Literature DB >> 11443548

Many roads lead to a broken heart: the genetics of dilated cardiomyopathy.

J Schönberger1, C E Seidman.   

Abstract

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Year:  2001        PMID: 11443548      PMCID: PMC1235300          DOI: 10.1086/321978

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  72 in total

1.  Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy.

Authors:  H Cao; R A Hegele
Journal:  Hum Mol Genet       Date:  2000-01-01       Impact factor: 6.150

2.  LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

Authors:  S Shackleton; D J Lloyd; S N Jackson; R Evans; M F Niermeijer; B M Singh; H Schmidt; G Brabant; S Kumar; P N Durrington; S Gregory; S O'Rahilly; R C Trembath
Journal:  Nat Genet       Date:  2000-02       Impact factor: 38.330

3.  The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14.

Authors:  D Li; F Ahmad; M J Gardner; D Weilbaecher; R Hill; A Karibe; O Gonzalez; T Tapscott; G P Sharratt; L L Bachinski; R Roberts
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

4.  Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C.

Authors:  R A Speckman; A Garg; F Du; L Bennett; R Veile; E Arioglu; S I Taylor; M Lovett; A M Bowcock
Journal:  Am J Hum Genet       Date:  2000-04       Impact factor: 11.025

5.  Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.

Authors:  D Fatkin; C MacRae; T Sasaki; M R Wolff; M Porcu; M Frenneaux; J Atherton; H J Vidaillet; S Spudich; U De Girolami; J G Seidman; C Seidman; F Muntoni; G Müehle; W Johnson; B McDonough
Journal:  N Engl J Med       Date:  1999-12-02       Impact factor: 91.245

6.  Desmin mutation responsible for idiopathic dilated cardiomyopathy.

Authors:  D Li; T Tapscoft; O Gonzalez; P E Burch; M A Quiñones; W A Zoghbi; R Hill; L L Bachinski; D L Mann; R Roberts
Journal:  Circulation       Date:  1999-08-03       Impact factor: 29.690

7.  Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy.

Authors:  S Minamisawa; M Hoshijima; G Chu; C A Ward; K Frank; Y Gu; M E Martone; Y Wang; J Ross; E G Kranias; W R Giles; K R Chien
Journal:  Cell       Date:  1999-10-29       Impact factor: 41.582

8.  Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group.

Authors:  L Mestroni; C Rocco; D Gregori; G Sinagra; A Di Lenarda; S Miocic; M Vatta; B Pinamonti; F Muntoni; A L Caforio; W J McKenna; A Falaschi; M Giacca
Journal:  J Am Coll Cardiol       Date:  1999-07       Impact factor: 24.094

9.  Dilated and failing cardiomyopathy in bradykinin B(2) receptor knockout mice.

Authors:  C Emanueli; R Maestri; D Corradi; R Marchione; A Minasi; M G Tozzi; M B Salis; S Straino; M C Capogrossi; G Olivetti; P Madeddu
Journal:  Circulation       Date:  1999-12-07       Impact factor: 29.690

10.  Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy.

Authors:  T Sullivan; D Escalante-Alcalde; H Bhatt; M Anver; N Bhat; K Nagashima; C L Stewart; B Burke
Journal:  J Cell Biol       Date:  1999-11-29       Impact factor: 10.539

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  36 in total

1.  Cardiac-specific NRAP overexpression causes right ventricular dysfunction in mice.

Authors:  Shajia Lu; Garland L Crawford; Justin Dore; Stasia A Anderson; Daryl Despres; Robert Horowits
Journal:  Exp Cell Res       Date:  2011-01-26       Impact factor: 3.905

2.  Progression of familial and non-familial dilated cardiomyopathy: long term follow up.

Authors:  V V Michels; D J Driscoll; F A Miller; T M Olson; E J Atkinson; C L Olswold; D J Schaid
Journal:  Heart       Date:  2003-07       Impact factor: 5.994

Review 3.  Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all.

Authors:  Thomas E Callis; Brian C Jensen; Karen E Weck; Monte S Willis
Journal:  Expert Rev Mol Diagn       Date:  2010-04       Impact factor: 5.225

4.  Organotypic heart slices for cell transplantation and physiological studies.

Authors:  Walter Habeler; Marc Peschanski; Christelle Monville
Journal:  Organogenesis       Date:  2009-04       Impact factor: 2.500

Review 5.  Methods in molecular cardiology: microarray technology.

Authors:  B van den Bosch; P A Doevendans; D Lips; H J M Smeets
Journal:  Neth Heart J       Date:  2003-05       Impact factor: 2.380

Review 6.  Role of various proteases in cardiac remodeling and progression of heart failure.

Authors:  Alison L Müller; Naranjan S Dhalla
Journal:  Heart Fail Rev       Date:  2012-05       Impact factor: 4.214

Review 7.  Molecular mechanisms of cardiomyopathy phenotypes associated with myosin light chain mutations.

Authors:  Wenrui Huang; Danuta Szczesna-Cordary
Journal:  J Muscle Res Cell Motil       Date:  2015-09-18       Impact factor: 2.698

8.  Functional and transcriptomic insights into pathogenesis of R9C phospholamban mutation using human induced pluripotent stem cell-derived cardiomyocytes.

Authors:  Delaine K Ceholski; Irene C Turnbull; Chi-Wing Kong; Simon Koplev; Joshua Mayourian; Przemek A Gorski; Francesca Stillitano; Angelos A Skodras; Mathieu Nonnenmacher; Ninette Cohen; Johan L M Björkegren; Daniel R Stroik; Razvan L Cornea; David D Thomas; Ronald A Li; Kevin D Costa; Roger J Hajjar
Journal:  J Mol Cell Cardiol       Date:  2018-05-09       Impact factor: 5.000

9.  Mapping genetic contributions to cardiac pathology induced by Beta-adrenergic stimulation in mice.

Authors:  Christoph D Rau; Jessica Wang; Rozeta Avetisyan; Milagros C Romay; Lisa Martin; Shuxun Ren; Yibin Wang; Aldons J Lusis
Journal:  Circ Cardiovasc Genet       Date:  2014-12-05

10.  Association of genetic polymorphisms on BTNL2 with susceptibility to and prognosis of dilated cardiomyopathy in a Chinese population.

Authors:  Liang Cheng; Rong Zhao; ZhenXiao Jin; Kai Ren; Chao Deng; Shiqiang Yu
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01
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