Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens - Wikidata - wikimedia - TriplyDB

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

http://www.wikidata.org/entity/Q42573684

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The elephant shark methylome reveals conservation of epigenetic regulation across jawed vertebrates.Zebrafish mll gene is essential for hematopoiesis.Cell-specific DNA methylation patterns of retina-specific genes The cellular and molecular mechanisms of vertebrate lens development.DNA hypomethylation induces a DNA replication-associated cell cycle arrest to block hepatic outgrowth in uhrf1 mutant zebrafish embryos Epigenetic control of intestinal barrier function and inflammation in zebrafish.The visual system of zebrafish and its use to model human ocular diseases.H3K9 methyltransferase G9a negatively regulates UHRF1 transcription during leukemia cell differentiation UHRF1 phosphorylation by cyclin A2/cyclin-dependent kinase 2 is required for zebrafish embryogenesis.Basic concepts of epigenetics: impact of environmental signals on gene expression.Eyes on DNA methylation: current evidence for DNA methylation in ocular development and disease.An ENU mutagenesis screen in zebrafish for visual system mutants identifies a novel splice-acceptor site mutation in patched2 that results in Colobomas.Changes in zebrafish (Danio rerio) lens crystallin content during development Zebrafish models of human liver development and disease UHRF1 regulation of Dnmt1 is required for pre-gastrula zebrafish development.Identification of HMX1 target genes: a predictive promoter model approach.Transient reduction of 5-methylcytosine and 5-hydroxymethylcytosine is associated with active DNA demethylation during regeneration of zebrafish fin.Pdgfra protects against ethanol-induced craniofacial defects in a zebrafish model of FASD.UHRF1 overexpression drives DNA hypomethylation and hepatocellular carcinoma Epigenetics, development, and cancer: zebrafish make their mark..The role of methyl-binding proteins in chromatin organization and epigenome maintenance.Epigenetics and ocular diseases: from basic biology to clinical study.Zebrafish as a model to study the role of DNA methylation in environmental toxicology.Examination of a palatogenic gene program in zebrafish.PIM1 induces cellular senescence through phosphorylation of UHRF1 at Ser311.The Role of DNA Methylation in Lens Development and Cataract Formation.DNA methyl transferases are differentially expressed in the human anterior eye segment.Loss of DNA methylation in zebrafish embryos activates retrotransposons to trigger antiviral signaling.Tet-mediated DNA hydroxymethylation regulates retinal neurogenesis by modulating cell-extrinsic signaling pathways.Lens development requires DNMT1 but takes place normally in the absence of both DNMT3A and DNMT3B activity.[Epigenetic regulation in neuronal differentiation and brain function].Expression of the de novo DNA methyltransferases (dnmt3 - dnmt8) during zebrafish lens development.Developmental Functions of the Dynamic DNA Methylome and Hydroxymethylome in the Mouse and Zebrafish: Similarities and Differences.Epigenetic therapy restores normal hematopoiesis in a zebrafish model of NUP98-HOXA9-induced myeloid disease.Aqp0a Regulates Suture Stability in the Zebrafish Lens.Uhrf1 regulates active transcriptional marks at bivalent domains in pluripotent stem cells through Setd1a.

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Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

http://www.wikidata.org/entity/Q42573684

description

2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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2010年论文

@zh-cn

name

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

@en

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

@nl

type

label

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

@en

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

@nl

prefLabel

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

@en

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

@nl

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J.YDBIO.2010.11.009

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Developmental Biology

P1476

Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens

@en

P2093

Anthony Ng

http://www.w3.org/2001/XMLSchema#string

Johann K Eberhart

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Justin Bosch

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Mary E Swartz

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Rachel K Tittle

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Richard J Nuckels

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Ryan M Anderson

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Ryan Sze

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P2860

DNA methylation patterns and epigenetic memory

The interaction of the SRA domain of ICBP90 with a novel domain of DNMT1 is involved in the regulation of VEGF gene expression

ICBP90, a novel methyl K9 H3 binding protein linking protein ubiquitination with heterochromatin formation

Np95 interacts with de novo DNA methyltransferases, Dnmt3a and Dnmt3b, and mediates epigenetic silencing of the viral CMV promoter in embryonic stem cells

UHRF1 plays a role in maintaining DNA methylation in mammalian cells

The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores

ICBP90, a novel human CCAAT binding protein, involved in the regulation of topoisomerase IIalpha expression

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

Down-regulation of nuclear protein ICBP90 by p53/p21Cip1/WAF1-dependent DNA-damage checkpoint signals contributes to cell cycle arrest at G1/S transition

The retinoblastoma gene and its product are targeted by ICBP90: a key mechanism in the G1/S transition during the cell cycle

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50-63

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scholarly article

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10.1016/J.YDBIO.2010.11.009

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1

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350

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Didier Stainier

Jeffrey M Gross

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2010-11-30T00:00:00Z

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49653443

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21126517

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3022120

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