The scientist’s investigation covers issues in Molecular biology, Hepatic stellate cell, Internal medicine, Cell culture and Fibrosis. Procollagen peptidase is the focus of his Molecular biology research. His Hepatic stellate cell study integrates concerns from other disciplines, such as Extracellular matrix, Transforming growth factor beta and Phagocytosis.
Mark A. Zern works mostly in the field of Internal medicine, limiting it down to concerns involving Endocrinology and, occasionally, Transplantation and Progenitor cell. Mark A. Zern combines subjects such as Epithelial–mesenchymal transition, Cyclopamine, Cancer stem cell, Telomerase and Aldehyde dehydrogenase with his study of Cell culture. His work carried out in the field of Gene expression brings together such families of science as Embryonic stem cell, Cellular differentiation and Hepatocyte.
The scientist’s investigation covers issues in Molecular biology, Cell biology, Internal medicine, Pathology and Hepatocyte. His study in Molecular biology is interdisciplinary in nature, drawing from both Cell culture, Gene expression, Hepatic stellate cell, Messenger RNA and Albumin. Mark A. Zern has included themes like Embryonic stem cell, Apoptosis and Cellular differentiation in his Cell biology study.
His Internal medicine research is multidisciplinary, incorporating elements of Gastroenterology, Endocrinology and In vivo. The Pathology study which covers Cirrhosis that intersects with Hepatitis and Liver disease. The Hepatocyte study combines topics in areas such as Tissue transglutaminase, Liver injury and Liver transplantation.
Mark A. Zern mostly deals with Cell biology, Stem cell, Cellular differentiation, Cancer research and Molecular biology. His studies deal with areas such as Embryonic stem cell and Hepatocyte as well as Cell biology. His study looks at the relationship between Cellular differentiation and topics such as Mesenchymal stem cell, which overlap with Cholangiocyte.
His Cancer research research includes elements of Epithelial–mesenchymal transition, Gene silencing, microRNA and Immunology. Mark A. Zern has researched Molecular biology in several fields, including Cell culture, Hepatic stellate cell, Hepatocyte growth factor, Apoptosis and Extracellular matrix. His Signal transduction research incorporates themes from Endocrinology and Internal medicine.
Stem cell, Cellular differentiation, Molecular biology, Embryonic stem cell and Hepatocyte are his primary areas of study. His research in Stem cell intersects with topics in Hepatoblastoma and Pathology. His studies deal with areas such as Gene silencing and Induced pluripotent stem cell as well as Cellular differentiation.
His study in Molecular biology is interdisciplinary in nature, drawing from both Epithelial–mesenchymal transition, Cell culture, Hepatic stellate cell, Hepatocyte growth factor and Extracellular matrix. His Hepatic stellate cell research incorporates elements of Apoptosis, Liver cell, Alcoholic liver disease and Liver injury. His work on Hepatocyte differentiation as part of general Hepatocyte study is frequently linked to Hepatocyte nuclear factor 4, bridging the gap between disciplines.
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In vitro and in vivo association of transforming growth factor-beta 1 with hepatic fibrosis.
Mark J. Czaja;Francis R. Weiner;Kathleen C. Flanders;Marie-Adele Giambrone.
Journal of Cell Biology (1989)
Reversal of hyperglycemia in mice by using human expandable insulin-producing cells differentiated from fetal liver progenitor cells
Michal Zalzman;Sanjeev Gupta;Ranjit K. Giri;Irina Berkovich.
Proceedings of the National Academy of Sciences of the United States of America (2003)
Hepatic stellate cells: a target for the treatment of liver fibrosis.
Jian Wu;Mark A. Zern.
Journal of Gastroenterology (2000)
Collagen chain mRNAs in isolated heart cells from young and adult rats
Mahboubeh Eghbali;Mark J. Czaja;Maria Zeydel;Francis R. Weiner.
Journal of Molecular and Cellular Cardiology (1988)
Phagocytosis of apoptotic bodies by hepatic stellate cells induces NADPH oxidase and is associated with liver fibrosis in vivo
Shan‐Shan Zhan;Joy X. Jiang;Jian Wu;Charles Halsted.
Hepatology (2006)
SYBR Green real-time telomeric repeat amplification protocol for the rapid quantification of telomerase activity
Henning Wege;Michael S. Chui;Hai T. Le;Julie M. Tran.
Nucleic Acids Research (2002)
γ‐interferon treatment inhibits collagen deposition in murine schistosomiasis
M. J. Czaja;F. R. Weiner;S. Takahashi;M. A. Giambrone.
Hepatology (1989)
Localization of types I, III and IV collagen mRNAs in rat heart cells by in situ hybridization
M. Eghbali;O. O. Blumenfeld;S. Seifter;P. M. Buttrick.
Journal of Molecular and Cellular Cardiology (1989)
Liver fibrosis causes downregulation of miRNA-150 and miRNA-194 in hepatic stellate cells, and their overexpression causes decreased stellate cell activation
Senthil Kumar Venugopal;Joy Jiang;Tae-Hun Kim;Yong Li.
American Journal of Physiology-gastrointestinal and Liver Physiology (2010)
Ito-cell gene expression and collagen regulation
Francis R. Weiner;Marie‐Adele ‐A Giambrone;Mark J. Czaja;Anish Shah.
Hepatology (1990)
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