scholarly article | Q13442814 |
P50 | author | Leah B Honor | Q57677573 |
Bin Zhou | Q59708703 | ||
P2093 | author name string | Qing Ma | |
Anna Petryk | |||
Alexander von Gise | |||
William T Pu | |||
P2860 | cites work | YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis | Q22009123 |
Slug is a direct Notch target required for initiation of cardiac cushion cellularization | Q24318449 | ||
GenePaint.org: an atlas of gene expression patterns in the mouse embryo | Q24600734 | ||
Characterization and in vivo pharmacological rescue of a Wnt2-Gata6 pathway required for cardiac inflow tract development | Q24610934 | ||
A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo | Q28505232 | ||
Coronary vessel development requires activation of the TrkB neurotrophin receptor by the Wilms' tumor transcription factor Wt1. | Q28507412 | ||
Cell adhesion events mediated by alpha 4 integrins are essential in placental and cardiac development | Q28507437 | ||
Fibroblast growth factor signals regulate a wave of Hedgehog activation that is essential for coronary vascular development | Q28511544 | ||
WT-1 is required for early kidney development | Q28512266 | ||
Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development | Q28513519 | ||
Rescue of cardiac defects in id knockout embryos by injection of embryonic stem cells | Q28589630 | ||
Defective development of the embryonic and extraembryonic circulatory systems in vascular cell adhesion molecule (VCAM-1) deficient mice | Q28590782 | ||
Wnt/beta-catenin/Tcf signaling induces the transcription of Axin2, a negative regulator of the signaling pathway | Q28640887 | ||
Complex networks orchestrate epithelial-mesenchymal transitions | Q29547478 | ||
A global double-fluorescent Cre reporter mouse | Q29616157 | ||
Mapping Wnt/beta-catenin signaling during mouse development and in colorectal tumors | Q29619814 | ||
Wt1 and retinoic acid signaling in the subcoelomic mesenchyme control the development of the pleuropericardial membranes and the sinus horns. | Q33821188 | ||
Endogenous retinoic acid regulates cardiac progenitor differentiation. | Q33927331 | ||
Epicardial retinoid X receptor alpha is required for myocardial growth and coronary artery formation | Q34234421 | ||
Adult mouse epicardium modulates myocardial injury by secreting paracrine factors | Q34875955 | ||
CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors | Q35103587 | ||
Epicardium-derived progenitor cells require beta-catenin for coronary artery formation | Q36156815 | ||
Epicardium-derived cells in cardiogenesis and cardiac regeneration | Q36767594 | ||
Epicardial progenitors contribute to the cardiomyocyte lineage in the developing heart. | Q36952843 | ||
An integrated genome screen identifies the Wnt signaling pathway as a major target of WT1. | Q37256912 | ||
Epicardial induction of fetal cardiomyocyte proliferation via a retinoic acid-inducible trophic factor | Q40701785 | ||
A myocardial lineage derives from Tbx18 epicardial cells | Q41213731 | ||
Wt1 controls retinoic acid signalling in embryonic epicardium through transcriptional activation of Raldh2. | Q42052856 | ||
Genetic fate mapping demonstrates contribution of epicardium-derived cells to the annulus fibrosis of the mammalian heart | Q42271204 | ||
Wt1 is required for cardiovascular progenitor cell formation through transcriptional control of Snail and E-cadherin. | Q42945812 | ||
Retinoic acid and VEGF delay smooth muscle relative to endothelial differentiation to coordinate inner and outer coronary vessel wall morphogenesis. | Q43044958 | ||
Erythropoietin and retinoic acid, secreted from the epicardium, are required for cardiac myocyte proliferation | Q44369644 | ||
A caudorostral wave of RALDH2 conveys anteroposterior information to the cardiac field | Q44586410 | ||
Wt1 and retinoic acid signaling are essential for stellate cell development and liver morphogenesis | Q46889320 | ||
Dynamic patterns of retinoic acid synthesis and response in the developing mammalian heart | Q47796138 | ||
