Citations for
1NOS1AP, SLC8A1
A Common Variant in SLC8A1 Is Associated with the Duration of the Electrocardiographic QT Interval.
Kim JW, Hong KW, Go MJ, Kim SS, Tabara Y, Kita Y, Tanigawa T, Cho YS, Han BG, Oh B.
Am J Hum Genet 91(1):180-4. Epub 2012 Jun 21. 2012
2CASQ2, NOS1AP
Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease.
Westaway SK, Reinier K, Huertas-Vazquez A, Evanado A, Teodorescu C, Navarro J, Sinner MF, Gunson K, Jui J, Spooner P, Kaab S, Chugh SS.
Circ Cardiovasc Genet 4(4):397-402. Epub 2011 Jun 17. 2011
3NOS1AP
The nuclear localization of CAPON in hippocampus and cerebral cortex neurons after lipopolysaccharide stimulation.
Shao B, Jiang J, Wu Q, Xu Y, Lv Q, Li X, Wang P, Shen A, Yan M.
Neuroimmunomodulation 18(2):89-97. Epub 2010 Oct 20. 2011
4NOS1AP, SCRIB
NOS1AP associates with Scribble and regulates dendritic spine development.
Richier L, Williton K, Clattenburg L, Colwill K, O'Brien M, Tsang C, Kolar A, Zinck N, Metalnikov P, Trimble WS, Krueger SR, Pawson T, Fawcett JP.
J Neurosci 30(13):4796-805. 2010
5NOS1AP
Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome.
Tomás M, Napolitano C, De Giuli L, Bloise R, Subirana I, Malovini A, Bellazzi R, Arking DE, Marban E, Chakravarti A, Spooner PM, Priori SG.
J Am Coll Cardiol 55(24):2745-52. 2010
6NOS1AP
Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration.
Eijgelsheim M, Aarnoudse AL, Rivadeneira F, Kors JA, Witteman JC, Hofman A, van Duijn CM, Uitterlinden AG, Stricker BH.
Hum Mol Genet 18(2):347-57. Epub 2008 Oct 16. 2009
7NOS1AP
Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.
Eijgelsheim M, Newton-Cheh C, Aarnoudse AL, van Noord C, Witteman JC, Hofman A, Uitterlinden AG, Stricker BH.
Hum Mol Genet 18(21):4213-8. Epub 2009 Jul 30.PMID: 19643915 2009
8NOS1AP, RGS4, SCZD9, UHMK1
Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.
Puri V, McQuillin A, Datta S, Choudhury K, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Crombie C, Fraser G, Walker N, Moorey H, Ray MK, Sule A, Curtis D, St Clair D, Gurling H.
Eur J Hum Genet 16(10):1275-82. Epub 2008 Apr 16. 2008
9NOS1AP, UHMK1
Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.
Puri V, McQuillin A, Datta S, Choudhury K, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Crombie C, Fraser G, Walker N, Moorey H, Ray MK, Sule A, Curtis D, St Clair D, Gurling H.
Eur J Hum Genet 16(10):1275-82. Epub 2008 Apr 16. 2008
10APBB1, NOS1AP, RASD1
Dexras1 interacts with FE65 to regulate FE65-amyloid precursor protein-dependent transcription.
Lau KF, Chan WM, Perkinton MS, Tudor EL, Chang RC, Chan HY, McLoughlin DM, Miller CC.
J Biol Chem 283(50):34728-37. Epub 2008 Oct 15. 2008
11NOS1, NOS1AP
CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart.
Chang KC, Barth AS, Sasano T, Kizana E, Kashiwakura Y, Zhang Y, Foster DB, Marbán E.
Proc Natl Acad Sci U S A 105(11):4477-82. Epub 2008 Mar 12. 2008
12NOS1AP
Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish.
Post W, Shen H, Damcott C, Arking DE, Kao WH, Sack PA, Ryan KA, Chakravarti A, Mitchell BD, Shuldiner AR.
Hum Hered 64(4):214-9. Epub 2007 Jun 12. 2007
13DAOA, PRODH, DTNBP1, NRG1, DISC1, NOS1Ap, ZDHHC8, CLINT1, TAAR6, COMT, GABRA1, GABRP, HPI
Schizophrenia genetics: uncovering positional candidate genes.
Karayiorgou M, Gogos JA.
Eur J Hum Genet 14(5):512-9. 2006
14NOS1AP
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Arking DE, Pfeufer A, Post W, Kao WH, Newton-Cheh C, Ikeda M, West K, Kashuk C, Akyol M, Perz S, Jalilzadeh S, Illig T, Gieger C, Guo CY, Larson MG, Wichmann HE, Marban E, O'Donnell CJ, Hirschhorn JN, Kaab S, Spooner PM, Meitinger T, Chakravarti A.
Nat Genet 38(6):644-51. Epub 2006 Apr 30. 2006
15NOS1AP , SCZD9
Linkage Disequilibrium Mapping of Schizophrenia Susceptibility to the CAPON Region of Chromosome 1q22.
Brzustowicz LM, Simone J, Mohseni P, Hayter JE, Hodgkinson KA, Chow EW, Bassett AS.
Am J Hum Genet 74(5):1057-63. Epub 2004 Apr 02. 2004
16NOS1AP
Neuronal nitric-oxide synthase localization mediated by a ternary complex with synapsin and CAPON.
Jaffrey SR, Benfenati F, Snowman AM, Czernik AJ, Snyder SH.
Proc Natl Acad Sci U S A 99(5):3199-204. Epub 2002 Feb 26. 2002
17NOS1AP, RASD1
Dexras1: a G protein specifically coupled to neuronal nitric oxide synthase via CAPON.
Fang M, Jaffrey SR, Sawa A, Ye K, Luo X, Snyder SH.
Neuron 28(1):183-93. 2000
18NOS1AP
CAPON: a protein associated with neuronal nitric oxide synthase that regulates its interactions with PSD95.
Jaffrey SR, Snowman AM, Eliasson MJ, Cohen NA, Snyder SH.
Neuron 20(1):115-24. 1998
19C1orf34, CDC42BPA, CEP170, CROCC, CROCC, CYHR1, DENND4B, DISC1, DNAJC6, FAM20B, FAM91A2, HS2ST1, IPP, KIF21B, MACF1, NMNAT2, NOS1AP, PDE4DIP, PLCH2, POGZ, RABGAP1L, RERE, RPRD2, SDC3, SLC35E2, SNX27, SRGAP2, SZT2, TMCC2, UBR4, ZBTB40
Characterization of cDNA clones in size-fractionated cDNA libraries from human brain.
Seki N, Ohira M, Nagase T, Ishikawa K, Miyajima N, Nakajima D, Nomura N,Ohara O.
DNA Res 4(5):345-9. 1997