P.1.h.017 Regulation of the level of LSAMP gene and protein by alternative promoters in mouse brain and implications in behavioral models von Philips, M, Lilleväli, K, Innos, J, Luuk, H, Hundahl, C.A, Heinla, I, Vasar, E

Volltext

Chronic SSRI administration in Lsamp deficient mice von Philips, M.A., Bregin, A., Innos, J., Lilleväli, K., Raudkivi, K., Harro, J., Vasar, E.

Volltext

Correction: GDNF Overexpression from the Native Locus Reveals its Role in the Nigrostriatal Dopaminergic System Function von Kumar, Anmol, Kopra, Jaakko, Varendi, Kärt, Porokuokka, Lauriina L, Panhelainen, Anne, Kuure, Satu, Marshall, Pepin, Karalija, Nina, Härma, Mari-Anne, Vilenius, Carolina, Lilleväli, Kersti, Tekko, Triin, Mijatovic, Jelena, Pulkkinen, Nita, Jakobson, Madis, Jakobson, Maili, Ola, Roxana, Palm, Erik, Lindahl, Maria, Strömberg, Ingrid, Võikar, Vootele, Piepponen, T Petteri, Saarma, Mart, Andressoo, Jaan-Olle

Volltext

GDNF Overexpression from the Native Locus Reveals its Role in the Nigrostriatal Dopaminergic System Function von Kumar, Anmol, Kopra, Jaakko, Varendi, Kärt, Porokuokka, Lauriina L, Panhelainen, Anne, Kuure, Satu, Marshall, Pepin, Karalija, Nina, Härma, Mari-Anne, Vilenius, Carolina, Lilleväli, Kersti, Tekko, Triin, Mijatovic, Jelena, Pulkkinen, Nita, Jakobson, Madis, Jakobson, Maili, Ola, Roxana, Palm, Erik, Lindahl, Maria, Strömberg, Ingrid, Võikar, Vootele, Piepponen, T Petteri, Saarma, Mart, Andressoo, Jaan-Olle

Volltext

[P1.30]: The role of Gata2 in the midbrain GABAergic neuron development von Kala, K., Haugas, M., Lilleväli, K., Salminen, M., Partanen, J.

Volltext

Partially overlapping expression of Gata2 and Gata3 during inner ear development von Lilleväli, Kersti, Matilainen, Tanja, Karis, Alar, Salminen, Marjo

Volltext

Depression-associated Negr1 gene-deficiency induces alterations in the monoaminergic neurotransmission enhancing time-dependent sensitization to amphetamine in mice von Kaare, M., Jayaram, M., Jagomäe, T., Singh, K., Kilk, K., Leevik, M., Varul, J., Leidmaa, E., Visnapuu, T., Nõmm, H., Rähn, K., Plaas, M., Lilleväli, K., Schäfer, M.K.E., Philips, M.A., Vasar, E.

Volltext

Comparative expression analysis of the genes encoding polypyrimidine tract binding protein (PTB) and its neural homologue (brPTB) in prenatal and postnatal mouse brain von Lilleväli, Kersti, Kulla, Andres, Örd, Tõnis

Volltext

Neural cell adhesion molecule Negr1 deficiency in mouse results in structural brain endophenotypes and behavioral deviations related to psychiatric disorders von Singh, Katyayani, Jayaram, Mohan, Kaare, Maria, Leidmaa, Este, Jagomäe, Toomas, Heinla, Indrek, Hickey, Miriam A., Kaasik, Allen, Schäfer, Michael K., Innos, Jürgen, Lilleväli, Kersti, Philips, Mari-Anne, Vasar, Eero

Volltext

The IgLON family of cell adhesion molecules expressed in developing neural circuits ensure the proper functioning of the sensory system in mice von Singh, Katyayani, Jayaram, Mohan, Hanumantharaju, Arpana, Tõnissoo, Tambet, Jagomäe, Toomas, Mikheim, Kaie, Muthuraman, Srirathi, Gilbert, Scott F., Plaas, Mario, Schäfer, Michael K. E., Innos, Jürgen, Lilleväli, Kersti, Philips, Mari-Anne, Vasar, Eero

