2022 - Research.com Best Female Scientist Award
2014 - Fellow of the American Academy of Arts and Sciences
Her primary scientific interests are in Cell biology, Transcription factor, Hypoxia, Biochemistry and Regulation of gene expression. Her work deals with themes such as Embryonic stem cell, Angiogenesis and Molecular biology, which intersect with Cell biology. Her Angiogenesis study is related to the wider topic of Cancer research.
M. Celeste Simon interconnects Intestinal epithelium, Homeostasis and Conditional gene knockout in the investigation of issues within Transcription factor. The concepts of her Hypoxia study are interwoven with issues in Cell growth, Cancer cell, Immunology, CD38 and Cell type. Her Regulation of gene expression study integrates concerns from other disciplines, such as Phenotype, Erythropoiesis, Hypoxia-inducible factors, Disease and Gene isoform.
M. Celeste Simon mostly deals with Cell biology, Cancer research, Hypoxia-inducible factors, Transcription factor and Molecular biology. Her Cell biology study incorporates themes from Embryonic stem cell, Endocrinology and Internal medicine, Angiogenesis. The Cancer research study combines topics in areas such as Carcinogenesis, Tumor progression, Immunology and Cell growth.
Her Hypoxia-inducible factors study combines topics from a wide range of disciplines, such as Inflammation, HIF1A and Pathology. Her Transcription factor research includes themes of Regulation of gene expression and Signal transduction. Her biological study spans a wide range of topics, including Cell culture and Transcription, Gene expression, Gene, Transactivation.
M. Celeste Simon mainly focuses on Cancer research, Cell biology, Cancer, Tumor microenvironment and Hypoxia. Her research integrates issues of Cell culture, Clear cell renal cell carcinoma, Metastasis, Sarcoma and Tumor progression in her study of Cancer research. Her Metastasis research focuses on EPAS1 and how it connects with Cell growth.
Her studies in Cell biology integrate themes in fields like Phenotype, Lipid metabolism, Transcription factor and Medical education. Her research in Tumor microenvironment intersects with topics in Liver cancer, Stromal cell, Gene expression and FBP1. The various areas that M. Celeste Simon examines in her Hypoxia study include Inflammation, Tumor tissue and Neuroscience.
M. Celeste Simon mainly investigates Cancer research, Cancer, Cell biology, Cancer cell and Tumor microenvironment. Her studies in Cancer research integrate themes in fields like KRAS, Metastasis, Sarcoma and Enzyme. Her studies deal with areas such as Phenotype, Malignancy and Clear cell renal cell carcinoma as well as Cancer.
Her Cell biology study integrates concerns from other disciplines, such as Lipid metabolism and Cellular adaptation, Hypoxia. Her Cancer cell study incorporates themes from Glutathione, Angiogenesis, Antioxidant and Tumor initiation. The Immunology study combines topics in areas such as Transcription factor and Hypoxia-inducible factors.
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.
Targeted Disruption of the Mouse Stat1 Gene Results in Compromised Innate Immunity to Viral Disease
Joan E Durbin;Renée Hackenmiller;M.Celeste Simon;David E Levy.
Cell (1996)
Hypoxia inducible factors and the response to hypoxic stress
Amar J. Majmundar;Waihay J. Wong;M. Celeste Simon.
Molecular Cell (2010)
The combined functions of proapoptotic Bcl-2 family members bak and bax are essential for normal development of multiple tissues.
Tullia Lindsten;Andrea J. Ross;Ayala King;Wei Xing Zong.
Molecular Cell (2000)
HIF1α and HIF2α: sibling rivalry in hypoxic tumour growth and progression
Brian Keith;Randall S. Johnson;M. Celeste Simon;M. Celeste Simon.
Nature Reviews Cancer (2012)
Mop3 Is an Essential Component of the Master Circadian Pacemaker in Mammals
Maureen K. Bunger;Lisa D. Wilsbacher;Susan M. Moran;Cynthia Clendenin.
Cell (2000)
Differential Roles of Hypoxia-Inducible Factor 1α (HIF-1α) and HIF-2α in Hypoxic Gene Regulation
Cheng-Jun Hu;Li-Yi Wang;Lewis A. Chodosh;Brian Keith.
Molecular and Cellular Biology (2003)
Erythroid differentiation in chimaeric mice blocked by a targeted mutation in the gene for transcription factor GATA-1
Larysa Pevny;M. Celeste Simon;Elizabeth Robertson;William H. Klein.
Nature (1991)
Mitochondrial complex III is required for hypoxia-induced ROS production and cellular oxygen sensing
Robert D. Guzy;Beatrice Hoyos;Emmanuel Robin;Hong Chen.
Cell Metabolism (2005)
The impact of O2 availability on human cancer.
Jessica A. Bertout;Shetal A. Patel;M. Celeste Simon.
Nature Reviews Cancer (2008)
Hypoxia-inducible factors, stem cells, and cancer.
Brian Keith;M. Celeste Simon;M. Celeste Simon.
Cell (2007)
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:
University of Cambridge
Memorial Sloan Kettering Cancer Center
Children's Hospital of Philadelphia
Case Western Reserve University
University of Pennsylvania
KU Leuven
University of Florida
Children's Hospital of Philadelphia
University of Pittsburgh
Cincinnati Children's Hospital Medical Center
University of Melbourne
Australian National University
Xi'an Jiaotong University
Roma Tre University
University of Canterbury
University of Zurich
Lund University
University of Nebraska–Lincoln
National and Kapodistrian University of Athens
Pablo de Olavide University
Tohoku University
Université Catholique de Louvain
Bedford Institute of Oceanography
University of Pittsburgh
University of California, Davis
Beth Israel Deaconess Medical Center