Research output per year
Research output per year
Personal profile
External positions
Tutkijatohtori, University of Lund
12 Feb 2015 → 30 Jun 2016Fields of Science
- 1182 Biochemistry, cell and molecular biology
International and National Collaboration
Publications and projects within past five years.
Publications
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Microglial phagocytosis dysfunction in the dentate gyrus is related to local neuronal activity in a genetic model of epilepsy
Sierra-Torre, V., Plaza-Zabala, A., Bonifazi, P., Abiega, O., Diaz-Aparicio, I., Tegelberg, S., Lehesjoki, A-E., Valero, J. & Sierra, A., Nov 2020, In : Epilepsia. 61, 11, p. 2593-2608 16 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
Alternative oxidase-mediated respiration prevents lethal mitochondrial cardiomyopathy
Rajendran, J., Purhonen, J., Tegelberg, S., Smolander, O-P., Mörgelin, M., Rozman, J., Gailus-Durner, V., Fuchs, H., de Angelis, M. H., Auvinen, P., Mervaala, E., Jacobs, H. T., Szibor, M., Fellman, V. & Kallijärvi, J., Jan 2019, In : EMBO molecular medicine. 11, 1, 19 p., 9456.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
NAD(+) repletion produces no therapeutic effect in mice with respiratory chain complex III deficiency and chronic energy deprivation
Purhonen, J., Rajendran, J., Tegelberg, S., Smolander, O-P., Pirinen, E., Kallijärvi, J. & Fellman, V., Nov 2018, In : FASEB Journal. 32, 11, p. 5913-5926 14 p.Research output: Contribution to journal › Article › Scientific › peer-review
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Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
Tegelberg, S., Tomasic, N., Kallijärvi, J., Purhonen, J., Elmer, E., Lindberg, E., Nord, D. G., Soller, M., Lesko, N., Wedell, A., Bruhn, H., Freyer, C., Stranneheim, H., Wibom, R., Nennesmo, I., Wredenberg, A., Eklund, E. A. & Fellman, V., 20 Apr 2017, In : Orphanet journal of rare diseases. 12, 14 p., 73.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile -
ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss
Anttonen, A-K., Laari, A., Kousi, M., Yang, Y. J., Jääskeläinen, T., Somer, M., Siintola, E., Jakkula, E., Muona, M., Tegelberg, S., Lönnqvist, T., Pihko, H., Valanne, L., Paetau, A., Lun, M. P., Hästbacka, J., Kopra, O., Joensuu, T., Katsanis, N., Lehtinen, M. K. & 2 others, , May 2017, In : Brain : a journal of neurology. 140, p. 1267-1279 13 p.Research output: Contribution to journal › Article › Scientific › peer-review
Open AccessFile