Understanding Lynch Syndrome: Genetic and Molecular Insights
Introduction Lynch syndrome, or Hereditary Non-Polyposis Colorectal Cancer (HNPCC), is a frequent hereditary cancer predisposition with a strong relationship with …
The Role of Mitochondrial DNA in Neurodegenerative Diseases
Introduction Heterochromatin and its known role in energy production and management of the cells make it vital in the body, …
Advances in Understanding Chromosomal Abnormalities in Livestock
Introduction Chromosome aberrations in livestock have over the decades generated substantial attention and interest to be detected as owing enormous …
Genetic and Environmental Factors in Congenital Heart Disease (CHD)
Introduction Congenital heart disease (CHD) remains one of the major dilemmas in pediatric cardiology and genetics. CHD affects about 1% …
Exploring the Neurobiological Mechanisms of Fragile X Syndrome
Introduction FXS is the only known cause of intellectual disability, being primarily inherited as well as being one of the …
Advancements in Iron Chelation Therapy for Thalassemia Patients
Introduction Thalassemia is one of the blood disorders passed on to the offspring in which the human body fails to …
Innovations in DNA Cloning and Sequencing
Introduction DNA cloning and sequencing have been an overwhelming game-changing field in the past 50 years, establishing our knowledge of …
Genetic and Molecular Insights into Sickle Cell Disease
Sickle cell disease is a congenital disease of the blood that has presented a lot of complications to researchers due …
Advancements in CFTR Modulators for Cystic Fibrosis Treatment
Cystic fibrosis is one of the hereditary diseases that run through genetics and, until now, was one of the biggest …
Advances in Genetic Research: Implications for Autism Diagnosis and Treatment
Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition characterized by challenges with social interaction, communication difficulties, and repetitive behaviors. …