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The Journal of Cell Biology|November 13, 1998
Paralemmin, a prenyl-palmitoyl-anchored phosphoprotein abundant in neurons and implicated in plasma membrane dynamics and cell process formationC Kutzleb, G Sanders, R Yamamoto, et al.
Brain Research. Molecular Brain Research|January 14, 1998
Differential regulation of genes encoding synaptic proteins by the Oct-2 transcription factorZ C Deans, S J Dawson, M W Kilimann, et al.
The Journal of Biological Chemistry|April 15, 2000
Inhibition of phospholipase D by amphiphysinsC Lee, S R Kim, J K Chung, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1988
cDNA cloning and complete primary structure of skeletal muscle phosphorylase kinase (alpha subunit)N F Zander, H E Meyer, E Hoffmann-Posorske, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 11, 2000
Neurobeachin: A protein kinase A-anchoring, beige/Chediak-higashi protein homolog implicated in neuronal membrane trafficX Wang, F W Herberg, M M Laue, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1988
The alpha and beta subunits of phosphorylase kinase are homologous: cDNA cloning and primary structure of the beta subunitM W Kilimann, N F Zander, C C Kuhn, et al.
Human Molecular Genetics|May 1, 1996
Mutation hotspots in the PHKA2 gene in X-linked liver glycogenosis due to phosphorylase kinase deficiency with atypical activity in blood cells (XLG2)B Burwinkel, Y S Shin, H D Bakker, et al.
Annals of Neurology|April 13, 2000
Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body diseaseF Ziemssen, E Sindern, J M Schröder, et al.
Brain Research. Molecular Brain Research|December 31, 1996
Differential regulation of genes encoding synaptic proteins by members of the Brn-3 subfamily of POU transcription factorsP J Morris, N D Lakin, S J Dawson, et al.
Human Molecular Genetics|July 1, 1997
Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB)B Burwinkel, A J Maichele, O Aagenaes, et al.
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