scholarly article | Q13442814 |
P2093 | author name string | Yuji Mishina | |
Murim Choi | |||
John Klingensmith | |||
Rolf W. Stottmann | |||
Erik N. Meyers | |||
P2860 | cites work | Heart specific expression of mouse BMP-10 a novel member of the TGF-beta superfamily | Q22009012 |
YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis | Q22009123 | ||
Bmp4 is required for the generation of primordial germ cells in the mouse embryo | Q24608134 | ||
Generalized lacZ expression with the ROSA26 Cre reporter strain | Q27860837 | ||
Fate of the mammalian cardiac neural crest | Q28139176 | ||
Requirement of Bmpr1a for Müllerian duct regression during male sexual development | Q28504908 | ||
The BMP antagonists Chordin and Noggin have essential but redundant roles in mouse mandibular outgrowth | Q28505692 | ||
Early embryonic lethality in Bmp5;Bmp7 double mutant mice suggests functional redundancy within the 60A subgroup | Q28506935 | ||
Cell adhesion events mediated by alpha 4 integrins are essential in placental and cardiac development | Q28507437 | ||
Overlapping expression domains of bone morphogenetic protein family members potentially account for limited tissue defects in BMP7 deficient embryos | Q28507860 | ||
Vitamin A deficiency and mutations of RXRalpha, RXRbeta and RARalpha lead to early differentiation of embryonic ventricular cardiomyocytes | Q28511999 | ||
WT-1 is required for early kidney development | Q28512266 | ||
Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development | Q28513337 | ||
Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development | Q28513519 | ||
The ActR-I activin receptor protein is expressed in notochord, lens placode and pituitary primordium cells in the mouse embryo | Q28585192 | ||
Pod-1, a mesoderm-specific basic-helix-loop-helix protein expressed in mesenchymal and glomerular epithelial cells in the developing kidney | Q28585814 | ||
The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain | Q28586297 | ||
Cerberus-like is a secreted factor with neutralizing activity expressed in the anterior primitive endoderm of the mouse gastrula | Q28587138 | ||
FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium | Q28587401 | ||
The type I serine/threonine kinase receptor ActRIA (ALK2) is required for gastrulation of the mouse embryo | Q28587737 | ||
BMP signaling is required for septation of the outflow tract of the mammalian heart | Q28592358 | ||
Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase | Q29615040 | ||
Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis | Q29616631 | ||
HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo | Q29618704 | ||
Cardiac neural crest in zebrafish embryos contributes to myocardial cell lineage and early heart function | Q30891539 | ||
Cardiac neural crest contributes to cardiomyogenesis in zebrafish. | Q31140343 | ||
Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis | Q33515610 | ||
Molecular mechanisms of neural crest formation. | Q33804299 | ||
The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain | Q33937596 | ||
A novel role for cardiac neural crest in heart development | Q33958910 | ||
Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3 | Q34014910 | ||
Molecular control of neural crest formation, migration and differentiation | Q34076847 | ||
BMP signaling is required locally to pattern the dorsal telencephalic midline | Q34152297 | ||
Divergence and convergence of TGF-beta/BMP signaling | Q34229726 | ||
Induction of the neural crest: a multigene process | Q34664846 | ||
Early induction of neural crest cells: lessons learned from frog, fish and chick | Q34723602 | ||
Induction and patterning of the cardiac conduction system. | Q34969544 | ||
Sequential actions of BMP receptors control neural precursor cell production and fate | Q35080582 | ||
Uniform vascular-endothelial-cell-specific gene expression in both embryonic and adult transgenic mice | Q36077023 | ||
Neural crest is involved in development of abnormal myocardial function. | Q39454956 | ||
The role of the epicardium and neural crest as extracardiac contributors to coronary vascular development | Q39697256 | ||
Creation and Characterization of E‐Selectin‐ and VCAM‐1‐Deficient Mice | Q40431914 | ||
Neural crest and cardiovascular patterning. | Q40447081 | ||
Epicardial induction of fetal cardiomyocyte proliferation via a retinoic acid-inducible trophic factor | Q40701785 | ||
Cadherin-6 expression transiently delineates specific rhombomeres, other neural tube subdivisions, and neural crest subpopulations in mouse embryos | Q40900471 | ||
Involvement of Bone Morphogenetic Protein-4 (BMP-4) and Vgr-1 in morphogenesis and neurogenesis in the mouse | Q41161285 | ||
Neural crest formation in the head of the mouse embryo as observed using a new histological technique | Q41469009 | ||
Inactivation of erythropoietin leads to defects in cardiac morphogenesis | Q41679719 | ||
Role of cardiac neural crest cells in cardiovascular development | Q41748295 | ||
The outflow tract of the heart is recruited from a novel heart-forming field | Q42819988 | ||
Bmp6 and Bmp7 are required for cushion formation and septation in the developing mouse heart | Q43661888 | ||
BMPR-IA signaling is required for the formation of the apical ectodermal ridge and dorsal-ventral patterning of the limb. | Q43683437 | ||
Experimental studies on the spatiotemporal expression of WT1 and RALDH2 in the embryonic avian heart: a model for the regulation of myocardial and valvuloseptal development by epicardially derived cells (EPDCs). | Q44042836 | ||
Fgf8 is required for pharyngeal arch and cardiovascular development in the mouse. | Q44132458 | ||
Erythropoietin and retinoic acid, secreted from the epicardium, are required for cardiac myocyte proliferation | Q44369644 | ||
Myocardial volume and organization are changed by failure of addition of secondary heart field myocardium to the cardiac outflow tract | Q44601570 | ||
RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis. | Q46123728 | ||
Vital dye analysis of cranial neural crest cell migration in the mouse embryo | Q46333344 | ||
Ventral and lateral regions of the zebrafish gastrula, including the neural crest progenitors, are established by a bmp2b/swirl pathway of genes | Q47073994 | ||
Targeted deletion of a branchial arch-specific enhancer reveals a role of dHAND in craniofacial development | Q47614302 | ||
epicardin: A novel basic helix-loop-helix transcription factor gene expressed in epicardium, branchial arch myoblasts, and mesenchyme of developing lung, gut, kidney, and gonads | Q48024565 | ||
[The epicardium and epicardial-derived cells: multiple functions in cardiac development]. | Q52113714 | ||
Generation of Bmpr/Alk3 conditional knockout mice. | Q52123530 | ||
BMP signaling is essential for development of skeletogenic and neurogenic cranial neural crest. | Q52171172 | ||
Transgenic rescue of congenital heart disease and spina bifida in Splotch mice. | Q52177459 | ||
Bmpr encodes a type I bone morphogenetic protein receptor that is essential for gastrulation during mouse embryogenesis. | Q52204129 | ||
Organogenesis and pattern formation in the mouse: RNA distribution patterns suggest a role for bone morphogenetic protein-2A (BMP-2A) | Q68581207 | ||
Origin and development of the epicardium in the mouse embryo | Q69193857 | ||
Mouse cellular retinoic acid binding protein: cloning, complementary DNA sequence, and messenger RNA expression during the retinoic acid-induced differentiation of F9 wild type and RA-3-10 mutant teratocarcinoma cells | Q69333784 | ||
Cardiac neural crest is essential for the persistence rather than the formation of an arch artery | Q71638225 | ||
Epicardial outgrowth inhibition leads to compensatory mesothelial outflow tract collar and abnormal cardiac septation and coronary formation | Q73221474 | ||
Recovery from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region | Q73773763 | ||
Misexpression of noggin leads to septal defects in the outflow tract of the chick heart | Q74040088 | ||
Conotruncal myocardium arises from a secondary heart field | Q77102388 | ||
The arterial pole of the mouse heart forms from Fgf10-expressing cells in pharyngeal mesoderm | Q77153201 | ||
Signal transduction by bone morphogenetic proteins | Q77163167 | ||
BMP-2 gene expression and effects on human vascular smooth muscle cells | Q77358428 | ||
A novel role for cardiac neural crest in heart development | Q77845998 | ||
A novel transgenic technique that allows specific marking of the neural crest cell lineage in mice | Q78038712 | ||
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Bone morphogenetic protein receptor, type 1A | Q14904969 |
negative regulation of neural crest cell differentiation | Q26248759 | ||
positive regulation of neural crest cell differentiation | Q26248765 | ||
regulation of neural crest cell differentiation | Q26248769 | ||
regulation of neural crest cell fate specification | Q26250134 | ||
positive regulation of neural crest cell fate specification | Q26250135 | ||
negative regulation of neural crest cell fate specification | Q26250177 | ||
P304 | page(s) | 2205–2218 | |
P577 | publication date | 2004-05-01 | |
P1433 | published in | Development | Q3025404 |
P1476 | title | BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium | |
P478 | volume | 131 |
Q34201469 | A Tlx2-Cre mouse line uncovers essential roles for hand1 in extraembryonic and lateral mesoderm |
Q28508787 | A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning |
Q38072446 | A molecular and genetic outline of cardiac morphogenesis. |
Q38267022 | A novel association of biventricular cardiac noncompaction and diabetic embryopathy: case report and review of the literature |
