Adipose tissue is inflamed in NAFLD due to obesity but not in NAFLD due to genetic variation in PNPLA3 von Lallukka, S., Sevastianova, K., Perttilä, J., Hakkarainen, A., Orho-Melander, M., Lundbom, N., Olkkonen, V. M., Yki-Järvinen, H.

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Differentiation of human adipose stromal cells in vitro into insulin-sensitive adipocytes von Huttala, Outi, Mysore, R., Sarkanen, J. R., Heinonen, T., Olkkonen, V. M., Ylikomi, T.

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Biosynthesis and Intracellular Targeting of the CLN3 Protein Defective in Batten Disease von Järvelä, Irma, Sainio, Markku, Rantamäki, Terhi, Olkkonen, Vesa M., Carpén, Olli, Peltonen, Leena, Jalanko, Anu

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In Vivo Interaction of the Adapter Protein CD2-associated Protein with the Type 2 Polycystic Kidney Disease Protein, Polycystin-2 von Lehtonen, Sanna, Ora, Ari, Olkkonen, Vesa M., Geng, Lin, Zerial, Marino, Somlo, Stefan, Lehtonen, Eero

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Human palmitoyl protein thioesterase: evidence for lysosomal targeting of the enzyme and disturbed cellular routing in infantile neuronal ceroid lipofuscinosis von Hellsten, E., Vesa, J., Olkkonen, V. M., Jalanko, A., Peltonen, L.

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Quantification of human plasma phospholipid transfer protein (PLTP): relationship between PLTP mass and phospholipid transfer activity von Huuskonen, Jarkko, Ekström, Minna, Tahvanainen, Esa, Vainio, Anu, Metso, Jari, Pussinen, Pirkko, Ehnholm, Christian, Olkkonen, Vesa M., Jauhiainen, Matti

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The impact of phospholipid transfer protein (PLTP) on HDL metabolism von Huuskonen, Jarkko, Olkkonen, Vesa M., Jauhiainen, Matti, Ehnholm, Christian

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Molecular cloning and subcellular localization of three GTP-binding proteins of the rab subfamily von OLKKONEN, V. M, DUPREE, P, KILLISCH, I, LÜTCKE, A, ZERIAL, M, SIMONS, K

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Phospholipid Transfer Is a Prerequisite for PLTP-Mediated HDL Conversion von Huuskonen, Jarkko, Olkkonen, Vesa M, Ehnholm, Christian, Metso, Jari, Julkunen, Ilkka, Jauhiainen, Matti

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The OSBP-related protein family in humans von Lehto, M, Laitinen, S, Chinetti, G, Johansson, M, Ehnholm, C, Staels, B, Ikonen, E, Olkkonen, V M

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Phospholipid transfer protein (PLTP) causes proteolytic cleavage of apolipoprotein A-I von Jauhiainen, M., Huuskonen, J., Baumann, M., Metso, J., Oka, T., Egashira, T., Hattori, H., Olkkonen, V.M., Ehnholm, C.

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Dissecting the Role of the Golgi Complex and Lipid Rafts in Biosynthetic Transport of Cholesterol to the Cell Surface von Heino, Sanna, Lusa, Sari, Somerharju, Pentti, Ehnholm, Christian, Olkkonen, Vesa M., Ikonen, Elina

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Effect of short-term carbohydrate overfeeding and long-term weight loss on liver fat in overweight humans von Sevastianova, Ksenia, Santos, Alexandre, Kotronen, Anna, Hakkarainen, Antti, Makkonen, Janne, Silander, Kaisa, Peltonen, Markku, Romeo, Stefano, Lundbom, Jesper, Lundbom, Nina, Olkkonen, Vesa M, Gylling, Helena, Fielding, Barbara A, Rissanen, Aila, Yki-Järvinen, Hannele

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Syntaxin 3 and Munc-18-2 in epithelial cells during kidney development von Lehtonen, Sanna, Riento, Kirsi, Olkkonen, Vesa M., Lehtonen, Eero

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Expression of heterologous proteins in cultured rat hippocampal neurons using the semliki forest virus vector von Olkkonen, V. M., Liljeström, P., Garoff, H., Simons, K., Dotti, C. G.

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Distribution of phospholipid transfer protein in human plasma: presence of two forms of phospholipid transfer protein, one catalytically active and the other inactive von Oka, T, Kujiraoka, T, Ito, M, Egashira, T, Takahashi, S, Nanjee, M N, Miller, N E, Metso, J, Olkkonen, V M, Ehnholm, C, Jauhiainen, M, Hattori, H

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Analysis of the Munc18b-syntaxin binding interface. Use of a mutant Munc18b to dissect the functions of syntaxins 2 and 3 von Kauppi, Maria, Wohlfahrt, Gerd, Olkkonen, Vesa M

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Munc18-2, a Functional Partner of Syntaxin 3, Controls Apical Membrane Trafficking in Epithelial Cells von Riento, Kirsi, Kauppi, Maria, Keränen, Sirkka, Olkkonen, Vesa M.

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Molecular cloning and functional expression of cDNA encoding the pig plasma phospholipid transfer protein von Pussinen, P.J. (National Public Health Institute, Helsinki, Finland.), Olkkonen, V.M, Jauhiainen, M, Ehnholm, C

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Osteoporosis and skeletal dysplasia caused by pathogenic variants in SGMS2 von Pekkinen, Minna, Terhal, Paulien A, Botto, Lorenzo D, Henning, Petra, Mäkitie, Riikka E, Roschger, Paul, Jain, Amrita, Kol, Matthijs, Kjellberg, Matti A, Paschalis, Eleftherios P, van Gassen, Koen, Murray, Mary, Bayrak-Toydemir, Pinar, Magnusson, Maria K, Jans, Judith, Kausar, Mehran, Carey, John C, Somerharju, Pentti, Lerner, Ulf H, Olkkonen, Vesa M, Klaushofer, Klaus, Holthuis, Joost Cm, Mäkitie, Outi

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