Projects per year
Search results
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Active
Integrative analysis of whole-genome noncoding and transcriptome sequencing data to improve diagnosis of innate immune disorders.
Rozevska, M. (Project leader) & Kurjāne, N. (Supervisor)
2/10/23 → 30/09/27
Project: PhD projects
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SARS-CoV-2 vakcinācija iedzimto imunitātes traucējumu pacientiem Latvijā: imūnā atbilde, vakcinācijas aptvere un iemesli atteikumam no rekomendētas vakcinācijas
Lucāne, Z. (Project leader) & Kurjāne, N. (Supervisor)
1/10/21 → 30/09/25
Project: PhD projects
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Peripheral nervous system damage and its biomarkers study in patients with systemic sclerosis.
Ivanova, K. (Project leader), Kurjāne, N. (Supervisor) & Ķēniņa, V. (Supervisor)
1/10/21 → 30/09/25
Project: PhD projects
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Finished
Hereditary angioedema: Research of genetic etiology
Kurjāne, N. (Project leader), Gailīte, L. (Participant), Kaņepa, A. (Participant), Rots, D. (Participant), Nartiša, I. (Participant) & Vīksne, K. (Participant)
12/07/21 → 11/07/22
Project: RSU grants
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Predominantly primary antibody deficiencies among adults: solving etiology and causes of clinical variability
Kurjāne, N. (Project leader), Gailīte, L. (Leading expert), Rots, D. (Participant), Kaņepa, A. (Assistant (student)), Lucāne, Z. (Assistant (student)), Nartiša, I. (Assistant (student)), Neiburga, K. D. (Assistant (student)), Ozola, L. (Participant) & Ķēniņa, V. (Expert)
1/01/21 → 31/12/23
Project: Fundamental and Applied Research Programme
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Hereditary angioedema: clinical and genetic research
Kaņepa, A. (Project leader) & Kurjāne, N. (Supervisor)
1/10/20 → 30/09/24
Project: PhD projects
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Predominant antibody deficiencies: in search of causes for clinical phenotypes and etiological diversity
Nartiša, I. (Project leader) & Kurjāne, N. (Supervisor)
1/10/20 → 30/09/24
Project: PhD projects