MOLECULAR-GENETICS OF NEUROLOGICAL DISEASES

被引:40
作者
MARTIN, JB
机构
[1] University of California, San Francisco, San Francisco, CA 94143-0402
关键词
D O I
10.1126/science.8235586
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
[No abstract available]
引用
收藏
页码:674 / 676
页数:3
相关论文
共 37 条
[1]   THE RELATIONSHIP BETWEEN TRINUCLEOTIDE (CAG) REPEAT LENGTH AND CLINICAL-FEATURES OF HUNTINGTONS-DISEASE [J].
ANDREW, SE ;
GOLDBERG, YP ;
KREMER, B ;
TELENIUS, H ;
THEILMANN, J ;
ADAM, S ;
STARR, E ;
SQUITIERI, F ;
LIN, BY ;
KALCHMAN, MA ;
GRAHAM, RK ;
HAYDEN, MR .
NATURE GENETICS, 1993, 4 (04) :398-403
[2]   CLONING OF THE ESSENTIAL MYOTONIC-DYSTROPHY REGION AND MAPPING OF THE PUTATIVE DEFECT [J].
ASLANIDIS, C ;
JANSEN, G ;
AMEMIYA, C ;
SHUTLER, G ;
MAHADEVAN, M ;
TSILFIDIS, C ;
CHEN, C ;
ALLEMAN, J ;
WORMSKAMP, NGM ;
VOOIJS, M ;
BUXTON, J ;
JOHNSON, K ;
SMEETS, HJM ;
LENNON, GG ;
CARRANO, AV ;
KORNELUK, RG ;
WIERINGA, B ;
DEJONG, PJ .
NATURE, 1992, 355 (6360) :548-551
[3]   INTRAGENIC DELETION OF THE KALIG-1 GENE IN KALLMANNS SYNDROME [J].
BICK, D ;
FRANCO, B ;
SHERINS, RJ ;
HEYE, B ;
PIKE, L ;
CRAWFORD, J ;
MADDALENA, A ;
INCERTI, B ;
PRAGLIOLA, A ;
MEITINGER, T ;
BALLABIO, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (26) :1752-1755
[4]   TRIPLET REPEAT MUTATIONS IN HUMAN-DISEASE [J].
CASKEY, CT ;
PIZZUTI, A ;
FU, YH ;
FENWICK, RG ;
NELSON, DL .
SCIENCE, 1992, 256 (5058) :784-789
[5]   TRIPLET REPEATS ON THE RISE [J].
DAVIES, K .
NATURE, 1993, 364 (6432) :88-88
[6]   TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE [J].
DUYAO, M ;
AMBROSE, C ;
MYERS, R ;
NOVELLETTO, A ;
PERSICHETTI, F ;
FRONTALI, M ;
FOLSTEIN, S ;
ROSS, C ;
FRANZ, M ;
ABBOTT, M ;
GRAY, J ;
CONNEALLY, P ;
YOUNG, A ;
PENNEY, J ;
HOLLINGSWORTH, Z ;
SHOULSON, I ;
LAZZARINI, A ;
FALEK, A ;
KOROSHETZ, W ;
SAX, D ;
BIRD, E ;
VONSATTEL, J ;
BONILLA, E ;
ALVIR, J ;
CONDE, JB ;
CHA, JH ;
DURE, L ;
GOMEZ, F ;
RAMOS, M ;
SANCHEZRAMOS, J ;
SNODGRASS, S ;
DEYOUNG, M ;
WEXLER, N ;
MOSCOWITZ, C ;
PENCHASZADEH, G ;
MACFARLANE, H ;
ANDERSON, M ;
JENKINS, B ;
SRINIDHI, J ;
BARNES, G ;
GUSELLA, J ;
MACDONALD, M .
NATURE GENETICS, 1993, 4 (04) :387-392
[7]   A GENE DELETED IN KALLMANNS SYNDROME SHARES HOMOLOGY WITH NEURAL CELL-ADHESION AND AXONAL PATH-FINDING MOLECULES [J].
FRANCO, B ;
GUIOLI, S ;
PRAGLIOLA, A ;
INCERTI, B ;
BARDONI, B ;
TONLORENZI, R ;
CARROZZO, R ;
MAESTRINI, E ;
PIERETTI, M ;
TAILLONMILLER, P ;
BROWN, CJ ;
WILLARD, HF ;
LAWRENCE, C ;
PERSICO, MG ;
CAMERINO, G ;
BALLABIO, A .
NATURE, 1991, 353 (6344) :529-536
[8]   DECREASED EXPRESSION OF MYOTONIN PROTEIN-KINASE MESSENGER-RNA AND PROTEIN IN ADULT FORM OF MYOTONIC-DYSTROPHY [J].
FU, YH ;
FRIEDMAN, DL ;
RICHARDS, S ;
PEARLMAN, JA ;
GIBBS, RA ;
PIZZUTI, A ;
ASHIZAWA, T ;
PERRYMAN, MB ;
SCARLATO, G ;
FENWICK, RG ;
CASKEY, CT .
SCIENCE, 1993, 260 (5105) :235-238
[9]   MOLECULAR-BASIS OF THOMSEN DISEASE (AUTOSOMAL DOMINANT MYOTONIA-CONGENITA) [J].
GEORGE, AL ;
CRACKOWER, MA ;
ABDALLA, JA ;
HUDSON, AJ ;
EBERS, GC .
NATURE GENETICS, 1993, 3 (04) :305-310
[10]   SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE [J].
GOATE, A ;
CHARTIERHARLIN, MC ;
MULLAN, M ;
BROWN, J ;
CRAWFORD, F ;
FIDANI, L ;
GIUFFRA, L ;
HAYNES, A ;
IRVING, N ;
JAMES, L ;
MANT, R ;
NEWTON, P ;
ROOKE, K ;
ROQUES, P ;
TALBOT, C ;
PERICAKVANCE, M ;
ROSES, A ;
WILLIAMSON, R ;
ROSSOR, M ;
OWEN, M ;
HARDY, J .
NATURE, 1991, 349 (6311) :704-706