Found: 12
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Nuclease Activity of the Junín Virus Nucleoprotein C-Terminal Domain.
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- Viruses (1999-4915), 2023, v. 15, n. 9, p. 1818, doi. 10.3390/v15091818
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- Article
Uncovering Causes of Childhood Death Using the Minimally Invasive Autopsy at the Community Level in an Urban Vulnerable Setting of Argentina: A Population-Based Study.
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- Clinical Infectious Diseases, 2021, v. 73, p. S435, doi. 10.1093/cid/ciab838
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- Article
Community Mortality Due to Respiratory Syncytial Virus in Argentina: Population-based Surveillance Study.
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- Clinical Infectious Diseases, 2021, v. 73, p. S210, doi. 10.1093/cid/ciab497
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- Article
Tolcapone, a potent aggregation inhibitor for the treatment of familial leptomeningeal amyloidosis.
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- FEBS Journal, 2021, v. 288, n. 1, p. 310, doi. 10.1111/febs.15339
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- Article
Structure and stability of the <italic>Human respiratory syncytial virus</italic> M<sub>2–1</sub> RNA‐binding core domain reveals a compact and cooperative folding unit.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2018, v. 74, n. 1, p. 23, doi. 10.1107/S2053230X17017381
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- Article
Cavity filling mutations at the thyroxine-binding site dramatically increase transthyretin stability and prevent its aggregation.
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- Scientific Reports, 2017, p. 44709, doi. 10.1038/srep44709
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- Article
Repositioning tolcapone as a potent inhibitor of transthyretin amyloidogenesis and associated cellular toxicity.
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- Nature Communications, 2016, v. 7, n. 2, p. 10787, doi. 10.1038/ncomms10787
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- Article
Identification and characterization of four PAX8 rare sequence variants (p.T225M, p.L233L, p.G336S and p.A439A) in patients with congenital hypothyroidism and dysgenetic thyroid glands.
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- Clinical Endocrinology, 2008, v. 68, n. 5, p. 828, doi. 10.1111/j.1365-2265.2007.03111.x
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- Article
Congenital hypothyroidism with goitre caused by new mutations in the thyroglobulin gene.
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- Clinical Endocrinology, 2007, v. 67, n. 3, p. 351, doi. 10.1111/j.1365-2265.2007.02889.x
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- Article
Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defectCommunicated by Mark H. PaalmanOnline Citation:Human Mutation, Mutation in Brief #646 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/646.pdf
- Published in:
- Human Mutation, 2003, v. 22, n. 3, p. 259, doi. 10.1002/humu.9175
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- Article
Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #646 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/646.pdf)
- Published in:
- Human Mutation, 2003, v. 22, n. 3, p. 259, doi. 10.1002/humu.9175
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- Publication type:
- Article
Detection of Mutations in Argentine Retinoblastoma Patients by Segregation of Polymorphisms, Exon Analysis and Cytogenetic Test.
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- Ophthalmic Research, 2001, v. 33, n. 6, p. 336, doi. 10.1159/000055690
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- Article