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5 results for uniprot:Q8N336 in Computationally mapped citations

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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

BRIGHT Consortium
Talmud P.J., Drenos F., Shah S., Shah T., Palmen J., Verzilli C., Gaunt T.R., Pallas J., Lovering R., Li K. et al.

Am. J. Hum. Genet. 85:628-642(2009) GeneRIF 55531 · Mapped (10,092)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 55531

Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.

Rose J.E., Behm F.M., Drgon T., Johnson C., Uhl G.R.

Mol. Med. 16:247-253(2010) GeneRIF 55531 · Mapped (10,283)
Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) GeneRIF 55531

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.

Bailey S.D., Xie C., Do R., Montpetit A., Diaz R., Mohan V., Keavney B., Yusuf S., Gerstein H.C., Engert J.C. et al.

Diabetes Care 33:2250-2253(2010) GeneRIF 55531 · Mapped (10,071)
Observational study of gene-disease association gene-environment interaction and pharmacogenomic / toxicogenomic. (HuGE Navigator) GeneRIF 55531

An approach based on a genome-wide association study reveals candidate loci for narcolepsy.

Shimada M., Miyagawa T., Kawashima M., Tanaka S., Honda Y., Honda M., Tokunaga K.

Hum. Genet. 128:433-441(2010) GeneRIF 55531 · Mapped (688)
Observational study of gene-disease association. (HuGE Navigator) GeneRIF 55531

Towards a proteome-scale map of the human protein-protein interaction network.

Rual J.F., Venkatesan K., Hao T., Hirozane-Kishikawa T., Dricot A., Li N., Berriz G.F., Gibbons F.D., Dreze M., Ayivi-Guedehoussou N. et al.

Nature 437:1173-1178(2005) MINT MINT-1460488 · UniProtKB (1) · Mapped (1,321)
MINT-66859. THG1L (uniprotkb:Q9NWX6) physically interacts (MI:0915) with ELMOD1 (uniprotkb:Q8N336) by two hybrid (MI:0018). From mint MINT MINT-1460488

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