puromycin sensitive aminopeptidase, partial [Homo sapiens]

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No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. [Hum Mol Genet. 2014]
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.
Goris A, van Setten J, Diekstra F, Ripke S, Patsopoulos NA, Sawcer SJ, International Multiple Sclerosis Genetics Consortium, van Es M, Australia and New Zealand MS Genetics Consortium, Andersen PM, et al. Hum Mol Genet. 2014 Apr 1; 23(7):1916-22. Epub 2013 Nov 13.
Analysis of conserved residues of the human puromycin-sensitive aminopeptidase. [Peptides. 2003]
Analysis of conserved residues of the human puromycin-sensitive aminopeptidase.
Thompson MW, Hersh LB. Peptides. 2003 Sep; 24(9):1359-65.
Human puromycin-sensitive aminopeptidase: cloning of 3' UTR, evidence for a polymorphism at a.a. 140 and refined chromosomal localization to 17q21. [Cytogenet Cell Genet. 2001]
Human puromycin-sensitive aminopeptidase: cloning of 3' UTR, evidence for a polymorphism at a.a. 140 and refined chromosomal localization to 17q21.
Bauer WO, Nanda I, Beck G, Schmid M, Jakob F. Cytogenet Cell Genet. 2001; 92(3-4):221-4.

RefSeq protein isoforms
See 9 reference sequence protein isoforms for the NPEPPS gene.

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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein