Her main research concerns Cell biology, Signal transduction, Molecular biology, Immunology and Immune system. Stephanie S. Watowich focuses mostly in the field of Cell biology, narrowing it down to matters related to Transcription factor and, in some cases, FOXP3. As a member of one scientific family, Stephanie S. Watowich mostly works in the field of Signal transduction, focusing on Receptor and, on occasion, Stem cell factor, Suppressor of cytokine signalling and Interleukin 10.
Her Molecular biology study incorporates themes from Fibrosis, Downregulation and upregulation, Messenger RNA and Cellular differentiation. Her study in the field of Acquired immune system and Immunity also crosses realms of Urea cycle. Her STAT3 study combines topics from a wide range of disciplines, such as Cancer research and Gene expression.
Her primary areas of study are Cell biology, Cancer research, Signal transduction, Immunology and STAT3. Her Cell biology research incorporates themes from Molecular biology, Dendritic cell, Transcription factor and Cellular differentiation. She interconnects Fms-Like Tyrosine Kinase 3, Interleukin 17, Adoptive cell transfer, CXCR5 and Regulation of gene expression in the investigation of issues within Cellular differentiation.
Her Cancer research study integrates concerns from other disciplines, such as Carcinogenesis, Tumor progression, Immunotherapy and Tumor microenvironment. Her research in Signal transduction tackles topics such as Receptor which are related to areas like Extracellular. Her studies deal with areas such as Haematopoiesis and Lung cancer as well as Immunology.
Her primary scientific interests are in Cancer research, Population, Tumor microenvironment, Tumor progression and Immune system. The study incorporates disciplines such as Immune checkpoint, Carcinogenesis, STAT3, Signal transduction and Antigen presentation in addition to Cancer research. Her Signal transduction research integrates issues from MTT assay and Estrogen.
In her study, Immunology is strongly linked to Receptor, which falls under the umbrella field of Microglia. Her Blood cell research incorporates elements of Myeloid, Proinflammatory cytokine and Cell biology. Her Cell biology study frequently draws connections between related disciplines such as OTUB1.
Stephanie S. Watowich mostly deals with Cancer research, Tumor progression, Tumor microenvironment, Cytokine and Carcinogenesis. Her studies in Cancer research integrate themes in fields like Brain tumor, Stem cell and Cellular differentiation, Dendritic cell differentiation. The Tumor progression study combines topics in areas such as Immune checkpoint, Dendritic cell, Immune tolerance, Immune system and Antigen presentation.
Her Tumor microenvironment study combines topics in areas such as Proinflammatory cytokine, Lung cancer, Mutant and Conditional gene knockout. Her Carcinogenesis research includes themes of Progenitor cell, CCL20, CXCL1, Peroxisome proliferator-activated receptor delta and STAT3. She integrates Progenitor cell and Population in her studies.
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T Helper 17 Lineage Differentiation Is Programmed by Orphan Nuclear Receptors RORα and RORγ
Xuexian O. Yang;Bhanu P. Pappu;Roza Nurieva;Askar Akimzhanov.
Essential autocrine regulation by IL-21 in the generation of inflammatory T cells
Roza Nurieva;Xuexian O. Yang;Gustavo Martinez;Yongliang Zhang.
STAT3 REGULATES CYTOKINE-MEDIATED GENERATION OF INFLAMMATORY HELPER T CELLS
Xuexian O. Yang;Athanasia D. Panopoulos;Roza Nurieva;Seon Hee Chang.
Journal of Biological Chemistry (2007)
Generation of T Follicular Helper Cells Is Mediated by Interleukin-21 but Independent of T Helper 1, 2, or 17 Cell Lineages
Roza I. Nurieva;Yeonseok Chung;Daehee Hwang;Xuexian O. Yang.
Critical Regulation of Early Th17 Cell Differentiation by Interleukin-1 Signaling
Yeonseok Chung;Seon Hee Chang;Gustavo J. Martinez;Xuexian O. Yang.
Molecular Antagonism and Plasticity of Regulatory and Inflammatory T Cell Programs
Xuexian O. Yang;Roza Nurieva;Gustavo J. Martinez;Hong Soon Kang.
CCR6 regulates the migration of inflammatory and regulatory T cells.
Tomohide Yamazaki;Xuexian O. Yang;Yeonseok Chung;Atsushi Fukunaga.
Journal of Immunology (2008)
HIF-1α, STAT3, CBP/p300 and Ref-1/APE are components of a transcriptional complex that regulates Src-dependent hypoxia-induced expression of VEGF in pancreatic and prostate carcinomas
Michael J Gray;Jing Zhang;Jing Zhang;Lee M Ellis;Gregg L Semenza.
Homodimerization and constitutive activation of the erythropoietin receptor.
Stephanie S. Watowich;Akihiko Yoshimura;Gregory D. Longmore;Gregory D. Longmore;Douglas J. Hilton.
Proceedings of the National Academy of Sciences of the United States of America (1992)
The transcriptional regulators Id2 and Id3 control the formation of distinct memory CD8+ T cell subsets.
Cliff Y Yang;J Adam Best;Jamie Knell;Edward Yang.
Nature Immunology (2011)
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