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Direction Name Project leader Period Funding
Human genetics and disease mechanisms
Functional and genetic research of rare unidentitied neuromuscular disorders Inna Iņaškina 2019.04.01.-2022.03.31 ERDF
Human genetics and disease mechanisms
The determination of rare inherited diseases' causative mechanisms using whole genome sequencing approach Inna Iņaškina 2019.04.01.-2022.03.31 ERDF
Human genetics and disease mechanisms
The characterization and analysis of mitochondrial DNA mutations and variants of unknown significance using transmitochondrial cytoplasmic hybrid cell models. Inna Iņaškina 2018.08.01.-2021.07.31. PFAR
Human genetics and disease mechanisms
Functional model for the mitochondrial disease evaluation and biomarker development Baiba Lāce , Inna Iņaškina 2015-2018 Taiwan-Latvian-Lithuanian collaboration project
Human genetics and disease mechanisms
Cancer research
Development of novel in vitro tests for diagnostics and prognostics of individualized therapies of tumors and mitochondrial disease treatment Jānis Kloviņš 2014.08.01.-2015.08.31. ERDF
Human genetics and disease mechanisms
Preparatory visit for project "Investigation, characterization and modeling of mitochondrial functions in patients with autism spectrum disorders" Baiba Lāce 2014 (23.02.14 - 26.02.14) EEA/Norway Grants
Human genetics and disease mechanisms
New tests for the diagnosis of inherited neuromuscular diseases Baiba Lāce 2010-2013 ERDF
Human genetics and disease mechanisms
The impact of risk factors on the development of nonsindromic cleft palate, lip and/or palate in the Latvian population Baiba Lāce 2010-2012 LCS GR
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Mājas lapas izstrādi finansēja ERAF 2.1.1.2. aktivitātes projekts Nr. 2010/0196/2DP/2.1.1.2.0/10/APIA/VIAA/004 "Latvijas biomedicīnas pētījumu integrācija Eiropas zinātnes telpā".