254 related articles for article (PubMed ID: 15465027)
1. Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations.
Da Pozzo P; Cardaioli E; Radi E; Federico A
Biochem Biophys Res Commun; 2004 Nov; 324(1):360-4. PubMed ID: 15465027
[TBL] [Abstract][Full Text] [Related]
2. A collection of 33 novel human mtDNA homoplasmic variants.
Crimi M; Sciacco M; Galbiati S; Bordoni A; Malferrari G; Del Bo R; Biunno I; Bresolin N; Comi GP
Hum Mutat; 2002 Nov; 20(5):409. PubMed ID: 12402350
[TBL] [Abstract][Full Text] [Related]
3. 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; 2(9):e942. PubMed ID: 17895983
[TBL] [Abstract][Full Text] [Related]
4. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.
Kornblum C; Zsurka G; Wiesner RJ; Schröder R; Kunz WS
Biosci Rep; 2008 Apr; 28(2):89-96. PubMed ID: 18384291
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 17637808
[TBL] [Abstract][Full Text] [Related]
6. Surveyor Nuclease: a new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects.
Bannwarth S; Procaccio V; Paquis-Flucklinger V
Hum Mutat; 2005 Jun; 25(6):575-82. PubMed ID: 15880407
[TBL] [Abstract][Full Text] [Related]
7. Yield of mtDNA mutation analysis in 2,000 patients.
Liang MH; Wong LJ
Am J Med Genet; 1998 Jun; 77(5):395-400. PubMed ID: 9632169
[TBL] [Abstract][Full Text] [Related]
8. Detection of mitochondrial DNA mutations using temporal temperature gradient gel electrophoresis.
Wong LJ; Chen TJ; Tan DJ
Electrophoresis; 2004 Aug; 25(15):2602-10. PubMed ID: 15300781
[TBL] [Abstract][Full Text] [Related]
9. A novel mutation in the mitochondrial tRNA for tryptophan causing a late-onset mitochondrial encephalomyopathy.
Sanaker PS; Nakkestad HL; Downham E; Bindoff LA
Acta Neurol Scand; 2010 Feb; 121(2):109-13. PubMed ID: 19744136
[TBL] [Abstract][Full Text] [Related]
10. Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients.
Kocaefe YC; Erdem S; Ozgüç M; Tan E
Eur J Hum Genet; 2003 Jan; 11(1):102-4. PubMed ID: 12529715
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial encephalomyopathies: an update.
DiMauro S; Hirano M
Neuromuscul Disord; 2005 Apr; 15(4):276-86. PubMed ID: 15792866
[TBL] [Abstract][Full Text] [Related]
12. Novel heteroplasmic frameshift and missense somatic mitochondrial DNA mutations in oral cancer of betel quid chewers.
Tan DJ; Chang J; Chen WL; Agress LJ; Yeh KT; Wang B; Wong LJ
Genes Chromosomes Cancer; 2003 Jun; 37(2):186-94. PubMed ID: 12696067
[TBL] [Abstract][Full Text] [Related]
13. Evidence of apoptosis via TUNEL staining in muscle biopsy from patients with mitochondrial encephaloneuromyopathies.
Formichi P; Battisti C; Bianchi S; Cardaioli E; Federico A
J Submicrosc Cytol Pathol; 2003 Jan; 35(1):29-34. PubMed ID: 12762649
[TBL] [Abstract][Full Text] [Related]
14. Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome.
Ruppert V; Nolte D; Aschenbrenner T; Pankuweit S; Funck R; Maisch B
Biochem Biophys Res Commun; 2004 May; 318(2):535-43. PubMed ID: 15120634
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.
Hirano M; Nishigaki Y; Martí R
Neurologist; 2004 Jan; 10(1):8-17. PubMed ID: 14720311
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 15639196
[TBL] [Abstract][Full Text] [Related]
17. The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations.
Marin-Garcia J; Goldenthal MJ; Ananthakrishnan R; Pierpont ME
J Card Fail; 2000 Dec; 6(4):321-9. PubMed ID: 11145757
[TBL] [Abstract][Full Text] [Related]
18. A cystic fibrosis patient with two novel mutations in mitochondrial DNA: mild disease led to delayed diagnosis of both disorders.
Wong LJ; Liang MH; Kwon H; Bai RK; Alper O; Gropman A
Am J Med Genet; 2002 Nov; 113(1):59-64. PubMed ID: 12400067
[TBL] [Abstract][Full Text] [Related]
19. Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy.
Bannwarth S; Procaccio V; Rouzier C; Fragaki K; Poole J; Chabrol B; Desnuelle C; Pouget J; Azulay JP; Attarian S; Pellissier JF; Gargus JJ; Abdenur JE; Mozaffar T; Calvas P; Labauge P; Pages M; Wallace DC; Lambert JC; Paquis-Flucklinger V
Mitochondrion; 2008 Mar; 8(2):136-45. PubMed ID: 18078792
[TBL] [Abstract][Full Text] [Related]
20. Diagnosis of mitochondrial disease: assessment of mitochondrial DNA heteroplasmy in blood.
Taylor RW; Taylor GA; Morris CM; Edwardson JM; Turnbull DM
Biochem Biophys Res Commun; 1998 Oct; 251(3):883-7. PubMed ID: 9791004
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
