The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy

Por Lonka, Liina, Aalto, Antti, Kopra, Outi, Kuronen, Mervi, Kokaia, Zaal, Saarma, Mart, Lehesjoki, Anna-Elina
Publicado em 2005

Progressive Volume Loss and White Matter Degeneration in Cstb-Deficient Mice: A Diffusion Tensor and Longitudinal Volumetry MRI Study

Por Manninen, Otto, Laitinen, Teemu, Lehtimäki, Kimmo K., Tegelberg, Saara, Lehesjoki, Anna-Elina, Gröhn, Olli, Kopra, Outi
Publicado em 2014

Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1) – distinct characteristics in neurons

Por Jauhiainen Matti, Saarela Jani, Kopra Outi, Salonen Tarja, von Schantz Carina, Lyly Annina, Kyttälä Aija, Jalanko Anu
Publicado em 2007-06-01

Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1) – distinct characteristics in neurons

Por Lyly, Annina, von Schantz, Carina, Salonen, Tarja, Kopra, Outi, Saarela, Jani, Jauhiainen, Matti, Kyttälä, Aija, Jalanko, Anu
Publicado em 2007

Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases

Por von Schantz, Carina, Saharinen, Juha, Kopra, Outi, Cooper, Jonathan D, Gentile, Massimiliano, Hovatta, Iiris, Peltonen, Leena, Jalanko, Anu
Publicado em 2008

Progressive thalamocortical neuron loss in Cln5 deficient mice: distinct effects in Finnish variant late infantile NCL

Por von Schantz, Carina, Kielar, Catherine, Hansen, Stine N, Pontikis, Charlie C, Alexander, Noreen A, Kopra, Outi, Jalanko, Anu, Cooper, Jonathan D
Publicado em 2009

Impaired osteoclast homeostasis in the cystatin B-deficient mouse model of progressive myoclonus epilepsy

Por Manninen, Otto, Puolakkainen, Tero, Lehto, Jemina, Harittu, Elina, Kallonen, Aki, Peura, Marko, Laitala-Leinonen, Tiina, Kopra, Outi, Kiviranta, Riku, Lehesjoki, Anna-Elina
Publicado no Bone Rep (2015)

Cystatin B Deficiency Sensitizes Neurons to Oxidative Stress in Progressive Myoclonus Epilepsy, EPM1

Por Lehtinen, Maria K., Tegelberg, Saara, Schipper, Hyman, Su, Haixiang, Zukor, Hillel, Manninen, Otto, Kopra, Outi, Joensuu, Tarja, Hakala, Paula, Bonni, Azad, Lehesjoki, Anna-Elina
Publicado em 2009

Gene Expression Alterations in the Cerebellum and Granule Neurons of Cstb(−/−) Mouse Are Associated with Early Synaptic Changes and Inflammation

Por Joensuu, Tarja, Tegelberg, Saara, Reinmaa, Eva, Segerstråle, Mikael, Hakala, Paula, Pehkonen, Heidi, Korpi, Esa R., Tyynelä, Jaana, Taira, Tomi, Hovatta, Iiris, Kopra, Outi, Lehesjoki, Anna-Elina
Publicado em 2014

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Por Kousi, Maria, Anttila, Verneri, Schulz, Angela, Calafato, Stella, Jakkula, Eveliina, Riesch, Erik, Myllykangas, Liisa, Kalimo, Hannu, Topcu, Meral, Gokben, Sarenur, Alehan, Fusun, Lemke, Johannes R, Alber, Michael, Palotie, Aarno, Kopra, Outi, Lehesjoki, Anna-Elina
Publicado em 2012