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Items: 1 to 20 of 91

1.

MitoBreak: the mitochondrial DNA breakpoints database.

Damas J, Carneiro J, Amorim A, Pereira F.

Nucleic Acids Res. 2014 Jan;42(Database issue):D1261-8. doi: 10.1093/nar/gkt982. Epub 2013 Oct 28.

2.

Mitochondrial DNA rearrangements in health and disease--a comprehensive study.

Damas J, Samuels DC, Carneiro J, Amorim A, Pereira F.

Hum Mutat. 2014 Jan;35(1):1-14. doi: 10.1002/humu.22452. Epub 2013 Oct 18. Review.

PMID:
24115352
3.

Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

Lakshmanan LN, Gruber J, Halliwell B, Gunawan R.

PLoS One. 2012;7(4):e35271. doi: 10.1371/journal.pone.0035271. Epub 2012 Apr 18.

4.

Mitochondrial DNA deletions are associated with non-B DNA conformations.

Damas J, Carneiro J, Gonçalves J, Stewart JB, Samuels DC, Amorim A, Pereira F.

Nucleic Acids Res. 2012 Sep;40(16):7606-21. doi: 10.1093/nar/gks500. Epub 2012 May 31.

5.

An enhanced MITOMAP with a global mtDNA mutational phylogeny.

Ruiz-Pesini E, Lott MT, Procaccio V, Poole JC, Brandon MC, Mishmar D, Yi C, Kreuziger J, Baldi P, Wallace DC.

Nucleic Acids Res. 2007 Jan;35(Database issue):D823-8. Epub 2006 Dec 18.

6.

MitoLSDB: a comprehensive resource to study genotype to phenotype correlations in human mitochondrial DNA variations.

K S, Jalali S, Scaria V, Bhardwaj A.

PLoS One. 2013 Apr 9;8(4):e60066. doi: 10.1371/journal.pone.0060066. Print 2013.

7.

dbCRID: a database of chromosomal rearrangements in human diseases.

Kong F, Zhu J, Wu J, Peng J, Wang Y, Wang Q, Fu S, Yuan LL, Li T.

Nucleic Acids Res. 2011 Jan;39(Database issue):D895-900. doi: 10.1093/nar/gkq1038. Epub 2010 Nov 4.

8.

SyStemCell: a database populated with multiple levels of experimental data from stem cell differentiation research.

Yu J, Xing X, Zeng L, Sun J, Li W, Sun H, He Y, Li J, Zhang G, Wang C, Li Y, Xie L.

PLoS One. 2012;7(7):e35230. doi: 10.1371/journal.pone.0035230. Epub 2012 Jul 13.

9.

Mitochondrial DNA alterations as ageing-associated molecular events.

Wei YH.

Mutat Res. 1992 Sep;275(3-6):145-55. Review.

PMID:
1383757
11.

YOGY: a web-based, integrated database to retrieve protein orthologs and associated Gene Ontology terms.

Penkett CJ, Morris JA, Wood V, Bähler J.

Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W330-4.

12.

Accumulation of deleted mitochondrial DNA in aging Drosophila melanogaster.

Yui R, Ohno Y, Matsuura ET.

Genes Genet Syst. 2003 Jun;78(3):245-51.

13.

Toward a mtDNA locus-specific mutation database using the LOVD platform.

Elson JL, Sweeney MG, Procaccio V, Yarham JW, Salas A, Kong QP, van der Westhuizen FH, Pitceathly RD, Thorburn DR, Lott MT, Wallace DC, Taylor RW, McFarland R.

Hum Mutat. 2012 Sep;33(9):1352-8. doi: 10.1002/humu.22118. Epub 2012 Jul 2.

14.
15.

Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease.

Nicholls TJ, Zsurka G, Peeva V, Schöler S, Szczesny RJ, Cysewski D, Reyes A, Kornblum C, Sciacco M, Moggio M, Dziembowski A, Kunz WS, Minczuk M.

Hum Mol Genet. 2014 Dec 1;23(23):6147-62. doi: 10.1093/hmg/ddu336. Epub 2014 Jun 30.

16.

Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acid.

Tengan CH, Kiyomoto BH, Rocha MS, Tavares VL, Gabbai AA, Moraes CT.

J Clin Endocrinol Metab. 1998 Jan;83(1):125-9. Review.

PMID:
9435428
17.

Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints.

Dong DW, Pereira F, Barrett SP, Kolesar JE, Cao K, Damas J, Yatsunyk LA, Johnson FB, Kaufman BA.

BMC Genomics. 2014 Aug 13;15:677. doi: 10.1186/1471-2164-15-677.

18.

Animal models for mitochondrial disease.

Wallace DC.

Methods Mol Biol. 2002;197:3-54. Review.

PMID:
12013805
19.

Mitochondrial DNA mutations in disease and aging.

Wallace DC.

Environ Mol Mutagen. 2010 Jun;51(5):440-50. doi: 10.1002/em.20586. Review.

PMID:
20544884
20.

MitoRes: a resource of nuclear-encoded mitochondrial genes and their products in Metazoa.

Catalano D, Licciulli F, Turi A, Grillo G, Saccone C, D'Elia D.

BMC Bioinformatics. 2006 Jan 24;7:36.

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