The serosal mesothelium is a major source of smooth muscle cells of the gut vasculature. | Q52034331 | ||
YAC transgenic analysis reveals Wilms' tumour 1 gene activity in the proliferating coelomic epithelium, developing diaphragm and limb. | Q52176765 | ||
Epicardial outgrowth inhibition leads to compensatory mesothelial outflow tract collar and abnormal cardiac septation and coronary formation | Q73221474 | ||
A mitogen gradient of dorsal midline Wnts organizes growth in the CNS | Q77960718 | ||
Wnt5a is required for cardiac outflow tract septation in mice | Q80362379 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | tretinoin | Q29417 |
P304 | page(s) | 421-431 | |
P577 | publication date | 2011-05-30 | |
P1433 | published in | Developmental Biology | Q3025402 |
P1476 | title | WT1 regulates epicardial epithelial to mesenchymal transition through β-catenin and retinoic acid signaling pathways | |
P478 | volume | 356 |
Q26859990 | "String theory" of c-kit(pos) cardiac cells: a new paradigm regarding the nature of these cells that may reconcile apparently discrepant results |
Q37642991 | A dynamic spatiotemporal extracellular matrix facilitates epicardial-mediated vertebrate heart regeneration |
Q43626717 | A glimpse of Cre-mediated controversies in epicardial signalling. |
Q88879573 | Alterations in retinoic acid signaling affect the development of the mouse coronary vasculature |
Q92438901 | Altered haemodynamics causes aberrations in the epicardium |
Q42001387 | Approaches to augment vascularisation and regeneration of the adult heart via the reactivated epicardium |
Q41126801 | BRG1-SWI/SNF-dependent regulation of the Wt1 transcriptional landscape mediates epicardial activity during heart development and disease |
Q36731334 | C/EBP transcription factors mediate epicardial activation during heart development and injury. |
Q55254109 | Cancer Stem Cells are Regulated by STAT3 Signalling in Wilms Tumour. |
Q50601069 | Cardiac endothelial cells express Wilms' tumor-1: Wt1 expression in the developing, adult and infarcted heart. |
Q34291299 | Cardiac explant-derived cells are regulated by Notch-modulated mesenchymal transition |
Q38337373 | Cellular origin and developmental program of coronary angiogenesis. |
Q36073691 | Characterisation of Cultured Mesothelial Cells Derived from the Murine Adult Omentum. |
Q38659781 | Coelomic epithelium-derived cells in visceral morphogenesis. |
Q37265937 | Conditional deletion of WT1 in the septum transversum mesenchyme causes congenital diaphragmatic hernia in mice |
Q38711945 | Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology--a position statement of the development, anatomy, and pathology ESC Working Group. |
Q36765923 | Contribution of Fetal, but Not Adult, Pulmonary Mesothelium to Mesenchymal Lineages in Lung Homeostasis and Fibrosis |
Q33557435 | Derivation of lung mesenchymal lineages from the fetal mesothelium requires hedgehog signaling for mesothelial cell entry |
Q38856926 | Discovering cardiac pericyte biology: From physiopathological mechanisms to potential therapeutic applications in ischemic heart disease |
Q38148527 | Embryonic heart progenitors and cardiogenesis |
Q26830155 | Endocardial and epicardial epithelial to mesenchymal transitions in heart development and disease |
Q26767045 | Epicardial Epithelial-to-Mesenchymal Transition in Heart Development and Disease |
Q53785255 | Epicardial Outgrowth Culture Assay and Ex Vivo Assessment of Epicardial-derived Cell Migration. |
Q90162709 | Epicardial TGFβ and BMP Signaling in Cardiac Regeneration: What Lesson Can We Learn from the Developing Heart? |
Q46355504 | Epicardial function of canonical Wnt-, Hedgehog-, Fgfr1/2-, and Pdgfra-signalling |
Q38015278 | Epicardial progenitor cells in cardiac development and regeneration |
Q41465394 | Epicardium is required for cardiac seeding by yolk sac macrophages, precursors of resident macrophages of the adult heart. |
