Tutkijat / Kuopio  | Airaksinen, O(lavi) |
| Alhava, E. |
| Alhonen, L. |
| Atalay, M(ustafa) |
| Cederberg, H. |
| Dunkel, L(eo) |
| Eskelinen, M(atti) |
| Giniatullin, R. |
| Gröhn, O(lli) |
| Harno, K. |
| Hartikainen, J(aana). |
| Hartikainen, J(uha). |
| Harvima, I. |
| Hiltunen, M(ikko) |
| Jääskeläinen, J(uha) E. |
| Jäkälä, P(ekka) |
| Jänne, J. |
| Jantunen, E(sa) |
| Järvinen, R. |
| Julkunen, P. |
| Kaikkonen, M(inna) U. |
| Kauhanen, J(ussi) |
| Kivipelto, M(iia) |
| Koistinaho, M. |
| Koivisto, T(imo) |
| Kokki, H. |
| Könönen, M. |
| Kosma, V(eli)-M(atti) |
| Kröger, H. |
| Kurl, S(udhir) |
| Kuusisto, J(ohanna) |
| Laakso, M(arkku) |
| Lakka, T(imo) A. |
| Lapinlampi, N(iina) |
| Laukkanen, J(ari) (UEF/KSSHP) |
| Levonen, A(nna)-L(iisa) |
| Lindgren, A(ntti) E. |
| Löppönen, H(eikki) |
| Mannermaa, A. |
| Manninen, H. |
| Mecklin, J(ukka)-P(ekka) |
| Moilanen, L(eena) |
| Mönkkönen, J. |
| Mykkänen, H. |
| Nuutinen, J. |
| Paajanen, H. |
| Paananen, J. |
| Palvimo, J.J. |
| Pelkonen, J(ukka) |
| Pihlajamäki, J(ussi) |
| Pihlajamäki, M. |
| Pitkänen, A(sla) |
| Punnonen, K. |
| Raatikainen K |
| Rauramaa, R. |
| Rissanen, T.T. |
| Roine, R(isto) P. |
| Ryynänen, O.P. |
| Saarikoski, S. |
| Schwab, U(rsula) |
| Sivenius, J. |
| Soininen, H(ilkka) |
| Soininen, P(asi) |
| Sorri, I. |
| Stancakova, A(lena) |
| Sulkava, R. |
| Sund, R(eijo) |
| Tammi, M. |
| Tanila, H(eikki) |
| Tiihonen, J(ari) |
| Uusaro, A. |
| Uusitupa, M. |
| Vanninen, R. |
| Vaskilampi, T. |
| Viinamäki, H(eimo) |
| Virtanen, M(arianna) |
| Voutilainen, R(aimo) |
| Voutilainen, S(ari) |
| Wahlfors, J. |
| Wirth, T. |
| Wong, G. |
| Ylä-Herttuala, S(eppo) |
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| | The calcium-activated chloride channel-associated protein rCLCA2 is expressed throughout rat epidermis, facilitates apoptosis and is downmodulated by UVB. | Tammi, M. | 273 days | save |  |  | |
| Cellular hyaluronan is associated with a poor prognosis in renal cell carcinoma. | Tammi, M. | 539 days | save | | | |
| Tumor microenvironment and breast cancer survival: combined effects of breast fat, M2 macrophages and hyaluronan create a dismal prognosis. | Tammi, M. | 711 days | save | | | |
| Peritumoral ADC values in breast cancer: region of interest selection, associations with hyaluronan intensity, and prognostic significance. | Tammi, M. | 818 days | save | | | |
| Hyaluronan synthesis supports glutamate transporter activity. | Tammi, M. | 866 days | save | | | |
| Melanocyte hyaluronan coat fragmentation enhances the UVB-induced TLR-4 receptor signaling and expression of proinflammatory mediators IL-6, IL-8, CXCL-1 and CXCL-10 via NF-κB activation. | Tammi, M. | 937 days | save | | | |
| Analysis of UDP-Sugars from Cultured Cells and Small Tissue Samples. | Tammi, M. | 968 days | save | | | |
| Effects of mutations in the post-translational modification sites on the trafficking of hyaluronan synthase 2 (HAS2). | Tammi, M. | 1084 days | save | | | |
| Single-Molecule Unbinding Forces between the Polysaccharide Hyaluronan and Its Binding Proteins. | Tammi, M. | 1222 days | save | | | |
| Activated hyaluronan metabolism in the tumor matrix - Causes and consequences. | Tammi, M. | 1273 days | save | | | |
