Literature DB >> 7668244

1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging.

D C Wallace1.   

Abstract

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Year:  1995        PMID： 7668244      PMCID： PMC1801540     

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


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  104 in total

1.  Native American mitochondrial DNA analysis indicates that the Amerind and the Nadene populations were founded by two independent migrations.

Authors:  A Torroni; T G Schurr; C C Yang; E J Szathmary; R C Williams; M S Schanfield; G A Troup; W C Knowler; D N Lawrence; K M Weiss
Journal:  Genetics       Date:  1992-01       Impact factor: 4.562

2.  Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations.

Authors:  S W Ballinger; T G Schurr; A Torroni; Y Y Gan; J A Hodge; K Hassan; K H Chen; D C Wallace
Journal:  Genetics       Date:  1992-01       Impact factor: 4.562

3.  Extensive mitochondrial diversity within a single Amerindian tribe.

Authors:  R H Ward; B L Frazier; K Dew-Jager; S Pääbo
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

4.  Y chromosome probe p49a detects complex PvuII haplotypes and many new TaqI haplotypes in southern African populations.

Authors:  A Spurdle; T Jenkins
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

5.  Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

Authors:  M D Brown; A S Voljavec; M T Lott; A Torroni; C C Yang; D C Wallace
Journal:  Genetics       Date:  1992-01       Impact factor: 4.562

6.  Cytochrome b mutations in Leber hereditary optic neuropathy.

Authors:  D R Johns; M J Neufeld
Journal:  Biochem Biophys Res Commun       Date:  1991-12-31       Impact factor: 3.575

7.  Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.

Authors:  N Howell; L A Bindoff; D A McCullough; I Kubacka; J Poulton; D Mackey; L Taylor; D M Turnbull
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

8.  Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Authors:  J M Shoffner; M T Lott; A M Lezza; P Seibel; S W Ballinger; D C Wallace
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

9.  The structure of human mitochondrial DNA variation.

Authors:  D A Merriwether; A G Clark; S W Ballinger; T G Schurr; H Soodyall; T Jenkins; S T Sherry; D C Wallace
Journal:  J Mol Evol       Date:  1991-12       Impact factor: 2.395

10.  Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.

Authors:  I J Holt; A E Harding; J A Morgan-Hughes
Journal:  Nature       Date:  1988-02-25       Impact factor: 49.962
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  55 in total

1.  Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue- or age-related variation.

Authors:  S L White; S Shanske; J J McGill; H Mountain; M T Geraghty; S DiMauro; H H Dahl; D R Thorburn
Journal:  J Inherit Metab Dis       Date:  1999-12       Impact factor: 4.982

2.  The biology of mitochondrial disease.

Authors:  A Clarke
Journal:  Arch Dis Child       Date:  2000-05       Impact factor: 3.791

Review 3.  Mitochondrial DNA analysis: polymorphisms and pathogenicity.

Authors:  P F Chinnery; N Howell; R M Andrews; D M Turnbull
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

4.  Male sperm motility dictated by mother's mtDNA.

Authors:  F L Moore; R A Reijo-Pera
Journal:  Am J Hum Genet       Date:  2000-08-09       Impact factor: 11.025

5.  A sensitive denaturing gradient-Gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region.

Authors:  L A Tully; T J Parsons; R J Steighner; M M Holland; M A Marino; V L Prenger
Journal:  Am J Hum Genet       Date:  2000-06-28       Impact factor: 11.025

6.  Interspecies subtractive hybridization of cDNA from human and chimpanzee brains.

Authors:  E V Nadezhdin; T V Vinogradova; E D Sverdlov
Journal:  Dokl Biochem Biophys       Date:  2001 Nov-Dec       Impact factor: 0.788

7.  Effect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseases.

Authors:  B Korzeniewski; M Malgat; T Letellier; J P Mazat
Journal:  Biochem J       Date:  2001-08-01       Impact factor: 3.857

8.  The presence of mitochondrial haplogroup x in Altaians from South Siberia.

Authors:  M V Derenko; T Grzybowski; B A Malyarchuk; J Czarny; D Miścicka-Sliwka; I A Zakharov
Journal:  Am J Hum Genet       Date:  2001-07       Impact factor: 11.025

9.  Genetic evidence on the origins of Indian caste populations.

Authors:  M Bamshad; T Kivisild; W S Watkins; M E Dixon; C E Ricker; B B Rao; J M Naidu; B V Prasad; P G Reddy; A Rasanayagam; S S Papiha; R Villems; A J Redd; M F Hammer; S V Nguyen; M L Carroll; M A Batzer; L B Jorde
Journal:  Genome Res       Date:  2001-06       Impact factor: 9.043

10.  Human mtDNA haplogroups associated with high or reduced spermatozoa motility.

Authors:  E Ruiz-Pesini; A C Lapeña; C Díez-Sánchez; A Pérez-Martos; J Montoya; E Alvarez; M Díaz; A Urriés; L Montoro; M J López-Pérez; J A Enríquez
Journal:  Am J Hum Genet       Date:  2000-08-09       Impact factor: 11.025
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