Human diseases with underlying defects in chromatin structure and modification.
about
Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)Isolation of human NURF: a regulator of Engrailed gene expressionCECR2, a protein involved in neurulation, forms a novel chromatin remodeling complex with SNF2LMutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardationProteomic investigation of epigenetics in neuropsychiatric disorders: a missing link between genetics and behavior?Immunologic and neurodevelopmental susceptibilities of autismX-linked mental retardation (XLMR): from clinical conditions to cloned genes.The methyl-CpG binding proteins Mecp2, Mbd2 and Kaiso are dispensable for mouse embryogenesis, but play a redundant function in neural differentiation.The new field of epigenomics: implications for cancer and other common disease research.Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?Proteomic interrogation of human chromatin.Perturbations of chromatin structure in human genetic disease: recent advances.Structural, Dynamical, and Energetical Consequences of Rett Syndrome Mutation R133C in MeCP2.Evolutionary conservation of histone modifications in mammals.Combination therapy: histone deacetylase inhibitors and platinum-based chemotherapeutics for cancerA Rising Cancer Prevention Target of RSK2 in Human Skin Cancer.Tension-Dependent Free Energies of Nucleosome Unwrapping.Proteolytic clipping of histone tails: the emerging role of histone proteases in regulation of various biological processes.Iterative Fragmentation Improves the Detection of ChIP-seq Peaks for Inactive Histone Marks.A chemical strategy for the cell-based detection of HDAC activity.BET bromodomain inhibition suppresses transcriptional responses to cytokine-Jak-STAT signaling in a gene-specific manner in human monocytes.Aggregation of population-based genetic variation over protein domain homologues and its potential use in genetic diagnostics.In silico evidence for sequence-dependent nucleosome sliding.Copy number variants in a population-based investigation of Klippel-Trenaunay syndrome.The relative effect of parasites and social status on sperm traits in Arctic charr
P2860
Q21203047-FD47F3A9-B583-439E-AE18-13DBF45ADC78Q24299509-5FD23902-57B5-4E8F-8A9D-DB964FD1190EQ24337637-E29AB5CF-EE94-4CE2-9605-FC29CF8DCBB8Q24532155-EC47EA71-4555-4205-B8A3-E3226C9F0771Q24603107-E758F415-B814-4283-9C3C-9F74397C46D2Q28275427-8E8F315B-A700-414B-A0FD-B2105E262F12Q33205129-88072C2A-8F1F-4FB0-B4DF-F9158EBB8A65Q33403744-704B62B5-7762-46F3-803F-61AEFBBFE303Q33698033-7ADD37A5-7ABC-4ECA-B93A-82FA0DF0EDD0Q33748887-D1CF059E-68B5-45E8-B602-3827A94E97CCQ34026216-55B8A7EC-E0FD-4E63-8E1A-0339B8614676Q35198386-054BB42C-0995-4573-87EB-B1A17CBB054EQ35606203-CE4FA42E-2B66-474B-9AB4-EDDEF936C4DAQ36032955-618DA845-F01A-4212-98B4-DC398174DE24Q36537920-227B5698-06D2-450A-95E9-F85071B8CC26Q37068772-F8C3F2B4-FB70-48D0-A881-14F37B7AF56EQ37299023-76088DE3-161B-4718-8F7C-6549E776BA4FQ38182451-349ECF92-2AA1-4575-97B9-6A599E674B27Q39216883-8F4E7160-0282-4D20-8506-D8B9216659BDQ41514784-490CF925-E37A-4DFC-8141-8362EB670FEFQ41904871-59645549-168D-4818-BB1F-FB6FF897A877Q47139191-21655AC7-39A0-498F-9882-CF0383C9D048Q47403190-D44D4F37-6ECD-4D38-AEF5-B2F4A7E35024Q52818380-FF35E1CE-D02B-48B5-914E-BC14A3B0FA25Q58771341-C1C67079-D9C1-4EF0-ABEF-2C5E6190E13F
P2860
Human diseases with underlying defects in chromatin structure and modification.
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Human diseases with underlying defects in chromatin structure and modification.
@ast
Human diseases with underlying defects in chromatin structure and modification.
@en
Human diseases with underlying defects in chromatin structure and modification.
@nl
type
label
Human diseases with underlying defects in chromatin structure and modification.
@ast
Human diseases with underlying defects in chromatin structure and modification.
@en
Human diseases with underlying defects in chromatin structure and modification.
@nl
prefLabel
Human diseases with underlying defects in chromatin structure and modification.
@ast
Human diseases with underlying defects in chromatin structure and modification.
@en
Human diseases with underlying defects in chromatin structure and modification.
@nl
P356
P1476
Human diseases with underlying defects in chromatin structure and modification
@en
P2093
W Bickmore
P304
P356
10.1093/HMG/10.20.2233
P577
2001-10-01T00:00:00Z