199 related articles for article (PubMed ID: 8138807)
1. Content of mutant mitochondrial DNA and organ dysfunction in a patient with a MELAS subgroup of mitochondrial encephalomyopathies.
Shiraiwa N; Ishii A; Iwamoto H; Mizusawa H; Kagawa Y; Ohta S
J Neurol Sci; 1993 Dec; 120(2):174-9. PubMed ID: 8138807
[TBL] [Abstract][Full Text] [Related]
2. Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
Shoji Y; Sato W; Hayasaka K; Takada G
J Inherit Metab Dis; 1993; 16(1):27-30. PubMed ID: 8487499
[TBL] [Abstract][Full Text] [Related]
3. Organ distribution of mutant mitochondrial tRNA(leu(UUR)) gene in a MELAS patient.
Hamazaki S; Koshiba M; Sugiyama T
Acta Pathol Jpn; 1993 Apr; 43(4):187-91. PubMed ID: 8493868
[TBL] [Abstract][Full Text] [Related]
4. Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function.
Hayashi J; Ohta S; Takai D; Miyabayashi S; Sakuta R; Goto Y; Nonaka I
Biochem Biophys Res Commun; 1993 Dec; 197(3):1049-55. PubMed ID: 8280119
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
Fabrizi GM; Cardaioli E; Grieco GS; Cavallaro T; Malandrini A; Manneschi L; Dotti MT; Federico A; Guazzi G
J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial diseases.
Nonaka I
Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
[TBL] [Abstract][Full Text] [Related]
8. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
Tokunaga M; Mita S; Sakuta R; Nonaka I; Araki S
Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
[TBL] [Abstract][Full Text] [Related]
9. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.
Chomyn A; Enriquez JA; Micol V; Fernandez-Silva P; Attardi G
J Biol Chem; 2000 Jun; 275(25):19198-209. PubMed ID: 10858457
[TBL] [Abstract][Full Text] [Related]
10. Sequencing and quantitative assessment of mutant and wild-type mitochondrial DNA in paraffin sections from cases of MELAS.
Love S; Nicoll JA; Kinrade E
J Pathol; 1993 May; 170(1):9-14. PubMed ID: 8326463
[TBL] [Abstract][Full Text] [Related]
11. mtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girl.
Topaloğlu H; Seyrantepe V; Kandemir N; Akçören Z; Ozgüç M
Pediatr Neurol; 1998 May; 18(5):429-31. PubMed ID: 9650685
[TBL] [Abstract][Full Text] [Related]
12. Temporal bone histopathological and quantitative analysis of mitochondrial DNA in MELAS.
Takahashi K; Merchant SN; Miyazawa T; Yamaguchi T; McKenna MJ; Kouda H; Iino Y; Someya T; Tamagawa Y; Takiyama Y; Nakano I; Saito K; Boyer P; Kitamura K
Laryngoscope; 2003 Aug; 113(8):1362-8. PubMed ID: 12897560
[TBL] [Abstract][Full Text] [Related]
13. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
Hammans SR; Sweeney MG; Hanna MG; Brockington M; Morgan-Hughes JA; Harding AE
Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089
[TBL] [Abstract][Full Text] [Related]
14. MELAS with the mitochondrial DNA 3243 point mutation: a neuropathological study.
Tanahashi C; Nakayama A; Yoshida M; Ito M; Mori N; Hashizume Y
Acta Neuropathol; 2000 Jan; 99(1):31-8. PubMed ID: 10651025
[TBL] [Abstract][Full Text] [Related]
15. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
Thajeb P; Lee HC; Pang CY; Jeng CM; Huang SF; Wei YH
Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
[TBL] [Abstract][Full Text] [Related]
16. Diabetes and mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): radiolabeled polymerase chain reaction is necessary for accurate detection of low percentages of mutation.
Smith ML; Hua XY; Marsden DL; Liu D; Kennaway NG; Ngo KY; Haas RH
J Clin Endocrinol Metab; 1997 Sep; 82(9):2826-31. PubMed ID: 9284704
[TBL] [Abstract][Full Text] [Related]
17. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
Liu CS; Cheng WL; Lee CF; Ma YS; Lin CY; Huang CC; Wei YH
Acta Neurol Scand; 2006 May; 113(5):334-41. PubMed ID: 16629770
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS-associated mtDNA mutations.
Gramegna LL; Evangelisti S; Di Vito L; La Morgia C; Maresca A; Caporali L; Amore G; Talozzi L; Bianchini C; Testa C; Manners DN; Cortesi I; Valentino ML; Liguori R; Carelli V; Tonon C; Lodi R
Ann Clin Transl Neurol; 2021 Jun; 8(6):1200-1211. PubMed ID: 33951347
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
Morgan-Hughes JA; Sweeney MG; Cooper JM; Hammans SR; Brockington M; Schapira AH; Harding AE; Clark JB
Biochim Biophys Acta; 1995 May; 1271(1):135-40. PubMed ID: 7599199
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
