Terkko Navigator / Saarela, J(ani) (FIMM)

Genome-wide siRNA screening reveals several host receptors for the binding of human gut commensal Bifidobacterium bifidum

Correction to: Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients

A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign

Forced Migration and the Childbearing of Women and Men: A Disruption of the Tempo and Quantum of Fertility?

Ethnic Composition of Couples and Mutual Health Benefit Receipt: Register-Based Evidence from Finland

Loss-of-function mutation in <em>IKZF2</em> leads to immunodeficiency with dysregulated germinal center reactions and reduction of MAIT cells

Implementing a functional precision medicine tumor board for acute myeloid leukemia

Minimal information for chemosensitivity assays (MICHA): a next-generation pipeline to enable the FAIRification of drug screening experiments

Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients

High-throughput compound screening identifies navitoclax combined with irradiation as a candidate therapy for HPV-negative head and neck squamous cell carcinoma

High miR-30 Expression Associates with Improved Breast Cancer Patient Survival and Treatment Outcome

Birth order and alcohol-related mortality by ethnic origin and national context: Within-family comparisons for Finland and Sweden

Do monogenic inborn errors of immunity cause susceptibility to severe COVID-19?

Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients

<em>In vitro</em> identification and <em>in vivo</em> confirmation of inhibitors for SPCSV RNA silencing suppressor, a viral RNase III

Life Expectancy of the Ethnically Mixed: Register-Based Evidence from Native Finns

Sickness Absence and Disability Pension in the Very Long Term: A Finnish Register-Based Study With 20 Years Follow-Up

Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and mitochondrial dysfunction

RhoG deficiency abrogates cytotoxicity of human lymphocytes and causes hemophagocytic lymphohistiocytosis

Alcohol-related mortality by ethnic origin of natives: a prospective cohort study based on multigenerational population register data from Finland and Sweden

Minimal information for Chemosensitivity assays (MICHA): A next-generation pipeline to enable the FAIRification of drug screening experiments

Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation

Somatic mutations and T-cell clonality in patients with immunodeficiency

High NRF2 Levels Correlate with Poor Prognosis in Colorectal Cancer Patients and with Sensitivity to the Kinase Inhibitor AT9283 In Vitro

Therapeutic targeting of KSP in preclinical models of high-risk neuroblastoma

Heterozygous TLR3 Mutation in Patients with Hantavirus Encephalitis

Recessive MYH3 variants cause "Contractures, pterygia, and variable skeletal fusions syndrome 1B" mimicking Escobar variant multiple pterygium syndrome

Morale in Old Age and Its Association with Sociodemographic, Social, and Health-Related Factors in Different Age Groups

Development of FRET-based high-throughput screening for viral RNase III inhibitors

Prediction of drug combination effects with a minimal set of experiments

Patient-Derived Organoids from Multiple Colorectal Cancer Liver Metastases Reveal Moderate Intra-patient Pharmacotranscriptomic Heterogeneity

Naturalization in a Context of Free Mobility: Evidence from Cross-National Data on Finnish Immigrants in Sweden

Vascular plants of Victoria Island (Northwest Territories and Nunavut, Canada): a specimen-based study of an Arctic flora

Breeze: an integrated quality control and data analysis application for high-throughput drug screening

Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency

A Family With A20 Haploinsufficiency Presenting With Novel Clinical Manifestations and Challenges for Treatment

Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma

Corrigendum to 'Combined gene essentiality scoring improves the prediction of cancer dependency maps' [EBioMedicine 50 (2019) 66-79]

Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

Non-native vascular flora of the Arctic: Taxonomic richness, distribution and pathways

Combined gene essentiality scoring improves the prediction of cancer dependency maps

Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutation

In sickness or in health? Register-based evidence on partners' mutual receipt of sickness allowance and disability pension

Network pharmacology modeling identifies synergistic Aurora B and ZAK interaction in triple-negative breast cancer

Childlessness and union histories: evidence from Finnish population register data

A nearly fatal primary Epstein-Barr virus infection associated with low NK-cell counts in a patient receiving azathioprine: a case report and review of literature

SLC18A3 variants lead to fetal akinesia deformation sequence early in pregnancy

Experience of sibling death in childhood and risk of psychiatric care in adulthood: a national cohort study from Sweden

Return to work after sickness absence: a register-based comparison of two indigenous population groups

Genetic Association and Altered Gene Expression of <em>CYBB</em> in Multiple Sclerosis Patients