z-logo
open-access-imgOpen Access
Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation
Author(s) -
Tassilo Kruis,
Jürgen Klammt,
Assimina GalliΤsinopoulou,
Tillmann Wallborn,
Marina Schlicke,
Eva Müller,
Jürgen Kratzsch,
Antje Körner,
Rasha Odeh,
Wieland Kieß,
Roland Pfäffle
Publication year - 2010
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/mend.24.2.9996
Subject(s) - biology , insulin like growth factor 1 receptor , autophosphorylation , endocrinology , insulin like growth factor , insulin receptor , medicine , protein kinase b , mutation , mapk/erk pathway , microbiology and biotechnology , genetics , kinase , protein kinase a , receptor , signal transduction , growth factor , gene , insulin , insulin resistance

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom