scholarly article | Q13442814 |
P2093 | author name string | Ileana M Cristea | |
Frank L Conlon | |||
Lauren M Kuchenbrod | |||
Panna Tandon | |||
Yana V Miteva | |||
P2860 | cites work | YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis | Q22009123 |
Modulation of the expression and transactivation of androgen receptor by the basic helix-loop-helix transcription factor Pod-1 through recruitment of histone deacetylase 1 | Q24303847 | ||
A novel C-terminal binding protein (CTBP2) is closely related to CTBP1, an adenovirus E1A-binding protein, and maps to human chromosome 21q21.3 | Q24312935 | ||
Basic helix-loop-helix transcription factor epicardin/capsulin/Pod-1 suppresses differentiation by negative regulation of transcription | Q24337398 | ||
Overlapping and unique roles for C-terminal binding protein 1 (CtBP1) and CtBP2 during mouse development. | Q24537603 | ||
A conserved motif N-terminal to the DNA-binding domains of myogenic bHLH transcription factors mediates cooperative DNA binding with pbx-Meis1/Prep1 | Q24548862 | ||
Helix-loop-helix proteins: regulators of transcription in eucaryotic organisms | Q24554353 | ||
Negative and positive regulation of gene expression by mouse histone deacetylase 1 | Q24672508 | ||
An atypical PKC directly associates and colocalizes at the epithelial tight junction with ASIP, a mammalian homologue of Caenorhabditis elegans polarity protein PAR-3 | Q24682973 | ||
Endocardial and epicardial epithelial to mesenchymal transitions in heart development and disease | Q26830155 | ||
Wnt11-R, a protein closely related to mammalian Wnt11, is required for heart morphogenesis in Xenopus | Q28307143 | ||
The basic-helix-loop-helix protein pod1 is critically important for kidney and lung organogenesis | Q28504626 | ||
Cloning of capsulin, a basic helix-loop-helix factor expressed in progenitor cells of the pericardium and the coronary arteries | Q28505293 | ||
Pod-1/Capsulin shows a sex- and stage-dependent expression pattern in the mouse gonad development and represses expression of Ad4BP/SF-1 | Q28507235 | ||
Capsulin: a novel bHLH transcription factor expressed in epicardial progenitors and mesenchyme of visceral organs | Q28507663 | ||
Kielin/chordin-like protein, a novel enhancer of BMP signaling, attenuates renal fibrotic disease | Q28508295 | ||
Pod1 is required in stromal cells for glomerulogenesis | Q28509812 | ||
The basic helix-loop-helix transcription factor capsulin controls spleen organogenesis | Q28510286 | ||
Pod-1, a mesoderm-specific basic-helix-loop-helix protein expressed in mesenchymal and glomerular epithelial cells in the developing kidney | Q28585814 | ||
Epicardial-derived cell epithelial-to-mesenchymal transition and fate specification require PDGF receptor signaling. | Q42137346 | ||
Cell surface glycoconjugates and the extracellular matrix of the developing mouse embryo epicardium | Q42481029 | ||
PAR3 is essential for cyst-mediated epicardial development by establishing apical cortical domains. | Q42491526 | ||
Epicardial development in lamprey supports an evolutionary origin of the vertebrate epicardium from an ancestral pronephric external glomerulus | Q42525372 | ||
Analysis of the proepicardium-epicardium transition during the malformation of the RXRalpha-/- epicardium | Q42734016 | ||
Distinct and redundant functions of histone deacetylases HDAC1 and HDAC2 in proliferation and tumorigenesis. | Q42757408 | ||
tcf21+ epicardial cells adopt non-myocardial fates during zebrafish heart development and regeneration | Q42766102 | ||
Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline | Q42868304 | ||
Wt1 is required for cardiovascular progenitor cell formation through transcriptional control of Snail and E-cadherin. | Q42945812 | ||
Small heat shock protein Hsp27 is required for proper heart tube formation | Q43146663 | ||
Regulation of neurocoel morphogenesis by Pard6 gamma b. | Q43198871 | ||
alpha4 integrin is expressed in a subset of cranial neural crest cells and in epicardial progenitor cells during early mouse development. | Q43512229 | ||
Distinct distribution of vimentin and cytokeratin in Xenopus oocytes and early embryos | Q44590561 | ||
Use of Kikume green-red fusions to study the influence of pharmacological chaperones on trafficking of G protein-coupled receptors | Q45011170 | ||
Inhibition of α4-integrin stimulates epicardial–mesenchymal transformation and alters migration and cell fate of epicardially derived mesenchyme | Q45258552 | ||
Communication between integrin receptors facilitates epicardial cell adhesion and matrix organization. | Q45267926 | ||
Transforming growth factor-beta induces loss of epithelial character and smooth muscle cell differentiation in epicardial cells | Q46782583 | ||
Development of the proepicardial organ in the zebrafish | Q46799857 | ||
Cloning and expression analysis of the mouse T-box gene Tbx18. | Q47807069 | ||
Wilms' tumor suppressor gene is involved in the development of disparate kidney forms: evidence from expression in the Xenopus pronephros | Q48063713 | ||
SM22 alpha, a marker of adult smooth muscle, is expressed in multiple myogenic lineages during embryogenesis | Q48066756 | ||
Distinct in vivo engraftment and growth patterns of t(1;19)+/E2A-PBX1+ and t(9;22)+/BCR-ABL+ human leukemia cells in SCID mice | Q48276056 | ||
Development of the proepicardium in Xenopus laevis | Q48743572 | ||
Morphological and molecular left-right asymmetries in the development of the proepicardium: a comparative analysis on mouse and chick embryos | Q48744477 | ||
Evidence for an extracellular matrix bridge guiding proepicardial cell migration to the myocardium of chick embryos. | Q50493507 | ||
Cellular characterization of MPZ mutations presenting with diverse clinical phenotypes. | Q50553666 | ||
Preservation of left ventricular function and attenuation of remodeling after transplantation of human epicardium-derived cells into the infarcted mouse heart. | Q50670579 | ||
Preparation of fixed Xenopus embryos for confocal imaging. | Q51909183 | ||
Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis. | Q51928742 | ||
A dynamic epicardial injury response supports progenitor cell activity during zebrafish heart regeneration. | Q52002879 | ||
A new direction for cardiac regeneration therapy: application of synergistically acting epicardium-derived cells and cardiomyocyte progenitor cells | Q39928426 | ||
PDGF-A as an epicardial mitogen during heart development | Q40009186 | ||
Pod1 induces myofibroblast differentiation in mesenchymal progenitor cells from mouse kidney | Q40123333 | ||
Induction of proepicardial marker gene expression by the liver bud. | Q40174197 | ||
The Wilms tumor suppressor Wt1 promotes cell adhesion through transcriptional activation of the alpha4integrin gene | Q40241736 | ||
Glomerular permeability is altered by loss of P0, a myelin protein expressed in glomerular epithelial cells | Q40373511 | ||
Does the subepicardial mesenchyme contribute myocardioblasts to the myocardium of the chick embryo heart? A quail-chick chimera study tracing the fate of the epicardial primordium | Q40810484 | ||
Cytokeratins as a marker for epicardial formation in the quail embryo | Q40984991 | ||
The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments | Q28586354 | ||
A Pbx1-dependent genetic and transcriptional network regulates spleen ontogeny | Q28590235 | ||
REVIGO summarizes and visualizes long lists of gene ontology terms | Q29614817 | ||
Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips | Q29614831 | ||
GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists | Q29615019 | ||
Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos | Q29620084 | ||
Mechanisms, mechanics and function of epithelial-mesenchymal transitions in early development | Q30311953 | ||
Transient early embryonic expression of Nkx2-5 mutations linked to congenital heart defects in human causes heart defects in Xenopus laevis | Q30480671 | ||
Use of KikGR a photoconvertible green-to-red fluorescent protein for cell labeling and lineage analysis in ES cells and mouse embryos | Q30494573 | ||
BMP signals promote proepicardial protrusion necessary for recruitment of coronary vessel and epicardial progenitors to the heart | Q30496194 | ||
Generation and characterization of iUBC-KikGR photoconvertible transgenic mice for live time-lapse imaging during development | Q30523832 | ||
Cell type-dependent transactivation or repression of mesoderm-restricted basic helix-loop-helix protein, POD-1/Capsulin | Q30872611 | ||
Analysis of TBX18 expression in chick embryos | Q33204809 | ||
Discovering motifs in ranked lists of DNA sequences | Q33279806 | ||
GATA4/FOG2 transcriptional complex regulates Lhx9 gene expression in murine heart development | Q33346498 | ||
SHP-2 is required for the maintenance of cardiac progenitors | Q33595597 | ||
Nuclear Import of Histone Deacetylase 5 by Requisite Nuclear Localization Signal Phosphorylation | Q33748395 | ||
The BMP pathway acts to directly regulate Tbx20 in the developing heart. | Q33840093 | ||
Histone deacetylase 1 (HDAC1), but not HDAC2, controls embryonic stem cell differentiation | Q33929178 | ||
Tbx5 and Bmp signaling are essential for proepicardium specification in zebrafish | Q33942656 | ||
Tazarotene-induced gene 1 inhibits prostaglandin E2-stimulated HCT116 colon cancer cell growth | Q34086015 | ||
Clusterin | Q34119745 | ||
Matrix remodeling in the ovary: regulation and functional role of the plasminogen activator and matrix metalloproteinase systems | Q34126544 | ||
Imbalance of Plasminogen Activator Inhibitor Type-1 (PAI-1) and Tissue Plasminogen Activator (t-PA) Activity in Patients With Noonan Syndrome | Q34129775 | ||
Depletion of the actin bundling protein SM22/transgelin increases actin dynamics and enhances the tumourigenic phenotypes of cells | Q34132416 | ||
Epigenetic deregulation of TCF21 inhibits metastasis suppressor KISS1 in metastatic melanoma | Q34201939 | ||
Distinct compartments of the proepicardial organ give rise to coronary vascular endothelial cells | Q34261674 | ||
The bHLH transcription factor Tcf21 is required for lineage-specific EMT of cardiac fibroblast progenitors. | Q34273888 | ||
Ubiquitin-Proteasome-mediated degradation of Id1 is modulated by MyoD. | Q34323067 | ||
Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation. | Q34405424 | ||
A novel fibroblast growth factor gene expressed in the developing nervous system is a downstream target of the chimeric homeodomain oncoprotein E2A-Pbx1. | Q34440327 | ||
Fluorescent proteins as proteomic probes. | Q34450046 | ||
Xenbase: a Xenopus biology and genomics resource | Q34584638 | ||
S100A11 mediates hypoxia-induced mitogenic factor (HIMF)-induced smooth muscle cell migration, vesicular exocytosis, and nuclear activation | Q34616744 | ||
Developmental expression of Pod 1 in Xenopus laevis. | Q52056112 | ||
Cloning of zebrafish T-box genes tbx15 and tbx18 and their expression during embryonic development. | Q52116128 | ||
YAC transgenic analysis reveals Wilms' tumour 1 gene activity in the proliferating coelomic epithelium, developing diaphragm and limb. | Q52176765 | ||
A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus. | Q52247943 | ||
Pericardial mesoderm generates a population of coronary smooth muscle cells migrating into the heart along with ingrowth of the epicardial organ. | Q53678848 | ||
Conditional inactivation of TGF-β type II receptor in smooth muscle cells and epicardium causes lethal aortic and cardiac defects. | Q54688073 | ||
Myocardial infarction induces embryonic reprogramming of epicardial c-kit(+) cells: role of the pericardial fluid. | Q54705281 | ||
Origin, fate, and function of epicardium-derived cells (EPDCs) in normal and abnormal cardiac development. | Q55282875 | ||
Formation of the Venous Pole of the Heart From an Nkx2-5-Negative Precursor Population Requires Tbx18 | Q56000972 | ||
Identification of Myocardial and Vascular Precursor Cells in Human and Mouse Epicardium | Q61824978 | ||
Changes in C-terminal binding protein 2 (CtBP2) corepressor complex induced by E1A and modulation of E1A transcriptional activity by CtBP2 | Q64377469 | ||
Origin and development of the epicardium in the mouse embryo | Q69193857 | ||
Early limb development of Xenopus laevis | Q70705541 | ||
Left and right contributions to the Xenopus heart: implications for asymmetric morphogenesis | Q73432592 | ||
Expression of smooth muscle alpha-actin in mesenchymal cells during formation of avian endocardial cushion tissue: A role for transforming growth factor β3 | Q73494345 | ||
Localization of the Wilm's tumour protein WT1 in avian embryos | Q73724818 | ||
Smooth muscle cells and fibroblasts of the coronary arteries derive from epithelial-mesenchymal transformation of the epicardium | Q77296275 | ||
Expression of the bHLH transcription factor Tcf12 (ME1) gene is linked to the expansion of precursor cell populations during neurogenesis | Q79773025 | ||
Rapid isolation of glomeruli coupled with gene expression profiling identifies downstream targets in Pod1 knockout mice | Q81316661 | ||
In vivo and in vitro analysis of the vasculogenic potential of avian proepicardial and epicardial cells | Q82462288 | ||
Ca2+-binding protein S100A11: a novel diagnostic marker for breast carcinoma | Q84013991 | ||
FGF-1 reverts epithelial-mesenchymal transition induced by TGF-{beta}1 through MAPK/ERK kinase pathway | Q84284635 | ||
The cysteine-rich domain protein KCP is a suppressor of transforming growth factor beta/activin signaling in renal epithelia | Q34718144 | ||
Roles of clusterin in progression, chemoresistance and metastasis of human ovarian cancer | Q34977601 | ||
CtBP family proteins: more than transcriptional corepressors | Q35036904 | ||
Xenopus: An emerging model for studying congenital heart disease | Q35075360 | ||
TBX5 is required for embryonic cardiac cell cycle progression | Q35129339 | ||
Transforming growth factor-beta stimulates epithelial-mesenchymal transformation in the proepicardium | Q35177514 | ||
The origins of cardiac tissue in the amphibian, Xenopus laevis | Q35201190 | ||
TCF12 protein functions as transcriptional repressor of E-cadherin, and its overexpression is correlated with metastasis of colorectal cancer | Q35710117 | ||
SHP-2 acts via ROCK to regulate the cardiac actin cytoskeleton | Q35741910 | ||
Efficient inducible Cre-mediated recombination in Tcf21 cell lineages in the heart and kidney. | Q35756001 | ||
Xenopus as a model system for vertebrate heart development | Q35793616 | ||
Non-synonymous variants in pre-B cell leukemia homeobox (PBX) genes are associated with congenital heart defects | Q35928623 | ||
Pod1/Tcf21 is regulated by retinoic acid signaling and inhibits differentiation of epicardium-derived cells into smooth muscle in the developing heart. | Q36148533 | ||
Tissue-type plasminogen activator promotes murine myofibroblast activation through LDL receptor-related protein 1-mediated integrin signaling | Q36151652 | ||
Functional proteomics establishes the interaction of SIRT7 with chromatin remodeling complexes and expands its role in regulation of RNA polymerase I transcription. | Q36163466 | ||
Instructive role of aPKCzeta subcellular localization in the assembly of adherens junctions in neural progenitors | Q36423540 | ||
Complementary proteomic analysis of protein complexes. | Q36739823 | ||
Immunoisolation of protein complexes from Xenopus | Q36808221 | ||
Morpholino injection in Xenopus | Q36808239 | ||
Adult cardiac-resident MSC-like stem cells with a proepicardial origin | Q36838490 | ||
Pbx/Meis deficiencies demonstrate multigenetic origins of congenital heart disease | Q37077784 | ||
Embryonic development of the proepicardium and coronary vessels | Q37098811 | ||
Pbx1 functions in distinct regulatory networks to pattern the great arteries and cardiac outflow tract | Q37188312 | ||
Lessons from the lily pad: Using Xenopus to understand heart disease | Q37353967 | ||
A bHLH code for cardiac morphogenesis | Q37662205 | ||
Xenopus explants as an experimental model system for studying heart development. | Q37728660 | ||
Myocardial lineage development | Q37819523 | ||
Signaling during epicardium and coronary vessel development. | Q37967123 | ||
The arterial and cardiac epicardium in development, disease and repair | Q38015007 | ||
Distinct enhancers regulate skeletal and cardiac muscle-specific expression programs of the cardiac alpha-actin gene in Xenopus embryos | Q38289939 | ||
Expression of the smooth muscle cell calponin gene marks the early cardiac and smooth muscle cell lineages during mouse embryogenesis | Q38360190 | ||
Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis | Q39096808 | ||
Developmental expression of the Xenopus laevis Tbx20 orthologue | Q39096883 | ||
Distinct roles of HDAC1 and HDAC2 in transcription and recombination at the immunoglobulin loci in the chicken B cell line DT40. | Q39698754 | ||
An ARF/CtBP2 complex regulates BH3-only gene expression and p53-independent apoptosis | Q39792504 | ||
Epicardium and myocardium separate from a common precursor pool by crosstalk between bone morphogenetic protein- and fibroblast growth factor-signaling pathways | Q39821385 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 13 | |
P304 | page(s) | 2409-2421 | |
P577 | publication date | 2013-05-01 | |
P1433 | published in | Development | Q3025404 |
P1476 | title | Tcf21 regulates the specification and maturation of proepicardial cells | |
P478 | volume | 140 |
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