nucleoporin 155kDa, isoform CRA_a [Homo sapiens]

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Heart failure induces significant changes in nuclear pore complex of human cardiomyocytes. [PLoS One. 2012]
Heart failure induces significant changes in nuclear pore complex of human cardiomyocytes.
Tarazón E, Rivera M, Roselló-Lletí E, Molina-Navarro MM, Sánchez-Lázaro IJ, España F, Montero JA, Lago F, González-Juanatey JR, Portolés M. PLoS One. 2012; 7(11):e48957. Epub 2012 Nov 12.
The "missing" link in atrial fibrillation heritability. [J Electrocardiol. 2011]
The "missing" link in atrial fibrillation heritability.
Parvez B, Darbar D. J Electrocardiol. 2011 Nov-Dec; 44(6):641-4. Epub 2011 Sep 15.
Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy. [Circulation. 2004]
Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.
Oberti C, Wang L, Li L, Dong J, Rao S, Du W, Wang Q. Circulation. 2004 Dec 21; 110(25):3753-9. Epub 2004 Dec 13.

RefSeq genomic sequence
See the genomic reference sequence for the NUP155 gene (NG_034131.2).
RefSeq protein isoforms
See 9 reference sequence protein isoforms for the NUP155 gene.

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