Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome

被引:69
作者
Tsai, TF
Armstrong, D
Beaudet, AL [1 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
关键词
D O I
10.1038/8722
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:15 / 16
页数:2
相关论文
共 15 条
[1]   A CANDIDATE MOUSE MODEL FOR PRADER-WILLI SYNDROME WHICH SHOWS AN ABSENCE OF SNRPN EXPRESSION [J].
CATTANACH, BM ;
BARR, JA ;
EVANS, EP ;
BURTENSHAW, M ;
BEECHEY, CV ;
LEFF, SE ;
BRANNAN, CI ;
COPELAND, NG ;
JENKINS, NA ;
JONES, J .
NATURE GENETICS, 1992, 2 (04) :270-274
[2]   Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome [J].
Conroy, JM ;
Grebe, TA ;
Becker, LA ;
Tsuchiya, K ;
Nicholls, RD ;
Buiting, K ;
Horsthemke, B ;
Cassidy, SB ;
Schwartz, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (02) :388-394
[3]   A FAMILY OF RAPIDLY EVOLVING GENES FROM THE SEX REVERSAL CRITICAL REGION IN XP21 [J].
DABOVIC, B ;
ZANARIA, E ;
BARDONI, B ;
LISA, A ;
BORDIGNON, C ;
RUSSO, V ;
MATESSI, C ;
TRAVERSARI, C ;
CAMERINO, G .
MAMMALIAN GENOME, 1995, 6 (09) :571-580
[4]   STRUCTURE, CHROMOSOMAL LOCALIZATION, AND EXPRESSION OF 12 GENES OF THE MAGE FAMILY [J].
DEPLAEN, E ;
ARDEN, K ;
TRAVERSARI, C ;
GAFORIO, JJ ;
SZIKORA, JP ;
DESMET, C ;
BRASSEUR, F ;
VANDERBRUGGEN, P ;
LETHE, B ;
LURQUIN, C ;
BRASSEUR, R ;
CHOMEZ, P ;
DEBACKER, O ;
CAVENEE, W ;
BOON, T .
IMMUNOGENETICS, 1994, 40 (05) :360-369
[5]   ARREST OF CELL-GROWTH BY NECDIN, A NUCLEAR-PROTEIN EXPRESSED IN POSTMITOTIC NEURONS [J].
HAYASHI, Y ;
MATSUYAMA, K ;
TAKAGI, K ;
SUGIURA, H ;
YOSHIKAWA, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 213 (01) :317-324
[6]   The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region [J].
Jay, P ;
Rougeulle, C ;
Massacrier, A ;
Moncla, A ;
Mattei, MG ;
Malzac, P ;
Roeckel, N ;
Taviaux, S ;
Lefranc, JLB ;
Cau, P ;
Berta, P ;
Lalande, M ;
Muscatelli, F .
NATURE GENETICS, 1997, 17 (03) :357-361
[7]   Mutation of the angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation [J].
Jiang, YH ;
Armstrong, D ;
Albrecht, U ;
Atkins, CM ;
Noebels, JL ;
Eichele, G ;
Sweatt, JD ;
Beaudet, AL .
NEURON, 1998, 21 (04) :799-811
[8]   Imprinting in Angelman and Prader-Willi syndromes [J].
Jiang, YH ;
Tsai, TF ;
Bressler, J ;
Beaudet, AL .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1998, 8 (03) :334-342
[9]   Prader-Willi syndrome is caused by disruption of the SNRPN gene [J].
Kuslich, CD ;
Kobori, JA ;
Mohapatra, G ;
Gregorio-King, C ;
Donlon, TA .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (01) :70-76
[10]   Parental imprinting and human disease [J].
Lalande, M .
ANNUAL REVIEW OF GENETICS, 1996, 30 :173-195