Biography
Aras N. Mattis, M.D., Ph.D., is a board-certified anatomic pathologist and clinical fellow in the Willenbring Lab. Dr. Mattis trained at the University of Illinois at Urbana-Champaign, earning both his doctorates, Biochemistry and Medicine, there in 2007. He continued his clinical training in Pathology at the University of California San Francisco completing residency in Anatomic Pathology with subsequent fellowship training in Surgical Pathology and Liver and gastrointestinal pathology under his clinical mentor, Dr. Linda Ferrell. Since 2010, he has worked in the Willenbring Lab, investigating the basic mechanisms of liver development and disease in the with a specific focus on liver metabolism and fatty liver disease as well as micro-RNA regulation of liver metabolism.
Education
Institution | Degree | Dept or School | End Date |
---|---|---|---|
University of Illinois Urbana-Champaign | PhD | Biochemistry | 2007 |
University of Illinois Urbana-Champaign | MD | Medicine | 2007 |
University of California Berkeley | BA | Molecular and Cell Biology - Genetics | 1998 |
Board Certifications
American Board of Pathology, Anatomic Pathology
Collaboration Interests
I am interested in:
- academic collaboration
- academic senate committee service
- companies and entrepreneurs
- multicenter clinical research
- press
- prospective donors
Clinical Expertise
Liver and Gastrointestinal Pathology
Program Affiliations
UCSF Department of Pathology
California Institute for Regenerative Medicine
In the News
Grants and Funding
- Establishing patient-derived iPSCs as a platform for discovery research in NAFLD | NIDDK | 2023-06-01 - 2028-05-30 | Role: MPI
- Modeling and Characterization of NAFLD Phenotypes in a Severely Affected Family | NIH/NIDDK | 2024-02-01 - 2027-11-30 | Role: PI
- Genetic Regulation of Nonalcoholic Fatty Liver Disease | NIH | 2021-06-08 - 2025-03-31 | Role: MPI
- Regulation of Lipid Metabolism by miR-29a within Hepatocytes | NIH | 2013-09-01 - 2019-07-31 | Role: Principal Investigator
Research Narrative
Dr. Mattis' postdoctoral work includes the use of translational human biopsy material as well as patient-derived induced pluripotent stem cell reprogramming to hepatocytes. As a long-term goal, this work aims to develop a humanized liver mouse model of fatty liver disease. Aras is supported by the UCSF CIRM clinical fellow training grant and continues to work closely with the UCSF Department of Pathology as a clinical researcher.
Research Interests
Liver diseases including metabolic, pediatric, fibrotic, idiopathic, stem cell derived
Hepatocytes for transplant and disease modeling, micro-RNA regulation of hepatocyte
Development and metabolism, liver and gastrointestinal tumors, site-specific recombination.
Publications
- Doxycycline Significantly Enhances Induction of Induced Pluripotent Stem Cells to Endoderm by Enhancing Survival Through Protein Kinase B Phosphorylation.| | PubMed
- Gastric Intestinal Metaplasia in Mucosa Adjacent to Gastric Cancers Is Rarely Associated With the Aneuploidy That Is Characteristic of Gastric Dysplasia or Cancer.| | PubMed
- Persistent or recurrent Barrett's neoplasia after an endoscopic therapy session is associated with DNA content abnormality and can be detected by DNA flow cytometric analysis of paraffin-embedded tissue.| | PubMed
- Induced Pluripotent Stem Cell-derived Hepatocytes From Patients With Nonalcoholic Fatty Liver Disease Display a Disease-specific Gene Expression Profile.| | PubMed
- Non-conventional dysplasia in inflammatory bowel disease is more frequently associated with advanced neoplasia and aneuploidy than conventional dysplasia.| | PubMed
- Hepatocyte-specific deletion of XBP1 sensitizes mice to liver injury through hyperactivation of IRE1α.| | PubMed
- Targeting acid ceramidase inhibits YAP/TAZ signaling to reduce fibrosis in mice.| | PubMed
- Ly6cLo non-classical monocytes promote resolution of rhesus rotavirus-mediated perinatal hepatic inflammation.| | PubMed
- Utility of DNA flow cytometry in distinguishing between malignant and benign intrahepatic biliary lesions.| | PubMed
- DNA flow cytometric analysis of paraffin-embedded tissue for the diagnosis of malignancy in bile duct biopsies.| | PubMed