A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development
about
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceMechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathiesChild health, developmental plasticity, and epigenetic programmingComparison of two related lines of tauGFP transgenic mice designed for lineage tracingDifferential regulation of the α-globin locus by Krüppel-like Factor 3 in erythroid and non-erythroid cells.An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouseThe first mouse mutants of D14Abb1e (Fam208a) show that it is critical for early development.Opposite effects on facial morphology due to gene dosage sensitivityModifier genes and the plasticity of genetic networks in mice.An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.Repeat-induced gene silencing of L1 transgenes is correlated with differential promoter methylation.The WSTF-ISWI chromatin remodeling complex transiently associates with the human inactive X chromosome during late S-phase prior to BRCA1 and γ-H2AXReduced levels of two modifiers of epigenetic gene silencing, Dnmt3a and Trim28, cause increased phenotypic noise.Genetic analysis of litter size in miceDGCR14 induces Il17a gene expression through the RORγ/BAZ1B/RSKS2 complex.Facioscapulohumeral muscular dystrophy as a model for epigenetic regulation and diseaseGenetic and epigenetic characteristics of FSHD-associated 4q and 10q D4Z4 that are distinct from non-4q/10q D4Z4 homologsThe contribution of CLIP2 haploinsufficiency to the clinical manifestations of the Williams-Beuren syndrome.BAZ1B is dispensable for H2AX phosphorylation on Tyrosine 142 during spermatogenesisIndependent Mechanisms Target SMCHD1 to Trimethylated Histone H3 Lysine 9-Modified Chromatin and the Inactive X Chromosome.Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevisDNA-binding sequence specificity of DUX4.The use of mouse models to study epigeneticsTranscriptional silencing and reactivation in transgenic zebrafish.Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits.Animal models of Williams syndrome.The hunt for the epiallele.WSTF does it all: a multifunctional protein in transcription, repair, and replication.5-hydroxymethylcytosine profiling as an indicator of cellular state.Loss of epigenetic silencing of the DUX4 transcription factor gene in facioscapulohumeral muscular dystrophy.Position-effect variegation revisited: HUSHing up heterochromatin in human cells.ATP-dependent chromatin remodeling during mammalian development.Modeling Williams syndrome with induced pluripotent stem cells.Hepcidin independent iron recycling in a mouse model of β-thalassaemia intermedia.Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families.A forward genetic screen identifies eukaryotic translation initiation factor 3, subunit H (eIF3h), as an enhancer of variegation in the mouse.Allele-specific DNA methylation in mouse strains is mainly determined by cis-acting sequences.Utility and limitations of animal models for the functional validation of human sequence variants.A missense mutation in the transcription factor Foxo3a causes teratomas and oocyte abnormalities in mice.Hypothesis: the female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural fold elevation.
P2860
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P2860
A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development
description
2008 nî lūn-bûn
@nan
2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
A genome-wide screen for modif ...... critical roles in development
@ast
A genome-wide screen for modif ...... critical roles in development
@en
A genome-wide screen for modif ...... critical roles in development
@nl
type
label
A genome-wide screen for modif ...... critical roles in development
@ast
A genome-wide screen for modif ...... critical roles in development
@en
A genome-wide screen for modif ...... critical roles in development
@nl
prefLabel
A genome-wide screen for modif ...... critical roles in development
@ast
A genome-wide screen for modif ...... critical roles in development
@en
A genome-wide screen for modif ...... critical roles in development
@nl
P2093
P2860
P50
P1433
P1476
A genome-wide screen for modif ...... critical roles in development
@en
P2093
Alyson Ashe
Daniel K Morgan
Emma Whitelaw
Liza L Cox
Marnie E Blewitt
Nadia C Whitelaw
Natalie C Butterfield
Nicola K Vickaryous
Sarah J Wilkins
Timothy C Cox
P2860
P2888
P356
10.1186/GB-2008-9-12-R182
P577
2008-12-19T00:00:00Z
P5875
P6179
1021525172