CA
CARLOS ANDRES ARANGO FRANCO
Inserm, Human Genetic of Infectious Diseases, Universidad de Antioquia, Institut Imagine Institut des Maladies Génétiques
Research areas: Immunology and Microbiology · Immunology · Immunodeficiency and Autoimmune Disorders · Blood disorders and treatments · T-cell and B-cell Immunology
Employment
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Inserm PhD Student2021 - 2024
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Human Genetic of Infectious Diseases PhD Student2019 - 2024
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Institut Imagine Institut des Maladies Génétiques PhD student2019 - 2021
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Group of Primary Immunodeficiencies PhD Student2015 - 2022
Education
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University of Antioquia PhD Student2017 - 2023
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University of Antioquia Master degree in Microbiology2015 - 2017
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University of Antioquia Bachelor in Microbiology2008 - 2014
Projects & Funding
Projects & funding information is unavailable.
Publications (12)
- Human inherited CCR2 deficiency underlies progressive polycystic lung disease Save
- Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency Save
- Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria Save
- Human IL-23 is essential for IFN-γ–dependent immunity to mycobacteria Save
- Anti-GM-CSF Neutralizing Autoantibodies in Colombian Patients with Disseminated Cryptococcosis Save
- Human genetic and immunological determinants of critical COVID-19 pneumonia. Save
- Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation. Save
- A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency Save
- Correction to: A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency (Journal of Clinical Immunology, (2020), 40, 8, (1093-1101), 10.1007/s10875-020-00842-2) Save
- Causal association of antibiotic use and resistant tuberculosis infection: Casecontrol meta-analysis,Factores de riesgo para la infección por tuberculosis resistente: Metanálisis de estudios de casos y controles Save
- Early-Onset Invasive Infection Due to Corynespora cassiicola Associated with Compound Heterozygous CARD9 Mutations in a Colombian Patient Save
- Inherited p40 phox deficiency differs from classic chronic granulomatous disease Save