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FOXP3 exon 2 controls Treg stability and autoimmunity

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