Search details
1.
Premature termination of reprogramming in vivo leads to cancer development through altered epigenetic regulation.
Cell
; 156(4): 663-77, 2014 Feb 13.
Article
in English
| MEDLINE | ID: mdl-24529372
2.
Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.
J Med Genet
; 61(6): 590-594, 2024 May 21.
Article
in English
| MEDLINE | ID: mdl-38228391
3.
Possible regulation of ganglioside GD3 synthase gene expression with DNA methylation in human glioma cells.
Glycoconj J
; 40(3): 323-332, 2023 06.
Article
in English
| MEDLINE | ID: mdl-36897478
4.
A novel role of helix-loop-helix transcriptional factor Bhlhe40 in osteoclast activation.
J Cell Physiol
; 237(10): 3912-3926, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35908202
5.
Short-term running exercise alters DNA methylation patterns in neuronal nitric oxide synthase and brain-derived neurotrophic factor genes in the mouse hippocampus and reduces anxiety-like behaviors.
FASEB J
; 35(8): e21767, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34325488
6.
Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome.
J Med Genet
; 58(6): 422-425, 2021 06.
Article
in English
| MEDLINE | ID: mdl-32447322
7.
An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease.
Ann Hum Genet
; 85(5): 166-177, 2021 09.
Article
in English
| MEDLINE | ID: mdl-34013582
8.
Mbf1 ensures Polycomb silencing by protecting E(z) mRNA from degradation by Pacman.
Development
; 145(5)2018 03 09.
Article
in English
| MEDLINE | ID: mdl-29523653
9.
DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancer.
FASEB J
; 34(1): 960-973, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31914674
10.
Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndrome.
Am J Med Genet A
; 185(10): 3062-3067, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34037318
11.
Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case series.
J Obstet Gynaecol Res
; 47(3): 1118-1125, 2021 Mar.
Article
in English
| MEDLINE | ID: mdl-33462953
12.
One week, but not 12 hours, of cast immobilization alters promotor DNA methylation patterns in the nNOS gene in mouse skeletal muscle.
J Physiol
; 597(21): 5145-5159, 2019 11.
Article
in English
| MEDLINE | ID: mdl-31490543
13.
The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome.
J Hum Genet
; 64(9): 937-943, 2019 Sep.
Article
in English
| MEDLINE | ID: mdl-31235774
14.
Habitual Light-intensity Physical Activity and ASC Methylation in a Middle-aged Population.
Int J Sports Med
; 40(10): 670-677, 2019 Sep.
Article
in English
| MEDLINE | ID: mdl-31342477
15.
Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11.
Hum Mol Genet
; 25(7): 1406-19, 2016 Apr 01.
Article
in English
| MEDLINE | ID: mdl-26908620
16.
CTCF deletion syndrome: clinical features and epigenetic delineation.
J Med Genet
; 54(12): 836-842, 2017 12.
Article
in English
| MEDLINE | ID: mdl-28848059
17.
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.
Hum Mutat
; 38(6): 637-648, 2017 06.
Article
in English
| MEDLINE | ID: mdl-28229514
18.
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment.
Genome Res
; 24(4): 554-69, 2014 Apr.
Article
in English
| MEDLINE | ID: mdl-24402520
19.
Long term survival of a patient with Perlman syndrome due to novel compound heterozygous missense mutations in RNB domain of DIS3L2.
Am J Med Genet A
; 173(4): 1077-1081, 2017 Apr.
Article
in English
| MEDLINE | ID: mdl-28328139
20.
The allele frequency of ALDH2*Glu504Lys and ADH1B*Arg47His for the Ryukyu islanders and their history of expansion among East Asians.
Am J Hum Biol
; 29(2)2017 Mar.
Article
in English
| MEDLINE | ID: mdl-27801545