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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
Genetics cause of heterogeneous inherited myopathies in a cohort of Greek patients
A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy.