| 1 | CALM2, HNF4A, TAF1
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| Identification of TAF1, HNF4A, and CALM2 as potential therapeutic target genes for liver fibrosis.
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| Ji D, Chen GF, Wang JC, Cao LH, Lu F, Mu XX, Zhang XY, Lu XJ.
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| J Cell Physiol 234(6):9045-9051. doi: 10.1002/jcp.27579. Epub 2018 Oct 14.
2019
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| 2 | CALM2, LQT15
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| Novel Association of a De Novo CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy.
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| Zahavich L, Tarnopolsky M, Yao R, Mital S.
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| Circ Genom Precis Med 11(10):e002255. doi: 10.1161/CIRCGEN.118.002255. No abstract available.
2018
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| 3 | CALM2, LQT15
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| Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation.
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| Yamamoto Y, Makiyama T, Harita T, Sasaki K, Wuriyanghai Y, Hayano M, Nishiuchi S, Kohjitani H, Hirose S, Chen J, Yokoi F, Ishikawa T, Ohno S, Chonabayashi K, Motomura H, Yoshida Y, Horie M, Makita N, Kimura T.
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| Hum Mol Genet 26(9):1670-1677. doi: 10.1093/hmg/ddx073.
2017
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| 4 | CALM1, CALM2, CALM3, LQT14, LQT15, LQT16
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| A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome.
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| Limpitikul WB, Dick IE, Tester DJ, Boczek NJ, Limphong P, Yang W, Choi MH, Babich J, DiSilvestre D, Kanter RJ, Tomaselli GF, Ackerman MJ, Yue DT.
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| Circ Res 120(1):39-48. doi: 10.1161/CIRCRESAHA.116.309283. Epub 2016 Oct 20.
2017
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| 5 | CALM1, CALM2, CALM3, LQT14, LQT15, LQT16
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| Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy.
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| Chaix MA, Koopmann TT, Goyette P, Alikashani A, Latour F, Fatah M, Hamilton RM, Rioux JD.
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| HeartRhythm Case Rep 2(3):250-254. doi: 10.1016/j.hrcr.2016.02.002. eCollection 2016 May. No abstract available.
2016
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| 6 | CALM1, CALM2, CALM3, LQT14, LQT15, LQT16
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| Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G.
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| Boczek NJ, Gomez-Hurtado N, Ye D, Calvert ML, Tester DJ, Kryshtal D, Hwang HS, Johnson CN, Chazin WJ, Loporcaro CG, Shah M, Papez AL, Lau YR, Kanter R, Knollmann BC, Ackerman MJ.
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| Circ Cardiovasc Genet 9(2):136-146. doi: 10.1161/CIRCGENETICS.115.001323. Epub 2016 Mar 11.
2016
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| 7 | CALM1, CALM2, LQT14, LQT15
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| Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes.
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| Pipilas DC, Johnson CN, Webster G, Schlaepfer J, Fellmann F, Sekarski N, Wren LM, Ogorodnik KV, Chazin DM, Chazin WJ, Crotti L, Bhuiyan ZA, George AL Jr.
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| Heart Rhythm 13(10):2012-9. doi: 10.1016/j.hrthm.2016.06.038. Epub 2016 Jul 1.
2016
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| 8 | CALM2
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| Calmodulin 2 Mutation N98S Is Associated with Unexplained Cardiac Arrest in Infants Due to Low Clinical Penetrance Electrical Disorders.
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| Jiménez-Jáimez J, Palomino Doza J, Ortega Á, Macías-Ruiz R, Perin F, Rodríguez-Vázquez del Rey MM, Ortiz-Genga M, Monserrat L, Barriales-Villa R, Blanca E, Álvarez M, Tercedor L.
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| PLoS One 11(4):e0153851. doi: 10.1371/journal.pone.0153851. eCollection 2016.
2016
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| 9 | CALM2, LQT15
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| Novel calmodulin mutations associated with congenital arrhythmia susceptibility.
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| Makita N, Yagihara N, Crotti L, Johnson CN, Beckmann BM, Roh MS, Shigemizu D, Lichtner P, Ishikawa T, Aiba T, Homfray T, Behr ER, Klug D, Denjoy I, Mastantuono E, Theisen D, Tsunoda T, Satake W, Toda T, Nakagawa H, Tsuji Y, Tsuchiya T, Yamamoto H, Miyamoto Y, Endo N, Kimura A, Ozaki K, Motomura H, Suda K, Tanaka T, Schwartz PJ, Meitinger T, Kääb S, Guicheney P, Shimizu W, Bhuiyan ZA, Watanabe H, Chazin WJ, George AL Jr.
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| Circ Cardiovasc Genet 7(4):466-74. doi: 10.1161/CIRCGENETICS.113.000459. Epub 2014 Jun 10.
2014
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| 10 | CALM1, CALM2, LQT14, LQT15
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| Calmodulin mutations associated with recurrent cardiac arrest in infants.