Q33755344 | A purified population of multipotent cardiovascular progenitors derived from primate pluripotent stem cells engrafts in postmyocardial infarcted nonhuman primates. |
Q36838490 | Adult cardiac-resident MSC-like stem cells with a proepicardial origin |
Q37407385 | An FGF autocrine loop initiated in second heart field mesoderm regulates morphogenesis at the arterial pole of the heart |
Q33370427 | An in vivo reporter of BMP signaling in organogenesis reveals targets in the developing kidney |
Q28507415 | Atrioventricular cushion transformation is mediated by ALK2 in the developing mouse heart |
Q52018698 | BMP is an important regulator of proepicardial identity in the chick embryo. |
Q37850773 | BMP signaling in congenital heart disease: new developments and future directions |
Q28511625 | BMP signaling regulates sympathetic nervous system development through Smad4-dependent and -independent pathways |
Q28512717 | BMP type II receptor regulates positioning of outflow tract and remodeling of atrioventricular cushion during cardiogenesis |
Q28594976 | BMP4 is required in the anterior heart field and its derivatives for endocardial cushion remodeling, outflow tract septation, and semilunar valve development |
Q48107893 | BMPR1a signaling determines numbers of oligodendrocytes and calbindin-expressing interneurons in the cortex |
Q34004677 | BMPRIA mediated signaling is essential for temporomandibular joint development in mice |
Q33761311 | Bmp2 and Bmp4 genetically interact to support multiple aspects of mouse development including functional heart development |
Q34543311 | Bmpr1a signaling plays critical roles in palatal shelf growth and palatal bone formation |
Q42161619 | BmprIa is required in mesenchymal tissue and has limited redundant function with BmprIb in tooth and palate development |
Q42710100 | Bone morphogenetic protein signaling is required in the dorsal neural folds before neurulation for the induction of spinal neural crest cells and dorsal neurons |
Q28588651 | Canonical Wnt signaling functions in second heart field to promote right ventricular growth |
Q42784094 | Cardiac neural crest ablation results in early endocardial cushion and hemodynamic flow abnormalities. |
Q38135363 | Cardiac outflow tract anomalies |
Q37253735 | Cardiac repair and regeneration: the Rubik's cube of cell therapy for heart disease |
Q51981254 | Cardiovascular development and the colonizing cardiac neural crest lineage. |
Q36125674 | Characterization of transcription factor AP-2 β mutations involved in familial isolated patent ductus arteriosus suggests haploinsufficiency |
Q35843311 | Combinatorial transcriptional interaction within the cardiac neural crest: a pair of HANDs in heart formation. |
Q36088538 | Cooperation between the PDGF receptors in cardiac neural crest cell migration |
Q42026011 | Cre reporter mouse expressing a nuclear localized fusion of GFP and beta-galactosidase reveals new derivatives of Pax3-expressing precursors |
Q27024905 | Current perspectives of the signaling pathways directing neural crest induction |
Q28506220 | Defective ALK5 signaling in the neural crest leads to increased postmigratory neural crest cell apoptosis and severe outflow tract defects |
Q35910986 | Defective decapentaplegic signaling results in heart overgrowth and reduced cardiac output in Drosophila |
Q51944236 | Developmental signaling in myocardial progenitor cells: a comprehensive view of Bmp- and Wnt/beta-catenin signaling. |
Q37258930 | Differential requirement for BMP signaling in atrial and ventricular lineages establishes cardiac chamber proportionality |
Q36618064 | Disruption of Smad4 in neural crest cells leads to mid-gestation death with pharyngeal arch, craniofacial and cardiac defects |
Q36276867 | Distinct roles of Wnt/beta-catenin and Bmp signaling during early cardiogenesis |
Q89914653 | Dullard-mediated Smad1/5/8 inhibition controls mouse cardiac neural crest cells condensation and outflow tract septation |
Q28256445 | Endogenous bone morphogenetic protein antagonists regulate mammalian neural crest generation and survival |
Q54365023 | Epicardium is required for sarcomeric maturation and cardiomyocyte growth in the ventricular compact layer mediated by transforming growth factor β and fibroblast growth factor before the onset of coronary circulation. |
Q81297429 | Essential role of Smad4 in maintaining cardiomyocyte proliferation during murine embryonic heart development |
Q41825988 | Evidence for an early role for BMP4 signaling in thymus and parathyroid morphogenesis |
Q24619522 | Factors controlling cardiac neural crest cell migration |
Q39673288 | Fibronectin and integrin alpha 5 play essential roles in the development of the cardiac neural crest |
