The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997)

被引:0
|
作者
Musco, G
Kharrat, A
Stier, G
Fraternali, F
Gibson, TJ
Nilges, M
Pastore, A
机构
关键词
D O I
10.1038/nsb1097-840c
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
引用
收藏
页码:840 / 840
页数:1
相关论文
共 32 条
  • [1] The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome
    Giovanna Musco
    Abdelhakim Kharrat
    Gunter Stier
    Franca Fraternali
    Toby J. Gibson
    Michael Nilges
    Annalisa Pastore
    Nature Structural Biology, 1997, 4 : 712 - 716
  • [3] The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome
    Musco, G
    Kharrat, A
    Stier, G
    Fraternali, F
    Gibson, TJ
    Nilges, M
    Pastore, A
    NATURE STRUCTURAL BIOLOGY, 1997, 4 (09) : 712 - 716
  • [4] Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains
    Adinolfi, S
    Bagni, C
    Musco, G
    Gibson, T
    Mazzarella, L
    Pastore, A
    RNA, 1999, 5 (09) : 1248 - 1258
  • [5] MUTATIONS IN THE CPG ISLAND OF THE FMR1 GENE - ARE THEY RESPONSIBLE FOR FRAGILE-X SYNDROME
    MILA, M
    CASTELLVIBEL, S
    BARCELO, A
    SANCHEZ, A
    JIMENEZ, D
    MANDEL, JL
    ESTIVILL, X
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1273 - 1273
  • [6] Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles
    Sergi Castellví-Bel
    Miguel Fernández-Burriel
    Maria Rifé
    Dolores Jiménez
    Judith Mallolas
    Aurora Sánchez
    Feliciano Ramos
    Montserrat Milà
    Human Genetics, 2000, 107 : 195 - 196
  • [7] Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles
    Castellví-Bel, S
    Fernández-Burriel, M
    Rifé, M
    Jiménez, D
    Mallolas, J
    Sánchez, A
    Ramos, F
    Milà, M
    HUMAN GENETICS, 2000, 107 (02) : 195 - 196
  • [8] FRAGILE X-SYNDROME IS ASSOCIATED WITH A LARGE DOMAIN OF DELAYED REPLICATION AT THE FMR1 LOCUS
    HANSEN, RS
    CANFIELD, TK
    LAMB, MM
    GARTLER, SM
    LAIRD, CD
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 31 - 31
  • [9] Differential impact of the FMR1 gene on visual processing in fragile X syndrome (vol 127, pg 591, 2004)
    Kogan, Cary S.
    Boutet, Isabelle
    Cornish, Kim
    Zangenehpour, Shahin
    Mullen, Kathy T.
    Holden, Jeanette J. A.
    Kaloustian, Vazken M. Der
    Andermann, Eva
    Chaudhuri, Avi
    BRAIN, 2018, 141 : E64 - E65
  • [10] Autistic Behavior, FMR1 Protein, and Developmental Trajectories in Young Males with Fragile X Syndrome
    Bailey Jr. D.B.
    Hatton D.D.
    Skinner M.
    Mesibov G.
    Journal of Autism and Developmental Disorders, 2001, 31 (2) : 165 - 174