Literature DB >> 2898614

Deletions of muscle mitochondrial DNA.

I J Holt, J M Cooper, J A Morgan-Hughes, A E Harding.   

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Year:  1988        PMID： 2898614     DOI： 10.1016/s0140-6736(88)92273-8

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  10 in total

1.  Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.

Authors:  D R Johns; S L Rutledge; O C Stine; O Hurko
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

Review 2.  Mitochondrial DNA in sickness and in health.

Authors:  L I Grossman
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

Review 3.  Mitochondrial myopathies.

Authors:  A H Schapira
Journal:  BMJ       Date:  1989-04-29

4.  Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanisms.

Authors:  I J Holt; A E Harding; J A Morgan-Hughes
Journal:  Nucleic Acids Res       Date:  1989-06-26       Impact factor: 16.971

5.  Age-related human mtDNA deletions: a heterogeneous set of deletions arising at a single pair of directly repeated sequences.

Authors:  A Baumer; C Zhang; A W Linnane; P Nagley
Journal:  Am J Hum Genet       Date:  1994-04       Impact factor: 11.025

6.  Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

Authors:  J M Shoffner; M T Lott; A S Voljavec; S A Soueidan; D A Costigan; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

7.  Mutation Analysis of the Mitochondrial tRNA Genes in Iranian Coronary Atherosclerosis Patients.

Authors:  Mohammad Mehdi Heidari; Mahboobe Derakhshani; Fatemeh Sedighi; Seyed Khalil Foruzan-Nia
Journal:  Iran J Public Health       Date:  2017-10       Impact factor: 1.429

Review 8.  Rolling-Circle Replication in Mitochondrial DNA Inheritance: Scientific Evidence and Significance from Yeast to Human Cells.

Authors:  Feng Ling; Minoru Yoshida
Journal:  Genes (Basel)       Date:  2020-05-06       Impact factor: 4.096

9.  POLRMT mutations impair mitochondrial transcription causing neurological disease.

Authors:  Monika Oláhová; Bradley Peter; Zsolt Szilagyi; Hector Diaz-Maldonado; Meenakshi Singh; Ewen W Sommerville; Emma L Blakely; Jack J Collier; Emily Hoberg; Viktor Stránecký; Hana Hartmannová; Anthony J Bleyer; Kim L McBride; Sasigarn A Bowden; Zuzana Korandová; Alena Pecinová; Hans-Hilger Ropers; Kimia Kahrizi; Hossein Najmabadi; Mark A Tarnopolsky; Lauren I Brady; K Nicole Weaver; Carlos E Prada; Katrin Õunap; Monica H Wojcik; Sander Pajusalu; Safoora B Syeda; Lynn Pais; Elicia A Estrella; Christine C Bruels; Louis M Kunkel; Peter B Kang; Penelope E Bonnen; Tomáš Mráček; Stanislav Kmoch; Gráinne S Gorman; Maria Falkenberg; Claes M Gustafsson; Robert W Taylor
Journal:  Nat Commun       Date:  2021-02-18       Impact factor: 14.919

Review 10.  The mitochondrial brain: From mitochondrial genome to neurodegeneration.

Authors:  Helen E Turnbull; Nichola Z Lax; Daria Diodato; Olaf Ansorge; Doug M Turnbull
Journal:  Biochim Biophys Acta       Date:  2009-08-06
  10 in total

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