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Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers

Cancer science, 2006-11, Vol.97 (11), p.1147-1154

2006

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Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase ( ) gene expression in human cancer

Oncogene, 2003-12, Vol.22 (55), p.8835-8844

2003

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A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q

Genome research, 2004-02, Vol.14 (2), p.247

2004

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Antisense Transcription Occurs at the Promoter of a Mouse Imprinted Gene, Commd1, on the Repressed Paternal Allele

Journal of biochemistry (Tokyo), 2009-12, Vol.146 (6), p.771-774

2009

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Role of DNA Methylation and Histone H3 Lysine 27 Methylation in Tissue-Specific Imprinting of Mouse Grb10

Molecular and Cellular Biology, 2007-01, Vol.27 (2), p.732-742

2007

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The Mouse Murr1 Gene Is Imprinted in the Adult Brain, Presumably Due to Transcriptional Interference by the Antisense-Oriented U2af1-rs1 Gene

Molecular and Cellular Biology, 2004-01, Vol.24 (1), p.270-279

2004

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Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer

Oncogene, 2004-05, Vol.23 (25), p.4380-4388

2004

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Essential Role of Histone H3 Lys9 Di-Methylation and MeCP2 Binding in MGMT Silencing with Poor DNA Methylation of the Promoter CpG Island

Journal of biochemistry (Tokyo), 2005-03, Vol.137 (3), p.431-440

2005

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Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Journal of medical genetics, 1999-07, Vol.36 (7), p.518-523

1999

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Gene silencing in phenomena related to DNA repair: DNA repair

Oncogene, 2002-12, Vol.21 (58), p.9033-9042

2002

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MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products

Genes & Genetic Systems, 2008, Vol.83(2), pp.199-208

2008

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Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome

Genes & Genomics, 2013, 35(2), , pp.141-147

2013

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Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11

Human molecular genetics, 2016-04, Vol.25 (7), p.1406-1419

2016

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Characterization and Imprinting Status of OBPH1/Obph1 Gene: Implications for an Extended Imprinting Domain in Human and Mouse

Genomics (San Diego, Calif.), 2002-12, Vol.80 (6), p.575-584

2002

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Significant Reduction of WT1 Gene Expression, Possibly Due to Epigenetic Alteration in Wilms’ Tumor

Journal of biochemistry (Tokyo), 2003-03, Vol.133 (3), p.303-308

2003

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Transcriptional Map of 170-kb Region at Chromosome 11p15.5: Identification and Mutational Analysis of the BWR1A Gene Reveals the Presence of Mutations in Tumor Samples

Proceedings of the National Academy of Sciences - PNAS, 1998-03, Vol.95 (7), p.3873-3878

1998

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A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors

Journal of biochemistry (Tokyo), 2000-11, Vol.128 (5), p.847-853

2000

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Restriction landmark genomic scanning method and its various applications

Electrophoresis, 1993, Vol.14 (1), p.251-258

1993

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Identification of a novel isoform of Murr1 transcript, U2mu, which is transcribed from the portions of two closely located but oppositely oriented genes

Genes & Genetic Systems, 2002, Vol.77(5), pp.377-381

2002

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Epigenetic silencing of the MGMT gene in cancer

Biochemistry and cell biology, 2005-08, Vol.83 (4), p.429

2005

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Allele-specific methylation and expression of an imprinted U2afl-rsl (SP2) gene

Nucleic acids research, 1995-01, Vol.23 (1), p.36-41

1995

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Japanese and North American European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterations

European journal of human genetics : EJHG, 2007-12, Vol.15 (12), p.1205-1210

2007

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Aberrant Methylation of an Imprinted Gene U2af1-rs1(SP2) Caused by Its Own Transgene

The Journal of biological chemistry, 1997-04, Vol.272 (14), p.9120-9122

1997

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C11orf21, a novel gene within the Beckwith–Wiedemann syndrome region in human chromosome 11p15.5

Gene, 2000-10, Vol.256 (1), p.311-317

2000

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Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers

Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase ( ) gene expression in human cancer

A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q

Antisense Transcription Occurs at the Promoter of a Mouse Imprinted Gene, Commd1, on the Repressed Paternal Allele

Role of DNA Methylation and Histone H3 Lysine 27 Methylation in Tissue-Specific Imprinting of Mouse Grb10

The Mouse Murr1 Gene Is Imprinted in the Adult Brain, Presumably Due to Transcriptional Interference by the Antisense-Oriented U2af1-rs1 Gene

Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer

Essential Role of Histone H3 Lys9 Di-Methylation and MeCP2 Binding in MGMT Silencing with Poor DNA Methylation of the Promoter CpG Island

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Gene silencing in phenomena related to DNA repair: DNA repair

MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products

Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome

Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11

Characterization and Imprinting Status of OBPH1/Obph1 Gene: Implications for an Extended Imprinting Domain in Human and Mouse

Significant Reduction of WT1 Gene Expression, Possibly Due to Epigenetic Alteration in Wilms’ Tumor

Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations

Transcriptional Map of 170-kb Region at Chromosome 11p15.5: Identification and Mutational Analysis of the BWR1A Gene Reveals the Presence of Mutations in Tumor Samples

A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors

Restriction landmark genomic scanning method and its various applications

Identification of a novel isoform of Murr1 transcript, U2mu, which is transcribed from the portions of two closely located but oppositely oriented genes

Epigenetic silencing of the MGMT gene in cancer

Allele-specific methylation and expression of an imprinted U2afl-rsl (SP2) gene

Japanese and North American European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterations

Aberrant Methylation of an Imprinted Gene U2af1-rs1(SP2) Caused by Its Own Transgene

C11orf21, a novel gene within the Beckwith–Wiedemann syndrome region in human chromosome 11p15.5

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