Kidere Dita: Difference between revisions
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Revision as of 09:15, 21 June 2016
Name | Pelnena Dita, MSc |
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Institution | Latvian Biomedical Research and Study Centre |
Address | Ratsupites Street 1, LV-1067 |
City | Riga |
State/Province | |
Country | Latvia |
[email protected] | |
Weblink | |
O2k-Network Lab |
Labels:
Publications
Published | Reference | |
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MitoEAGLE blood cells 1 | 2020 | Γ sander Frostner Eleonor*, Aburel Oana M*, Avram Vlad F*, Calabria Elisa, Castelo Rueda Maria Paulina*, Chamkha Imen*, ΔiΕΎmΓ‘rovΓ‘ Beata, Danila Maria-Daniela*, Doerrier Carolina*, Eckert Gunter P*, Ehinger Johannes K, Elmer Eskil*, Garcia-Souza Luiz F*, Gnaiger Erich*, Hoppel Florian*, Karabatsiakis Alexander*, Keppner Gloria, Kidere Dita*, Krako JakovljeviΔ Nina, Labieniec-Watala Magdalena*, Lelcu Theia*, Micankova Petra, Michalak Slawomir*, Molina Anthony JA*, Pavlovic Kasja, Pichler Irene*, Piel Sarah, Rousar Tomas, Rybacka-Mossakowska Joanna, Schartner Melanie, Siewiera Karolina*, Silaidos Carmina*, SjΓΆvall Fredrik*, Sobotka Ondrej*, Sumbalova Zuzana*, Swiniuch Daria, Vernerova Andrea*, Volani Chiara*, Vujacic-Mirski Ksenija*, Watala Cezary* (2020) Interlaboratory guide to mitochondrial respiratory studies with peripheral blood mononuclear cells and platelets. - Updated: 2020-03-06 - *Confirmed |
BEC 2020.1 doi10.26124bec2020-0001.v1 | 2020 | Gnaiger E et al β MitoEAGLE Task Group (2020) Mitochondrial physiology. Bioenerg Commun 2020.1. https://doi.org/10.26124/bec:2020-0001.v1 |
Abstracts
Published | Reference | |
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Kidere 2019 MiP2019 | 2019 | No abstract |
Kidere 2018 MiP2018 | 2018 | Cytoplasmic hybrid cells as a model to characterize the effect of the mtDNA mutations on the OXPHOS system. |
Kidere 2018 MiPschool Tromso E2 | 2018 | Cytoplasmic hybrid cells as a model to characterize the OXPHOS system: control sample with glutamate metabolism defect. |
Pelnena 2016 Abstract MitoFit Science Camp 2016 | 2016 | OXPHOS enzyme activity measurements in mitochondria isolated from peripheral blood leukocytes in control group and patients with suspected mitochondrial disease. |