Dr. Omer H Yilmaz MD, PHD
Pathologist | Anatomic Pathology & Clinical Pathology
Massachusetts General Hospital 55 Fruit Street Boston MA, 02114About
Dr. Omer Yilmaz is a pathologist practicing in Boston, MA. Dr. Yilmaz is a doctor who specializes in the study of bodily fluids and tissues. As a pathologist, Dr. Yilmaz can help your primary care doctor make a diagnosis about your medical condition. Dr. Yilmaz may perform a tissue biopsy to determine if a patient has cancer, practice genetic testing, and complete a number of laboratory examinations. Pathologists can also perform autopsies which can determine a persons cause of death and gain information about genetic progression of a disease.
Board Certification
PathologyAmerican Board of PathologyABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- CD144 (VE-cadherin) is transiently expressed by fetal liver hematopoietic stem cells.
- Spatial differences in hematopoiesis but not in stem cells indicate a lack of
- The PI-3kinase pathway in hematopoietic stem cells and leukemia-initiating cells: a mechanistic difference between normal and cancer stem cells.
- CD150- cells are transiently reconstituting multipotent progenitors with little or no stem cell activity.
- Aldehyde dehydrogenase 1a1 is dispensable for stem cell function in the mouse
- Pten-null tumors cohabiting the same lung display differential AKT activation and
- Depletion of Rictor, an essential protein component of mTORC2, decreases male lifespan.
- Intestinal colonization by Candida albicans alters inflammatory responses in Bruton's tyrosine kinase-deficient mice.
- Pathology and Genetics of Pancreatic Neoplasms.
- Mule Regulates the Intestinal Stem Cell Niche via the Wnt Pathway and Targets EphB3 for Proteasomal and Lysosomal Degradation.
- Comprehensive Electrocardiographic Analysis of Lead Exposed Workers: An Arrhythmic Risk Assessment Study.
- Fasting-Mimicking Diet Promotes Ngn3-Driven β-Cell Regeneration to Reverse Diabetes.
- Mex3a Marks a Slowly Dividing Subpopulation of Lgr5+ Intestinal Stem Cells.
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