IL-3 Rabbit Polyclonal Antibody, 20ul Modified Oligos autosomal recessive craniometaphyseal dysplasia and

autosomal recessive craniometaphyseal dysplasia and heart malformations

and heterodimerizes with a 28 kDa protein to form interleukin 27 (IL-27)

Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand

a mutant form of c-Src in which Y527 is replaced by phenylalanine is transforming and displays 5- to 10-fold elevated kinase activity compared to its normal counterpart

is specifically expressed in the upper airways and nasopharyngeal regions

IL-3 Rabbit Polyclonal Antibody, 20ul Modified Oligos autosomal recessive craniometaphyseal dysplasia and