Literature DB >> 1434520

Defects of mitochondrial respiratory enzymes in cloned cells from MELAS fibroblasts.

S Miyabayashi1, H Hanamizu, R Nakamura, H Endo, K Tada.   

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Year:  1992        PMID： 1434520     DOI： 10.1007/bf01800024

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  7 in total

1.  Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies.

Authors:  J F Hess; M A Parisi; J L Bennett; D A Clayton
Journal:  Nature       Date:  1991-05-16       Impact factor: 49.962

2.  A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

Authors:  Y Goto; I Nonaka; S Horai
Journal:  Nature       Date:  1990-12-13       Impact factor: 49.962

3.  Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

Authors:  J Hayashi; S Ohta; A Kikuchi; M Takemitsu; Y Goto; I Nonaka
Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-01       Impact factor: 11.205

4.  Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy.

Authors:  S Miyabayashi; K Haginoya; H Hanamizu; K Iinuma; K Narisawa; K Tada
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

5.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

6.  Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples.

Authors:  S R Hammans; M G Sweeney; M Brockington; J A Morgan-Hughes; A E Harding
Journal:  Lancet       Date:  1991-06-01       Impact factor: 79.321

7.  Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).

Authors:  Y Kobayashi; M Y Momoi; K Tominaga; H Shimoizumi; K Nihei; M Yanagisawa; Y Kagawa; S Ohta
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025
  7 in total
  9 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.  Clinical and biochemical phenotype of the MELAS mutation.

Authors:  S Miyabayashi; H Hanamizu; R Nakamura; J I Hayashi; K Tada
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

3.  Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues.

Authors:  P M Matthews; J Hopkin; R M Brown; J B Stephenson; D Hilton-Jones; G K Brown
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

4.  Unravelling the Effects of the Mutation m.3571insC/MT-ND1 on Respiratory Complexes Structural Organization.

Authors:  Luisa Iommarini; Anna Ghelli; Concetta Valentina Tropeano; Ivana Kurelac; Giulia Leone; Sara Vidoni; Anne Lombes; Massimo Zeviani; Giuseppe Gasparre; Anna Maria Porcelli
Journal:  Int J Mol Sci       Date:  2018-03-07       Impact factor: 5.923

5.  Late-onset MELAS syndrome with mtDNA 14453G→A mutation masquerading as an acute encephalitis: a case report.

Authors:  Yuki Yokota; Makoto Hara; Takayoshi Akimoto; Tomotaka Mizoguchi; Yu-Ichi Goto; Ichizo Nishino; Satoshi Kamei; Hideto Nakajima
Journal:  BMC Neurol       Date:  2020-06-17       Impact factor: 2.474

Review 6.  Mitochondrial Heterogeneity.

Authors:  Juvid Aryaman; Iain G Johnston; Nick S Jones
Journal:  Front Genet       Date:  2019-01-25       Impact factor: 4.599

Review 7.  Oxygen toxicity: cellular mechanisms in normobaric hyperoxia.

Authors:  Ricardo Alva; Maha Mirza; Adam Baiton; Lucas Lazuran; Lyuda Samokysh; Ava Bobinski; Cale Cowan; Alvin Jaimon; Dede Obioru; Tala Al Makhoul; Jeffrey A Stuart
Journal:  Cell Biol Toxicol       Date:  2022-09-16       Impact factor: 6.819

8.  Mitochondrial DNA density homeostasis accounts for a threshold effect in a cybrid model of a human mitochondrial disease.

Authors:  Juvid Aryaman; Iain G Johnston; Nick S Jones
Journal:  Biochem J       Date:  2017-11-24       Impact factor: 3.857

9.  Sexual conflict explains the extraordinary diversity of mechanisms regulating mitochondrial inheritance.

Authors:  Arunas L Radzvilavicius; Nick Lane; Andrew Pomiankowski
Journal:  BMC Biol       Date:  2017-10-26       Impact factor: 7.431
  9 in total

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