Nipbl and mediator cooperatively regulate gene expression to control limb development.
about
Mediator kinase module and human tumorigenesisThe Mediator complex: a central integrator of transcriptionDisorders of Transcriptional Regulation: An Emerging Category of Multiple Malformation SyndromesImproved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndromeConditional Creation and Rescue of Nipbl-Deficiency in Mice Reveals Multiple Determinants of Risk for Congenital Heart DefectsIdentification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development.NIPBL Controls RNA Biogenesis to Prevent Activation of the Stress Kinase PKR.Genetic enhancement of limb defects in a mouse model of Cornelia de Lange syndrome.Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange SyndromeEtiology and pathogenesis of the cohesinopathies.5C analysis of the Epidermal Differentiation Complex locus reveals distinct chromatin interaction networks between gene-rich and gene-poor TADs in skin epithelial cells.The two domain hypothesis of limb prepattern and its relevance to congenital limb anomalies.Resolving the Genomic Localization of the Kollerin Cohesin-Loader Complex.How many roads lead to cohesinopathies?Structure of the cohesin loader Scc2.The cohesin complex prevents Myc-induced replication stress.mRNA Quantification of NIPBL Isoforms A and B in Adult and Fetal Human Tissues, and a Potentially Pathological Variant Affecting Only Isoform A in Two Patients with Cornelia de Lange Syndrome.Zebrafish as a Model to Study Cohesin and Cohesinopathies.Neural EGFL-Like 1 Regulates Cartilage Maturation through Runt-Related Transcription Factor 3-Mediated Indian Hedgehog Signaling.Chl1 DNA helicase and Scc2 function in chromosome condensation through cohesin deposition.Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome.Connected Gene Communities Underlie Transcriptional Changes in Cornelia de Lange Syndrome.NIPBL+/- haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states.
P2860
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P2860
Nipbl and mediator cooperatively regulate gene expression to control limb development.
description
2014 nî lūn-bûn
@nan
2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@ast
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@en
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@nl
type
label
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@ast
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@en
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@nl
prefLabel
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@ast
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@en
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@nl
P2093
P2860
P1433
P1476
Nipbl and mediator cooperatively regulate gene expression to control limb development.
@en
P2093
Akihiko Muto
Anne L Calof
Arthur D Lander
Martha E Lopez-Burks
Shingo Ikeda
Thomas F Schilling
Yutaka Kikuchi
P2860
P304
P356
10.1371/JOURNAL.PGEN.1004671
P577
2014-09-25T00:00:00Z