central nervous system disease

Literature (2)

Literature for DOID 331: central nervous system disease

Xenbase Articles Publications associated with this Disease Ontology entry or its descendants

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NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter., Goytain A,Hines RM,El-Husseini A,Quamme GA, J Biol Chem. March 16, 2007; 282(11):1083-351X.
RG3487, a novel nicotinic α7 receptor partial agonist, improves cognition and sensorimotor gating in rodents., Wallace TL,Callahan PM,Tehim A,Bertrand D,Tombaugh G,Wang S,Xie W,Rowe WB,Ong V,Graham E,Terry AV,Rodefer JS,Herbert B,Murray M,Porter R,Santarelli L,Lowe DA, J Pharmacol Exp Ther. January 1, 2011; 336(1):1521-0103.

RG3487, a novel nicotinic α7 receptor partial agonist, improves cognition and sensorimotor gating in rodents., Wallace TL,Callahan PM,Tehim A,Bertrand D,Tombaugh G,Wang S,Xie W,Rowe WB,Ong V,Graham E,Terry AV,Rodefer JS,Herbert B,Murray M,Porter R,Santarelli L,Lowe DA, J Pharmacol Exp Ther. January 1, 2011; 336(1):1521-0103.