303 related articles for article (PubMed ID: 8582049)
21. No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.
Gerbitz KD; Paprotta A; Obermaier-Kusser B; Rietschel M; Zerres K
FEBS Lett; 1992 Dec; 314(3):251-5. PubMed ID: 1361456
[TBL] [Abstract][Full Text] [Related]
22. [Development of a DNA biochip for detection of known mtDNA mutations associated with MELAS and MERRF syndromes.].
Chen G; Li W; DU WD; Cao HM; Tang HY; Tang XF; Sun ZW; Zhao H; Jin QH; Zhao JL; Zhang XJ
Yi Chuan; 2008 Oct; 30(10):1279-86. PubMed ID: 18930887
[TBL] [Abstract][Full Text] [Related]
23. Molecular analysis of mitochondrial DNA point mutations by polymerase chain reaction.
Wong LJ; Cobb BR; Chen TJ
Methods Mol Biol; 2006; 336():135-43. PubMed ID: 16916259
[TBL] [Abstract][Full Text] [Related]
24. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
Jean-Francois MJ; Lertrit P; Berkovic SF; Crimmins D; Morris J; Marzuki S; Byrne E
Aust N Z J Med; 1994 Apr; 24(2):188-93. PubMed ID: 8042948
[TBL] [Abstract][Full Text] [Related]
25. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
Chinnery PF; Brown DT; Andrews RM; Singh-Kler R; Riordan-Eva P; Lindley J; Applegarth DA; Turnbull DM; Howell N
Brain; 2001 Jan; 124(Pt 1):209-18. PubMed ID: 11133798
[TBL] [Abstract][Full Text] [Related]
26. Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP.
Tanno Y; Yoneda M; Tanaka K; Tanaka H; Yamazaki M; Nishizawa M; Wakabayashi K; Ohama E; Tsuji S
Muscle Nerve; 1995 Dec; 18(12):1390-7. PubMed ID: 7477061
[TBL] [Abstract][Full Text] [Related]
27. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T
Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
[TBL] [Abstract][Full Text] [Related]
28. Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.
Pang CY; Huang CC; Yen MY; Wang EK; Kao KP; Chen SS; Wei YH
J Formos Med Assoc; 1999 May; 98(5):326-34. PubMed ID: 10420700
[TBL] [Abstract][Full Text] [Related]
29. Identifying allogeneic platelets by resolution of point mutations in mitochondrial DNA using single-stranded conformational polymorphism PCR.
Garritsen HS; Hellenkamp F; Hoerning A; Mittmann K; Sibrowski W
Transfusion; 2001 Dec; 41(12):1531-8. PubMed ID: 11778068
[TBL] [Abstract][Full Text] [Related]
30. The expanding clinical spectrum of mitochondrial diseases.
De Vivo DC
Brain Dev; 1993; 15(1):1-22. PubMed ID: 8338207
[TBL] [Abstract][Full Text] [Related]
31. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
Pénisson-Besnier I; Moreau C; Jacques C; Roger JC; Dubas F; Reynier P
Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
[TBL] [Abstract][Full Text] [Related]
32. Molecular epidemiology of childhood mitochondrial encephalomyopathies in a Finnish population: sequence analysis of entire mtDNA of 17 children reveals heteroplasmic mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) genes.
Uusimaa J; Finnilä S; Remes AM; Rantala H; Vainionpää L; Hassinen IE; Majamaa K
Pediatrics; 2004 Aug; 114(2):443-50. PubMed ID: 15286228
[TBL] [Abstract][Full Text] [Related]
33. The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS.
Pulkes T; Eunson L; Patterson V; Siddiqui A; Wood NW; Nelson IP; Morgan-Hughes JA; Hanna MG
Ann Neurol; 1999 Dec; 46(6):916-9. PubMed ID: 10589546
[TBL] [Abstract][Full Text] [Related]
34. Screening for mutations by RNA single-strand conformation polymorphism (rSSCP): comparison with DNA-SSCP.
Sarkar G; Yoon HS; Sommer SS
Nucleic Acids Res; 1992 Feb; 20(4):871-8. PubMed ID: 1371869
[TBL] [Abstract][Full Text] [Related]
35. Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy.
Houshmand M; Larsson NG; Holme E; Oldfors A; Tulinius MH; Andersen O
Biochim Biophys Acta; 1994 Apr; 1226(1):49-55. PubMed ID: 8155739
[TBL] [Abstract][Full Text] [Related]
36. Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations.
Fauser S; Luberichs J; Besch D; Leo-Kottler B
Biochem Biophys Res Commun; 2002 Jul; 295(2):342-7. PubMed ID: 12150954
[TBL] [Abstract][Full Text] [Related]
37. Mitochondrial diseases.
Nonaka I
Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
[TBL] [Abstract][Full Text] [Related]
38. The detection of mitochondrial DNA mutations using single stranded conformation polymorphism (SSCP) analysis and heteroduplex analysis.
Thomas AW; Morgan R; Sweeney M; Rees A; Alcolado J
Hum Genet; 1994 Dec; 94(6):621-3. PubMed ID: 7989037
[TBL] [Abstract][Full Text] [Related]
39. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
Seibel P; Flierl A; Kottlors M; Reichmann H
Biochem Biophys Res Commun; 1994 Apr; 200(2):938-42. PubMed ID: 8179630
[TBL] [Abstract][Full Text] [Related]
40. Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.
Qi Y; Zhang Y; Wang Z; Yang Y; Yuan Y; Niu S; Pei P; Wang S; Ma Y; Bu D; Zou L; Fang F; Xiao J; Sun F; Zhang Y; Wu Y; Wang S; Xiong H; Wu X
Mitochondrion; 2007; 7(1-2):147-50. PubMed ID: 17276742
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]