Found: 75
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Evaluation of serum MicroRNA 21, MicroRNA 192 and serum TGFβ1 in type 2 diabetes mellitus patients and their relation to diabetic nephropathy.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00544-z
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- Publication type:
- Article
Association of ARMS2, HTRA1 and CFH genes polymorphisms in patients with age-related macular degeneration in the Malaysian population.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00549-8
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- Publication type:
- Article
Genetic association study for three single nucleotide polymorphisms related to type 2 diabetes in Egyptian population.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00546-x
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- Publication type:
- Article
Serum mir-31-5p is a reliable biomarker in patients with oral squamous cell carcinoma and oral lichen planus.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00531-4
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- Publication type:
- Article
A cost-efficient algorithm for diagnosing children with dysmorphic features.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00545-y
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- Publication type:
- Article
Correction: Emanuel syndrome due to unusual pattern.
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- 2024
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- Publication type:
- Correction Notice
miR-146a and miR-155 as promising biomarkers for prognosis and diagnosis of multiple sclerosis: systematic review.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00543-0
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- Publication type:
- Article
Preliminary study: nutrigenomics analysis results of COVID-19 survivors.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00547-w
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- Publication type:
- Article
Novel TRPV6 variant linked with transient neonatal hyperparathyroidism.
- Published in:
- 2024
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- Publication type:
- Case Study
Deciphering the landscape of lncRNA-driven ceRNA network in schizophrenia etiology.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00542-1
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- Publication type:
- Article
The potentials of nonlinear polarization with hyperspectral imaging of RNA for hepatocellular carcinoma early diagnosis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00541-2
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- Publication type:
- Article
VHL mutation as a cause of three generations familial pheochromocytoma.
- Published in:
- 2024
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- Publication type:
- Case Study
Genetic analysis of BRPF1 exon deletion variant causing intellectual developmental disorder with dysmorphic facies and ptosis in a Chinese family.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00539-w
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- Publication type:
- Article
Causal associations between gut microbiota and chronic prostatitis/chronic pelvic pain syndrome: a two-sample Mendelian randomization study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00540-3
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- Publication type:
- Article
Association of insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme gene (ACE) with Parkinson's disease and factors risk in eastern Algeria: case–control study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00536-z
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- Publication type:
- Article
Association of VEGF-2549I/D promoter polymorphism with gastrointestinal tract cancer risk: a meta-analysis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00535-0
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- Publication type:
- Article
Evaluation of the biomarker potential of miR-650 and miR-663b in tumor tissues and plasma specimens of colon cancer patients living in northwest of Iran.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00534-1
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- Publication type:
- Article
Evaluation of adropin, fibroblast growth factor-1 (FGF-1), and Toll-like receptor-1 (TLR1) biomarkers in patients with inflammatory bowel disease: gene expression of TNF-α as a marker of disease severity.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00533-2
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- Publication type:
- Article
Diagnostic biomarkers for ST-segment elevation myocardial infarction using RNA methylation regulators.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00532-3
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- Publication type:
- Article
Challenges in blood transfusion caused by anti-Hr<sub>0</sub>: A rare case of D-- Phenotype in Asia Abstract.
- Published in:
- 2024
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- Publication type:
- Case Study
Insights into the structural and functional analysis of impact of the missense mutations on α-synuclein: an in silico study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00530-5
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- Publication type:
- Article
Genetic-driven biomarkers for liver fibrosis through bioinformatic approach.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00528-z
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- Publication type:
- Article
Identification of circRNA–miRNA–mRNA regulatory network associated to the autism spectrum disorder in children through integrated bioinformatics analysis.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00527-0
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- Publication type:
- Article
A bioinformatics approach to reveal common genes and molecular pathways shared by cutaneous melanoma and uveal melanoma.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00526-1
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- Publication type:
- Article
Association of leptin–melanocortin gene polymorphisms with the risk of obesity in northwest Indian population.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00529-y
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- Publication type:
- Article
Retinoic Acid-Induced 1 gene variants associated with Smith–Magenis syndrome circadian phenotypes enriched in autism spectrum disorder: whole-genome sequencing study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00508-3
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- Publication type:
- Article
Association between genetic polymorphisms and other attributing factors with lipid profiles among statin users: a cross-sectional retrospective study.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00523-4
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- Publication type:
- Article
Exploring the potential of phytoconstituents from Phaseolus vulgaris L against C-X-C motif chemokine receptor 4 (CXCR4): a bioinformatic and molecular dynamic simulations approach.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00510-9
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- Publication type:
- Article
Artificial intelligence-driven enhanced skin cancer diagnosis: leveraging convolutional neural networks with discrete wavelet transformation.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00522-5
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- Publication type:
- Article
Turkish population-based screening for first identified changes of BRCA1 and BRCA2 genes in breast and/or ovarian cancer patients.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00525-2
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- Publication type:
- Article
The potential anticancer effect of bee venom in combination with sorafenib against HepG2 cell lines via induction of apoptosis and autophagy candidate genes.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00524-3
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- Publication type:
- Article
The causal relationship between anxiety and tinnitus severity: a Mendelian randomization study.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00520-7
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- Publication type:
- Article
Four microRNA gene polymorphisms are associated with Iraqi patients with colorectal cancer.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00521-6
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- Publication type:
- Article
Association of single nucleotide polymorphism at BMP2 gene with iron deficiency status among anaemic patients in Hospital Universiti Sains Malaysia.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00511-8
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- Publication type:
- Article
Prognosis and immunological characteristics of HDAC family in pan-cancer through integrative multi-omic analysis.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00518-1
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- Publication type:
- Article
ACE I/D polymorphism in cognitive impairment and depression among North Indian adults: a pilot study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00515-4
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- Publication type:
- Article
Clinical impact of IDH1 mutations and MGMT methylation in adult glioblastoma.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00516-3
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- Publication type:
- Article
Genomic susceptibility to gastric cancer in Northwest Iran: population-based and case–control studies.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00474-w
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- Publication type:
- Article
Mowat-Wilson syndrome: unraveling the complexities of diagnosis, treatment, and symptom management.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00517-2
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- Publication type:
- Article
Potential biomarker signatures in male infertility: integrative genomic analysis.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00512-7
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- Publication type:
- Article
The homozygous pathogenic variant of the POMGNT1 gene identified using whole-exome sequencing in Iranian family with congenital hydrocephalus.
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- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00513-6
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- Publication type:
- Article
Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00514-5
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- Publication type:
- Article
Low heterozygosity for rs3811050, a 5 prime untranslated region variant of the gene encoding interleukin-38 (IL1F10), is associated with a reduced risk of systemic lupus erythematosus.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00503-8
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- Publication type:
- Article
Germline variants in the Von Hippel-Lindau tumor suppressor gene in Cuban patients.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00506-5
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- Publication type:
- Article
Exploring the interplay of MTHFR and FGG polymorphisms with serum levels of adiponectin and leptin in pediatric lupus nephritis: a pilot study.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00507-4
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- Publication type:
- Article
Genetic factors and the role of pancreatic amylase in the pathogenesis of type 2 diabetes.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00505-6
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- Publication type:
- Article
Analysis of the CYP21A2 gene pathogenic variants in CAH patients from Surgut using next-generation sequencing (NGS).
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00502-9
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- Publication type:
- Article
Irreversible methadone-induced GSTP1 downregulation in SH-SY5Y cells.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00504-7
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- Publication type:
- Article
Technologies of gene editing and related clinical trials for the treatment of genetic and acquired diseases: a systematic review.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00501-w
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- Publication type:
- Article
Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00490-w
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- Publication type:
- Article