Competitive edge at the imprinted Prader-Willi/Angelman region?

被引:18
作者
Tilghman, SM [1 ]
Caspary, T
Ingram, RS
机构
[1] Princeton Univ, Howard Hughes Med Inst, Princeton, NJ 08544 USA
[2] Princeton Univ, Dept Biol Mol, Princeton, NJ 08544 USA
关键词
D O I
10.1038/ng0398-206
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:206 / 208
页数:3
相关论文
共 20 条
[1]   Competition - a common motif for the imprinting mechanism? [J].
Barlow, DP .
EMBO JOURNAL, 1997, 16 (23) :6899-6905
[2]  
Bartolomei M.S., 1992, SEMIN DEV BIOL, V3, P107
[3]   INHERITED MICRODELETIONS IN THE ANGELMAN AND PRADER-WILLI SYNDROMES DEFINE AN IMPRINTING CENTER ON HUMAN-CHROMOSOME-15 [J].
BUITING, K ;
SAITOH, S ;
GROSS, S ;
DITTRICH, B ;
SCHWARTZ, S ;
NICHOLLS, RD ;
HORSTHEMKE, B .
NATURE GENETICS, 1995, 9 (04) :395-400
[4]   Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene [J].
Dittrich, B ;
Buiting, K ;
Korn, B ;
Rickard, S ;
Buxton, J ;
Saitoh, S ;
Nicholls, RD ;
Poustka, A ;
Winterpacht, A ;
Zabel, B ;
Horsthemke, B .
NATURE GENETICS, 1996, 14 (02) :163-170
[5]   Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans [J].
Forne, T ;
Oswald, J ;
Dean, W ;
Saam, JR ;
Bailleul, B ;
Dandolo, L ;
Tilghman, SM ;
Walter, J ;
Reik, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (19) :10243-10248
[6]   Genomic imprinting: Potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes [J].
Glenn, CC ;
Driscoll, DJ ;
Yang, TP ;
Nicholls, RD .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (04) :321-332
[7]   TISSUE-SPECIFIC AND ALLELE-SPECIFIC REPLICATION TIMING CONTROL IN THE IMPRINTED HUMAN PRADER-WILLI-SYNDROME REGION [J].
GUNARATNE, PH ;
NAKAO, M ;
LEDBETTER, DH ;
SUTCLIFFE, JS ;
CHINAULT, AC .
GENES & DEVELOPMENT, 1995, 9 (07) :808-820
[8]   UBE3A/E6-AP mutations cause Angelman syndrome [J].
Kishino, T ;
Lalande, M ;
Wagstaff, J .
NATURE GENETICS, 1997, 15 (01) :70-73
[9]   Parental imprinting and human disease [J].
Lalande, M .
ANNUAL REVIEW OF GENETICS, 1996, 30 :173-195
[10]   DISRUPTION OF IMPRINTING CAUSED BY DELETION OF THE H19 GENE REGION IN MICE [J].
LEIGHTON, PA ;
INGRAM, RS ;
EGGENSCHWILER, J ;
EFSTRATIADIS, A ;
TILGHMAN, SM .
NATURE, 1995, 375 (6526) :34-39