about
Tumor transcriptome sequencing reveals allelic expression imbalances associated with copy number alterationsMaternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndromeA novel DNA damage-inducible transcript, gadd7, inhibits cell growth, but lacks a protein productImprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15The product of the imprinted H19 gene is an oncofetal RNAEpigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defectsA maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeHypomethylation and aberrant expression of the glioma pathogenesis-related 1 gene in Wilms tumorsTranscriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samplesH19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and Ki-67 expressionLoss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprintingMutations in the IGF-II pathway that confer resistance to lytic reovirus infectionBlockade of EphA receptor tyrosine kinase activation inhibits vascular endothelial cell growth factor-induced angiogenesis.Epigenetics of cervical cancer. An overview and therapeutic perspectivesEpigenetic modulators, modifiers and mediators in cancer aetiology and progressionDNA methylation data analysis and its application to cancer researchNutrition, epigenetics, and diseasesTwo novel genes in the center of the 11p15 imprinted domain escape genomic imprintingFrequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinomaAntioncogenes and human cancer.IGF2 is critical for tumorigenesis by synovial sarcoma oncoprotein SYT-SSX1Gain of allelic gene expression for IGF-II occurs frequently in Barrett's esophagusThe expression of the imprinted H19 and IGF-2 genes in human bladder carcinomaLoss of H19 imprinting in adult T-cell leukaemia/lymphomaEstablishment of functional imprinting of the H19 gene in human developing placentaeImprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegalyMethylation mattersEpigenetics in cancerAntisense transcripts with FANTOM2 clone set and their implications for gene regulation.Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors.The evolution of epigenetic regulators CTCF and BORIS/CTCFL in amniotes.Genomic imprinting: implications for human disease.Birth characteristics and the risk of childhood rhabdomyosarcoma based on histological subtype.Loss of IGF2 imprinting is associated with abrogation of long-range intrachromosomal interactions in human cancer cells.New insights into the molecular pathogenesis of colorectal cancer.Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsThe new field of epigenomics: implications for cancer and other common disease research.Genetic susceptibility to non-polyposis colorectal cancer.cis-Acting signal for inheritance of imprinted DNA methylation patterns in the preimplantation mouse embryo
P2860
Q21562666-A3380314-D29C-4AC4-B9C1-D380B3CD43E9Q24305283-6F6656F6-DC63-496A-A399-E6DEFC88B63DQ24546216-6CDEDFD5-7AA1-4C66-916B-C3AA6368480EQ24568014-8A9CA3BD-7A21-4002-A53D-33C3A1761607Q24609254-5468DEC8-1D93-44C0-AAFD-25204E9FB655Q24632842-E6EC2FDA-5A46-4B89-A291-F004FC6753D1Q24644175-549BE2E4-9C5F-41B7-BB85-755B02C2B603Q24678285-A15E796C-0386-49A3-9352-DA65A43DCA74Q24681580-77F29441-5310-4A2E-83FE-E744894062C6Q24682023-1BF7D261-3D6A-457A-96EF-441B2CAC92E0Q24684284-C01DFB53-80A9-46D0-B6AC-748C23AAE813Q24791505-88B850A4-801C-48A6-84C7-2E70C1B3ABB2Q24798922-89DA41DC-BD82-4A3D-9D7F-64BBDD32A4E9Q24812104-C1AD3432-0D06-42A9-AB00-639762A45B3EQ26766149-234E0CCB-8123-4C2D-B548-170EB6B72F0CQ26996466-D68078AA-5F1C-43FF-AE71-2C51BC7DC58EQ27021924-9DF4D458-50BB-4A15-9944-B87F9BC99712Q28138506-A0A54616-3D14-4F35-BC46-E90783D142ABQ28140252-A7A8420A-0B79-45D6-A139-89AE5FAE3FA9Q28237050-D02C1593-F66C-4FF3-B86D-7D5266B48AC5Q28278853-26331BEB-0E0F-4EF1-808D-CE5935DCA764Q28285950-1B80F6F4-D80F-443E-95CB-1C108C5AA009Q28291512-C0779132-96A4-4755-A24D-F55A446F8A1CQ28296472-1AEB9B30-F9CF-409A-AD6C-CCB5CFD3459CQ28297145-047D252C-A8F6-4617-8B40-C5631228A5E6Q28360510-0573D9D4-48A9-42A5-9D10-82DA8ECA846DQ28364163-17332C61-AD66-43EA-8A94-D39071F213DEQ29617139-DB0DB976-913E-472E-82F3-54EEF55691DFQ31147226-5B59D195-5B83-4414-96C6-18692DD2034FQ33327077-2AB68F74-873C-456D-A8EC-D64FA9F61591Q33366534-554C89B4-C427-4AFF-8131-7E1150AC589DQ33541538-A8EEE48E-FAD4-489C-9A2B-123083203C3BQ33620152-27AAF10B-17D9-4600-9246-04C74D90E2E5Q33630697-8321D670-46D2-466D-9929-01B67D76DD65Q33640592-8A4A9832-EAF2-4208-B472-BBC0AC750DB5Q33675226-B4516FFA-BA32-48B2-BCE6-518DA6821529Q33681805-8C060008-264B-42F4-8680-54B947BDD4B9Q33698033-906ED39A-AF4E-4D9E-9DBB-B3DF6B2FE5E1Q33764029-D67D4653-DCF7-44F2-810A-5FC8FFEA3F4DQ33774966-E9FACC08-2A59-414E-A254-E0F15372EE19
P2860
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
Relaxation of imprinted genes in human cancer.
@en
Relaxation of imprinted genes in human cancer.
@nl
type
label
Relaxation of imprinted genes in human cancer.
@en
Relaxation of imprinted genes in human cancer.
@nl
prefLabel
Relaxation of imprinted genes in human cancer.
@en
Relaxation of imprinted genes in human cancer.
@nl
P2093
P356
P1433
P1476
Relaxation of imprinted genes in human cancer.
@en
P2093
P2888
P304
P356
10.1038/362747A0
P407
P577
1993-04-01T00:00:00Z
P5875
P6179
1010381628