PubMed

Next generation sequence analysis for mitochondrial disorders.

Vasta V, Ng SB, Turner EH, Shendure J, Hahn SH.

Genome Med. 2009 Oct 23;1(10):100.PMID: 19852779 [PubMed - in process]Free PMC ArticleFree textRelated citations

Mitochondrial DNA Variant Discovery and Evaluation in Human Cardiomyopathies through Next-Generation Sequencing.

Zaragoza MV, Fass J, Diegoli M, Lin D, Arbustini E.

PLoS One. 2010 Aug 20;5(8). pii: e12295.PMID: 20808834 [PubMed - in process]Related citations

Facile whole mitochondrial genome resequencing from nipple aspirate fluid using MitoChip v2.0.

Jakupciak JP, Maggrah A, Maragh S, Maki J, Reguly B, Maki K, Wittock R, Robinson K, Wagner PD, Thayer RE, Gehman K, Gehman T, Srivastava S, Ngom A, Dakubo GD, Parr RL.

BMC Cancer. 2008 Apr 10;8:95.PMID: 18402686 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Performance of mitochondrial DNA mutations detecting early stage cancer.

Jakupciak JP, Maragh S, Markowitz ME, Greenberg AK, Hoque MO, Maitra A, Barker PE, Wagner PD, Rom WN, Srivastava S, Sidransky D, O'Connell CD.

BMC Cancer. 2008 Oct 3;8:285.PMID: 18834532 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Quantitation of heteroplasmy of mtDNA sequence variants identified in a population of AD patients and controls by array-based resequencing.

Coon KD, Valla J, Szelinger S, Schneider LE, Niedzielko TL, Brown KM, Pearson JV, Halperin R, Dunckley T, Papassotiropoulos A, Caselli RJ, Reiman EM, Stephan DA.

Mitochondrion. 2006 Aug;6(4):194-210. Epub 2006 Jul 21.PMID: 16920408 [PubMed - indexed for MEDLINE]Related citations

Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.

Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, Obstoy MF, Dollfus H, Eliot MM, Faivre L, Duvillard C, Couderc R, Garabedian EN, Petit C, Feldmann D, Denoyelle F.

Eur J Hum Genet. 2007 Nov;15(11):1145-55. Epub 2007 Jul 18.PMID: 17637808 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

Comprehensive molecular diagnosis of mitochondrial disorders: qualitative and quantitative approach.

Wong LJ.

Ann N Y Acad Sci. 2004 Apr;1011:246-58.PMID: 15126301 [PubMed - indexed for MEDLINE]Related citations

Mitochondrial DNA mutations in pancreatic cancer.

Kassauei K, Habbe N, Mullendore ME, Karikari CA, Maitra A, Feldmann G.

Int J Gastrointest Cancer. 2006;37(2-3):57-64.PMID: 17827523 [PubMed - in process]Related citations

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.PMID: 19728970 [PubMed - indexed for MEDLINE]Related citations

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing.

Lee H, O'Connor BD, Merriman B, Funari VA, Homer N, Chen Z, Cohn DH, Nelson SF.

BMC Genomics. 2009 Dec 31;10:646.PMID: 20043857 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography.

Biggin A, Henke R, Bennetts B, Thorburn DR, Christodoulou J.

Mol Genet Metab. 2005 Jan;84(1):61-74. Epub 2004 Nov 11.PMID: 15639196 [PubMed - indexed for MEDLINE]Related citations

[Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes]

Zhang DL, Ji L, Li YD.

Yi Chuan Xue Bao. 2004 May;31(5):431-43. Chinese. PMID: 15478601 [PubMed - indexed for MEDLINE]Related citations

DNA sequence capture and enrichment by microarray followed by next-generation sequencing for targeted resequencing: neurofibromatosis type 1 gene as a model.

Chou LS, Liu CS, Boese B, Zhang X, Mao R.

Clin Chem. 2010 Jan;56(1):62-72. Epub 2009 Nov 12.PMID: 19910506 [PubMed - indexed for MEDLINE]Related citations

Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes.

Li M, Schönberg A, Schaefer M, Schroeder R, Nasidze I, Stoneking M.

Am J Hum Genet. 2010 Aug 13;87(2):237-49.PMID: 20696290 [PubMed - indexed for MEDLINE]Related citations

Current molecular diagnostic algorithm for mitochondrial disorders.

Wong LJ, Scaglia F, Graham BH, Craigen WJ.

Mol Genet Metab. 2010 Jun;100(2):111-7. Epub 2010 Mar 4. Review.PMID: 20359921 [PubMed - indexed for MEDLINE]Related citations

Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.

Marotta R, Chin J, Quigley A, Katsabanis S, Kapsa R, Byrne E, Collins S.

Intern Med J. 2004 Jan-Feb;34(1-2):10-9.PMID: 14748908 [PubMed - indexed for MEDLINE]Related citations

Analysis of mitochondrial DNA sequences in childhood encephalomyopathies reveals new disease-associated variants.

Wani AA, Ahanger SH, Bapat SA, Rangrez AY, Hingankar N, Suresh CG, Barnabas S, Patole MS, Shouche YS.

PLoS One. 2007 Sep 26;2(9):e942.PMID: 17895983 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

[DNA diagnosis in the age of individual made-to-order medications]

Mashima Y.

Nippon Ganka Gakkai Zasshi. 2004 Dec;108(12):863-85; discussion 886. Review. Japanese. PMID: 15656090 [PubMed - indexed for MEDLINE]Related citations

Screening for mitochondrial DNA (mtDNA) point mutations using nonradioactive single strand conformation polymorphism (SSCP) analysis.

Jaksch M, Gerbitz KD, Kilger C.

Clin Biochem. 1995 Oct;28(5):503-9.PMID: 8582049 [PubMed - indexed for MEDLINE]Related citations

Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.

van Eijsden RG, Gerards M, Eijssen LM, Hendrickx AT, Jongbloed RJ, Wokke JH, Hintzen RQ, Rubio-Gozalbo ME, De Coo IF, Briem E, Tiranti V, Smeets HJ.

Genet Med. 2006 Oct;8(10):620-7.PMID: 17079878 [PubMed - indexed for MEDLINE]Related citations