THE MUTANT MITOCHONDRIAL GENES IN MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS AND STROKE-LIKE EPISODES (MELAS) WERE SELECTIVELY AMPLIFIED THROUGH GENERATIONS

被引：25

作者：

KOBAYASHI, Y

ICHIHASHI, K

OHTA, S

NIHEI, K

KAGAWA, Y

YANAGISAWA, M

MOMOI, MY

机构：

[1] JICHI MED SCH,DEPT PEDIAT,MINAMI KAWACHI,TOCHIGI 32904,JAPAN

[2] NATL CHILDRENS HOSP,DEPT NEUROL,TOKYO 154,JAPAN

[3] JICHI MED SCH,DEPT BIOCHEM,MINAMI KAWACHI,TOCHIGI 32904,JAPAN

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1992年 / 15卷 / 05期

关键词：

D O I：

10.1007/BF01800025

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：803 / 808

页数：6

共 17 条

[1]

DAVIS LG, 1986, BASIC METHODS MOL BI, P44

[2] A MUTATION IN THE TRANSFER RNALEU(UUR) GENE ASSOCIATED WITH THE MELAS SUBGROUP OF MITOCHONDRIAL ENCEPHALOMYOPATHIES [J].

GOTO, Y ;

NONAKA, I ;

HORAI, S .

NATURE, 1990, 348 (6302) :651-653

[3] DELETIONS OF MUSCLE MITOCHONDRIAL-DNA IN PATIENTS WITH MITOCHONDRIAL MYOPATHIES [J].

HOLT, IJ ;

HARDING, AE ;

MORGANHUGHES, JA .

NATURE, 1988, 331 (6158) :717-719

[4] MITOCHONDRIAL MYOPATHIES - CLINICAL AND BIOCHEMICAL FEATURES OF 30 PATIENTS WITH MAJOR DELETIONS OF MUSCLE MITOCHONDRIAL-DNA [J].

HOLT, IJ ;

HARDING, AE ;

COOPER, JM ;

SCHAPIRA, AHV ;

TOSCANO, A ;

CLARK, JB ;

MORGANHUGHES, JA .

ANNALS OF NEUROLOGY, 1989, 26 (06) :699-708

[5] A POINT MUTATION IN THE MITOCHONDRIAL TRANSFER RNALEU(UUR) GENE IN MELAS (MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS AND STROKE-LIKE EPISODES) [J].

KOBAYASHI, Y ;

MOMOI, MY ;

TOMINAGA, K ;

MOMOI, T ;

NIHEI, K ;

YANAGISAWA, M ;

KAGAWA, Y ;

OHTA, S .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (03) :816-822

[6]

KOBAYASHI Y, 1991, AM J HUM GENET, V49, P590

[7] MELAS SYNDROME - CHARACTERISTIC MIGRAINOUS AND EPILEPTIC FEATURES AND MATERNAL TRANSMISSION [J].

MONTAGNA, P ;

GALLASSI, R ;

MEDORI, R ;

GOVONI, E ;

ZEVIANI, M ;

DIMAURO, S ;

LUGARESI, E ;

ANDERMANN, F .

NEUROLOGY, 1988, 38 (05) :751-754

[8] MITOCHONDRIAL-DNA DELETIONS IN PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND KEARNS-SAYRE SYNDROME [J].

MORAES, CT ;

DIMAURO, S ;

ZEVIANI, M ;

LOMBES, A ;

SHANSKE, S ;

MIRANDA, AF ;

NAKASE, H ;

BONILLA, E ;

WERNECK, LC ;

SERVIDEI, S ;

NONAKA, I ;

KOGA, Y ;

SPIRO, AJ ;

BROWNELL, AKW ;

SCHMIDT, B ;

SCHOTLAND, DL ;

ZUPANC, M ;

DEVIVO, DC ;

SCHON, EA ;

ROWLAND, LP .

NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (20) :1293-1299

[9] GENERATION OF HUMAN MYOGENIC CELL-LINES BY THE TRANSFORMATION OF PRIMARY CULTURE WITH ORIGIN-DEFECTIVE SV40 DNA [J].

NAKAMIGAWA, T ;

MOMOI, MY ;

MOMOI, T ;

YANAGISAWA, M .

JOURNAL OF THE NEUROLOGICAL SCIENCES, 1988, 83 (2-3) :305-319

[10] MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC-ACIDOSIS, AND STROKELIKE EPISODES - A DISTINCTIVE CLINICAL SYNDROME [J].

PAVLAKIS, SG ;

PHILLIPS, PC ;

DIMAURO, S ;

DEVIVO, DC ;

ROWLAND, LP .

ANNALS OF NEUROLOGY, 1984, 16 (04) :481-488

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