Scopus h-index:36
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Jose M Silva, PhD
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About Me
Language
Position
Research Topics
Cancer, Cancer Genetics, Tumorigenesis
Multi-Disciplinary Training Areas
Cancer Biology [CAB]
About Me
Language
Position
Research Topics
Cancer, Cancer Genetics, Tumorigenesis
Multi-Disciplinary Training Areas
Cancer Biology [CAB]
About Me
Language
Position
Research Topics
Cancer, Cancer Genetics, Tumorigenesis
Multi-Disciplinary Training Areas
Cancer Biology [CAB]
Education
BSc, Complutense University of Madrid, Spain
PhD, Autonoma University of Madrid, Spain
PostDoc, Cold Spring Harbor Laboratory, NY
Senior Fellow, Cold Spring Harbor Laboratory, NY
Assistant Professor of Pathology, Columbia University Medical School
Adjunct Faculty, Columbia University Medical School
Research
Updated October-2015 -We are looking for a molecular cell biologist with experience in breast cancer research. Previous experience in genetic manipulation of cellular models, basic biochemistry and mouse models of breast cancer will be beneficial. -Applicants must have shown research abilities and capabilities to perform collaborative project within a team, and possess good written and verbal communication skills in English. Applicants must have a Ph.D. and evidence of research productivity. Please send your C.V., contact information for two references, and a brief motivation letter including a summary of research experience to: Jose M. Silva; E-mail:jose.silva@mssm.edu
Locations
Publications
Article:81
Review Article:3
Comment/Debate:2
Letter:5
Chapter:3
Recent Artifacts
- Pseudo-temporal dynamics of chemoresistant triple negative breast cancer cells reveal EGFR/HER2 inhibition as synthetic lethal during mid-neoadjuvant chemotherapy
- Network-based assessment of HDAC6 activity predicts preclinical and clinical responses to the HDAC6 inhibitor ricolinostat in breast cancer
- The Breast Cancer Single-Cell Atlas: Defining cellular heterogeneity within model cell lines and primary tumors to inform disease subtype, stemness, and treatment options
- Smurf2 inhibition enhances chemotherapy and radiation sensitivity in non-small-cell lung cancer
- Single-cell analysis reveals the Comma-1D cell line as a unique model for mammary gland development and breast cancer
- A microRNA Cluster Controls Fat Cell Differentiation and Adipose Tissue Expansion By Regulating SNCG
- miR-424/503 modulates Wnt/β-catenin signaling in the mammary epithelium by targeting LRP6
- UV-induced reduction in Polycomb repression promotes epidermal pigmentation
- Phase I/II trial of ruxolitinib in combination with trastuzumab in metastatic HER2 positive breast cancer
- The miR-424(322)/503 gene cluster regulates pro- versus anti-inflammatory skin DC subset differentiation by modulating TGF-β signaling