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| Crotti L, Johnson CN, Graf E, De Ferrari GM, Cuneo BF, Ovadia M, Papagiannis J, Feldkamp MD, Rathi SG, Kunic JD, Pedrazzini M, Wieland T, Lichtner P, Beckmann BM, Clark T, Shaffer C, Benson DW, Kääb S, Meitinger T, Strom TM, Chazin WJ, Schwartz PJ, George AL Jr.
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| Circulation 127(9):1009-17. doi: 10.1161/CIRCULATIONAHA.112.001216. Epub 2013 Feb 6.
2013
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| 11 | CALM1, CALM2, LQT14, LQT15
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| Calmodulin mutations associated with recurrent cardiac arrest in infants.
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| Crotti L, Johnson CN, Graf E, De Ferrari GM, Cuneo BF, Ovadia M, Papagiannis J, Feldkamp MD, Rathi SG, Kunic JD, Pedrazzini M, Wieland T, Lichtner P, Beckmann BM, Clark T, Shaffer C, Benson DW, Kääb S, Meitinger T, Strom TM, Chazin WJ, Schwartz PJ, George AL Jr.
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| Circulation 127(9):1009-17. doi: 10.1161/CIRCULATIONAHA.112.001216. Epub 2013 Feb 6.
2013
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| 12 | CACNA1E, CALM2
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| The C-terminus of human Ca(v)2.3 voltage-gated calcium channel interacts with alternatively spliced calmodulin-2 expressed in two human cell lines.
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| Kamp MA, Shakeri B, Tevoufouet EE, Krieger A, Henry M, Behnke K, Herzig S, Hescheler J, Radhakrishnan K, Parent L, Schneider T.
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| Biochim Biophys Acta 1824(9):1045-57. doi: 10.1016/j.bbapap.2012.05.008. Epub 2012 May 24.
2012
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| 13 | CALM1, CALM2, CALM3
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| A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy.
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| Friedrich FW, Bausero P, Sun Y, Treszl A, Krämer E, Juhr D, Richard P, Wegscheider K, Schwartz K, Brito D, Arbustini E, Waldenström A, Isnard R, Komajda M, Eschenhagen T, Carrier L; EUROGENE Heart Failure Project.
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| Eur Heart J 30(13):1648-55. doi: 10.1093/eurheartj/ehp153. Epub 2009 May 8.
2009
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| 14 | CALM2
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| Involvement of calmodulin in neuronal cell death.
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| Shirasaki Y, Kanazawa Y, Morishima Y, Makino M.
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| Brain Res 1083(1):189-95. Epub 2006 Mar 20. 2006
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| 15 | CALM2, RELA
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| Gene expression profiling of human placentas from preeclamptic and normotensive pregnancies.
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| Hansson SR, Chen Y, Brodszki J, Chen M, Hernandez-Andrade E, Inman JM, Kozhich OA, Larsson I, Mars‡l K, Medstrand P, Xiang CC, Brownstein MJ.
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| Mol Hum Reprod 12(3):169-79. Epub 2006 Mar 23. 2006
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| 16 | DLG1, CALM2
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| Formation of complexes between Ca2+.calmodulin and the synapse-associated protein SAP97 requires the SH3 domain-guanylate kinase domain-connecting HOOK region.
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| Paarmann I, Spangenberg O, Lavie A, Konrad M.
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| J Biol Chem 277(43):40832-8. Epub 2002 Aug 19. 2002
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| 17 | CALM1, CALM2, CALM3, RAB3B
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| Rab3B in human platelet is membrane bound and interacts with Ca(2+)/calmodulin.
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| Sidhu RS, Bhullar RP.
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| Biochem Biophys Res Commun 289(5):1039-43. 2001
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| 18 | CALM1, CALM2, CALM3
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| Characterization of the human CALM2 calmodulin gene and comparison of the transcriptional activity of CALM1, CALM2 and CALM3.
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| Toutenhoofd SL, Foletti D, Wicki R, Rhyner JA, Garcia F, Tolon R, Strehler EE.
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| Cell Calcium 23(5):323-38. 1998
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| 19 | CALM1, CALM2, CALM3
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| Localization of the human bona fide calmodulin genes CALM1, CALM2, and CALM3 to chromosomes 14q24-q31, 2p21.1-p21.3, and 19q13.2-q13.3.
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| Berchtold MW, et al.
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| Genomics 16 : 461-465. 1993
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| 20 | CALM2, CALM3, CALML1, CALML3
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| Chromosomal localization of multiple genes encoding calmodulin.
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| McPherson JD, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 1951. 1991
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| 21 | CALM1, CALM2, CALM3
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| Multiple mRNAs encoding human calmodulin.
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| Pegues JC, Friedberg F.
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| Biochem Biophys Res Commun 172(3):1145-9. 1990
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