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Results: 1 to 20 of 100

1.

Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis.

Purevjav E, Varela J, Morgado M, Kearney DL, Li H, Taylor MD, Arimura T, Moncman CL, McKenna W, Murphy RT, Labeit S, Vatta M, Bowles NE, Kimura A, Boriek AM, Towbin JA.

J Am Coll Cardiol. 2010 Oct 26;56(18):1493-502. doi: 10.1016/j.jacc.2010.05.045.

PMID:
20951326
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Altered regional cardiac wall mechanics are associated with differential cardiomyocyte calcium handling due to nebulette mutations in preclinical inherited dilated cardiomyopathy.

Maiellaro-Rafferty K, Wansapura JP, Mendsaikhan U, Osinska H, James JF, Taylor MD, Robbins J, Kranias EG, Towbin JA, Purevjav E.

J Mol Cell Cardiol. 2013 Jul;60:151-60. doi: 10.1016/j.yjmcc.2013.04.021. Epub 2013 Apr 28.

PMID:
23632046
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Nebulette mutations in cardiac remodeling: big effects from a small mechanosensor.

Ram R, Blaxall BC.

J Am Coll Cardiol. 2010 Oct 26;56(18):1503-5. doi: 10.1016/j.jacc.2010.06.031. No abstract available.

PMID:
20951327
[PubMed - indexed for MEDLINE]
Free Article
4.

Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis.

Mohapatra B, Jimenez S, Lin JH, Bowles KR, Coveler KJ, Marx JG, Chrisco MA, Murphy RT, Lurie PR, Schwartz RJ, Elliott PM, Vatta M, McKenna W, Towbin JA, Bowles NE.

Mol Genet Metab. 2003 Sep-Oct;80(1-2):207-15.

PMID:
14567970
[PubMed - indexed for MEDLINE]
5.

A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathy.

Li Z, Ai T, Samani K, Xi Y, Tzeng HP, Xie M, Wu S, Ge S, Taylor MD, Dong JW, Cheng J, Ackerman MJ, Kimura A, Sinagra G, Brunelli L, Faulkner G, Vatta M.

Circ Arrhythm Electrophysiol. 2010 Dec;3(6):646-56. doi: 10.1161/CIRCEP.109.929240. Epub 2010 Sep 18.

PMID:
20852297
[PubMed - indexed for MEDLINE]
Free Article
6.

Cardiac-specific ablation of Cypher leads to a severe form of dilated cardiomyopathy with premature death.

Zheng M, Cheng H, Li X, Zhang J, Cui L, Ouyang K, Han L, Zhao T, Gu Y, Dalton ND, Bang ML, Peterson KL, Chen J.

Hum Mol Genet. 2009 Feb 15;18(4):701-13. doi: 10.1093/hmg/ddn400. Epub 2008 Nov 21.

PMID:
19028670
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Sarcomere protein gene mutations and inherited heart disease: a beta-cardiac myosin heavy chain mutation causing endocardial fibroelastosis and heart failure.

Kamisago M, Schmitt JP, McNamara D, Seidman C, Seidman JG.

Novartis Found Symp. 2006;274:176-89; discussion 189-95, 272-6. Review.

PMID:
17019812
[PubMed - indexed for MEDLINE]
8.

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

Arimura T, Onoue K, Takahashi-Tanaka Y, Ishikawa T, Kuwahara M, Setou M, Shigenobu S, Yamaguchi K, Bertrand AT, Machida N, Takayama K, Fukusato M, Tanaka R, Somekawa S, Nakano T, Yamane Y, Kuba K, Imai Y, Saito Y, Bonne G, Kimura A.

Cardiovasc Res. 2013 Aug 1;99(3):382-94. doi: 10.1093/cvr/cvt106. Epub 2013 Apr 30.

PMID:
23631840
[PubMed - indexed for MEDLINE]
Free Article
9.

Architecture of the thin filament-Z-line junction: lessons from nebulette and nebulin homologies.

Moncman CL, Wang K.

J Muscle Res Cell Motil. 2000 Feb;21(2):153-69.

PMID:
10961839
[PubMed - indexed for MEDLINE]
10.

Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity.

Rajan S, Ahmed RP, Jagatheesan G, Petrashevskaya N, Boivin GP, Urboniene D, Arteaga GM, Wolska BM, Solaro RJ, Liggett SB, Wieczorek DF.

Circ Res. 2007 Jul 20;101(2):205-14. Epub 2007 Jun 7. Erratum in: Circ Res. 2007 Sep 14;101(6):e80.

PMID:
17556658
[PubMed - indexed for MEDLINE]
Free Article
11.

The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.

