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Dietary total antioxidant capacity interacts with a variant of chromosome 5q13-14 locus to influence cardio-metabolic risk factors among obese adults.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00328-3
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- Publication type:
- Article
Secure framework for IoT technology based on RSA and DNA cryptography.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00326-5
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- Publication type:
- Article
Characterization of the expressed RNA variants from young patients with critical and non-critical SARS-CoV-2 infection.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00327-4
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- Publication type:
- Article
Evaluation of the soldier's physical fitness test results (strength endurance) ın relation to genotype: longitudinal study.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00325-6
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- Publication type:
- Article
Analysis of real-time PCR Melanocortin 3 (MC3R) gene expression to identify new biomarkers inflammation in tuberculosis.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00323-8
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- Publication type:
- Article
Evaluation of the soldier's physical fitness test results (strength endurance) ın relation to genotype: longitudinal study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00325-6
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- Publication type:
- Article
Polymorphism of the IL-10 gene in Azeri population of Iran.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00324-7
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- Publication type:
- Article
Correction to: The genetic influence of PD-1/PD-L1 axis single nucleotide polymorphisms on the incidence of type 1 diabetes mellitus in pediatric Egyptian patients.
- Published in:
- 2022
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- Publication type:
- Correction Notice
The genetic influence of PD-1/PD-L1 axis single nucleotide polymorphisms on the incidence of type 1 diabetes mellitus in pediatric Egyptian patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00302-z
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- Publication type:
- Article
Wilms tumor 1 gene expression in acute myeloid leukemia: prognostic significance and usefulness in minimal residual disease monitoring—a case–control study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00291-z
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- Publication type:
- Article
Correction to: The genetic influence of PD-1/PD-L1 axis single nucleotide polymorphisms on the incidence of type 1 diabetes mellitus in pediatric Egyptian patients.
- Published in:
- 2022
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- Publication type:
- Correction Notice
A single-nucleotide polymorphism of IL12A gene (rs582537 A/C/G) and susceptibility to chronic hepatitis B virus infection among Iraqi patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00322-9
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- Publication type:
- Article
The association between variant rs9939609 in the FTO gene with free leptin index and the risk of obesity in the Indonesian children population.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00321-w
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- Publication type:
- Article
Generation of muscle progenitors from human-induced pluripotent stem cells.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00319-4
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- Publication type:
- Article
Clinical implications of PON1 (rs662) and TNF-α (rs1799964) genes polymorphism in patients with coronary artery disease.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00318-5
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- Publication type:
- Article
MicroRNAs influence and longevity.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00316-7
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- Publication type:
- Article
Intermittent white noise exposure is associated with rat cochleae damage and changes in the gene expression.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00317-6
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- Publication type:
- Article
Role of microRNAs in regulation of WNT signaling pathway in urothelial and prostate cancers.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00315-8
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- Publication type:
- Article
The efficacy of clopidogrel in preventing recurrent cardiovascular events among Arab population carrying different CYP2C19 mutations: systematic review and meta-analysis.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00313-w
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- Publication type:
- Article
The role of angiotensin-converting enzyme 2 (ACE2) genetic variations in COVID-19 infection: a literature review.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00309-6
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- Publication type:
- Article
Identifying the potential role of curcumin analogues as anti-breast cancer agents; an in silico approach.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00312-x
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- Publication type:
- Article
Receptor of advanced glycation end product (RAGE) polymorphism and oxidative status in Hashimoto's thyroiditis in Egyptian female patients: case control study.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00311-y
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- Publication type:
- Article
The role of radiogenomics in the diagnosis of breast cancer: a systematic review.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00310-z
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- Publication type:
- Article
Understanding the pivotal roles of ACE2 in SARS-CoV-2 infection: from structure/function to therapeutic implication.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00314-9
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- Publication type:
- Article
Genetic polymorphisms and gene expression of one-carbon metabolizing enzymes and their relation to breast cancer.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00296-8
