Found: 22
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Intestinal microbiome analysis demonstrates azithromycin post-treatment effects improve when combined with lactulose.
- Published in:
- World Journal of Pediatrics, 2020, v. 16, n. 2, p. 168, doi. 10.1007/s12519-019-00315-6
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- Article
Phenotypic variability of hyperandrogenemia in females heterozygous for CYP21A2 mutations.
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- Indian Journal of Endocrinology & Metabolism, 2014, v. 18, p. 572, doi. 10.4103/2230-8210.145077
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- Article
Variations in the 3′UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia.
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- International Journal of Endocrinology, 2017, p. 1, doi. 10.1155/2017/8984365
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- Article
Bifidobacterium Is Enriched in Gut Microbiome of Kashmiri Women with Polycystic Ovary Syndrome.
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- Genes, 2022, v. 13, n. 2, p. 379, doi. 10.3390/genes13020379
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- Article
Tackling the pathogenesis of RNA nuclear retention in myotonic dystrophy.
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- Biology of the Cell (Wiley-Blackwell), 2010, v. 102, n. 9, p. 515
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- Article
Molecular Defects of the CYP21A2 Gene in Greek-Cypriot Patients with Congenital Adrenal Hyperplasia.
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- Hormone Research in Paediatrics, 2011, v. 75, n. 3, p. 180, doi. 10.1159/000320040
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- Article
Familial Mediterranean Fever Associated with MEFV Mutations in a Large Cohort of Cypriot Patients.
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- Annals of Human Genetics, 2015, v. 79, n. 1, p. 1, doi. 10.1111/ahg.12087
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- Article
A family with Camurati-Engelman disease: the role of the missense p.R218C mutation in TGFbeta1 in bones and endocrine glands.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 11/12, p. 1189, doi. 10.1515/jpem-2013-0150
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- Article
A family with Camurati-Engelman disease. The role of the missense p.R218C mutation in TGFB1 in bones and endocrine glands.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 9/10, p. 987, doi. 10.1515/jpem-2013-0019
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- Article
NMR structure of the peptidyl transferase RNA inhibitor antibiotic amicetin.
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- Magnetic Resonance in Chemistry, 2007, v. 45, n. 2, p. 133, doi. 10.1002/mrc.1932
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- Article
NMR and Molecular Modelling Studies of the Binding of Amicetin Antibiotic to Conserved Secondary Structural Motifs of 23S Ribosomal RNAs.
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- Journal of Antibiotics, 2006, v. 59, n. 3, p. 177, doi. 10.1038/ja.2006.25
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- Article
CDKN2A and MC1R variants found in Cypriot patients diagnosed with cutaneous melanoma.
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- Journal of Genetics, 2017, v. 96, n. 1, p. 155, doi. 10.1007/s12041-017-0742-6
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- Article
Evidence of digenic inheritance in autoinflammation-associated genes.
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- Journal of Genetics, 2016, v. 95, n. 4, p. 761, doi. 10.1007/s12041-016-0691-5
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- Article
Fecal Microbiota and Associated Volatile Organic Compounds Distinguishing No-Adenoma from High-Risk Colon Adenoma Adults.
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- Metabolites (2218-1989), 2023, v. 13, n. 7, p. 819, doi. 10.3390/metabo13070819
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- Article
ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia.
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- Clinical Chemistry & Laboratory Medicine, 2010, v. 48, n. 12, p. 1713, doi. 10.1515/CCLM.2010.331
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- Article
Microform holoprosencephaly with bilateral congenital elbow dislocation; increasing the phenotypic spectrum of Steinfeld syndrome.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 3, p. 754, doi. 10.1002/ajmg.a.37511
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- Article
A systematic review of miRNAs as biomarkers for chemotherapy-induced cardiotoxicity in breast cancer patients reveals potentially clinically informative panels as well as key challenges in miRNA research.
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- Cardio-Oncology, 2022, v. 8, n. 1, p. 1, doi. 10.1186/s40959-022-00142-1
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- Article
In silico analysis of a novel MKRN3 missense mutation in familial central precocious puberty.
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- Clinical Endocrinology, 2016, v. 84, n. 1, p. 80, doi. 10.1111/cen.12854
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- Article
Unraveling the Dynamics of Omicron (BA.1, BA.2, and BA.5) Waves and Emergence of the Deltacton Variant: Genomic Epidemiology of the SARS-CoV-2 Epidemic in Cyprus (Oct 2021–Oct 2022).
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- Viruses (1999-4915), 2023, v. 15, n. 9, p. 1933, doi. 10.3390/v15091933
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- Article
Genomic Epidemiology of the SARS-CoV-2 Epidemic in Cyprus from November 2020 to October 2021: The Passage of Waves of Alpha and Delta Variants of Concern.
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- Viruses (1999-4915), 2023, v. 15, n. 1, p. 108, doi. 10.3390/v15010108
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- Article
Genetic screening of EXT1 and EXT2 in Cypriot families with hereditary multiple osteochondromas.
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- Journal of Genetics, 2015, v. 94, n. 4, p. 749, doi. 10.1007/s12041-015-0564-3
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- Article
Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects.
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- Journal of Genetics, 2014, v. 93, n. 2, p. 471, doi. 10.1007/s12041-014-0365-0
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- Article