Found: 20
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Effect of Hydrocortisone on Angiotensinogen (AGT) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 4, p. 782, doi. 10.3390/cells10040782
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- Publication type:
- Article
Integration of metagenomics‐metabolomics reveals specific signatures and functions of airway microbiota in mite‐sensitized childhood asthma.
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- Allergy, 2020, v. 75, n. 11, p. 2846, doi. 10.1111/all.14438
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- Publication type:
- Article
Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms.
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- Genome Biology & Evolution, 2014, v. 6, n. 9, p. 2258, doi. 10.1093/gbe/evu181
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- Article
Genome-Wide Patterns of Genetic Variation in Two Domestic Chickens.
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- Genome Biology & Evolution, 2013, v. 5, n. 7, p. 1376, doi. 10.1093/gbe/evt097
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- Publication type:
- Article
Whole-Exome Sequencing Identified Novel CLMP Mutations in a Family With Congenital Short Bowel Syndrome Presenting Differently in Two Probands.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.574943
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- Publication type:
- Article
Characteristics and genetic analysis of patients suspected with early-onset systemic lupus erythematosus.
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- Pediatric Rheumatology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12969-022-00722-6
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- Publication type:
- Article
Whole-Genome Sequencing of a Family with Hereditary Pulmonary Alveolar Proteinosis Identifies a Rare Structural Variant Involving CSF2RA/CRLF2/IL3RA Gene Disruption.
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- Scientific Reports, 2017, p. 43469, doi. 10.1038/srep43469
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- Publication type:
- Article
Leptin Is Associated with Poor Clinical Outcomes and Promotes Clear Cell Renal Cell Carcinoma Progression.
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- Biomolecules (2218-273X), 2021, v. 11, n. 3, p. 431, doi. 10.3390/biom11030431
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- Publication type:
- Article
Long-Term Outcome of Neonatal Seizure with PACS2 Mutation: Case Series and Literature Review.
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- Children, 2023, v. 10, n. 4, p. 621, doi. 10.3390/children10040621
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- Publication type:
- Article
HLA Association with Drug-Induced Adverse Reactions.
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- 2017
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- Publication type:
- journal article
Lipopolysaccharide stimulation test on cultured PBMCs assists the discrimination of cryopyrin-associated periodic syndrome from systemic juvenile idiopathic arthritis.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91354-5
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- Publication type:
- Article
A combined analysis of maximum standardized uptake value on FDG-PET, genetic markers, and clinicopathological risk factors in the prognostic stratification of patients with resected oral cavity squamous cell carcinoma.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2020, v. 47, n. 1, p. 84, doi. 10.1007/s00259-019-04453-x
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- Publication type:
- Article
Author Correction: The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth.
- Published in:
- 2023
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- Publication type:
- Correction Notice
The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31486-y
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- Publication type:
- Article
Prognostic Genetic Biomarkers Based on Oncogenic Signaling Pathways for Outcome Prediction in Patients with Oral Cavity Squamous Cell Carcinoma.
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- Cancers, 2021, v. 13, n. 11, p. 2709, doi. 10.3390/cancers13112709
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- Publication type:
- Article
Ghrelin Upregulates Oncogenic Aurora A to Promote Renal Cell Carcinoma Invasion.
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- Cancers, 2019, v. 11, n. 3, p. 303, doi. 10.3390/cancers11030303
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- Publication type:
- Article
HLA Alleles and CYP2C9*3 as Predictors of Phenytoin Hypersensitivity in East Asians.
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- Clinical Pharmacology & Therapeutics, 2019, v. 105, n. 2, p. 476, doi. 10.1002/cpt.1190
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- Publication type:
- Article
A Novel CD3G Mutation in a Taiwanese Patient With Normal T Regulatory Function Presenting With the CVID Phenotype Free of Autoimmunity—Analysis of all Genotypes and Phenotypes.
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- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02833
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- Publication type:
- Article
Novel discovery of association between the mutation in exon 14 of the ATP2A2 gene and Darier's disease.
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- Dermatologica Sinica, 2018, v. 36, n. 4, p. 236, doi. 10.1016/j.dsi.2018.04.001
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- Publication type:
- Article
Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome.
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- Pediatric Rheumatology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12969-022-00743-1
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- Publication type:
- Article