Kirsi Määttä

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Genetic Variant Coding for Iron Regulatory Protein HFE Contributes to Hypertension, the TAMRISK Study

S. Nikkari, Kirsi Määttä, T. Kunnas, 2015, Medicine.

Growth In Vitro and Reduces Oxidative Stress in Rabbit Aorta In Vivo Nrf2 Gene Transfer Induces Antioxidant Enzymes and Suppresses Smooth Muscle Cell

S. Ylä-Herttuala, T. Heikura, S. Jauhiainen, 2007 .

Nrf2 Gene Transfer Induces Antioxidant Enzymes and Suppresses Smooth Muscle Cell Growth In Vitro and Reduces Oxidative Stress in Rabbit Aorta In Vivo

S. Ylä-Herttuala, T. Heikura, S. Jauhiainen, 2007, Arteriosclerosis, thrombosis, and vascular biology.

Periodic cohort health examinations in the TAMRISK study show untoward increases in body mass index and blood pressure during 15 years of follow-up

S. Nikkari, Kirsi Määttä, T. Kunnas, 2012, BMC Public Health.

Abnormal Bone Tissue Organization and Osteocyte Lacunocanalicular Network in Early‐Onset Osteoporosis Due to SGMS2 Mutations

O. Mäkitie, S. Blouin, R. Mäkitie, 2021, JBMR plus.

Decorin Genotypes, Serum Glucose, Heart Rate, and Cerebrovascular Events: The Tampere Adult Population Cardiovascular Risk Study.

S. Nikkari, T. Solakivi, Kirsi Määttä, 2016, Genetic testing and molecular biomarkers.

Minor variant of rs 16827043 in the iron regulator hemojuvelin gene (HJV) contributes to hypertension

S. Nikkari, Kirsi Määttä, T. Kunnas, 2017, Medicine.

Genetic Polymorphisms of Transcription Factor NRF2 and of its Host Gene Sulfiredoxin (SRXN1) are Associated with Cerebrovascular Disease in a Finnish Cohort, the TAMRISK Study

S. Nikkari, Kirsi Määttä, T. Kunnas, 2016, International journal of medical sciences.

Functional Inducible Nitric Oxide Synthase Gene Variants Associate With Hypertension

S. Nikkari, Kirsi Määttä, T. Kunnas, 2015, Medicine.

A multi-omics study to characterize the transdifferentiation of human dermal fibroblasts to osteoblast-like cells

O. Mäkitie, M. Varjosalo, T. Öhman, 2022, Frontiers in Molecular Biosciences.

Glucuronic Acid Epimerase (GLCE) Variant rs3865014 (A>G) Is Associated with BMI, Blood Hemoglobin, Hypertension, and Cerebrovascular Events, the TAMRISK Study

S. Nikkari, T. Solakivi, Kirsi Määttä, 2016, Annals of human genetics.

Genetic predisposition to breast and ovarian cancer - BRCA1/2-negative families

Kirsi Määttä, 2016 .

Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families

Riikka Nurminen, Anne Kallioniemi, Johanna Schleutker, 2017, BMC Cancer.

NLR family pyrin domain containing 3 (NLRP3) inflammasome gene polymorphism rs7512998 (C>T) predicts aging-related increase of blood pressure, the TAMRISK study

S. Nikkari, Kirsi Määttä, T. Kunnas, 2015, Immunity & Ageing.

Whole-exome sequencing of Finnish hereditary breast cancer families

M. Nykter, J. Schleutker, T. Rantapero, 2016, European Journal of Human Genetics.

Microbial community dynamics during a demonstration-scale bioheap leaching operation

J. Puhakka, A. Kaksonen, Nelli J. Beecroft, 2012 .

A functional variant in the serine-threonine kinase coding gene is associated with hypertension: a case–control study in a Finnish population, the Tampere adult population cardiovascular risk study

S. Nikkari, Kirsi Määttä, T. Kunnas, 2013, Journal of hypertension.

Microbial Community of the Talvivaara Demonstration-Scale Bioheap

J. Puhakka, A. Kaksonen, N. Rahunen, 2007 .

Variant rs6749447 (T > G) in the serine threonine kinase gene is associated with cardiovascular complications, the Tampere adult population cardiovascular risk study

S. Nikkari, Kirsi Määttä, T. Kunnas, 2021, Medicine.

Contribution of SLC7A1 genetic variant to hypertension, the TAMRISK study

S. Nikkari, Kirsi Määttä, T. Kunnas, 2013, BMC Medical Genetics.