Targeted Deletion of CASK-Interacting Nucleosome Assembly Protein Causes Higher Locomotor and Exploratory Activities

CASK phosphorylation by PKA regulates the protein-protein interactions of CASK and expression of the NMDAR2b gene

(2010) Tzyy-Nan Huang et al.   JOURNAL OF NEUROCHEMISTRY

Brain distribution of genes related to changes in locomotor activity

(2010) Pasquale Mignogna et al.   PHYSIOLOGY & BEHAVIOR

A Missense Mutation in CASK Causes FG Syndrome in an Italian Family

(2009) Giulio Piluso et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Calcium/calmodulin-dependent serine protein kinase and mental retardation

(2009) Yi-Ping Hsueh   ANNALS OF NEUROLOGY

CASK point mutation regulates protein–protein interactions and NR2b promoter activity

(2009) Tzyy-Nan Huang et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Cell division autoantigen 1 plays a profibrotic role by modulating downstream signalling of TGF-β in a murine diabetic model of atherosclerosis

(2009) Y. Pham et al.   DIABETOLOGIA

CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes

(2009) Anna Hackett et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

(2009) Patrick S Tarpey et al.   NATURE GENETICS

Differentially expressed nucleolar transforming growth factor-β1 target (DENTT) exhibits an inhibitory role on tumorigenesis

(2008) Lana E. Kandalaft et al.   CARCINOGENESIS

Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum

(2008) Juliane Najm et al.   NATURE GENETICS