Research at the Institute of Biomedicine is divided into three functional units: 1) Infection and Immunity, 2) Integrative Physiology and Pharmacology and 3) Cancer research. Research at our Institute includes both biomedical basic research and translational research, and the unit division expresses our research priorities.
We encourage creative interdisciplinary combination of research topics via collaboration of the individual research groups and the three units. In addition, we collaborate locally with clinical researchers, with other institutes of our university and with the Åbo Akademi University. We are also widely networked with numerous national and international universities and public and private research institutes.
Research services
Recent publications
Development of an Image-Guided Orthotopic Xenograft Mouse Model of Endometrial Cancer with Controllable Estrogen Exposure (2018)
International Journal of Molecular Sciences
(Refereed journal article or data article (A1))
SIRT1 mediates obesity- and nutrient-dependent perturbation of pubertal timing by epigenetically controlling Kiss1 expression (2018)
Nature Communications
(Refereed journal article or data article (A1))
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism (2018)
JCI Insight
(Refereed journal article or data article (A1))
Functional Characterization of MicroRNA-27a-3p Expression in Human Polycystic Ovary Syndrome (2018)
Endocrinology
(Refereed journal article or data article (A1))
Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene (2018)
Neuromuscular Disorders
(Refereed journal article or data article (A1))
Recent doctoral dissertations
Development of an Image-Guided Orthotopic Xenograft Mouse Model of Endometrial Cancer with Controllable Estrogen Exposure (2018)
International Journal of Molecular Sciences
(Refereed journal article or data article (A1))
SIRT1 mediates obesity- and nutrient-dependent perturbation of pubertal timing by epigenetically controlling Kiss1 expression (2018)
Nature Communications
(Refereed journal article or data article (A1))
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism (2018)
JCI Insight
(Refereed journal article or data article (A1))
Functional Characterization of MicroRNA-27a-3p Expression in Human Polycystic Ovary Syndrome (2018)
Endocrinology
(Refereed journal article or data article (A1))
Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene (2018)
Neuromuscular Disorders
(Refereed journal article or data article (A1))