Literature DB >> 11001802

Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders.

N Fischel-Ghodsian1.   

Abstract

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Year:  2000        PMID： 11001802     DOI： 10.1006/mgme.2000.3014

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN： 1096-7192            Impact factor:   4.797


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  4 in total

Review 1.  Mitochondrial threshold effects.

Authors:  Rodrigue Rossignol; Benjamin Faustin; Christophe Rocher; Monique Malgat; Jean-Pierre Mazat; Thierry Letellier
Journal:  Biochem J       Date:  2003-03-15       Impact factor: 3.857

2.  Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains.

Authors:  Michal Pravenec; Masaya Hyakukoku; Josef Houstek; Vaclav Zidek; Vladimir Landa; Petr Mlejnek; Ivan Miksik; Kristyna Dudová-Mothejzikova; Petr Pecina; Marek Vrbacky; Zdenek Drahota; Alena Vojtiskova; Tomas Mracek; Ludmila Kazdova; Olena Oliyarnyk; Jiaming Wang; Christopher Ho; Nathan Qi; Ken Sugimoto; Theodore Kurtz
Journal:  Genome Res       Date:  2007-08-10       Impact factor: 9.043

3.  Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins.

Authors:  Yelena Bykhovskaya; Emebet Mengesha; Nathan Fischel-Ghodsian
Journal:  Mol Genet Metab       Date:  2009-05-13       Impact factor: 4.797

4.  An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations.

Authors:  Sonia Emperador; David Pacheu-Grau; M Pilar Bayona-Bafaluy; Nuria Garrido-Pérez; Antonio Martín-Navarro; Manuel J López-Pérez; Julio Montoya; Eduardo Ruiz-Pesini
Journal:  Front Genet       Date:  2015-01-14       Impact factor: 4.599
  4 in total

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