Ahmad F, Banerjee SK, Lage ML, Huang XN, Smith SH, Saba S, Rager J, Conner DA, Janczewski AM, Tobita K, Tinney JP, Moskowitz IP, Perez-Atayde AR, Keller BB, Mathier MA, Shroff SG, Seidman CE, Seidman JG.

PLoS One. 2008 Jul 9;3(7):e2642. doi: 10.1371/journal.pone.0002642.

PMID:
18612386
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction.

Vatta M, Mohapatra B, Jimenez S, Sanchez X, Faulkner G, Perles Z, Sinagra G, Lin JH, Vu TM, Zhou Q, Bowles KR, Di Lenarda A, Schimmenti L, Fox M, Chrisco MA, Murphy RT, McKenna W, Elliott P, Bowles NE, Chen J, Valle G, Towbin JA.

J Am Coll Cardiol. 2003 Dec 3;42(11):2014-27.

PMID:
14662268
[PubMed - indexed for MEDLINE]
Free Article
13.

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.

Purevjav E, Arimura T, Augustin S, Huby AC, Takagi K, Nunoda S, Kearney DL, Taylor MD, Terasaki F, Bos JM, Ommen SR, Shibata H, Takahashi M, Itoh-Satoh M, McKenna WJ, Murphy RT, Labeit S, Yamanaka Y, Machida N, Park JE, Alexander PM, Weintraub RG, Kitaura Y, Ackerman MJ, Kimura A, Towbin JA.

Hum Mol Genet. 2012 May 1;21(9):2039-53. doi: 10.1093/hmg/dds022. Epub 2012 Jan 27.

PMID:
22286171
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding.

van de Meerakker JB, Christiaans I, Barnett P, Lekanne Deprez RH, Ilgun A, Mook OR, Mannens MM, Lam J, Wilde AA, Moorman AF, Postma AV.

Biochim Biophys Acta. 2013 Apr;1833(4):833-9. doi: 10.1016/j.bbamcr.2012.11.003. Epub 2012 Nov 9.

PMID:
23147248
[PubMed - indexed for MEDLINE]
Free Article
15.

EH-myomesin splice isoform is a novel marker for dilated cardiomyopathy.

Schoenauer R, Emmert MY, Felley A, Ehler E, Brokopp C, Weber B, Nemir M, Faggian GG, Pedrazzini T, Falk V, Hoerstrup SP, Agarkova I.

Basic Res Cardiol. 2011 Mar;106(2):233-47. doi: 10.1007/s00395-010-0131-2. Epub 2010 Nov 11.

PMID:
21069531
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Expression of nebulette during early cardiac development.

Esham M, Bryan K, Milnes J, Holmes WB, Moncman CL.

Cell Motil Cytoskeleton. 2007 Apr;64(4):258-73.

PMID:
17238151
[PubMed - indexed for MEDLINE]
17.

Molecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathy.

Rodriguez G, Ueyama T, Ogata T, Czernuszewicz G, Tan Y, Dorn GW 2nd, Bogaev R, Amano K, Oh H, Matsubara H, Willerson JT, Marian AJ.

Circ Cardiovasc Genet. 2011 Aug 1;4(4):349-58. doi: 10.1161/CIRCGENETICS.111.959866. Epub 2011 Jun 3.

PMID:
21642240
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Prevalence of desmin mutations in dilated cardiomyopathy.

Taylor MR, Slavov D, Ku L, Di Lenarda A, Sinagra G, Carniel E, Haubold K, Boucek MM, Ferguson D, Graw SL, Zhu X, Cavanaugh J, Sucharov CC, Long CS, Bristow MR, Lavori P, Mestroni L; Familial Cardiomyopathy Registry; BEST (Beta-Blocker Evaluation of Survival Trial) DNA Bank.

Circulation. 2007 Mar 13;115(10):1244-51. Epub 2007 Feb 26.

PMID:
17325244
[PubMed - indexed for MEDLINE]
Free Article
19.

Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes.

Arimura T, Ishikawa T, Nunoda S, Kawai S, Kimura A.

Hum Mutat. 2011 Dec;32(12):1481-91. doi: 10.1002/humu.21603. Epub 2011 Sep 29.

PMID:
21898660
[PubMed - indexed for MEDLINE]
20.

Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy.

Arimura T, Nakamura T, Hiroi S, Satoh M, Takahashi M, Ohbuchi N, Ueda K, Nouchi T, Yamaguchi N, Akai J, Matsumori A, Sasayama S, Kimura A.

Hum Genet. 2000 Nov;107(5):440-51.

PMID:
11140941
[PubMed - indexed for MEDLINE]

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