Literature DB >> 7473670

The COX8 gene is not the disease gene of the CMH4 locus in familial hypertrophic cardiomyopathy.

G Bonne, L Carrier, K Schwartz, M Komajda.   

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Year:  1995        PMID: 7473670      PMCID: PMC1051658          DOI: 10.1136/jmg.32.8.670

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  12 in total

Review 1.  Ultrastructural features of hypertrophied human ventricular myocardium.

Authors:  B J Maron; V J Ferrans
Journal:  Prog Cardiovasc Dis       Date:  1978 Nov-Dec       Impact factor: 8.194

2.  A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

Authors:  A A Geisterfer-Lowrance; S Kass; G Tanigawa; H P Vosberg; W McKenna; C E Seidman; J G Seidman
Journal:  Cell       Date:  1990-09-07       Impact factor: 41.582

Review 3.  The mitochondrial electron transport and oxidative phosphorylation system.

Authors:  Y Hatefi
Journal:  Annu Rev Biochem       Date:  1985       Impact factor: 23.643

4.  Expression of human cytochrome c oxidase subunits during fetal development.

Authors:  G Bonne; P Seibel; S Possekel; C Marsac; B Kadenbach
Journal:  Eur J Biochem       Date:  1993-11-01

5.  Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography.

Authors:  B J Maron; P F Nichols; L W Pickle; Y E Wesley; J J Mulvihill
Journal:  Am J Cardiol       Date:  1984-04-01       Impact factor: 2.778

6.  A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissues.

Authors:  R Rizzuto; H Nakase; B Darras; U Francke; G M Fabrizi; T Mengel; F Walsh; B Kadenbach; S DiMauro; E A Schon
Journal:  J Biol Chem       Date:  1989-06-25       Impact factor: 5.157

Review 7.  Mitochondrial cardiomyopathy.

Authors:  T Ozawa
Journal:  Herz       Date:  1994-04       Impact factor: 1.443

8.  Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Authors:  L Thierfelder; H Watkins; C MacRae; R Lamas; W McKenna; H P Vosberg; J G Seidman; C E Seidman
Journal:  Cell       Date:  1994-06-03       Impact factor: 41.582

9.  Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11.

Authors:  L Carrier; C Hengstenberg; J S Beckmann; P Guicheney; C Dufour; J Bercovici; E Dausse; I Berebbi-Bertrand; C Wisnewsky; D Pulvenis
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

10.  [Hypertrophic cardiomyopathy caused by cytochrome-oxidase deficiency].

Authors:  V Gournay-Toulemonde; A Munnich; J B Bouhour; M Lefèvre; M Potiron; J M Saudubray
Journal:  Presse Med       Date:  1994-10-22       Impact factor: 1.228

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