انگلیسی مرکز تحقیقات اختلالات متابولیک | Home

انگلیسی مرکز تحقیقات اختلالات متابولیک | Home

| Sep 25 2025

Metabolic Disorders Research Center

Metabolic Disorders Research Center

Metabolic Disorders Research Center

Address in Articles

Molecular Genetics Coursework

Research plans

Jan 8 2025

The Next-generation sequencing of obesity genes using the bioinformatics approach for genotype and haplotype study

Jan 8 2025

Genetic and clinical evaluation of patients suspected to Primordial dwarfism

Jan 8 2025

The study of new genotypes and haplotypes related to monogenic diabetes using whole exome sequencing (WES) and bioinformatics approach

Jan 8 2025

inborn errors of metabolism information registry

Jan 8 2025

Metformin and long non-coding RNAs in breast cancer

Jan 8 2025

Investigating the Mutual Influence of Colorectal Cancer and Metabolic Syndrome at the Molecular Level Through the Integration of Whole Exome Sequencing and Systems Biology Approach

Jan 8 2025

Investigation of PvuII polymorphism of estrogen receptor alpha (ERα) gene in patients with osteoporosis in Bushehr elderly health study

Jan 8 2025

Analysis of the association between SIRT6 gene polymorphisms with Lifespan in the Bushehr elderly health study

Scientific articles

Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes

Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes

Hyperglycemic Memory: Observational Evidence to Experimental Inference

Hyperglycemic Memory: Observational Evidence to Experimental Inference

ACE I/D gene polymorphisms and polycystic ovary syndrome manifestations

ACE I/D gene polymorphisms and polycystic ovary syndrome manifestations

Four Patients with Neonatal Diabetes Mellitus and their Outcomes: A Case Series

Four Patients with Neonatal Diabetes Mellitus and their Outcomes: A Case Series

Novel mutation in Patients with Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)

Novel mutation in Patients with Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)

Recognition of GCK Homozygote missense (His424Tyr) variant in a female patient with neonatal hyperglycemia

Recognition of GCK Homozygote missense (His424Tyr) variant in a female patient with neonatal hyperglycemia

Ethical Approaches in Secondary Findings Report from Exome Sequencing Analysis

Ethical Approaches in Secondary Findings Report from Exome Sequencing Analysis

Neural EGFL like 1 as a novel gene for Trabecular Bone Score in older adults: The Bushehr Elderly Health (BEH) program

Neural EGFL like 1 as a novel gene for Trabecular Bone Score in older adults: The Bushehr Elderly Health (BEH) program

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