The CB1 cannabinoid receptor signals striatal neuroprotection via a PI3K/Akt/mTORC1/BDNF pathway von Blázquez, C, Chiarlone, A, Bellocchio, L, Resel, E, Pruunsild, P, García-Rincón, D, Sendtner, M, Timmusk, T, Lutz, B, Galve-Roperh, I, Guzmán, M

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Neurotrophins: Transcription and Translation von West, A. E., Pruunsild, P., Timmusk, T.

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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia von FRANCKS, C, MAEGAWA, S, TIMMUSK, T, PRUUNSILD, P, KOPPEL, I, LIND, P. A, MATSUMOTO-ITABA, N, NICOD, J, XIONG, L, JOOBER, R, ENARD, W, KRINSKY, B, LAUREN, J, NANBA, E, RICHARDSON, A. J, RILEY, B. P, MARTIN, N. G, STRITTMATTER, S. M, MÖLLER, H.-J, RUJESCU, D, ST CLAIR, D, MUGLIA, P, ROOS, J. L, ABRAHAMS, B. S, FISHER, S. E, WADE-MARTINS, R, ROULEAU, G. A, STEIN, J. F, KARAYIORGOU, M, GESCHWIND, D. H, RAGOUSSIS, J, KENDLER, K. S, AIRAKSINEN, M. S, OSHIMURA, M, VELAYOS-BAEZA, A, DELISI, L. E, MONACO, A. P, MEDLAND, S. E, COLELLA, S, GROSZER, M, MCAULEY, E. Z, CAFFREY, T. M

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Dissecting the human BDNF locus: Bidirectional transcription, complex splicing, and multiple promoters von Pruunsild, Priit, Kazantseva, Anna, Aid, Tamara, Palm, Kaia, Timmusk, Tõnis

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Subcellular localization and transcription regulatory potency of KCNIP/Calsenilin/DREAM/KChIP proteins in cultured primary cortical neurons do not provide support for their role in... von Pruunsild, Priit, Timmusk, Tõnis

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Alternative splicing and expression of human and mouse NFAT genes von Vihma, Hanna, Pruunsild, Priit, Timmusk, Tõnis

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Structure, alternative splicing, and expression of the human and mouse KCNIP gene family von Pruunsild, Priit, Timmusk, Tõnis

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LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells von Francks, C, Maegawa, S, Laurén, J, Abrahams, B S, Velayos-Baeza, A, Medland, S E, Colella, S, Groszer, M, McAuley, E Z, Caffrey, T M, Timmusk, T, Pruunsild, P, Koppel, I, Lind, P A, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, A J, Riley, B P, Martin, N G, Strittmatter, S M, Möller, H-J, Rujescu, D, St Clair, D, Muglia, P, Roos, J L, Fisher, S E, Wade-Martins, R, Rouleau, G A, Stein, J F, Karayiorgou, M, Geschwind, D H, Ragoussis, J, Kendler, K S, Airaksinen, M S, Oshimura, M, DeLisi, L E, Monaco, A P

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The CB sub(1) cannabinoid receptor signals striatal neuroprotection via a PI3K/Akt/mTORC1/BDNF pathway von Blazquez, C, Chiarlone, A, Bellocchio, L, Resel, E, Pruunsild, P, Garcia-Rincon, D, Sendtner, M, Timmusk, T, Lutz, B, Galve-Roperh, I, Guzman, M

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Neuronal K+/Cl– co‐transporter (KCC2) transgenes lacking neurone restrictive silencer element recapitulate CNS neurone‐specific expression and developmental up‐regulation of endoge... von Uvarov, Pavel, Pruunsild, Priit, Timmusk, Tõnis, Airaksinen, Matti S.

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The ColR–ColS two‐component signal transduction system is involved in regulation of Tn4652 transposition in Pseudomonas putida under starvation conditions von Hõrak, Rita, Ilves, Heili, Pruunsild, Priit, Kuljus, Martin, Kivisaar, Maia

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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia von Francks, C, Maegawa, S, Laurén, J, Abrahams, B S, Velayos-Baeza, A, Medland, S E, Colella, S, Groszer, M, McAuley, E Z, Caffrey, T M, Timmusk, T, Pruunsild, P, Koppel, I, Lind, P A, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, A J, Riley, B P, Martin, N G, Strittmatter, S M, Möller, H-J, Rujescu, D, St Clair, D, Muglia, P, Roos, J L, Fisher, S E, Wade-Martins, R, Rouleau, G A, Stein, J F, Karayiorgou, M, Geschwind, D H, Ragoussis, J, Kendler, K S, Airaksinen, M S, Oshimura, M, DeLisi, L E, Monaco, A P

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Results of NOPHO ALL2008 treatment for patients aged 1–45 years with acute lymphoblastic leukemia von Toft, N, Birgens, H, Abrahamsson, J, Griškevičius, L, Hallböök, H, Heyman, M, Klausen, T W, Jónsson, ÓG, Palk, K, Pruunsild, K, Quist-Paulsen, P, Vaitkeviciene, G, Vettenranta, K, Åsberg, A, Frandsen, T L, Marquart, H V, Madsen, H O, Norén-Nyström, U, Schmiegelow, K

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Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritis von Niibo, P., Nikopensius, T., Jagomägi, T., Voog, Ü., Haller, T., Tõnisson, N., Metspalu, A., Saag, M., Pruunsild, C.

