Human Chordin-like Protein 2, CHRDL2 ELISA Kit , 96T Antisense Oligonucleotides An extremely rare recessive genetic

An extremely rare recessive genetic disorder

Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lact

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Isoform MXI2 activation is stimulated by mitogens and oxidative stress and only poorly phosphorylates ELK1 and ATF2

and male pseudohermaphtoditism with Leydig cell hypoplasia

Human Chordin-like Protein 2, CHRDL2 ELISA Kit , 96T Antisense Oligonucleotides An extremely rare recessive geneticMay inhibit BMPs activity by blocking their interaction with their receptors. Has a negative regulator effect on the cartilage formation regeneration from immature mesenchymal cells, by preventing or reducing the rate of matrix accumulation (By similarity). Implicated in tumor angiogenesis. May play a role during myoblast and osteoblast differentiation, and maturation.