Q38603614 | Epicardium-derived fibroblasts in heart development and disease. |
Q35906030 | Epithelial-to-mesenchymal and endothelial-to-mesenchymal transition: from cardiovascular development to disease. |
Q50778667 | Epithelial-to-mesenchymal transition in epicardium is independent of Snail1. |
Q37090676 | Fibrosis of the Neonatal Mouse Heart After Cryoinjury Is Accompanied by Wnt Signaling Activation and Epicardial-to-Mesenchymal Transition |
Q64984213 | Functional Role of Non-Coding RNAs during Epithelial-To-Mesenchymal Transition. |
Q26823949 | Functional Role of WT1 in Prostate Cancer |
Q62663831 | Functional molecules in mesothelial-to-mesenchymal transition revealed by transcriptome analyses |
Q34316132 | Generation of the epicardial lineage from human pluripotent stem cells |
Q42434214 | Genetic Cre-loxP assessment of epicardial cell fate using Wt1-driven Cre alleles. |
Q38654054 | Heart regeneration and repair after myocardial infarction: translational opportunities for novel therapeutics |
Q27001686 | Heart repair and regeneration: recent insights from zebrafish studies |
Q27301898 | Helicase-like transcription factor (Hltf) regulates G2/M transition, Wt1/Gata4/Hif-1a cardiac transcription networks, and collagen biogenesis |
Q36913611 | Hippo Signaling Mediators Yap and Taz Are Required in the Epicardium for Coronary Vasculature Development |
Q37456851 | Human fetal and adult epicardial-derived cells: a novel model to study their activation. |
Q39209922 | Human induced pluripotent stem cell-derived ectodermal precursor cells contribute to hair follicle morphogenesis in vivo |
Q47120885 | Identification of WT1 as determinant of heptatocellular carcinoma and its inhibition by Chinese herbal medicine Salvia chinensis Benth and its active ingredient protocatechualdehyde |
Q34048743 | Implications of the Wnt5a/CaMKII pathway in retinoic acid-induced myogenic tongue abnormalities of developing mice |
Q37998444 | Importance of myocyte-nonmyocyte interactions in cardiac development and disease |
Q24630155 | Increased dietary intake of vitamin A promotes aortic valve calcification in vivo |
Q58786498 | Injury-induced fetal reprogramming imparts multipotency and reparative properties to pericardial adipose stem cells |
Q36179651 | Insulin-Like Growth Factor 1 Receptor-Dependent Pathway Drives Epicardial Adipose Tissue Formation After Myocardial Injury |
Q37503436 | Lamin-B1 contributes to the proper timing of epicardial cell migration and function during embryonic heart development |
Q92844784 | Maternal voluntary exercise mitigates oxidative stress and incidence of congenital heart defects in pre-gestational diabetes |
Q36598066 | Mesothelial cells give rise to hepatic stellate cells and myofibroblasts via mesothelial-mesenchymal transition in liver injury |
Q57814182 | Mesothelial to mesenchyme transition as a major developmental and pathological player in trunk organs and their cavities |
Q51146170 | Micro RNAs are involved in activation of epicardium during zebrafish heart regeneration. |
Q38953681 | MicroRNA-191, by promoting the EMT and increasing CSC-like properties, is involved in neoplastic and metastatic properties of transformed human bronchial epithelial cells |
Q30580723 | Modified mRNA directs the fate of heart progenitor cells and induces vascular regeneration after myocardial infarction |
Q37371548 | Myc overexpression enhances of epicardial contribution to the developing heart and promotes extensive expansion of the cardiomyocyte population |
Q46348323 | Myocardial Infarct Scar: Hunting Down the Responsible Cells, But Then What? |
Q34985191 | Myocardin-related transcription factors control the motility of epicardium-derived cells and the maturation of coronary vessels |
Q38738993 | Navigating the labyrinth of cardiac regeneration |
Q92546203 | Neuropilin 1 mediates epicardial activation and revascularization in the regenerating zebrafish heart |
