Found: 16
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Retrotransposons and Diabetes Mellitus.
- Published in:
- Epigenomes, 2024, v. 8, n. 3, p. 35, doi. 10.3390/epigenomes8030035
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- Publication type:
- Article
Developmental Dyslexia: Insights from EEG-Based Findings and Molecular Signatures—A Pilot Study.
- Published in:
- Brain Sciences (2076-3425), 2024, v. 14, n. 2, p. 139, doi. 10.3390/brainsci14020139
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- Publication type:
- Article
Gender association of the angiotensin-converting enzyme gene with ischaemic stroke.
- Published in:
- 2011
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- Publication type:
- Journal Article
Gender association of the angiotensin-converting enzyme gene with ischaemic stroke.
- Published in:
- Journal of the Renin-Angiotensin-Aldosterone System, 2011, v. 12, n. 4, p. 510, doi. 10.1177/1470320310391333
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- Publication type:
- Article
Biological and Clinical Significance of Mosaicism in Human Preimplantation Embryos.
- Published in:
- Journal of Developmental Biology, 2021, v. 9, n. 2, p. 18, doi. 10.3390/jdb9020018
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- Publication type:
- Article
Sequence Motif Analysis of PRDM9 and Short Inverted Repeats Suggests Their Contribution to Human Microdeletion and Microduplication Syndromes.
- Published in:
- BioMedInformatics, 2023, v. 3, n. 2, p. 267, doi. 10.3390/biomedinformatics3020018
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- Publication type:
- Article
ATG16L1 T300A polymorphism is associated with Crohn's disease in a Northwest Greek cohort, but ECM1 T130M and G290S polymorphisms are not associated with ulcerative colitis.
- Published in:
- Annals of Gastroenterology, 2020, v. 33, n. 1, p. 38, doi. 10.20524/aog.2019.0434
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- Publication type:
- Article
An open study of valproate in subfertile men with epilepsy.
- Published in:
- Acta Neurologica Scandinavica, 2020, v. 142, n. 4, p. 317, doi. 10.1111/ane.13311
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- Publication type:
- Article
A mutation in NOTCH2 gene first associated with Hajdu–Cheney syndrome in a Greek family: diversity in phenotype and response to treatment.
- Published in:
- Endocrine (1355008X), 2021, v. 71, n. 1, p. 208, doi. 10.1007/s12020-020-02446-7
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- Publication type:
- Article
Correction to: A mutation in NOTCH2 gene first associated with Hajdu–Cheney syndrome in a Greek family: diversity in phenotype and response to treatment.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Unusual N Gene Dropout and Ct Value Shift in Commercial Multiplex PCR Assays Caused by Mutated SARS-CoV-2 Strain.
- Published in:
- Diagnostics (2075-4418), 2022, v. 12, n. 4, p. 973, doi. 10.3390/diagnostics12040973
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- Publication type:
- Article
Development and Validation of a Targeted 'Liquid' NGS Panel for Treatment Customization in Patients with Metastatic Colorectal Cancer.
- Published in:
- Diagnostics (2075-4418), 2021, v. 11, n. 12, p. 2375, doi. 10.3390/diagnostics11122375
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- Publication type:
- Article
Alu Methylation Patterns in Type 1 Diabetes: A Case-Control Study.
- Published in:
- Genes, 2023, v. 14, n. 12, p. 2149, doi. 10.3390/genes14122149
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- Publication type:
- Article
The Ratio of cf-mtDNA vs. cf-nDNA in the Follicular Fluid of Women Undergoing IVF Is Positively Correlated with Age.
- Published in:
- Genes, 2023, v. 14, n. 7, p. 1504, doi. 10.3390/genes14071504
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- Publication type:
- Article
The Role of One-Carbon Metabolism and Methyl Donors in Medically Assisted Reproduction: A Narrative Review of the Literature.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 9, p. 4977, doi. 10.3390/ijms25094977
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- Publication type:
- Article
Cancer Associated PRDM9: Implications for Linking Genomic Instability and Meiotic Recombination.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 22, p. 16522, doi. 10.3390/ijms242216522
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- Publication type:
- Article