Literature DB >> 8965716

Detection and quantification of point mutations in mitochondrial DNA by PCR.

M Yoneda1, Y Tanno, S Tsuji, G Attardi.   

Abstract

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Year:  1996        PMID： 8965716     DOI： 10.1016/s0076-6879(96)64039-7

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN： 0076-6879            Impact factor:   1.600


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  5 in total

1.  Sequence polymorphisms within the human mitochondrial genes MTATP6, MTATP8 and MTND4.

Authors:  Sabine Lutz-Bonengel; Ulrike Schmidt; Tanja Schmitt; Stefan Pollak
Journal:  Int J Legal Med       Date:  2003-05-06       Impact factor: 2.686

2.  Isolated cytochrome c oxidase deficiency as a cause of MELAS.

Authors:  Walter Rossmanith; Michael Freilinger; Julia Roka; Thomas Raffelsberger; Karin Moser-Their; Daniela Prayer; Günther Bernert; Reginald Bittner
Journal:  BMJ Case Rep       Date:  2009-01-23

3.  Establishment of a heteroplasmic mouse strain with interspecific mitochondrial DNA haplotypes and improvement of a PCR-RFLP-based measurement system for estimation of mitochondrial DNA heteroplasmy.

Authors:  Hiroshi Shitara; Liqin Cao; Midori Yamaguchi; Hiromichi Yonekawa; Choji Taya
Journal:  Transgenic Res       Date:  2017-02-20       Impact factor: 2.788

4.  Selective propagation of functional mitochondrial DNA during oogenesis restricts the transmission of a deleterious mitochondrial variant.

Authors:  Jahda H Hill; Zhe Chen; Hong Xu
Journal:  Nat Genet       Date:  2014-03-09       Impact factor: 38.330

5.  Mitochondrial DNA mutation detection by electrospray mass spectrometry.

Authors:  Yun Jiang; Thomas A Hall; Steven A Hofstadler; Robert K Naviaux
Journal:  Clin Chem       Date:  2006-12-07       Impact factor: 8.327
  5 in total

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