Q38498581 | Frs2alpha-deficiency in cardiac progenitors disrupts a subset of FGF signals required for outflow tract morphogenesis |
Q33938401 | Genetic interaction between Bmp2 and Bmp4 reveals shared functions during multiple aspects of mouse organogenesis |
Q35916112 | Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome |
Q24309588 | Identification of BMP9 and BMP10 as functional activators of the orphan activin receptor-like kinase 1 (ALK1) in endothelial cells |
Q36320719 | Identification of exercise capacity QTL using association mapping in inbred mice |
Q24310450 | Identification of receptors and signaling pathways for orphan bone morphogenetic protein/growth differentiation factor ligands based on genomic analyses |
Q44928146 | Inactivation of Cdc42 in neural crest cells causes craniofacial and cardiovascular morphogenesis defects |
Q81729304 | Insertion of Cre into the Pax3 locus creates a new allele of Splotch and identifies unexpected Pax3 derivatives |
Q36330450 | Maternal diabetes induces congenital heart defects in mice by altering the expression of genes involved in cardiovascular development |
Q90697209 | Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms |
Q26785404 | Mesenchymal Stem Cells for Cardiac Regenerative Therapy: Optimization of Cell Differentiation Strategy |
Q36708506 | Model systems for the study of heart development and disease. Cardiac neural crest and conotruncal malformations |
Q37383073 | Mouse models of congenital cardiovascular disease |
Q28587718 | Msx1 and Msx2 regulate survival of secondary heart field precursors and post-migratory proliferation of cardiac neural crest in the outflow tract |
Q36585449 | Multiple essential roles for primary cilia in heart development |
Q48020248 | Multiple lineage-specific roles of Smad4 during neural crest development |
Q28504710 | Murine Jagged1/Notch signaling in the second heart field orchestrates Fgf8 expression and tissue-tissue interactions during outflow tract development |
Q41834366 | N-cadherin is required for neural crest remodeling of the cardiac outflow tract |
Q33813000 | Neural crest cell signaling pathways critical to cranial bone development and pathology |
Q36497251 | Neural crest cell-autonomous roles of fibronectin in cardiovascular development. |
Q38117118 | Neural crest specification: tissues, signals, and transcription factors |
Q36321576 | Neural crest stem cell maintenance by combinatorial Wnt and BMP signaling |
Q51904000 | Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome. |
Q39406800 | Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation |
Q37702403 | Notch and cardiac outflow tract development |
Q30478829 | Outflow tract cushions perform a critical valve-like function in the early embryonic heart requiring BMPRIA-mediated signaling in cardiac neural crest |
Q54719719 | Pathways to embryonic heart failure. |
Q35127152 | Pax3 is essential for normal cardiac neural crest morphogenesis but is not required during migration nor outflow tract septation |
Q33555111 | Precardiac deletion of Numb and Numblike reveals renewal of cardiac progenitors |
Q36877617 | Rac1 Signaling Is Required for Anterior Second Heart Field Cellular Organization and Cardiac Outflow Tract Development. |
Q36359280 | Reduced bone morphogenetic protein receptor type 1A signaling in neural-crest-derived cells causes facial dysmorphism |
Q35127060 | Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular development |
Q28589696 | Regionalization of cell fates and cell movement in the endoderm of the mouse gastrula and the impact of loss of Lhx1(Lim1) function |
Q27863405 | Retracted: Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner |
Q38086222 | Signaling and transcriptional networks in heart development and regeneration |
Q37758308 | Signals controlling neural crest contributions to the heart |
Q42107846 | Smad signaling in the neural crest regulates cardiac outflow tract remodeling through cell autonomous and non-cell autonomous effects |
Q37247522 | Smad4 is required to regulate the fate of cranial neural crest cells |
Q28506949 | Sonic hedgehog is required for cardiac outflow tract and neural crest cell development |
Q39308262 | TGF-β Family Signaling in Mesenchymal Differentiation |
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Q27024385 | The neural crest in cardiac congenital anomalies |
Q37663823 | Tissue-tissue interactions during morphogenesis of the outflow tract |
Q24293493 | Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development. [corrected] |
Q34017313 | Trigenic neural crest-restricted Smad7 over-expression results in congenital craniofacial and cardiovascular defects. |
Q36657000 | c-kit+ Cardiac Stem Cells: Spontaneous Creation or a Perplexing Reality |
Q36207283 | cKit+ cardiac progenitors of neural crest origin |
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