Literature DB >> 9399813

MITOMAP: a human mitochondrial genome database--1998 update.

A M Kogelnik1, M T Lott, M D Brown, S B Navathe, D C Wallace.   

Abstract

We have continued to develop MITOMAP (http://www.gen.emory. edu/MITOMAP ), a comprehensive database for the human mitochondrial DNA (mtDNA). MITOMAP uses the mtDNA sequence as the unifying element for bringing together information on mitochondrial genome structure and function, pathogenic mutations and their clinical characteristics, population associated variation, and gene-gene interactions. Over the past year we have increased the degree of interlinking of MITOMAP information available on the web page, by using our generalized information management system, GENOME. As increasingly larger regions of the human genome are sequenced and characterized, the need for integrating such information is growing. Consequently, MITOMAP and GENOME provide a valuable reference for the mitochondrial biologist, in addition to being a model for the development of comprehensive, information storage and retrieval systems for other components of the human genome. This paper documents the changes to MITOMAP which have been implemented over the past year.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9399813      PMCID: PMC147233          DOI: 10.1093/nar/26.1.112

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  6 in total

Review 1.  Diseases of the mitochondrial DNA.

Authors:  D C Wallace
Journal:  Annu Rev Biochem       Date:  1992       Impact factor: 23.643

2.  Improvements to the GDB Human Genome Data Base.

Authors:  K H Fasman; S I Letovsky; R W Cottingham; D T Kingsbury
Journal:  Nucleic Acids Res       Date:  1996-01-01       Impact factor: 16.971

3.  MITOMAP: a human mitochondrial genome database.

Authors:  A M Kogelnik; M T Lott; M D Brown; S B Navathe; D C Wallace
Journal:  Nucleic Acids Res       Date:  1996-01-01       Impact factor: 16.971

4.  The status of online Mendelian inheritance in man (OMIM) medio 1994.

Authors:  P Pearson; C Francomano; P Foster; C Bocchini; P Li; V McKusick
Journal:  Nucleic Acids Res       Date:  1994-09       Impact factor: 16.971

5.  1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging.

Authors:  D C Wallace
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

6.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

  6 in total
  23 in total

1.  A novel method for estimating substitution rate variation among sites in a large dataset of homologous DNA sequences.

Authors:  G Pesole; C Saccone
Journal:  Genetics       Date:  2001-02       Impact factor: 4.562

2.  Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorder.

Authors:  R Kirk; R A Furlong; W Amos; G Cooper; J S Rubinsztein; C Walsh; E S Paykel; D C Rubinsztein
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

Review 3.  Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases.

Authors:  A Brega; J Narula; E Arbustini
Journal:  J Nucl Cardiol       Date:  2001 Jan-Feb       Impact factor: 5.952

Review 4.  Disease-related versus polymorphic mutations in human mitochondrial tRNAs. Where is the difference?

Authors:  C Florentz; M Sissler
Journal:  EMBO Rep       Date:  2001-06       Impact factor: 8.807

5.  Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication.

Authors:  Y Wang; Y Michikawa; C Mallidis; Y Bai; L Woodhouse; K E Yarasheski; C A Miller; V Askanas; W K Engel; S Bhasin; G Attardi
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

6.  A compositional segmentation of the human mitochondrial genome is related to heterogeneities in the guanine mutation rate.

Authors:  David C Samuels; Richard J Boys; Daniel A Henderson; Patrick F Chinnery
Journal:  Nucleic Acids Res       Date:  2003-10-15       Impact factor: 16.971

Review 7.  Progressive myoclonic epilepsies: review of clinical, molecular and therapeutic aspects.

Authors:  Luis Felipe Mendonça de Siqueira
Journal:  J Neurol       Date:  2010-07-01       Impact factor: 4.849

8.  MITOP, the mitochondrial proteome database: 2000 update.

Authors:  C Scharfe; P Zaccaria; K Hoertnagel; M Jaksch; T Klopstock; M Dembowski; R Lill; H Prokisch; K D Gerbitz; W Neupert; H W Mewes; T Meitinger
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

9.  Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.

Authors:  Hui Zhao; Ronghua Li; Qiuju Wang; Qingfeng Yan; Jian-Hong Deng; Dongyi Han; Yidong Bai; Wie-Yen Young; Min-Xin Guan
Journal:  Am J Hum Genet       Date:  2003-12-12       Impact factor: 11.025

10.  MitoP2, an integrated database on mitochondrial proteins in yeast and man.

Authors:  C Andreoli; H Prokisch; K Hörtnagel; J C Mueller; M Münsterkötter; C Scharfe; T Meitinger
Journal:  Nucleic Acids Res       Date:  2004-01-01       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.