Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy.
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G-protein Coupled Receptor Signaling in Pluripotent Stem Cell-derived Cardiovascular Cells: Implications for Disease ModelingMoving domain computational fluid dynamics to interface with an embryonic model of cardiac morphogenesisTargeted inactivation of Cerberus like-2 leads to left ventricular cardiac hyperplasia and systolic dysfunction in the mouseLoss of Function Mutations in NNT Are Associated With Left Ventricular NoncompactionThe embryological basis of subclinical hypertrophic cardiomyopathyHeart Failure in Pediatric Patients With Congenital Heart Disease.Wnt/β-catenin signaling directs the regional expansion of first and second heart field-derived ventricular cardiomyocytes.Numb family proteins are essential for cardiac morphogenesis and progenitor differentiationTRAPLINE: a standardized and automated pipeline for RNA sequencing data analysis, evaluation and annotationCardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families.Critical roles of miRNA-mediated regulation of TGFβ signalling during mouse cardiogenesis.Multifaceted roles of miR-1s in repressing the fetal gene program in the heartNkx2-5 and Sarcospan genetically interact in the development of the muscular ventricular septum of the heartHow to take autophagy and endocytosis up a notch.MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.A tail of two sites: a bipartite mechanism for recognition of notch ligands by mind bomb E3 ligases.Directed differentiation of patient-specific induced pluripotent stem cells identifies the transcriptional repression and epigenetic modification of NKX2-5, HAND1, and NOTCH1 in hypoplastic left heart syndrome.Biventricular Noncompaction Cardiomyopathy in an Adult with Unique Facial Dysmorphisms: Case Report and Brief ReviewPLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompactionFractal Analysis of Myocardial Trabeculations in 2547 Study Participants: Multi-Ethnic Study of AtherosclerosisThe complex genetics of hypoplastic left heart syndrome.The Dynamic Nature of Hypertrophic and Fibrotic Remodeling of the Fish Ventricle.Single-Cell Lineage Tracing Reveals that Oriented Cell Division Contributes to Trabecular Morphogenesis and Regional Specification.Molecular mechanism of ventricular trabeculation/compaction and the pathogenesis of the left ventricular noncompaction cardiomyopathy (LVNC)Morphogenesis of myocardial trabeculae in the mouse embryo.Cardioprotective actions of Notch1 against myocardial infarction via LKB1-dependent AMPK signaling pathway.iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy.Genetic and functional genomics approaches targeting the Notch pathway in cardiac development and congenital heart disease.The role of Notch pathway in cardiovascular diseases.The Notch pathway: a novel target for myocardial remodelling therapy?Non-compaction cardiomyopathy: prevalence, prognosis, pathoetiology, genetics, and risk of cardioembolism.Insights into the Giardia intestinalis enolase and human plasminogen interaction.Molecular regulation of cardiomyocyte differentiation.Prolonged QTc indicates the clinical severity and poor prognosis in patients with isolated left ventricular non-compaction.Untangling the Biology of Genetic Cardiomyopathies with Pluripotent Stem Cell Disease Models.GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway.Notch signalling in ventricular chamber development and cardiomyopathy.Structure and function of the Mind bomb E3 ligase in the context of Notch signal transduction.The ClusPro web server for protein-protein docking.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.
P2860
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P2860
Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
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2013年學術文章
@zh-hant
name
Mutations in the NOTCH pathway ...... noncompaction cardiomyopathy.
@en
Mutations in the NOTCH pathway ...... noncompaction cardiomyopathy.
@nl
type
label
Mutations in the NOTCH pathway ...... noncompaction cardiomyopathy.
@en
Mutations in the NOTCH pathway ...... noncompaction cardiomyopathy.
@nl
prefLabel
Mutations in the NOTCH pathway ...... noncompaction cardiomyopathy.
@en
Mutations in the NOTCH pathway ...... noncompaction cardiomyopathy.
@nl
P2093
P50
P356
P1433
P1476
Mutations in the NOTCH pathway ...... noncompaction cardiomyopathy.
@en
P2093
Beatriz Martínez-Poveda
Belén Prados
Borja Ibañez
Constancio Medrano
David Dobarro
Gonzalo Pizarro
Guillermo Luxán
Jesús C Casanova
Juan R Gimeno
Leticia Fernández-Friera
P2888
P304
P356
10.1038/NM.3046
P407
P50
P577
2013-01-13T00:00:00Z