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Brain Research|October 31, 1998
Cytosolic phospholipase A2 (cPLA2) distribution in murine brain and functional studies indicate that cPLA2 does not participate in muscarinic receptor-mediated signaling in neuronsL L Lautens, X G Chiou, J D Sharp, et al.Molecular Genetics and Metabolism|April 7, 1999
A new locus for variant late infantile neuronal ceroid lipofuscinosis-CLN7R B Wheeler, J D Sharp, W A Mitchell, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1981
Insulin synthesis in a clonal cell line of simian virus 40-transformed hamster pancreatic beta cellsR F Santerre, R A Cook, R M Crisel, et al.Neurology|February 9, 2005
Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated casesN G Laing, C Ceuterick-de Groote, D E Dye, et al.Neurology|February 17, 2010
CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCLW Xin, T E Mullen, R Kiely, et al.Human Molecular Genetics|April 1, 1997
Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23J D Sharp, R B Wheeler, B D Lake, et al.Neurology|December 29, 2005
A mutation in myotilin causes spheroid body myopathyT Foroud, N Pankratz, A P Batchman, et al.Molecular Genetics and Metabolism|December 28, 2016
Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dogM Hirz, M Drögemüller, A Schänzer, et al.Proceedings of the National Academy of Sciences of the United States of America|December 10, 1996
Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophyB Hess, P Saftig, D Hartmann, et al.Stroke|March 1, 1996
Reactive glia express cytosolic phospholipase A2 after transient global forebrain ischemia in the ratJ A Clemens, D T Stephenson, E B Smalstig, et al.Pageof 29