THE D90A MUTATION RESULTS IN A POLYMORPHISM OF CU,ZN SUPEROXIDE-DISMUTASE THAT IS PREVALENT IN NORTHERN SWEDEN AND FINLAND

被引:38
|
作者
SJALANDER, A
BECKMAN, G
DENG, HX
IQBAL, Z
TAINER, JA
SIDDIQUE, T
机构
[1] NORTHWESTERN UNIV, SCH MED, DEPT NEUROL, CHICAGO, IL 60611 USA
[2] NORTHWESTERN UNIV, SCH MED, DEPT CELL & MOLEC BIOL, CHICAGO, IL 60611 USA
[3] NORTHWESTERN UNIV, SCH MED, INST NEUROSCI, CHICAGO, IL 60611 USA
[4] SCRIPPS RES INST, DEPT MOLEC BIOL, LA JOLLA, CA 92037 USA
关键词
D O I
10.1093/hmg/4.6.1105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:1105 / 1108
页数:4
相关论文
共 35 条
  • [21] The physiological basis of conduction slowing in amyotrophic lateral sclerosis patients homozygous for the autosomal recessive D90A copper/Zinc superoxide dismutase mutation
    Weber, M
    Eisen, A
    Stewart, HG
    Andersen, PM
    Hirota, N
    ANNALS OF NEUROLOGY, 2000, 48 (03) : 470 - 470
  • [22] VARIANCE OF AGE AT ONSET IN A JAPANESE FAMILY WITH AMYOTROPHIC-LATERAL-SCLEROSIS ASSOCIATED WITH A NOVEL CU/ZN SUPEROXIDE-DISMUTASE MUTATION
    AOKI, M
    ABE, K
    HOUI, K
    OGASAWARA, M
    MATSUBARA, Y
    KOBAYASHI, T
    MOCHIO, S
    NARISAWA, K
    ITOYAMA, Y
    ANNALS OF NEUROLOGY, 1995, 37 (05) : 676 - 679
  • [23] VARIABLE CLINICAL SYMPTOMS IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS WITH A NOVEL POINT MUTATION IN THE CU/ZN SUPEROXIDE-DISMUTASE GENE
    IKEDA, M
    ABE, K
    AOKI, M
    SAHARA, M
    WATANABE, M
    SHOJI, M
    STGEORGEHYSLOP, PH
    HIRAI, S
    ITOYAMA, Y
    NEUROLOGY, 1995, 45 (11) : 2038 - 2042
  • [24] Mutation-dependent Polymorphism of Cu,Zn-Superoxide Dismutase Aggregates in the Familial Form of Amyotrophic Lateral Sclerosis
    Furukawa, Yoshiaki
    Kaneko, Kumi
    Yamanaka, Koji
    Nukina, Nobuyuki
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (29) : 22221 - 22231
  • [26] A HOMOZYGOUS MUTATION DETECTED IN EXON-4 OF THE CU,ZN SUPEROXIDE-DISMUTASE GENE ASSOCIATED WITH FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS
    DENG, G
    DENG, HX
    ALSTON, S
    CAMPBELL, W
    KAPLAN, J
    ZU, J
    CALIENDO, J
    HUNG, WY
    SIDDIQUE, T
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1912 - 1912
  • [27] CuZn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala (D90A) mutation and novel rare polymorphism IVS3+35 A>C
    Slominsky, Petr A.
    Shadrina, Marya I.
    Kondratyeva, Ekaterina A.
    Tupitsina, Tatiana V.
    Levitsky, Gleb N.
    Skvortsova, Veronika I.
    Limborska, Svetlana A.
    HUMAN MUTATION, 2000, 16 (03) : 277 - 278
  • [28] Asp90Ala (A90D) mutation and novel rare normal polymorphism IVS3+35 AC in Cu-Zn superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia.
    Slominsky, PA
    Shadrina, MI
    Kondratyeva, EA
    Tupitsina, TV
    Levitsky, GN
    Skvortsova, VI
    Limborska, SA
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 341 - 341
  • [29] EVOLUTIONARY CONSERVATIVENESS OF ELECTRIC-FIELD IN THE CU,ZN SUPEROXIDE-DISMUTASE ACTIVE-SITE - EVIDENCE FOR COORDINATED MUTATION OF CHARGED AMINO-ACID-RESIDUES
    DESIDERI, A
    FALCONI, M
    POLTICELLI, F
    BOLOGNESI, M
    DJINOVIC, K
    ROTILIO, G
    JOURNAL OF MOLECULAR BIOLOGY, 1992, 223 (01) : 337 - 342
  • [30] AMPLIFICATION OF D-IMMITIS CDNA WITH AN ONCHOCERCA-VOLVULUS SPLICED LEADER PRIMER IDENTIFIES 2 PUTATIVE CU/ZN SUPEROXIDE-DISMUTASE CDNAS
    JAMES, ER
    MCLEAN, DL
    PERLER, FB
    MCREYNOLDS, LA
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, : 115 - 115