SCOPUS 정보 검색 플랫폼

Volumn 38, Issue 10, 2001, Pages 703-705

Functional characterisation of mitochondrial tRNATyr mutation (5877G→A) associated with familial chronic progressive external ophthalmoplegia [4]

(5) Sahashi, K a Yoneda, M a Ohno, K a Tanaka, M a Ibi, T a

a AICHI MEDICAL UNIVERSITY SCHOOL OF MEDICINE (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL RNA; TRANSFER RNA;

ADULT; AMINO ACID SUBSTITUTION; CASE REPORT; CHRONIC DISEASE; CLINICAL FEATURE; DNA DETERMINATION; DNA SEQUENCE; FAMILIAL DISEASE; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; LETTER; MITOCHONDRION; OPHTHALMOPLEGIA; PHENOTYPE; PRIORITY JOURNAL; RNA STRUCTURE;

ADULT; BASE SEQUENCE; CELL SURVIVAL; CELLS, CULTURED; DNA MUTATIONAL ANALYSIS; ELECTRON TRANSPORT; FEMALE; FIBROBLASTS; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MITOCHONDRIA, MUSCLE; MUSCLES; MUTATION; NUCLEIC ACID CONFORMATION; OPHTHALMOPLEGIA, CHRONIC PROGRESSIVE EXTERNAL; OXYGEN; OXYGEN CONSUMPTION; PHENOTYPE; RNA; RNA, TRANSFER, TYR;

EID: 0034796328 PISSN: 00222593 EISSN: None Source Type: Journal
DOI: None Document Type: Letter

Times cited : (12)

References (11)

1
- 0021798888
- Mitochondrial myopathies
- (1985) Ann Neurol , vol.17 , pp. 521-538
- DiMauro, S.¹ Bonilla, E.² Zeviani, M.³ Nakagawa, M.⁴ DeVivo, D.C.⁵

2
- 0025931788
- Neurological disorders due to mutations of the mitochondrial genome
- (1991) Neuromusc Disord , vol.1 , pp. 165-172
- Zeviani, M.¹ DiDonato, S.²

3
- 0030679561
- A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn)
- (1997) Mol Cell Biol , vol.17 , pp. 6831-6837
- Hao, H.¹ Moraes, C.T.²

4
- 0029086910
- Extensive tissue oxygenation associated with mitochondrial DNA mutations
- (1995) Biochem Biophys Res Commun , vol.213 , pp. 432-438
- Ozawa, T.¹ Sahashi, K.² Nakase, Y.³ Chance, B.⁴

5
- 0021940365
- 10 in Kearns-Sayre syndrome
- (1985) Neurology , vol.35 , pp. 372-377
- Ogasahara, S.¹ Yorifuji, S.² Nishikawa, Y.³ Takahashi, M.⁴ Wada, K.⁵ Hazama, T.⁶ Nakamura, Y.⁷ Hashimoto, S.⁸ Kono, N.⁹ Tarui, S.¹⁰

6
- 0016146021
- Three-dimensional tertiary structure of yeast phenylalanine transfer RNA
- (1974) Science , vol.185 , pp. 435-440
- Kim, S.H.¹ Suddath, F.L.² Quigley, G.J.³ McPherson, A.⁴ Sussman, J.L.⁵ Wang, A.H.⁶ Seeman, N.C.⁷ Rich, A.⁸

7
- 0026457825
- Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
- (1992) Proc Natl Acad Sci USA , vol.89 , pp. 11164-11168
- Yoneda, M.¹ Chomyn, A.² Martinuzzi, A.³ Hurko, O.⁴ Attardi, G.⁵

8
- 0031668586
- Peroxide production and apoptosis in cultured cells carrying mtDNA mutation causing encephalomyopathy
- (1998) Biochem Mol Biol Int , vol.46 , pp. 71-79
- Zhang, J.¹ Yoneda, M.² Naruse, K.³ Borgeld, H.J.⁴ Gong, J.S.⁵ Obata, S.⁶ Tanaka, M.⁷ Yagi, K.⁸

9
- 0027991050
- Free radicals and antioxidants: A personal view
- (1994) Nutr Rev , vol.52 , pp. 253-265
- Halliwell, B.¹

10
- 0026608057
- MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
- (1992) Proc Natl Acad Sci USA , vol.89 , pp. 4221-4225
- Chomyn, A.¹ Martinuzzi, A.² Yoneda, M.³ Daga, A.⁴ Hurko, O.⁵ Johns, D.⁶ Lai, S.T.⁷ Nonaka, I.⁸ Angelini, C.⁹ Attardi, G.¹⁰

11
- 0025666322
- Leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathy
- (1990) Nature , vol.348 , pp. 651-653
- Goto, Y.¹ Nonaka, I.² Horai, S.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.