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A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family
Coordinated responses to individual tumor antigens by IgG antibody and CD8+ T cells following cancer vaccination
Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family
The Fungal bZIP Transcription Factor AtfB Controls Virulence-Associated Processes in Aspergillus parasiticus
SIRT1/HERC4 locus associated with Bisphosphonate-induced osteonecrosis of the jaw: an exome-wide association analysis
BRCA1-mimetic compound NSC35446.HCL inhibits IKKBexpression by reducing estrogen receptor-a occupancy in the IKKB promoter and inhibits NF-kB activity in antiestrogen resistant human breast cancer cells
Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant
Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability
Differentially expressed genes in PPARg-deficient MSCs
Homozygous mutations in PJVK and MYO15A genes associated with nonsyndromic hearing loss in Moroccan families
