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Quoted phrase not found in phrase index: "Dilated cardiomyopathy 1B"
Page 1
The nuclear muscular dystrophies.
Wehnert MS, Bonne G. Wehnert MS, et al. Semin Pediatr Neurol. 2002 Jun;9(2):100-7. doi: 10.1053/spen.2002.33806. Semin Pediatr Neurol. 2002. PMID: 12138994 Review.
Phenotypically, they present as Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscle dystrophy 1B (LGMD1B), or dilated cardiomyopathy with conduction defects (DCM-CD). ...Although structural abnormalities of nuclei in animal and cell models have been …
Phenotypically, they present as Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscle dystrophy 1B (LGMD1B), or dilated …
The nuclear envelope in muscular dystrophy and cardiovascular diseases.
Burke B, Mounkes LC, Stewart CL. Burke B, et al. Traffic. 2001 Oct;2(10):675-83. doi: 10.1034/j.1600-0854.2001.21001.x. Traffic. 2001. PMID: 11576443 Free article. Review.
These disorders, described as laminopathies or nuclear envelopathies, include both X-linked and autosomal dominant forms of Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy with conduction system defects, limb girdle muscular dystrophy 1B with atriov …
These disorders, described as laminopathies or nuclear envelopathies, include both X-linked and autosomal dominant forms of Emery-Dreifuss m …
Predictors of disease progression in pediatric dilated cardiomyopathy.
Molina KM, Shrader P, Colan SD, Mital S, Margossian R, Sleeper LA, Shirali G, Barker P, Canter CE, Altmann K, Radojewski E, Tierney ES, Rychik J, Tani LY; Pediatric Heart Network Investigators. Molina KM, et al. Circ Heart Fail. 2013 Nov;6(6):1214-22. doi: 10.1161/CIRCHEARTFAILURE.113.000125. Epub 2013 Oct 16. Circ Heart Fail. 2013. PMID: 24132734 Free PMC article. Clinical Trial.
BACKGROUND: Despite medical advances, children with dilated cardiomyopathy (DCM) remain at high risk of death or need for cardiac transplantation. ...Multivariable analysis identified older age at diagnosis (hazard ratio=1.14 per year; P<0.001), larger left ventr …
BACKGROUND: Despite medical advances, children with dilated cardiomyopathy (DCM) remain at high risk of death or need for card …
Cardiac-specific LRP6 knockout induces lipid accumulation through Drp1/CPT1b pathway in adult mice.
Wang Y, Yin C, Chen Z, Li Y, Zou Y, Wang X, An Y, Wu F, Zhang G, Yang C, Tang H, Zou Y, Gong H. Wang Y, et al. Cell Tissue Res. 2020 Apr;380(1):143-153. doi: 10.1007/s00441-019-03126-3. Epub 2019 Dec 7. Cell Tissue Res. 2020. PMID: 31811407
We recently reported low-density lipoprotein receptor-related protein 6 (LRP6) decreased in dilated cardiomyopathy hearts, and cardiac-specific knockout mice displayed lethal heart failure through activation of dynamin-related protein 1 (Drp1). We also observed …
We recently reported low-density lipoprotein receptor-related protein 6 (LRP6) decreased in dilated cardiomyopathy hearts, and …
Urinary Proteomics in Predicting Heart Transplantation Outcomes (uPROPHET)-Rationale and database description.
Huang QF, Trenson S, Zhang ZY, Yang WY, Van Aelst L, Nkuipou-Kenfack E, Wei FF, Mujaj B, Thijs L, Ciarka A, Zoidakis J, Droogné W, Vlahou A, Janssens S, Vanhaecke J, Van Cleemput J, Staessen JA. Huang QF, et al. PLoS One. 2017 Sep 7;12(9):e0184443. doi: 10.1371/journal.pone.0184443. eCollection 2017. PLoS One. 2017. PMID: 28880921 Free PMC article.
RESULTS: Of 352 participants in the UP study (24.4% women), 38.9%, 40.3%, 5.7% and 15.1% had ischemic, dilated, hypertrophic or other cardiomyopathy. The median interval between HTx and first UP assessment (baseline) was 7.8 years. ...The TP study currently includes …
RESULTS: Of 352 participants in the UP study (24.4% women), 38.9%, 40.3%, 5.7% and 15.1% had ischemic, dilated, hypertrophic or other …
Laminopathies in Russian families.
