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Isolation of novel heart-specific genes using the BodyMap databasecDNA cloning and chromosomal mapping of human N-acetylglucosaminyltransferase V+The human ASCL2 gene escaping genomic imprinting and its expression patternGenomic organization and chromosomal assignment of the human beta1, 4-N-acetylgalactosaminyltransferase gene. Identification of multiple transcription unitsMapping of the bone morphogenetic protein 1 gene (BMP1) to 8p21: removal of BMP1 from candidacy for the bone disorder in Langer-Giedion syndromeMeCP2-dependent repression of an imprinted miR-184 released by depolarizationMutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndromeA novel imprinted gene, KCNQ1DN, within the WT2 critical region of human chromosome 11p15.5 and its reduced expression in Wilms' tumors.Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.Characterization and imprinting status of OBPH1/Obph1 gene: implications for an extended imprinting domain in human and mouse.Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment.Premature termination of reprogramming in vivo leads to cancer development through altered epigenetic regulation.A SacII polymorphism in the human ASCL2 (HASH2) gene region.Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene.Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers.Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsComprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma.Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole.Gene silencing in DNA damage repair.The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infants.The allele frequency of ALDH2*Glu504Lys and ADH1B*Arg47His for the Ryukyu islanders and their history of expansion among East Asians.Epigenetic silencing of the MGMT gene in cancer.CpG methylation of MGMT and hMLH1 promoter in hepatocellular carcinoma associated with hepatitis viral infection.Heme requirement for production of active endothelial nitric oxide synthase in baculovirus-infected insect cells.A comparison of GC content and the proportion of Alu/KpnI-repetitive sequences in a single dark- and light-band region from a human chromosome.Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract polycomb silencingInsulin-like growth factor 2 gene imprinting in clear cell sarcoma of the kidney.The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.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.An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression.Retinoic acid receptor beta2 is epigenetically silenced either by DNA methylation or repressive histone modifications at the promoter in cervical cancer cells.The essential role of histone H3 Lys9 di-methylation and MeCP2 binding in MGMT silencing with poor DNA methylation of the promoter CpG island.Epigenetic inactivation of class II transactivator (CIITA) is associated with the absence of interferon-gamma-induced HLA-DR expression in colorectal and gastric cancer cells.Fifty novel sequence-tagged sites (STSs) on human chromosome 11q13.4-->q25 identified from microclones generated by microdissection.Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours.A new organotypic culture of adipose tissue fragments maintains viable mature adipocytes for a long term, together with development of immature adipocytes and mesenchymal stem cell-like cells.Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10.A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.
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P50
description
researcher
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wetenschapper
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հետազոտող
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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Hidenobu Soejima
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P106
P1153
13409579700
P21
P31
P496
0000-0001-5076-6563