Latest Physician Education Resources
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
Exome sequencing identifies targets in the treatment-resistant phathalmoplegic subphenotype of Myasthenia Gravis
Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy