Julie Teruya-Feldstein mostly deals with Cancer research, Cell biology, Tumor suppressor gene, Carcinogenesis and Lymphoma. Her Cancer research research incorporates themes from Ubiquitin, Immunology, microRNA, Tumor progression and In vivo. Her Cell biology research integrates issues from Cancer cell, Molecular biology, Transcription factor and Genetics.
Her study in Tumor suppressor gene is interdisciplinary in nature, drawing from both Cell cycle, RHEB, Neovascularization and RPTOR. The Carcinogenesis study combines topics in areas such as Cell aging, B cell, B-cell lymphoma, Phosphorylation and Proto-Oncogene Proteins c-myc. Her Lymphoma study is related to the wider topic of Pathology.
Her main research concerns Cancer research, Pathology, Lymphoma, Internal medicine and Immunology. Her work investigates the relationship between Cancer research and topics such as Carcinogenesis that intersect with problems in Cell biology. Her study brings together the fields of Immunophenotyping and Pathology.
In Lymphoma, Julie Teruya-Feldstein works on issues like B cell, which are connected to Molecular biology. Her work carried out in the field of Internal medicine brings together such families of science as Gastroenterology, Surgery and Oncology. Her work in Immunology addresses subjects such as Haematopoiesis, which are connected to disciplines such as Myeloid leukemia, Bone marrow and Cellular differentiation.
Her primary areas of study are Cancer research, Lymphoma, Pathology, Internal medicine and Cell biology. Julie Teruya-Feldstein has included themes like Myeloproliferative neoplasm, Cell growth, Progenitor cell, Regulation of gene expression and PTEN in her Cancer research study. Her studies deal with areas such as Tumor microenvironment, HMGA1, Germinal center and Synthetic lethality as well as Lymphoma.
Her Internal medicine study integrates concerns from other disciplines, such as Orthopedic surgery and Oncology. Her research in Cell biology intersects with topics in Myeloid, Cellular differentiation and Lethality. The various areas that Julie Teruya-Feldstein examines in her Haematopoiesis study include Myeloid leukemia and Immunology.
Julie Teruya-Feldstein mostly deals with Cancer research, Myeloid leukemia, Haematopoiesis, PTEN and Cancer. Her biological study spans a wide range of topics, including Ubiquitin, Progenitor cell, Suppressor, Carcinogenesis and Phosphatase. Her study with Haematopoiesis involves better knowledge in Cell biology.
Her work deals with themes such as Cell growth, Sterol regulatory element-binding protein, Metastasis, Prostate cancer and MAPK/ERK pathway, which intersect with PTEN. The study incorporates disciplines such as Myelodysplastic syndromes and Pathology in addition to Stem cell. Her Human leukocyte antigen study combines topics from a wide range of disciplines, such as Internal medicine and Lymphoma.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Tumour invasion and metastasis initiated by microRNA-10b in breast cancer
Li Ma;Julie Teruya-Feldstein;Robert A. Weinberg.
Nature (2007)
Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer
Arkaitz Carracedo;Li Ma;Li Ma;Li Ma;Julie Teruya-Feldstein;Federico Rojo.
Journal of Clinical Investigation (2008)
miR-9, a MYC/MYCN-activated microRNA, regulates E-cadherin and cancer metastasis
Li Ma;Jennifer Young;Harsha Prabhala;Elizabeth Pan.
Nature Cell Biology (2010)
Therapeutic silencing of miR-10b inhibits metastasis in a mouse mammary tumor model
Li Ma;Ferenc Reinhardt;Elizabeth Pan;Jürgen Soutschek.
Nature Biotechnology (2010)
Ubiquitination regulates PTEN nuclear import and tumor suppression
Lloyd C. Trotman;Xinjiang Wang;Andrea Alimonti;Zhenbang Chen.
Cell (2007)
SIRT3 Opposes Reprogramming of Cancer Cell Metabolism through HIF1α Destabilization
Lydia W.S. Finley;Arkaitz Carracedo;Jaewon Lee;Amanda Souza.
Cancer Cell (2011)
p63 Expression Profiles in Human Normal and Tumor Tissues
Charles J. Di Como;Marshall J. Urist;Irina Babayan;Marija Drobnjak.
Clinical Cancer Research (2002)
Mad2 Overexpression Promotes Aneuploidy and Tumorigenesis in Mice
Rocío Sotillo;Eva Hernando;Elena Díaz-Rodríguez;Julie Teruya-Feldstein.
Cancer Cell (2007)
PML targeting eradicates quiescent leukaemia-initiating cells.
Keisuke Ito;Rosa Bernardi;Alessandro Morotti;Sahoko Matsuoka.
Nature (2008)
Evasion of the p53 tumour surveillance network by tumour-derived MYC mutants
Michael T. Hemann;Anka Bric;Julie Teruya-Feldstein;Andreas Herbst.
Nature (2005)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Beth Israel Deaconess Medical Center
Memorial Sloan Kettering Cancer Center
National Institutes of Health
National Institutes of Health
University of Miami
Memorial Sloan Kettering Cancer Center
National Institutes of Health
Emory University
Columbia University
Memorial Sloan Kettering Cancer Center
Université Catholique de Louvain
University of Stirling
University of Michigan–Ann Arbor
University of Minnesota
MIT
PSL University
Tulane University
University of Sydney
Ghent University
CSL (United Kingdom)
University of Oslo
Washington University in St. Louis
Keio University
University of Southern California
European Southern Observatory
Stanford University