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

[1] Competition - a common motif for the imprinting mechanism? [J]. 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]. NATURE GENETICS, 1995, 9 (04) : 395 - 400

[4] Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene [J]. 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]. 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]. 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]. GENES & DEVELOPMENT, 1995, 9 (07) : 808 - 820

[8] UBE3A/E6-AP mutations cause Angelman syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 70 - 73

[9] Parental imprinting and human disease [J]. ANNUAL REVIEW OF GENETICS, 1996, 30 : 173 - 195

[10] DISRUPTION OF IMPRINTING CAUSED BY DELETION OF THE H19 GENE REGION IN MICE [J]. NATURE, 1995, 375 (6526) : 34 - 39

[1] Competition - a common motif for the imprinting mechanism? [J]. 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]. NATURE GENETICS, 1995, 9 (04) : 395 - 400

[4] Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene [J]. 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]. 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]. 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]. GENES & DEVELOPMENT, 1995, 9 (07) : 808 - 820

[8] UBE3A/E6-AP mutations cause Angelman syndrome [J]. NATURE GENETICS, 1997, 15 (01) : 70 - 73

[9] Parental imprinting and human disease [J]. ANNUAL REVIEW OF GENETICS, 1996, 30 : 173 - 195

[10] DISRUPTION OF IMPRINTING CAUSED BY DELETION OF THE H19 GENE REGION IN MICE [J]. NATURE, 1995, 375 (6526) : 34 - 39