Q36108192 | Numb family proteins: novel players in cardiac morphogenesis and cardiac progenitor cell differentiation |
Q35775407 | PDGFRα demarcates the cardiogenic clonogenic Sca1+ stem/progenitor cell in adult murine myocardium |
Q62607845 | Pan-epicardial lineage tracing reveals that epicardium derived cells give rise to myofibroblasts and perivascular cells during zebrafish heart regeneration |
Q36148533 | Pod1/Tcf21 is regulated by retinoic acid signaling and inhibits differentiation of epicardium-derived cells into smooth muscle in the developing heart. |
Q91640846 | Pre-existing fibroblasts of epicardial origin are the primary source of pathological fibrosis in cardiac ischemia and aging |
Q38825941 | Probing early heart development to instruct stem cell differentiation strategies |
Q36875332 | Prokineticin receptor-1 signaling promotes Epicardial to Mesenchymal Transition during heart development |
Q92877879 | Rational Reprogramming of Cellular States by Combinatorial Perturbation |
Q49239010 | Recapitulation of developmental mechanisms to revascularize the ischemic heart |
Q91843151 | Recent insights on the role and regulation of retinoic acid signaling during epicardial development |
Q35782005 | Regional differences in WT-1 and Tcf21 expression during ventricular development: implications for myocardial compaction |
Q38698079 | Regulation of retinoic acid synthetic enzymes by WT1 and HDAC inhibitors in 293 cells |
Q92445859 | Reiterative Mechanisms of Retinoic Acid Signaling during Vertebrate Heart Development |
Q37577416 | Retinoic acid alters the proliferation and survival of the epithelium and mesenchyme and suppresses Wnt/β-catenin signaling in developing cleft palate |
Q90297521 | Retinoic acid signaling in heart development |
Q49982092 | Retinoic acid signaling promotes the cytoskeletal rearrangement of embryonic epicardial cells |
Q30638155 | Robust derivation of epicardium and its differentiated smooth muscle cell progeny from human pluripotent stem cells |
Q41266029 | Snai1 is important for avian epicardial cell transformation and motility |
Q41903030 | Tbx18 regulates development of the epicardium and coronary vessels. |
Q36503371 | Tbx5 is required for avian and Mammalian epicardial formation and coronary vasculogenesis |
Q89427974 | Temporary, Systemic Inhibition of the WNT/β-Catenin Pathway promotes Regenerative Cardiac Repair following Myocardial Infarct |
Q33732860 | The Epicardium and the Development of the Atrioventricular Junction in the Murine Heart |
Q38897318 | The Role of WT1 in Embryonic Development and Normal Organ Homeostasis |
Q98224256 | The Roles of Noncardiomyocytes in Cardiac Remodeling |
Q50551462 | The epicardium as modulator of the cardiac autonomic response during early development. |
Q50543643 | The roadmap of WT1 protein expression in the human fetal heart. |
Q34612490 | The transcription factors Tbx18 and Wt1 control the epicardial epithelial-mesenchymal transition through bi-directional regulation of Slug in murine primary epicardial cells |
Q38013063 | Thymosin β4 and cardiac regeneration: are we missing a beat? |
Q39007418 | Transcriptional Control of Cell Lineage Development in Epicardium-Derived Cells. |
Q50971977 | Turning back the Wheel: Inducing Mesenchymal to Epithelial Transition via Wilms Tumor 1 Knockdown in Human Mesothelioma Cell Lines to Influence Proliferation, Invasiveness, and Chemotaxis. |
Q47948619 | Wilms' tumour 1 (WT1) in development, homeostasis and disease. |
Q47280595 | Wnt inhibition promotes vascular specification of embryonic cardiac progenitors |
Q64236020 | Wnt signaling in orofacial clefts: crosstalk, pathogenesis and models |
Q38659755 | Wnt signaling in the heart fields: Variations on a common theme |
Q52655129 | Wnt5a is necessary for normal kidney development in zebrafish and mice. |
Q36271500 | Wt1 and β-catenin cooperatively regulate diaphragm development in the mouse |
Q37190836 | Wtip is required for proepicardial organ specification and cardiac left/right asymmetry in zebrafish |
Search more.