| Extracellular ATP activates hyaluronan synthase 2 ( HAS2 ) in epidermal keratinocytes via P2Y2, Ca2+-signaling, and MAPK pathways. | Tammi, M. | 1296 days | save | | | |
| Hyaluronan metabolism enhanced during epidermal differentiation is suppressed by vitamin C. | Tammi, M. | 1357 days | save | | | |
| UDP-sugar accumulation drives hyaluronan synthesis in breast cancer. | Tammi, M. | 1379 days | save | | | |
| Transmembrane Pickets Connect Cyto- and Pericellular Skeletons Forming Barriers to Receptor Engagement. | Tammi, M. | 1382 days | save | | | |
| Evaluation of methods and marker Systems in Genomic Selection of oil palm (Elaeis guineensis Jacq.). | Tammi, M. | 1413 days | save | | | |
| Genomic Selection in Commercial Perennial Crops: Applicability and Improvement in Oil Palm (Elaeis guineensis Jacq.). | Tammi, M. | 1600 days | save | | | |
| Human Keratinocytes Respond to Extracellular UTP by Induction of Hyaluronan Synthase 2 Expression and Increased Hyaluronan Synthesis. | Tammi, M. | 1716 days | save | | | |
| High extent of O-GlcNAcylation in breast cancer cells correlates with the levels of HAS enzymes, accumulation of hyaluronan, and poor outcome. | Tammi, M. | 1851 days | save | | | |
| Hexosamine biosynthesis in keratinocytes - roles of GFAT and GNPDA enzymes in the maintenance of UDP-GlcNAc content and hyaluronan synthesis. | Tammi, M. | 2075 days | save | | | |
| UDP-sugar substrates of HAS3 regulate its O-GlcNAcylation, intracellular traffic, extracellular shedding and correlate with melanoma progression. | Tammi, M. | 2076 days | save | | | |
| Hyaluronan-positive plasma membrane protrusions exist on mesothelial cells in vivo. | Tammi, M. | 2096 days | save | | | |
| The organic osmolyte betaine induces keratin 2 expression in rat epidermal keratinocytes - A genome-wide study in UVB irradiated organotypic 3D cultures. | Tammi, M. | 2224 days | save | | | |
| The reciprocal association between mammographic breast density, hyaluronan synthesis and patient outcome. | Tammi, M. | 2235 days | save | | | |
| Hyaluronan synthase 3 (HAS3) overexpression downregulates MV3 melanoma cell proliferation, migration and adhesion. | Tammi, M. | 2280 days | save | | | |
| Cell protrusions induced by hyaluronan synthase 3 (HAS3) resemble mesothelial microvilli and share cytoskeletal features of filopodia. | Tammi, M. | 2295 days | save | | | |
| Interleukin-1β-induced Reduction of CD44 S325 Phosphorylation in Human Epidermal Keratinocytes Promotes CD44 Homomeric Complexes and Binding to Ezrin, and Extended, Monocyte-adhesive Hyaluronan Coats. | Tammi, M. | 2405 days | save | | | |
| Fluorescence Resonance Energy Transfer (FRET) and Proximity Ligation Assays Reveal Functionally Relevant Homo- and Heteromeric Complexes among Hyaluronan Synthases HAS1, HAS2 and HAS3. | Tammi, M. | 2410 days | save | | | |
| Decreased Hyaluronidase 1 Expression is Associated with Early Disease Recurrence in Human Endometrial Cancer. | Tammi, M. | 2475 days | save | | | |
| High numbers of macrophages, especially M2-like (CD163-positive), correlate with hyaluronan accumulation and poor outcome in breast cancer. | Tammi, M. | 2538 days | save | | | |
| Hyaluronan-coated extracellular vesicles-a novel link between hyaluronan and cancer. | Tammi, M. | 2642 days | save | | | |
