Imprinting moves to the centre

被引:22
作者
FergusonSmith, AC
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D O I
10.1038/ng1096-119
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Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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页码:119 / 121
页数:3
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共 18 条
[1]   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
[2]   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
[3]  
ELLIOT M, 1994, J MED GENET, V7, P560
[4]   EMBRYOLOGICAL AND MOLECULAR INVESTIGATIONS OF PARENTAL IMPRINTING ON MOUSE CHROMOSOME-7 [J].
FERGUSONSMITH, AC ;
CATTANACH, BM ;
BARTON, SC ;
BEECHEY, CV ;
SURANI, MA .
NATURE, 1991, 351 (6328) :667-670
[5]   An imprinted gene p57(KIP2) is mutated in Beckwith-Wiedemann syndrome [J].
Hatada, I ;
Ohashi, H ;
Fukushima, Y ;
Kaneko, Y ;
Inoue, M ;
Komoto, Y ;
Okada, A ;
Ohishi, S ;
Nabetani, A ;
Morisaki, H ;
Nakayama, M ;
Niikawa, N ;
Mukai, T .
NATURE GENETICS, 1996, 14 (02) :171-173
[6]   Genomic imprinting of human p57(KIP2) and its reduced expression in Wilms' tumors [J].
Hatada, I ;
Inazawa, J ;
Abe, T ;
Nakayama, M ;
Kaneko, Y ;
Jinno, Y ;
Niikawa, N ;
Ohashi, H ;
Fukushima, Y ;
Iida, K ;
Yutani, C ;
Takahashi, S ;
Chiba, Y ;
Ohishi, S ;
Mukai, T .
HUMAN MOLECULAR GENETICS, 1996, 5 (06) :783-788
[7]   Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments [J].
Hoovers, JMN ;
Kalikin, LM ;
Johnson, LA ;
Alders, M ;
Redeker, B ;
Law, DJ ;
Bliek, J ;
Steenman, M ;
Benedict, M ;
Wiegant, J ;
Lengauer, C ;
TaillonMiller, P ;
Schlessinger, D ;
Edwards, MC ;
Elledge, SJ ;
Ivens, A ;
Westerveld, A ;
Little, P ;
Mannens, M ;
Feinberg, AP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) :12456-12460
[8]   LOSS OF THE IMPRINTED IGF2/CATION-INDEPENDENT MANNOSE 6-PHOSPHATE RECEPTOR RESULTS IN FETAL OVERGROWTH AND PERINATAL LETHALITY [J].
LAU, MMH ;
STEWART, CEH ;
LIU, ZY ;
BHATT, H ;
ROTWEIN, P ;
STEWART, CL .
GENES & DEVELOPMENT, 1994, 8 (24) :2953-2963
[9]   UNIPARENTAL DISOMY IN HUMANS - DEVELOPMENT OF AN IMPRINTING MAP AND ITS IMPLICATIONS FOR PRENATAL-DIAGNOSIS [J].
LEDBETTER, DH ;
ENGEL, E .
HUMAN MOLECULAR GENETICS, 1995, 4 :1757-1764
[10]   P57(KIP2), A STRUCTURALLY DISTINCT MEMBER OF THE P21(CIP1) CDK INHIBITOR FAMILY, IS A CANDIDATE TUMOR-SUPPRESSOR GENE [J].
MATSUOKA, S ;
EDWARDS, MC ;
BAI, C ;
PARKER, S ;
ZHANG, PM ;
BALDINI, A ;
HARPER, JW ;
ELLEDGE, SJ .
GENES & DEVELOPMENT, 1995, 9 (06) :650-662