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Items: 1 to 20 of 32

1.

Rebooting the human mitochondrial phylogeny: an automated and scalable methodology with expert knowledge.

Blanco R, Mayordomo E, Montoya J, Ruiz-Pesini E.

BMC Bioinformatics. 2011 May 19;12:174. doi: 10.1186/1471-2105-12-174.

2.

Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva.

Bartoletti-Stella A, Salfi NC, Ceccarelli C, Attimonelli M, Romeo G, Gasparre G.

Arch Ophthalmol. 2011 May;129(5):664-6. doi: 10.1001/archophthalmol.2011.95. No abstract available.

PMID:
21555623
3.

DNA repair deficiency in neurodegeneration.

Jeppesen DK, Bohr VA, Stevnsner T.

Prog Neurobiol. 2011 Jul;94(2):166-200. doi: 10.1016/j.pneurobio.2011.04.013. Epub 2011 Apr 30. Review.

4.

Placing mitochondrial DNA mutations within the progression model of type I endometrial carcinoma.

Guerra F, Kurelac I, Cormio A, Zuntini R, Amato LB, Ceccarelli C, Santini D, Cormio G, Fracasso F, Selvaggi L, Resta L, Attimonelli M, Gadaleta MN, Gasparre G.

Hum Mol Genet. 2011 Jun 15;20(12):2394-405. doi: 10.1093/hmg/ddr146. Epub 2011 Apr 5.

PMID:
21470976
5.

Parkinson's syndrome and Parkinson's disease in mitochondrial disorders.

Finsterer J.

Mov Disord. 2011 Apr;26(5):784-91. doi: 10.1002/mds.23651. Epub 2011 Mar 7. Review.

PMID:
21384429
6.

The International Nucleotide Sequence Database Collaboration.

Cochrane G, Karsch-Mizrachi I, Nakamura Y; International Nucleotide Sequence Database Collaboration.

Nucleic Acids Res. 2011 Jan;39(Database issue):D15-8. doi: 10.1093/nar/gkq1150. Epub 2010 Nov 23.

7.

MitoTool: a web server for the analysis and retrieval of human mitochondrial DNA sequence variations.

Fan L, Yao YG.

Mitochondrion. 2011 Mar;11(2):351-6. doi: 10.1016/j.mito.2010.09.013. Epub 2010 Oct 7.

PMID:
20933105
8.

Clinical features and pathogenesis of Alzheimer's disease: involvement of mitochondria and mitochondrial DNA.

Mancuso M, Orsucci D, LoGerfo A, Calsolaro V, Siciliano G.

Adv Exp Med Biol. 2010;685:34-44. Review.

PMID:
20687493
9.

Late-onset Leber hereditary optic neuropathy mimicking Susac's syndrome.

Zoccolella S, Petruzzella V, Prascina F, Artuso L, Pacillo F, Dell'Aglio R, Avolio C, Delle Noci N, Attimonelli M, Specchio LM.

J Neurol. 2010 Dec;257(12):1999-2003. doi: 10.1007/s00415-010-5649-6. Epub 2010 Jul 15.

PMID:
20632027
10.

The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization.

Porcelli AM, Ghelli A, Ceccarelli C, Lang M, Cenacchi G, Capristo M, Pennisi LF, Morra I, Ciccarelli E, Melcarne A, Bartoletti-Stella A, Salfi N, Tallini G, Martinuzzi A, Carelli V, Attimonelli M, Rugolo M, Romeo G, Gasparre G.

Hum Mol Genet. 2010 Mar 15;19(6):1019-32. doi: 10.1093/hmg/ddp566. Epub 2009 Dec 22.

PMID:
20028790
11.

mtDNA data mining in GenBank needs surveying.

Yao YG, Salas A, Logan I, Bandelt HJ.

Am J Hum Genet. 2009 Dec;85(6):929-33; author reply 933. doi: 10.1016/j.ajhg.2009.10.023. No abstract available.

12.

SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building.

Gouy M, Guindon S, Gascuel O.

Mol Biol Evol. 2010 Feb;27(2):221-4. doi: 10.1093/molbev/msp259. Epub 2009 Oct 23.

PMID:
19854763
13.

Evaluating the mitochondrial timescale of human evolution.

Endicott P, Ho SY, Metspalu M, Stringer C.

Trends Ecol Evol. 2009 Sep;24(9):515-21. doi: 10.1016/j.tree.2009.04.006. Epub 2009 Aug 12. Review.

PMID:
19682765
14.

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm.

Kumar P, Henikoff S, Ng PC.

Nat Protoc. 2009;4(7):1073-81. doi: 10.1038/nprot.2009.86. Epub 2009 Jun 25.

PMID:
19561590
15.

The diversity present in 5140 human mitochondrial genomes.

Pereira L, Freitas F, Fernandes V, Pereira JB, Costa MD, Costa S, Máximo V, Macaulay V, Rocha R, Samuels DC.

Am J Hum Genet. 2009 May;84(5):628-40. doi: 10.1016/j.ajhg.2009.04.013. Epub 2009 May 7.

16.

Multiple alignment of DNA sequences with MAFFT.

Katoh K, Asimenos G, Toh H.

Methods Mol Biol. 2009;537:39-64. doi: 10.1007/978-1-59745-251-9_3.

PMID:
19378139
17.

EMPOP--a forensic mtDNA database.

Parson W, Dür A.

Forensic Sci Int Genet. 2007 Jun;1(2):88-92. doi: 10.1016/j.fsigen.2007.01.018. Epub 2007 Mar 7.

PMID:
19083735
18.

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation.

van Oven M, Kayser M.

Hum Mutat. 2009 Feb;30(2):E386-94. doi: 10.1002/humu.20921.

PMID:
18853457
19.

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.

20.

High penetrance of sequencing errors and interpretative shortcomings in mtDNA sequence analysis of LHON patients.

Bandelt HJ, Yao YG, Salas A, Kivisild T, Bravi CM.

Biochem Biophys Res Commun. 2007 Jan 12;352(2):283-91. Epub 2006 Nov 3.

PMID:
17123466

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