Tag: Gene

Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification – Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous Mutations

Lingjuan Liu, et al.

Introduction Dyschromatosis symmetrica hereditaria (DSH) shows the pattern of autosomal dominant inheritance. It is characterized by the freckle-like pigmentation or hypopigmentation spots on the backs of hands and feet, presenting…

Intermittent white noise exposure is associated with rat cochleae damage and changes in the gene expression – Egyptian Journal of Medical Human Genetics

Study design and setting The present study is an experimental and case–control type to investigate the association between noise exposure and changes in gene expression in male Wistar rats which…

Population genetic structure and evolutionary genetics of Anopheles sinensis based on knockdown resistance (kdr) mutations and mtDNA-COII gene in China–Laos, Thailand–Laos, and Cambodia–Laos borders – Parasites & Vectors

Sequence polymorphisms of the An. sinensis vgsc gene The 267-bp DNA fragments individually amplified from a total of 89 An. sinensis mosquitoes were used for sequence polymorphism analysis. This sequence…