| Evidence of endoplasmic reticulum stress and liver inflammation in the American mink Neovison vison with benign hepatic steatosis. | Tammi, M. | 2642 days | save | | | |
| Isothiocyanate analogs targeting CD44 receptor as an effective strategy against colon cancer. | Tammi, M. | 2663 days | save | | | |
| Extracellular UDP-Glucose Activates P2Y14 Receptor, Induces Signal Transducer and Activator of Transcription 3 (STAT3) T705 Phosphorylation and Binding to Hyaluronan Synthase 2 (HAS2) Promoter, Stimulating Hyaluronan Synthesis of Keratinocytes. | Tammi, M. | 2713 days | save | | | |
| rCLCA2 is associated with epidermal differentiation and strongly downregulated by UV radiation. | Tammi, M. | 2758 days | save | | | |
| Rab10-Mediated Endocytosis of the Hyaluronan Synthase HAS3 Regulates Hyaluronan Synthesis and Cell Adhesion to Collagen. | Tammi, M. | 2813 days | save | | | |
| The Dynamic Metabolism of Hyaluronan Regulates the Cytosolic Concentration of UDP-GlcNAc. | Tammi, M. | 2820 days | save | | | |
| Extensive CD44-dependent hyaluronan coats on human bone marrow-derived mesenchymal stem cells produced by hyaluronan synthases HAS1, HAS2 and HAS3. | Tammi, M. | 2845 days | save | | | |
| OGT and OGA expression in postmenopausal skeletal muscle associates with hormone replacement therapy and muscle cross-sectional area. | Tammi, M. | 2862 days | save | | | |
| Hyaluronan synthases (HAS1-3) in stromal and malignant cells correlate with breast cancer grade and predict patient survival. | Tammi, M. | 2868 days | save | | | |
| Borate-aided anion exchange high-performance liquid chromatography of uridine diphosphate-sugars in brain, heart, adipose and liver tissues. | Tammi, M. | 2880 days | save | | | |
| Manifestations of Fasting-Induced Fatty Liver and Rapid Recovery from Steatosis in Voles Fed Lard or Flaxseed Oil Lipids. | Tammi, M. | 2923 days | save | | | |
| Hyaluronan synthase 1 (HAS1) produces a cytokine-and glucose-inducible, CD44-dependent cell surface coat. | Tammi, M. | 2939 days | save | | | |
| Tissue distribution and subcellular localization of hyaluronan synthase isoenzymes. | Tammi, M. | 2954 days | save | | | |
| Hyaluronan production enhances shedding of plasma membrane-derived microvesicles. | Tammi, M. | 3065 days | save | | | |
| Low-dose ultraviolet B irradiation increases hyaluronan synthesis in epidermal keratinocytes via sequential induction of hyaluronan synthases Has1-3 mediated by p38 and Ca2+/calmodulin-dependent protein kinase II (CaMKII) signaling. | Tammi, M. | 3094 days | save | | | |
| Mannose reduces hyaluronan and leukocytes in wound granulation tissue and inhibits migration and hyaluronan-dependent monocyte binding. | Tammi, M. | 3154 days | save | | | |
| Plasma hyaluronan and hemorheology in patients with septic shock: a clinical and experimental study. | Tammi, M. | 3184 days | save | | | |
| Hyaluronan synthase 1 (HAS1) requires higher cellular UDP-GlcNAc concentration than HAS2 and HAS3. | Tammi, M. | 3210 days | save | | | |
| Hyaluronan in cytosol - microinjection-based probing of its existence and suggested functions. | Tammi, M. | 3290 days | save | | | |
| Role of UDP-GlcNAc and O-GlcNAcylation of hyaluronan synthase 2 in the control of chondroitin sulfate and hyaluronan synthesis. | Tammi, M. | 3360 days | save | | | |
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