Human transcription factor protein interaction networks von Göös, Helka, Kinnunen, Matias, Salokas, Kari, Tan, Zenglai, Liu, Xiaonan, Yadav, Leena, Zhang, Qin, Wei, Gong-Hong, Varjosalo, Markku

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An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic Differentiation von Saarimäki-Vire, Jonna, Balboa, Diego, Russell, Mark A., Saarikettu, Juha, Kinnunen, Matias, Keskitalo, Salla, Malhi, Amrinder, Valensisi, Cristina, Andrus, Colin, Eurola, Solja, Grym, Heli, Ustinov, Jarkko, Wartiovaara, Kirmo, Hawkins, R. David, Silvennoinen, Olli, Varjosalo, Markku, Morgan, Noel G., Otonkoski, Timo

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GATA-targeted compounds modulate cardiac subtype cell differentiation in dual reporter stem cell line von Valimaki, Mika J., Leigh, Robert S., Kinnunen, Sini M., March, Alexander R., de Sande, Ana Hernandez, Kinnunen, Matias, Varjosalo, Markku, Heinaniemi, Merja, Kaynak, Bogac L., Ruskoaho, Heikki

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Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations von Staels, Frederik, De Keukeleere, Kerstin, Kinnunen, Matias, Keskitalo, Salla, Lorenzetti, Flaminia, Vanmeert, Michiel, Prezzemolo, Teresa, Pasciuto, Emanuela, Lescrinier, Eveline, Bossuyt, Xavier, Gerbaux, Margaux, Willemsen, Mathijs, Neumann, Julika, Van Loo, Sien, Corveleyn, Anniek, Willekens, Karen, Stalmans, Ingeborg, Meyts, Isabelle, Liston, Adrian, Humblet-Baron, Stephanie, Seppänen, Mikko, Varjosalo, Markku, Schrijvers, Rik

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Human transcription factor protein interaction networks von Varjosalo, Markku, Göös, Helka, Kinnunen, Matias, Salokas, Kari, Liu, Xiaonan

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The Impact of ETV6-NTRK3 Oncogenic Gene Fusions on Molecular and Signaling Pathway Alterations von Kinnunen, Matias, Liu, Xiaonan, Niemelä, Elina, Öhman, Tiina, Gawriyski, Lisa, Salokas, Kari, Keskitalo, Salla, Varjosalo, Markku

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Abstract LB006: Interactome analysis identifies signaling pathways activated by ETV6-NTRK3 oncogenic gene fusions von Kinnunen, Matias, Liu, Xiaonan, Salokas, Kari, Keskitalo, Salla, Varjosalo, Markku

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Loss-of-function mutation in IKZF2 leads to immunodeficiency with dysregulated germinal center reactions and reduction of MAIT cells von Hetemaki, I, Kaustio, M, Kinnunen, M, Heikkila, N, Keskitalo, S, Nowlan, K, Miettinen, S, Sarkkinen, J, Glumoff, V, Andersson, N, Kettunen, K, Vanhanen, R, Nurmi, K, Eklund, KK, Dunkel, J, Mayranpaa, MI, Schlums, H, Arstila, TP, Kisand, K, Bryceson, YT, Peterson, P, Otava, U, Syrjanen, J, Saarela, J, Varjosalo, M, Kekalainen, E

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Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations von Staels, Frederik, De Keukeleere, Kerstin, Kinnunen, Matias, Keskitalo, Salla, Lorenzetti, Flaminia, Vanmeert, Michiel, Prezzemolo, Teresa, Pasciuto, Emanuela, Lescrinier, Eveline, Bossuyt, Xavier, Gerbaux, Margaux, Willemsen, Mathijs, Neumann, Julika, Van Loo, Sien, Corveleyn, Anniek, Willekens, Karen, Stalmans, Ingeborg, Meyts, Isabelle, Liston, Adrian, Humblet-Baron, Stephanie, Seppanen, Mikko, Varjosalo, Markku, Schrijvers, Rik

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Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50 von Fliegauf, Manfred, Kinnunen, Matias, Posadas-Cantera, Sara, Camacho-Ordonez, Nadezhda, Abolhassani, Hassan, Alsina, Laia, Atschekzei, Faranaz, Bogaert, Delfien, Burns, Siobhan O, Church, Joseph A, Dueckers, Gregor, Freeman, Alexandra F, Hammarstroem, Lennart, Hanitsch, Leif Gunnar, Kerre, Tessa, Kobbe, Robin, Sharapova, Svetlana O, Siepermann, Kathrin, Speckmann, Carsten, Steiner, Sophie, Verma, Nisha, Walter, Jolan E, Westermann-Clark, Emma, Goldacker, Sigune, Warnatz, Klaus, Varjosalo, Markku, Grimbacher, Bodo

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Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear Entry von Heikkinen, Tuomas, Kämpjärvi, Kati, Keskitalo, Salla, von Nandelstadh, Pernilla, Liu, Xiaonan, Rantanen, Ville, Pitkänen, Esa, Kinnunen, Matias, Kuusanmäki, Heikki, Kontro, Mika, Turunen, Mikko, Mäkinen, Netta, Taipale, Jussi, Heckman, Caroline, Lehti, Kaisa, Mustjoki, Satu, Varjosalo, Markku, Vahteristo, Pia

