QuickView for KLHL31;jsessionid=DE4E0C148F45692259CEDA63456D514B;jsessionid=4BF67817606E13B40CC539982DD1AF17;jsessionid=56161C28362EB70C70866AF0D9791FDE;jsessionid=5B3AFC448151D1FEEBA76B977E6B4D34 (gene)

1. Genomic and Transcriptional Profiles of Kelch-like (klhl) Gene Family in Polyploid Carassius Complex…
2. Epigenetics of Muscle- and Brain-Specific Expression of KLHL Family Genes.
3. Deficiency in Kelch protein Klhl31 causes congenital myopathy in mice.
4. Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis.
5. Targeting kelch-like (KLHL) proteins: achievements, challenges and perspectives.

There were no clinical trials for KLHL31;jsessionid=DE4E0C148F45692259CEDA63456D514B;jsessionid=4BF67817606E13B40CC539982DD1AF17;jsessionid=56161C28362EB70C70866AF0D9791FDE;jsessionid=5B3AFC448151D1FEEBA76B977E6B4D34