
16%
Western Blot
16%
Antiproliferative Activity
16%
Acid Phosphatase
16%
Caspase 3
16%
Trastuzumab Emtansine
16%
Lapatinib
16%
Neratinib
16%