Literature DB >> 8023848

Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy.

Y Kobayashi, H Sharpe, N Brown.   

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Year:  1994        PMID: 8023848      PMCID: PMC1918233     

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


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  20 in total

1.  Routine use of hair root or buccal swab specimens for PCR analysis: advantages over using blood.

Authors:  D M Thomson; N N Brown; A E Clague
Journal:  Clin Chim Acta       Date:  1992-05-15       Impact factor: 3.786

2.  Improved molecular-genetic diagnosis of Leber's hereditary optic neuropathy.

Authors:  D R Johns
Journal:  N Engl J Med       Date:  1990-11-22       Impact factor: 91.245

3.  The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

Authors:  N J Newman; M T Lott; D C Wallace
Journal:  Am J Ophthalmol       Date:  1991-06-15       Impact factor: 5.258

4.  Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy.

Authors:  N Howell; D McCullough; I Bodis-Wollner
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

5.  Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

Authors:  I J Holt; D H Miller; A E Harding
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

6.  In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.

Authors:  A Chomyn; G Meola; N Bresolin; S T Lai; G Scarlato; G Attardi
Journal:  Mol Cell Biol       Date:  1991-04       Impact factor: 4.272

7.  Variable genotype of Leber's hereditary optic neuropathy patients.

Authors:  M T Lott; A S Voljavec; D C Wallace
Journal:  Am J Ophthalmol       Date:  1990-06-15       Impact factor: 5.258

8.  Leber's hereditary optic neuropathy and complex I deficiency in muscle.

Authors:  N G Larsson; O Andersen; E Holme; A Oldfors; J Wahlström
Journal:  Ann Neurol       Date:  1991-11       Impact factor: 10.422

9.  Mitochondrial gene segregation in mammals: is the bottleneck always narrow?

Authors:  N Howell; S Halvorson; I Kubacka; D A McCullough; L A Bindoff; D M Turnbull
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

10.  Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy.

Authors:  E M Stone; J M Coppinger; R H Kardon; J Donelson
Journal:  Arch Ophthalmol       Date:  1990-10
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  2 in total

1.  Single lymphocytes from two healthy individuals with mitochondrial point heteroplasmy are mainly homoplasmic.

Authors:  Sabine Lutz-Bonengel; Timo Sänger; Walther Parson; Helena Müller; Joachim W Ellwart; Marie Follo; Bernhard Bonengel; Harald Niederstätter; Marielle Heinrich; Ulrike Schmidt
Journal:  Int J Legal Med       Date:  2007-10-06       Impact factor: 2.686

2.  Multiplex fluorescence-based primer extension method for quantitative mutation analysis of mitochondrial DNA and its diagnostic application for Alzheimer's disease.

Authors:  E Fahy; R Nazarbaghi; M Zomorrodi; C Herrnstadt; W D Parker; R E Davis; S S Ghosh
Journal:  Nucleic Acids Res       Date:  1997-08-01       Impact factor: 16.971

  2 in total

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