about
Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)CECR2, a protein involved in neurulation, forms a novel chromatin remodeling complex with SNF2L2003 William Allan Award address. The Thalassemias: the role of molecular genetics in an evolving global health problemDifferential repression by freud-1/CC2D1A at a polymorphic site in the dopamine-D2 receptor geneDyrk1A potentiates steroid hormone-induced transcription via the chromatin remodeling factor Arip4DNA methylation in the human cerebral cortex is dynamically regulated throughout the life span and involves differentiated neurons.Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndromeHuman intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic markingDisruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.Glaucoma related Proteomic Alterations in Human Retina SamplesLsh, a guardian of heterochromatin at repeat elements.Implication of abnormal epigenetic patterns for human diseases.ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulationGene clusters, molecular evolution and disease: a speculation.Epigenetics and ncRNAs in brain function and disease: mechanisms and prospects for therapy.Decoding the epigenetic language of neuronal plasticity.Epigenetics in the nervous system: An overview of its essential roleMalformation syndromes associated with disorders of sex development.Epigenetic regulation of myofibroblast differentiation and extracellular matrix production in nasal polyp-derived fibroblasts.Histone modifying enzymes: novel disease biomarkers and assay development.Identification of putative targets of DNA (cytosine-5) methylation-mediated transcriptional silencing using a novel conditionally active form of DNA methyltransferase 3a.MBD4-mediated glycosylase activity on a chromatin template is enhanced by acetylation.Epigenetic dynamics and interplay during spermatogenesis and embryogenesis: implications for male fertility and offspring health.Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain of ATRX.Contribution of CAF-I to anaphase-promoting-complex-mediated mitotic chromatin assembly in Saccharomyces cerevisiaeMeCP2 preferentially binds to methylated linker DNA in the absence of the terminal tail of histone H3 and independently of histone acetylation.WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy.IL-13 regulates human nasal epithelial cell differentiation via H3K4me3 modification.Histone modification analysis by chromatin immunoprecipitation from a low number of cells on a microfluidic platform.Patient mutations alter ATRX targeting to PML nuclear bodies.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Syndromes of disordered chromatin remodeling.
@ast
Syndromes of disordered chromatin remodeling.
@en
type
label
Syndromes of disordered chromatin remodeling.
@ast
Syndromes of disordered chromatin remodeling.
@en
prefLabel
Syndromes of disordered chromatin remodeling.
@ast
Syndromes of disordered chromatin remodeling.
@en
P2093
P2860
P1433
P1476
Syndromes of disordered chromatin remodeling.
@en
P2093
P2860
P356
10.1034/J.1399-0004.2003.00124.X
P577
2003-08-01T00:00:00Z