A5044291362- Pregnancy and preeclampsia studies
- Neonatal Respiratory Health Research
- COVID-19 and healthcare impacts
- COVID-19 Impact on Reproduction
- RNA and protein synthesis mechanisms
- Blood Coagulation and Thrombosis Mechanisms
- Birth, Development, and Health
- Genetics and Neurodevelopmental Disorders
- Growth Hormone and Insulin-like Growth Factors
- Protease and Inhibitor Mechanisms
- Gestational Diabetes Research and Management
- Cleft Lip and Palate Research
- Congenital Diaphragmatic Hernia Studies
- Metabolism and Genetic Disorders
- DNA Repair Mechanisms
- Cytokine Signaling Pathways and Interactions
- Genomic variations and chromosomal abnormalities
- Folate and B Vitamins Research
- Streptococcal Infections and Treatments
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Kawasaki Disease and Coronary Complications
- Inflammasome and immune disorders
- Mitochondrial Function and Pathology
- Helicobacter pylori-related gastroenterology studies
Shiraz University of Medical Sciences
2016-2025
Iranshahr University
2025
Imam Khomeini Hospital
2021
Tehran University of Medical Sciences
2021
Faghihi Hospital
2019
Background: The tumorigenesis of lung cancer is complicated, and genetic factor may have the role in malignant transformation cells. IL-10 gene polymorphisms been evaluated for their potential roles cancer. However, those studies results are controversial. To clarify effects rs1800871, rs1800872 rs1800896 on risk cancer, a meta-analysis was performed with eligible individual studies. Methods: Eligible publications were gathered by retrieving PubMed, Web Science, Embase, Wan Fang, CNKI up to...
<title>Abstract</title> Background This study aims to perform a comprehensive meta-analysis of existing literature elucidate the associations between genetic variations in XPD gene and risk prostate cancer development. Methods A systematic search multiple databases, including PubMed, Scopus, EMBASE, CNKI, was executed up until January 1, 2025, collect pertinent information. The utilized relevant keywords MeSH terms pertaining factors. Inclusion criteria were established for original...
<title>Abstract</title> Background Idiopathic short stature (ISS) poses substantial challenges in pediatric growth assessment due to its multifactorial origins. This meta-analysis explores the relationship between IGF1R polymorphisms and risk of ISS children. Methods A comprehensive literature review was performed utilizing PubMed, Web Knowledge, CNKI, culminating on January 1, 2025, focusing studies published before this date. The search employed relevant keywords MeSH terms related...
The use of machine learning (ML) in biomarker analysis for predicting Down syndrome exemplifies an innovative strategy that enhances diagnostic accuracy and enables early detection. Recent studies demonstrate the effectiveness ML algorithms identifying genetic variations expression patterns associated with by comparing genomic data from affected individuals their typically developing peers. This review examines how improve prenatal screening syndrome. Advancements show integrating maternal...
The Pediatric Buccal Epigenetic (PedBE) and Neonatal Estimator of Age (NEOage) clocks provide a novel method for assessing the biological age young individuals, enhancing our comprehension their health development. By analyzing DNA methylation patterns, these identify risk factors various conditions guide personalized interventions to promote optimal growth in children infants. With ongoing research validation, PedBE NEOage could revolutionize pediatric neonatal healthcare by facilitating...