Volltext

Neuronal Growth and Behavioral Alterations in Mice Deficient for the Psychiatric Disease-Associated Negr1 Gene von Singh, Katyayani, Loreth, Desirée, Pöttker, Bruno, Hefti, Kyra, Innos, Jürgen, Schwald, Kathrin, Hengstler, Heidi, Menzel, Lutz, Sommer, Clemens J, Radyushkin, Konstantin, Kretz, Oliver, Philips, Mari-Anne, Haas, Carola A, Frauenknecht, Katrin, Lilleväli, Kersti, Heimrich, Bernd, Vasar, Eero, Schäfer, Michael K E

Volltext

Depression-Associated Negr1 Gene-Deficiency Induces Alterations in the Monoaminergic Neurotransmission Enhancing Time-Dependent Sensitization to Amphetamine in Male Mice von Kaare, Maria, Jayaram, Mohan, Jagomäe, Toomas, Singh, Katyayani, Kilk, Kalle, Mikheim, Kaie, Leevik, Marko, Leidmaa, Este, Varul, Jane, Nõmm, Helis, Rähn, Kristi, Visnapuu, Tanel, Plaas, Mario, Lilleväli, Kersti, Schäfer, Michael K E, Philips, Mari-Anne, Vasar, Eero

Volltext

FLAD1‐associated multiple acyl‐CoA dehydrogenase deficiency identified by newborn screening von Muru, Kai, Reinson, Karit, Künnapas, Kadi, Lilleväli, Hardo, Nochi, Zahra, Mosegaard, Signe, Pajusalu, Sander, Olsen, Rikke K. J., Õunap, Katrin

Volltext

High-Fat Diet Induces Pre-Diabetes and Distinct Sex-Specific Metabolic Alterations in Negr1-Deficient Mice von Kaare, Maria, Mikheim, Kaie, Lilleväli, Kersti, Kilk, Kalle, Jagomäe, Toomas, Leidmaa, Este, Piirsalu, Maria, Porosk, Rando, Singh, Katyayani, Reimets, Riin, Taalberg, Egon, Schäfer, Michael K E, Plaas, Mario, Vasar, Eero, Philips, Mari-Anne

Volltext

Neuronal Growth and Behavioral Alterations in Mice Deficient for the Psychiatric Disease-Associated Negr1 Gene von Singh, Katyayani, Loreth, Desirée, Pöttker, Bruno, Hefti, Kyra, Innos, Jürgen, Schwald, Kathrin, Hengstler, Heidi, Menzel, Lutz, Sommer, Clemens J, Radyushkin, Konstantin, Kretz, Oliver, Philips, Mari-Anne, Haas, Carola A, Frauenknecht, Katrin, Lilleväli, Kersti, Heimrich, Bernd, Vasar, Eero, Schäfer, Michael K E

Volltext

Characterization of MYG1 gene and protein: subcellular distribution and function von Philips, Mari-Anne, Vikeså, Jonas, Luuk, Hendrik, Jønson, Lars, Lilleväli, Kersti, Rehfeld, Jens F., Vasar, Eero, Kõks, Sulev, Nielsen, Finn C.

Volltext

Mutation 985A>G in the MCAD gene shows low incidence in Estonian population von Lilleväli, Hardo, Margus, Külli, Õunap, Katrin, Metspalu, Andres

Volltext

Phenylalanine hydroxylase gene mutation R408W is present on 84% of Estonian phenylketonuria chromosomes von Lilleväli, H, Ounap, K, Metspalu, A

Volltext

Development of the phenylketonuria screening programme in Estonia von Ounap, K, Lilleväli, H, Metspalu, A, Lipping-Sitska, M

Volltext

The incidence and characterization of phenylketonuric patients in Estonia von õunap, K., Lilleväli, H., Klaassen, T., Metspalu, A., Sitska, M.

Volltext