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Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss.

Identification of a genetic variant underlying familial cases of recurrent benign paroxysmal positional vertigo

Parallel Evolution of Enhanced Biofilm Formation and Phage-Resistance in Pseudomonas aeruginosa during Adaptation Process in Spatially Heterogeneous Environments

Missense variant of endoplasmic reticulum region of WFS1 gene causes autosomal dominant hearing loss without syndromic phenotype

The transcriptome characteristics of vestibular organs from delayed endolymphatic hydrops patients (Menieres disease)

A novel stop-gain mutation in MSH2 gene among a Persian family fulfilling classic Amsterdam criteria for Lynch Syndrome

Pericytes contribute to the islet basement membranes to promote beta-cell gene expression

Inactivation of GaIU leads to a cell wall-associated polysaccharide defect that reduces the susceptibility of Enterococcus faecalis to bacteriolytic agents

Novel mutations in AIFM1 gene associated with X-linked deafness in a Moroccan family

Radixin modulates the function of outer hair cell stereocilia

Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant Patients

Deletion of Exon 1 in AMER1 in Osteopathia Striata with Cranial Sclerosis

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