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Genetic predisposition to PEG‐asparaginase hypersensitivity in children treated according to NOPHO ALL2008 von Højfeldt, Sofie G., Wolthers, Benjamin O., Tulstrup, Morten, Abrahamsson, Jonas, Gupta, Ramneek, Harila‐Saari, Arja, Heyman, Mats, Henriksen, Louise T., Jónsson, Òlafur G., Lähteenmäki, Päivi M., Lund, Bendik, Pruunsild, Kaie, Vaitkeviciene, Goda, Schmiegelow, Kjeld, Albertsen, Birgitte K.

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Complying with the European Clinical Trials directive while surviving the administrative pressure – An alternative approach to toxicity registration in a cancer trial von Frandsen, Thomas Leth, Heyman, Mats, Abrahamsson, Jonas, Vettenranta, Kim, Åsberg, Ann, Vaitkeviciene, Goda, Pruunsild, Kaie, Toft, Nina, Birgens, Henrik, Hallböök, Helena, Quist-Paulsen, Petter, Griškevičius, Laimonas, Helt, Louise, Hansen, Birgitte Vilsbøll, Schmiegelow, Kjeld

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Toxicity profile and treatment delays in NOPHO ALL2008-comparing adults and children with Philadelphia chromosome-negative acute lymphoblastic leukemia von Toft, Nina, Birgens, Henrik, Abrahamsson, Jonas, Griškevičius, Laimonas, Hallböök, Helene, Heyman, Mats, Klausen, Tobias Wirenfeldt, Jónsson, Ólafur Gísli, Palk, Katrin, Pruunsild, Kaie, Quist-Paulsen, Petter, Vaitkeviciene, Goda, Vettenranta, Kim, Asberg, Ann, Helt, Louise Rold, Frandsen, Thomas, Schmiegelow, Kjeld

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NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia von Tulstrup, Morten, Grosjean, Marie, Nielsen, Stine Nygaard, Grell, Kathrine, Wolthers, Benjamin Ole, Wegener, Peder Skov, Jonsson, Olafur Gisli, Lund, Bendik, Harila-Saari, Arja, Abrahamsson, Jonas, Vaitkeviciene, Goda, Pruunsild, Kaie, Toft, Nina, Holm, Mette, Hulegårdh, Erik, Liestøl, Sigurd, Griskevicius, Laimonas, Punab, Mari, Wang, Jinhua, Carroll, William L., Zhang, Zeyu, Dalgaard, Marlene D., Gupta, Ramneek, Nersting, Jacob, Schmiegelow, Kjeld

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The added value of a European Reference Network on rare and complex connective tissue and musculoskeletal diseases: insights after the first 5 years of the ERN ReCONNET von Talarico, Rosaria, Aguilera, Silvia, Alexander, Tobias, Amoura, Zahir, Andersen, Janette, Arnaud, Laurent, Avcin, Tadej, Marsal Barril, Sara, Beretta, Lorenzo, Bombardieri, Stefano, Bortoluzzi, Alessandra, Bouillot, Coralie, Bulina, Inita, Burmester, Gerd R, Cannizzo, Sara, Cavagna, Lorenzo, Chaigne, Benjamin, Cornet, Alain, Corti, Paolo, Costedoat-Chalumeau, Nathalie, Dāvidsone, Zane, Doria, Andrea, Fenech, Carol, Ferraris, Alessandro, Fischer-Betz, Rebecca, Fonseca, João Eurico, Frank, Charissa, Gaglioti, Andrea, Galetti, Ilaria, Guimarães, Vera, Hachulla, Eric, Holmner, Monica, Houssiau, Frederic, Iaccarino, Luca, Jacobsen, Søren, Limper, Maarten, Malfait, Fransiska, Mariette, Xavier, Marinello, Diana, Martin, Thierry, Matthews, Lisa, Matucci-Cerinic, Marco, Meyer, Alain, Milas-Ahić, Jasminka, Moinzadeh, Pia, Montecucco, Carlomaurizio, Mouthon, Luc, Müller-Ladner, Ulf, Nagy, György, Patarata, Eunice, Pileckyte, Margarita, Pruunsild, Chris, Rednic, Simona, Romão, Vasco C, Schneider, Matthias, Scirè, Carlo Alberto, Smith, Vanessa, Sulli, Alberto, Tamirou, Farah, Tani, Chiara, Taruscio, Domenica, Taulaigo, Anna V, Tincani, Angela, Ticciati, Simone, Turchetti, Giuseppe, van Hagen, P Martin, van Laar, Jacob M, Viera, Ana, de Vries-Bouwstra, Jeska K, Zschocke, Johannes, Cutolo, Maurizio, Mosca, Marta

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Effects of germ line DHFR and FPGS variants on methotrexate metabolism and relapse of leukemia von Tulstrup, M., Moriyama, T., Jiang, C., Grosjean, M., Nersting, J., Abrahamsson, Jonas, Grell, K., Hjalgrim, L. L., Jonsson, O. G., Kanerva, J., Lund, B., Nielsen, S. N., Nielsen, R. L., Quist-Paulsen, P., Pruunsild, K., Wolthers, B. O., Zhang, H., Gupta, R., Yang, J. J., Schmiegelow, K.

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