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- Publication type:
- Article
Role of engrailed homeobox 2 (EN2) gene in the development of the cerebellum and effects of its altered and ectopic expressions.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00307-8
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- Publication type:
- Article
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00308-7
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- Publication type:
- Article
Vascular endothelial growth factor A with two genetic variants for prediction of mixed microvascular diabetic complications.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00303-y
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- Publication type:
- Article
Analysis of missense SNPs in the SLC47A1 and SLC47A2 genes affecting the pharmacokinetics of metformin: Computational approach.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00306-9
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- Publication type:
- Article
The genetic influence of PD-1/PD-L1 axis single nucleotide polymorphisms on the incidence of type 1 diabetes mellitus in pediatric Egyptian patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00302-z
- By:
- Publication type:
- Article
A novel variant luteinizing hormone receptor in the first transmembrane helix of two homozygous Iranian patients: case report.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00305-w
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- Publication type:
- Article
P2X7 1513A/C loss-of-function polymorphism and active tuberculosis disease in a cohort of Egyptian population: a pilot study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00304-x
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- Publication type:
- Article
Toll-like receptor 10 gene polymorphism and risk of multiple sclerosis among Iraqi patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00301-0
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- Publication type:
- Article
Beta Thalassemia and Klinefelter syndrome: a rare occurrence.
- Published in:
- 2022
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- Publication type:
- Case Study
Comparative frequency distribution of glutathione S-transferase mu (GSTM1) and theta (GSTT1) allelic forms in Himachal Pradesh population.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00298-6
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- Publication type:
- Article
Genetic Counselling: the biomedical bridge between molecular diagnosis and precision treatment.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00297-7
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- Publication type:
- Article
Investigating expressed RNA variants that are related to disease severity in SARS-CoV-2-infected patients with mild-to-severe disease.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00299-5
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- Publication type:
- Article
Detection of intestinal colonization by carbapenem-resistant Enterobacteriaceae (CRE) among patients admitted to a tertiary care hospital in Egypt.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00295-9
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- Publication type:
- Article
Co-segregation of variant NSUN2 Lue198Arg among Iranian family with intellectual disability: a case report.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00293-x
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- Publication type:
- Article
An actualized screening of schizophrenia-associated genes.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00269-x
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- Publication type:
- Article
Shedding light on the phenotypic–genotypic correlation of rare treatable and potentially treatable pediatric movement disorders.
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- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00286-w
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- Publication type:
- Article
Association of FTO gene variant rs9939609 with hyperandrogenemia and fasting glucose levels in South Indian women with polycystic ovarian syndrome.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00236-6
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- Publication type:
- Article
Prevalence and population genetic data of colour vision deficiency among students from selected tertiary institutions in Lagos State, Nigeria.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00287-9
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- Publication type:
- Article
Investigating pathogenic SNPs in androgen receptor with direct influence on polycystic ovary syndrome (PCOS) in women.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00292-y
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- Publication type:
- Article
Fibroblast growth factor-23 rs7955866 polymorphism and risk of chronic kidney disease.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00289-7
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- Publication type:
- Article
Three uncommon mutations of the SLC12A3 gene in gitelman syndrome: case reports and review of the literature.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00288-8
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- Publication type:
- Article
Becker congenital myotonia in black African with molecular findings.
- Published in:
- 2022
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- Publication type:
- Case Study
Prevalence and population genetic data of colour vision deficiency among students from selected tertiary institutions in Lagos State, Nigeria.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00287-9
- By:
- Publication type:
- Article
The potential application of probiotics for the prevention and treatment of COVID-19.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, p. 1, doi. 10.1186/s43042-022-00252-6
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- Publication type:
- Article
Association of Keap1 (rs11085735) polymorphism and lncRNA MEG3 hypermethylation status with the risk of preeclampsia.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00251-7
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- Publication type:
- Article