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Truncating NFKB1 variants cause combined NLRP3 inflammasome activation and type I interferon signaling and predispose to necrotizing fasciitis von Nurmi, Katariina, Silventoinen, Kristiina, Keskitalo, Salla, Rajamäki, Kristiina, Kouri, Vesa-Petteri, Kinnunen, Matias, Jalil, Sami, Maldonado, Rocio, Wartiovaara, Kirmo, Nievas, Elma Inés, Denita-Juárez, Silvina Paola, Duncan, Christopher J.A., Kuismin, Outi, Saarela, Janna, Romo, Inka, Martelius, Timi, Parantainen, Jukka, Beklen, Arzu, Bilicka, Marcelina, Matikainen, Sampsa, Nordström, Dan C., Kaustio, Meri, Wartiovaara-Kautto, Ulla, Kilpivaara, Outi, Klein, Christoph, Hauck, Fabian, Jahkola, Tiina, Hautala, Timo, Varjosalo, Markku, Barreto, Goncalo, Seppänen, Mikko R.J., Eklund, Kari K.

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Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50 von Fliegauf, Manfred, Kinnunen, Matias, Posadas-Cantera, Sara, Camacho-Ordonez, Nadezhda, Abolhassani, Hassan, Alsina, Laia, Atschekzei, Faranaz, Bogaert, Delfien J, Burns, Siobhan O, Church, Joseph A, Dueckers, Gregor, Freeman, Alexandra F, Hammarstroem, Lennart, Hanitsch, Leif Gunnar, Kerre, Tessa, Kobbe, Robin, Sharapova, Svetlana O, Siepermann, Kathrin, Speckmann, Carsten, Steiner, Sophie, Verma, Nisha, Walter, Jolan E, Westermann-Clark, Emma, Goldacker, Sigune, Warnatz, Klaus, Varjosalo, Markku, Grimbacher, Bodo

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Common variable immunodeficiency in two families with heterogenous phenotypes caused by novel heterozygous NFKB1 mutations von Staels, Frederik, De Keukeleere, Kerstin, Kinnunen, Matias, Lorenzetti, Flaminia, Keskitalo, Salla, Van Meert, Michiel, Prezzemolo, Teresa, Lescrinier, Eveline, Bossuyt, Xavier, Gerbaux, Margaux, Willemsen, Mathijs, Neumann, Julika, Loo, Sien Van, Corveleyn, Anniek, Stalmans, Ingeborg, Liston, Adrian, Humblet-Baron, Stephanie, Seppanen, Mikko, Meyts, Isabelle, Varjosalo, Markku, Schrijvers, Rik

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Increased probability of hot and dry weather extremes during the growing season threatens global crop yields von Heino, Matias, Kinnunen, Pekka, Anderson, Weston, Ray, Deepak K., Puma, Michael J., Varis, Olli, Siebert, Stefan, Kummu, Matti

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Effect of a behavioural intervention in obese pregnant women (the UPBEAT study): a multicentre, randomised controlled trial von Poston, Lucilla, Prof, Bell, Ruth, MD, Croker, Helen, PhD, Flynn, Angela C, MSc, Godfrey, Keith M, Prof, Goff, Louise, PhD, Hayes, Louise, PhD, Khazaezadeh, Nina, MSc, Nelson, Scott M, Prof, Oteng-Ntim, Eugene, PhD, Pasupathy, Dharmintra, PhD, Patel, Nashita, MBBS, Robson, Stephen C, Prof, Sandall, Jane, Prof, Sanders, Thomas A B, Prof, Sattar, Naveed, Prof, Seed, Paul T, CStat, Wardle, Jane, Prof, Whitworth, Melissa K, MD, Briley, Annette L, PhD

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Early Antenatal Prediction of Gestational Diabetes in Obese Women: Development of Prediction Tools for Targeted Intervention von White, Sara L, Lawlor, Debbie A, Briley, Annette L, Godfrey, Keith M, Nelson, Scott M, Oteng-Ntim, Eugene, Robson, Stephen C, Sattar, Naveed, Seed, Paul T, Vieira, Matias C, Welsh, Paul, Whitworth, Melissa, Poston, Lucilla, Pasupathy, Dharmintra

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The potential of water security in leveraging Agenda 2030 von Taka, Maija, Ahopelto, Lauri, Fallon, Amy, Heino, Matias, Kallio, Marko, Kinnunen, Pekka, Niva, Venla, Varis, Olli

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Lifestyle intervention in obese pregnancy and cardiac remodelling in 3-year olds: children of the UPBEAT RCT von Taylor, Paul D., Gu, Haotian, Saunders, Hannah, Fiori, Federico, Dalrymple, Kathryn V., Sethupathi, Priyanka, Yamanouchi, Liana, Miller, Faith, Jones, Bethany, Vieira, Matias C., Singh, Claire, Briley, Annette, Seed, Paul T., Pasupathy, Dharmintra, Santosh, Paramala J., Groves, Alan M., Sinha, Manish D., Chowienczyk, Philip J., Poston, Lucilla

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Demand response events in district heating: Results from field tests in a university building von Mishra, Asit Kumar, Jokisalo, Juha, Kosonen, Risto, Kinnunen, Tuomas, Ekkerhaugen, Matias, Ihasalo, Heikki, Martin, Kristian

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