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Latest

hnRNPH1 recruites PTBP2 and SRSF3 to modulate alternative splicing in germ cells

DNA damage-induced block of sporulation in Streptomyces venezuelae involves downregulation of ssgB

Staphylococcus aureus a-toxin effect on acinetobacter baumannii behavior

New COL6A6 Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family

Pseudomonas aerugiosa transcriptome adaptations from colonization to biofilm infection of skin wounds

Regulator of Cell Cycle Protein (RGCC/RGC-32) Protects Against Pulmonary Fibrosis

Helicase-like transcription factor-deletion from the tumor microenvironment in a cell line-derived xenograft model of colorectal cancer reprogrammed the human transcriptome-S-nitroso-proteome to promote inflammation and redirect metastasis.

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)

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