INSULIN SENSITIVITY IN PATIENTS WITH NIDDM AND THE A-TO-G MUTATION AT NUCLEOTIDE-3,243 OF THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE

被引：3
|
作者：
IWASAKI, N [1 ]
WASADA, T [1 ]
TAKAHASHI, Y [1 ]
BABAZONO, T [1 ]
OHGAWARA, H [1 ]
OMORI, Y [1 ]
机构：
[1] TOKYO WOMENS MED COLL,MED RES INST,TOKYO 162,JAPAN
来源：
DIABETES CARE | 1995年 / 18卷 / 06期
关键词：
D O I：
10.2337/diacare.18.6.886b
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：886 / 888
页数：3
相关论文
共 50 条
  • [41] Insulin resistance in patients with the mitochondrial tRNALeu(UUR) gene mutation at position 3243
    Becker, R
    Laube, H
    Linn, T
    Damian, MS
    EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2002, 110 (06) : 291 - 297
  • [42] The expanding clinical phenotype of the tRNA(Leu(UUR)) A->G mutation at np 3243 of mitochondrial DNA: Diabetic embryopathy associated with mitochondrial cytopathy
    Feigenbaum, A
    Chitayat, D
    Robinson, B
    MacGregor, D
    Myint, T
    Arbus, G
    Nowaczyk, MJM
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 62 (04): : 404 - 409
  • [43] Overexpressed mitochondrial leucyl-tRNA synthetase suppresses the A3243G mutation in the mitochondrial tRNALeu(UUR) gene
    Park, Hyejeong
    Davidson, Edgar
    King, Michael P.
    RNA, 2008, 14 (11) : 2407 - 2416
  • [44] High prevalence of mitochondrial tRNA Leu(UUR) mutation at position 3243 in the diabetic patients with painful or posttreatment polyneuropathy in Japanese
    Suzuki, S
    Hinokio, Y
    Hirai, M
    Oka, Y
    DIABETES, 2004, 53 : A214 - A215
  • [45] THE MITOCHONDRIAL TRNA(LEU(UUR)) MUTATION AT NT-3243 IS ASSOCIATED WITH MITOCHONDRIAL PROLIFERATION AND ABNORMAL PROCESSING IN TISSUES FROM MELAS PATIENTS
    KAUFMANN, P
    KOGA, Y
    HIRANO, M
    KING, MP
    DIMAURO, S
    SCHON, EA
    ANNALS OF NEUROLOGY, 1994, 36 (02) : 317 - 317
  • [46] EXTRA-PANCREATIC MANIFESTATIONS IN DIABETES SECONDARY TO MITOCHONDRIAL-DNA POINT MUTATION WITHIN THE TRNA(LEU(UUR)) GENE
    VIALETTES, B
    PAQUISFLUCKINGER, V
    SILVESTREAILLAUD, P
    BENDAHAN, D
    PELISSIER, JF
    ETCHARYBOUYX, F
    RACCAH, D
    GIN, H
    GUILLAUSSEAU, PJ
    VANUXEN, D
    ORSINI, F
    POUGET, J
    COZZONE, P
    DESNUELLE, C
    DIABETES CARE, 1995, 18 (07) : 1023 - 1028
  • [47] Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNALys
    Kameoka, K
    Isotani, H
    Tanaka, K
    Kitaoka, H
    Ohsawa, N
    DIABETES CARE, 1998, 21 (11) : 2034 - 2035
  • [48] MATERNALLY INHERITED DIABETES AND DEAFNESS (MIDD) - A DISTINCT SUBTYPE OF DIABETES-ASSOCIATED WITH A MITOCHONDRIAL TRNA(LEU(UUR)) GENE POINT MUTATION
    VANDENOUWELAND, JMW
    LEMKES, HHPJ
    GERBITZ, KD
    MAASSEN, JA
    MUSCLE & NERVE, 1995, : S124 - S130
  • [49] MATERNALLY INHERITED DIABETES AND DEAFNESS IS A DISTINCT SUBTYPE OF DIABETES AND ASSOCIATES WITH A SINGLE-POINT MUTATION IN THE MITOCHONDRIAL TRNA(LEU(UUR)) GENE
    VANDENOUWELAND, JMW
    LEMKES, HHPJ
    TREMBATH, RC
    ROSS, R
    VELHO, G
    COHEN, D
    FROGUEL, P
    MAASSEN, JA
    DIABETES, 1994, 43 (06) : 746 - 751
  • [50] beta-cell loss and glucose induced signalling defects in diabetes mellitus caused by mitochondrial tRNA(Leu)(UUR) gene mutation
    Oka, Y
    Katagiri, H
    Ishihara, H
    Asano, T
    Kobayashi, T
    Kikuchi, M
    DIABETIC MEDICINE, 1996, 13 (09) : S98 - S102
12345