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A vaccine based on the yeast-expressed receptor-binding domain (RBD) elicits broad immune responses against SARS-CoV-2 variants.
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- Frontiers in Immunology, 2022, v. 13, p. 01, doi. 10.3389/fimmu.2022.1011484
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- Article
Development of an Adeno-Associated Virus-Vectored SARS-CoV-2 Vaccine and Its Immunogenicity in Mice.
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- Frontiers in Cellular & Infection Microbiology, 2022, v. 12, p. 1, doi. 10.3389/fcimb.2022.802147
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Prevalence of abnormal glucose metabolism in pediatric acute, acute recurrent and chronic pancreatitis.
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- PLoS ONE, 2018, v. 13, n. 10, p. 1, doi. 10.1371/journal.pone.0204979
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Comparison of medical management and genetic counseling options pre‐ and post‐whole exome sequencing for patients with positive and negative results.
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- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 182, doi. 10.1002/jgc4.1054
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- Article
Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual Understanding.
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- Journal of Genetic Counseling, 2017, v. 26, n. 4, p. 792, doi. 10.1007/s10897-016-0052-9
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- Article
mRNA-Display-Based Selections for Proteins with Desired Functions: A Protease-Substrate Case Study.
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- Biotechnology Progress, 2008, v. 24, n. 3, p. 561
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- Article
Enhanced sensitivity of neutralizing antibody detection for different AAV serotypes using HeLa cells with overexpressed AAVR.
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- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1188290
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- Article
An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticist.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 4, p. 996, doi. 10.1002/ajmg.c.31859
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- Article
Comprehensive Mutation Analysis for Congenital Muscular Dystrophy: A Clinical PCR-Based Enrichment and Next-Generation Sequencing Panel.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053083
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- Article
Heptameric Targeting Ligands against EGFR and HER2 with High Stability and Avidity.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043077
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- Article
The 253-kb inversion and deep intronic mutations in UNC13D are present in North American patients with familial hemophagocytic lymphohistiocytosis 3.
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- Pediatric Blood & Cancer, 2014, v. 61, n. 6, p. 1034, doi. 10.1002/pbc.24955
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- Article
A superior heterologous prime‐boost vaccination strategy against COVID‐19: A bivalent vaccine based on yeast‐derived RBD proteins followed by a heterologous vaccine.
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- Journal of Medical Virology, 2024, v. 96, n. 3, p. 1, doi. 10.1002/jmv.29454
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- Article
Characterization and expression of the Neurospora crassa nmt-1 gene.
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- Current Genetics, 2003, v. 44, n. 4, p. 216, doi. 10.1007/s00294-003-0441-0
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- Article
Identification of glucocorticoid receptor in Drosophila melanogaster.
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- BMC Microbiology, 2020, v. 20, n. 1, p. 1, doi. 10.1186/s12866-020-01848-x
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- Article
Pathogenesis of ELANE-mutant severe neutropenia revealed by induced pluripotent stem cells.
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- Journal of Clinical Investigation, 2015, v. 125, n. 8, p. 3103, doi. 10.1172/JCI80924
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- Article
Centenarians Alleviate Inflammaging by Changing the Ratio and Secretory Phenotypes of T Helper 17 and Regulatory T Cells.
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- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.877709
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- Article
PAX1 is essential for development and function of the human thymus.
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- Science Immunology, 2020, v. 5, n. 44, p. 1, doi. 10.1126/sciimmunol.aax1036
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- Article
Bilateral cataracts in a 6-yr-old with new onset diabetes: a novel presentation of a known INS gene mutation.
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- Pediatric Diabetes, 2016, v. 17, n. 7, p. 535, doi. 10.1111/pedi.12335
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- Article
Clinical Applications and Implications of Common and Founder Mutations in Indian Subpopulations.
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- Human Mutation, 2015, v. 36, n. 1, p. 1, doi. 10.1002/humu.22704
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Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy.
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- Human Molecular Genetics, 2017, v. 26, n. 24, p. 4937, doi. 10.1093/hmg/ddx377
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- Article
Optimization of miR-22 expression cassette for rAAV delivery on diabetes.
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- Molecular Biomedicine, 2022, p. 1, doi. 10.1186/s43556-021-00063-y
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Transfer of microRNAs by extracellular membrane microvesicles: a nascent crosstalk model in tumor pathogenesis, especially tumor cell-microenvironment interactions.
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- Journal of Hematology & Oncology, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13045-015-0111-y
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- Article
Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism.
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- PLoS ONE, 2016, v. 11, n. 8, p. 1, doi. 10.1371/journal.pone.0156738
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- Article
Modulation of nucleobindin-1 and nucleobindin-2 by caspases
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- FEBS Letters, 2008, v. 582, n. 2, p. 286, doi. 10.1016/j.febslet.2007.12.019
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- Article