Literature DB >> 7668245

Transmission of mtDNA: cracks in the bottleneck.

J Poulton.   

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Year:  1995        PMID： 7668245      PMCID： PMC1801550     

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


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  12 in total

1.  Unequal partitioning of bovine mitochondrial genotypes among siblings.

Authors:  P J Laipis; M J Van de Walle; W W Hauswirth
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

2.  Length heteroplasmy in the first hypervariable segment of the human mtDNA control region.

Authors:  K E Bendall; B C Sykes
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

3.  mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.

Authors:  A Torroni; M T Lott; M F Cabell; Y S Chen; L Lavergne; D C Wallace
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

4.  Length heterogeneity of a conserved displacement-loop sequence in human mitochondrial DNA.

Authors:  W W Hauswirth; D A Clayton
Journal:  Nucleic Acids Res       Date:  1985-11-25       Impact factor: 16.971

5.  Nucleotide sequence preservation of human mitochondrial DNA.

Authors:  R J Monnat; L A Loeb
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

6.  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

7.  Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

Authors:  N G Larsson; M H Tulinius; E Holme; A Oldfors; O Andersen; J Wahlström; J Aasly
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

8.  Rearranged mitochondrial genomes are present in human oocytes.

Authors:  X Chen; R Prosser; S Simonetti; J Sadlock; G Jagiello; E A Schon
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

9.  A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues.

Authors:  G A Cortopassi; D Shibata; N W Soong; N Arnheim
Journal:  Proc Natl Acad Sci U S A       Date:  1992-08-15       Impact factor: 11.205

10.  A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies.

Authors:  M Brockington; M G Sweeney; S R Hammans; J A Morgan-Hughes; A E Harding
Journal:  Nat Genet       Date:  1993-05       Impact factor: 38.330
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  6 in total

1.  Heteroplasmy and organelle gene dynamics.

Authors:  R K Chesser
Journal:  Genetics       Date:  1998-11       Impact factor: 4.562

2.  mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.

Authors:  S Mumm; M P Whyte; R V Thakker; K H Buetow; D Schlessinger
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

3.  A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissues.

Authors:  F Degoul; D François; M Diry; G Ponsot; I Desguerre; B Héron; C Marsac; M L Moutard
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

Review 4.  Transmission of mitochondrial DNA diseases and ways to prevent them.

Authors:  Joanna Poulton; Marcos R Chiaratti; Flávio V Meirelles; Stephen Kennedy; Dagan Wells; Ian J Holt
Journal:  PLoS Genet       Date:  2010-08-12       Impact factor: 5.917

5.  Stability of the m.8993T->G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome.

Authors:  J Steffann; N Gigarel; J Corcos; M Bonnière; F Encha-Razavi; M Sinico; S Prevot; Y Dumez; A Yamgnane; R Frydman; A Munnich; J P Bonnefont
Journal:  J Med Genet       Date:  2007-06-01       Impact factor: 6.318

6.  Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation.

Authors:  Yuhua Zhu; Shasha Huang; Dongyang Kang; Mingyu Han; Guojian Wang; Yongyi Yuan; Yu Su; Huijun Yuan; Suoqiang Zhai; Pu Dai
Journal:  BMC Genet       Date:  2014-02-17       Impact factor: 2.797
  6 in total

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