GHR Polyclonal Antibody, 20ul DNA Fragments Birt-Hogg-Dube syndrome and Canavan disease

Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17

G-protein coupled receptor (GPCR) family

sgRNA (single-guide RNA) is a key component in the CRISPR-Cas9 gene-editing system

4 N-acetylgalactosaminyltransferase 1 catalyzes the transfer of GalNAc into G(M3) and G(D3) by a beta-1

The type II cytokeratins are clustered in a region of chromosome 12q12-q13

GHR Polyclonal Antibody, 20ul DNA Fragments Birt-Hogg-Dube syndrome and Canavan diseaseGHR encodes a member of the type I cytokine receptor family, which is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra and intercellular signal transduction pathway leading to growth. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature.