Found: 11
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MicroRNAs as the actors in the atherosclerosis scenario.
- Published in:
- Journal of Physiology & Biochemistry, 2020, v. 76, n. 1, p. 1, doi. 10.1007/s13105-019-00710-7
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- Publication type:
- Article
The Epigenetic Overlap between Obesity and Mood Disorders: A Systematic Review.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 18, p. 6758, doi. 10.3390/ijms21186758
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- Publication type:
- Article
Genetic variation in salt taste receptors impact salt intake and blood pressure.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-022-23827-0
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- Publication type:
- Article
Isfahan Twins Registry (ITR): An Invaluable Platform for Epidemiological and Epigenetic Studies: Design and Methodology of ITR - Corrigendum.
- Published in:
- 2020
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- Publication type:
- journal article
Isfahan Twins Registry (ITR): An Invaluable Platform for Epidemiological and Epigenetic Studies: Design and Methodology of ITR.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genetic linkage analysis of DFNB22 in families with autosomal recessive non-syndromic hearing loss in Khuzestan province.
- Published in:
- Journal of Shahrekord University of Medical Sciences, 2019, v. 21, n. 5, p. 200, doi. 10.34172/jsums.2019.35
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- Publication type:
- Article
Precision medicine and metabolic syndrome.
- Published in:
- ARYA Atherosclerosis, 2022, v. 18, p. 1, doi. 10.22122/arya.v18i0.2475
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- Publication type:
- Article
Polymorphisms of LPA gene, rs1801693 and rs7765781, are not associated with premature myocardial infarction in the Iranian population.
- Published in:
- ARYA Atherosclerosis, 2021, v. 17, n. 1, p. 1, doi. 10.22122/arya.v17i0.2369
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- Publication type:
- Article
Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00578-3
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- Publication type:
- Article
FREQUENCY OF GJB2 MUTATIONS IN FAMILIES WITH AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING LOSS IN KHUZESTAN PROVINCE.
- Published in:
- Genetika (0534-0012), 2018, v. 50, n. 3, p. 837, doi. 10.2298/GENSR1803837T
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- Publication type:
- Article
Apolipoprotein B gene mutation related to familial hypercholesterolemia in an Iranian population: With or without hypothyroidism.
- Published in:
- Journal of Research in Medical Sciences, 2021, p. 1, doi. 10.4103/jrms.JRMS_970_19
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- Publication type:
- Article