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Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders

Journal of human genetics, 2013-07, Vol.58 (7), p.402-409

2013

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Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome

Cancers, 2022-11, Vol.14 (22), p.5563

2022

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Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome

Human mutation, 2017-06, Vol.38 (6), p.637-648

2017

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Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case series

The journal of obstetrics and gynaecology research, 2021-03, Vol.47 (3), p.1118-1125

2021

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Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome

Journal of medical genetics, 2021-06, Vol.58 (6), p.422-425

2021

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The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome

Journal of human genetics, 2019-09, Vol.64 (9), p.937-943

2019

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Donor cord blood aging accelerates in recipients after transplantation

Scientific reports, 2023-02, Vol.13 (1), p.2603-2603, Article 2603

2023

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Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract polycomb silencing

PLoS genetics, 2013-11, Vol.9 (11), p.e1003897-e1003897

2013

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Phosphorylation-mediated inactivation of coactivator-associated arginine methyltransferase 1

Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (30), p.12318-12323

2007

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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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Habitual Light-intensity Physical Activity and ASC Methylation in a Middle-aged Population

International journal of sports medicine, 2019-09, Vol.40 (10), p.670-677

2019

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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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Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR

Epigenetics & chromatin, 2018-06, Vol.11 (1), p.28-28, Article 28

2018

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Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia

Clinical epigenetics, 2022-05, Vol.14 (1), p.64-64, Article 64

2022

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TYK2 Promoter Variant Is Associated with Impaired Insulin Secretion and Lower Insulin Resistance in Japanese Type 2 Diabetes Patients

Genes, 2021-03, Vol.12 (3), p.400

2021

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The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants

Gene, 2016-06, Vol.583 (2), p.141-146

2016

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Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer

Clinical epigenetics, 2018-12, Vol.10 (1), p.150-150, Article 150

2018

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Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan

Neurologia medico-chirurgica, 2017, Vol.57(11), pp.607-611

2017

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Fibroadenoma in Beckwith–Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5

Pediatrics international, 2014-12, Vol.56 (6), p.931-934

2014

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Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: Few clinical features suggestive of Beckwith-Wiedemann syndrome

Endocrine Journal, 2013, Vol.60(4), pp.403-408

2013

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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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Exploration of genetic causes of biparental placenta mesenchymal dysplasia

Placenta (Eastbourne), 2023-09, Vol.141, p.106

2023

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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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Beckwith–Wiedemann syndrome with placental chorangioma due to H19‐differentially methylated region hypermethylation: A case report

The journal of obstetrics and gynaecology research, 2011-12, Vol.37 (12), p.1872-1876

2011

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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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Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders

Placental Mesenchymal Dysplasia and Beckwith-Wiedemann Syndrome

Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome

Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case series

Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome

The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome

Donor cord blood aging accelerates in recipients after transplantation

Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract polycomb silencing

Phosphorylation-mediated inactivation of coactivator-associated arginine methyltransferase 1

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

Habitual Light-intensity Physical Activity and ASC Methylation in a Middle-aged Population

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

Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR

Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia

TYK2 Promoter Variant Is Associated with Impaired Insulin Secretion and Lower Insulin Resistance in Japanese Type 2 Diabetes Patients

The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants

Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer

Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan

Fibroadenoma in Beckwith–Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5

Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: Few clinical features suggestive of Beckwith-Wiedemann syndrome

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

Exploration of genetic causes of biparental placenta mesenchymal dysplasia

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

Beckwith–Wiedemann syndrome with placental chorangioma due to H19‐differentially methylated region hypermethylation: A case report

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

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