NOR-1 Polyclonal Antibody, 50ul Pipette Holder Osteopetrosis is a rare genetic

Osteopetrosis is a rare genetic disease characterized by abnormally dense bone

is developmentally regulated

This gene encodes a member of the non-histone lysine methyltransferases

A single nucleotide polymorphism in this gene is associated with an aggressive form of prostate cancer

NOR-1 Polyclonal Antibody, 50ul Pipette Holder Osteopetrosis is a rare geneticNR4A3 (nuclear receptor subfamily 4 group A member 3) encodes a member of the steroid thyroid hormone retinoid receptor superfamily. The encoded protein may act as a transcriptional activator. The protein can efficiently bind the NGFI B Response Element (NBRE). Three different versions of extraskeletal myxoid chondrosarcomas (EMCs) are the result of reciprocal translocations between this gene and other genes. The translocation breakpoints are