Rudenskaya GE, Polyakov AV, Tverskaya SM, Zaklyazminskaya EV, Chukhrova AL, Groznova OE, Ginter EK. Rudenskaya GE, et al. Clin Genet. 2008 Aug;74(2):127-33. doi: 10.1111/j.1399-0004.2008.01045.x. Epub 2008 Jun 28. Clin Genet. 2008. PMID: 18564364
Because this mutation occurred de novo also in other reported cases, a mutational 'hot spot' was supposed. Three phenotypes were observed: autosomal dominant (AD) Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle MD type 1B, and AD dilated cardiomyopat …
Because this mutation occurred de novo also in other reported cases, a mutational 'hot spot' was supposed. Three phenotypes were observed …
The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases.
Mounkes LC, Burke B, Stewart CL. Mounkes LC, et al. Trends Cardiovasc Med. 2001 Oct;11(7):280-5. doi: 10.1016/s1050-1738(01)00126-8. Trends Cardiovasc Med. 2001. PMID: 11709282 Review.
Mutations in the lamin A (LMNA) gene are associated with the tissue-specific diseases Emery-Dreifuss muscular dystrophy (EDMD), limb girdle muscular dystrophy (LGMD-1B), dilated cardiomyopathy with conduction system disease (DCM-CD), and Dunnigan's familial p …
Mutations in the lamin A (LMNA) gene are associated with the tissue-specific diseases Emery-Dreifuss muscular dystrophy (EDMD), limb girdle …
Different expression of adrenoceptors and GRKs in the human myocardium depends on heart failure etiology and correlates to clinical variables.
Montó F, Oliver E, Vicente D, Rueda J, Agüero J, Almenar L, Ivorra MD, Barettino D, D'Ocon P. Montó F, et al. Am J Physiol Heart Circ Physiol. 2012 Aug 1;303(3):H368-76. doi: 10.1152/ajpheart.01061.2011. Epub 2012 Jun 8. Am J Physiol Heart Circ Physiol. 2012. PMID: 22685168 Free article.
To analyze these questions, we quantified the mRNA/protein expressions of six ARs (alpha(1A), alpha(1B), alpha(1D), beta(1), beta(2), and beta(3)) and three GRKs (GRK2, GRK3, and GRK5) in left (LV) and right ventricle (RV) from four donors, 10 patients with ischemic car …
To analyze these questions, we quantified the mRNA/protein expressions of six ARs (alpha(1A), alpha(1B), alpha(1D), beta(1), beta(2), …
Matrix metalloproteinase-9, tissue inhibitor of metalloproteinase-1, B+ tenascin-C and ED-A+ fibronectin in dilated cardiomyopathy: potential impact on disease progression and patients' prognosis.
Franz M, Berndt A, Neri D, Galler K, Grün K, Porrmann C, Reinbothe F, Mall G, Schlattmann P, Renner A, Figulla HR, Jung C, Küthe F. Franz M, et al. Int J Cardiol. 2013 Oct 15;168(6):5344-51. doi: 10.1016/j.ijcard.2013.08.005. Epub 2013 Aug 15. Int J Cardiol. 2013. PMID: 23998545
BACKGROUND: Dilated cardiomyopathy (DCM) is associated with heart failure and increased mortality and there is no reliable biomarker to estimate patients' prognosis. ...In a multivariate analysis, TIMP-1 is the superior parameter to predict transplantation fr …
BACKGROUND: Dilated cardiomyopathy (DCM) is associated with heart failure and increased mortality and there is no reliable bio …
Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
Jakobs PM, Hanson EL, Crispell KA, Toy W, Keegan H, Schilling K, Icenogle TB, Litt M, Hershberger RE. Jakobs PM, et al. J Card Fail. 2001 Sep;7(3):249-56. doi: 10.1054/jcaf.2001.26339. J Card Fail. 2001. PMID: 11561226
Mutations in lamin A/C cause 4 diseases: Emery-Dreifuss muscular dystrophy, limb girdle muscular dystrophy type 1B, Dunnigan-type familial partial lipodystrophy, and dilated cardiomyopathy. ...Death was caused by heart failure and sudden cardiac death. Skelet …
Mutations in lamin A/C cause 4 diseases: Emery-Dreifuss muscular dystrophy, limb girdle muscular dystrophy type 1B, Dunnigan-type fam …
18 results