scholarly article | Q13442814 |
P2093 | author name string | Simon M Hughes | |
Michael S Marber | |||
Yaniv Hinits | |||
Duvaraka Kula-Alwar | |||
P2860 | cites work | HRC is a direct transcriptional target of MEF2 during cardiac, skeletal, and arterial smooth muscle development in vivo | Q24623607 |
mef2ca is required in cranial neural crest to effect Endothelin1 signaling in zebrafish | Q24670788 | ||
The transcription factor MEF2C is required for craniofacial development | Q24672010 | ||
Functional modulation of cardiac form through regionally confined cell shape changes | Q27334821 | ||
An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation | Q27863351 | ||
Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart | Q28190508 | ||
MEF2C transcription factor controls chondrocyte hypertrophy and bone development | Q28505927 | ||
MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function | Q28507026 | ||
The transcription factor MEF2C-null mouse exhibits complex vascular malformations and reduced cardiac expression of angiopoietin 1 and VEGF | Q28508964 | ||
Regulation of skeletal muscle sarcomere integrity and postnatal muscle function by Mef2c | Q28513098 | ||
Chamber formation and morphogenesis in the developing mammalian heart | Q28566310 | ||
Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C | Q28589290 | ||
Building the mammalian heart from two sources of myocardial cells | Q29618590 | ||
Patterning of the heart field in the chick | Q30483203 | ||
Distinct phases of cardiomyocyte differentiation regulate growth of the zebrafish heart | Q30487250 | ||
High-resolution cardiovascular function confirms functional orthology of myocardial contractility pathways in zebrafish | Q30498064 | ||
A dual role for ErbB2 signaling in cardiac trabeculation | Q30498335 | ||
Role of mef2ca in developmental buffering of the zebrafish larval hyoid dermal skeleton. | Q30564456 | ||
Analysis of postembryonic heart development and maturation in the zebrafish, Danio rerio | Q30651967 | ||
An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein | Q33184506 | ||
Cell tracking using a photoconvertible fluorescent protein | Q33280951 | ||
Cabin1 expression suggests roles in neuronal development | Q33638732 | ||
Histone modifications and mitosis: countermarks, landmarks, and bookmarks | Q34318120 | ||
Heart fields and cardiac morphogenesis | Q34355325 | ||
Cardiac patterning and morphogenesis in zebrafish | Q34465794 | ||
Zebrafish cardiac development requires a conserved secondary heart field | Q34966448 | ||
eIF4EBP3L acts as a gatekeeper of TORC1 in activity-dependent muscle growth by specifically regulating Mef2ca translational initiation. | Q35021553 | ||
An early requirement for nkx2.5 ensures the first and second heart field ventricular identity and cardiac function into adulthood | Q35181554 | ||
Myocyte enhancer factor 2C function in skeletal muscle is required for normal growth and glucose metabolism in mice. | Q35190729 | ||
Rapid BAC selection for tol2-mediated transgenesis in zebrafish. | Q50513824 | ||
Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis. | Q51928742 | ||
A retrospective clonal analysis of the myocardium reveals two phases of clonal growth in the developing mouse heart. | Q52103466 | ||
Structure and function of the developing zebrafish heart. | Q52165184 | ||
Glypican4 promotes cardiac specification and differentiation by attenuating canonical Wnt and Bmp signaling. | Q52660013 | ||
A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle. | Q52691186 | ||
Targeted gene expression by the Gal4-UAS system in zebrafish. | Q53477164 | ||
Regionalized sequence of myocardial cell growth and proliferation characterizes early chamber formation. | Q53607310 | ||
Establishment of cardiac cytoarchitecture in the developing mouse heart | Q58200978 | ||
The deployment of cell lineages that form the mammalian heart | Q59755253 | ||
Using modified length–weight relationships to assess the condition of fish | Q62927106 | ||
The arterial pole of the mouse heart forms from Fgf10-expressing cells in pharyngeal mesoderm | Q77153201 | ||
Generation of conditional Mef2cloxP/loxP mice for temporal- and tissue-specific analyses | Q81075221 | ||
Cardiovascular development and survival require Mef2c function in the myocardial but not the endothelial lineage | Q90308691 | ||
In vivo analysis of cardiomyocyte proliferation during trabeculation | Q90644495 | ||
Scleraxis genes are required for normal musculoskeletal development and for rib growth and mineralization in zebrafish | Q92112739 | ||
Emerging roles for MEF2 in brain development and mental disorders | Q92297269 | ||
Cardiac chamber formation: development, genes, and evolution. | Q35541868 | ||
Multiple influences of blood flow on cardiomyocyte hypertrophy in the embryonic zebrafish heart | Q35758199 | ||
Latent TGF-β binding protein 3 identifies a second heart field in zebrafish | Q35869406 | ||
Clonally dominant cardiomyocytes direct heart morphogenesis | Q35921775 | ||
Cardiac contraction activates endocardial Notch signaling to modulate chamber maturation in zebrafish | Q36462525 | ||
A chemical method for fast and sensitive detection of DNA synthesis in vivo | Q36497275 | ||
Evolutionary conservation of Nkx2.5 autoregulation in the second heart field | Q36545329 | ||
In vivo monitoring of cardiomyocyte proliferation to identify chemical modifiers of heart regeneration | Q36580281 | ||
Zebrafish second heart field development relies on progenitor specification in anterior lateral plate mesoderm and nkx2.5 function. | Q36648675 | ||
The heart-forming fields: one or multiple? | Q36854392 | ||
Tbx1 is required for second heart field proliferation in zebrafish | Q36914162 | ||
Nkx genes are essential for maintenance of ventricular identity | Q37209154 | ||
Zebrafish as a model to study cardiac development and human cardiac disease | Q37878169 | ||
Mef2s are required for thick filament formation in nascent muscle fibres. | Q38301246 | ||
Germ-line transmission of a myocardium-specific GFP transgene reveals critical regulatory elements in the cardiac myosin light chain 2 promoter of zebrafish | Q38350936 | ||
Methodologies for Inducing Cardiac Injury and Assaying Regeneration in Adult Zebrafish | Q39553846 | ||
Notochord induction of zebrafish slow muscle mediated by Sonic hedgehog. | Q40240062 | ||
Mesoderm progenitor cells of common origin contribute to the head musculature and the cardiac outflow tract | Q40290155 | ||
Restricted expression of cardiac myosin genes reveals regulated aspects of heart tube assembly in zebrafish. | Q40797201 | ||
Regulation of cardiomyocyte behavior in zebrafish trabeculation by Neuregulin 2a signaling | Q41089472 | ||
Isl2b regulates anterior second heart field development in zebrafish. | Q41782390 | ||
Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations | Q41846618 | ||
A caudal proliferating growth center contributes to both poles of the forming heart tube | Q41881568 | ||
Zebrafish Mef2ca and Mef2cb are essential for both first and second heart field cardiomyocyte differentiation. | Q41962292 | ||
MEF2 transcription factors are key regulators of sprouting angiogenesis | Q42368143 | ||
The outflow tract of the heart is recruited from a novel heart-forming field | Q42819988 | ||
Cadm4 restricts the production of cardiac outflow tract progenitor cells | Q42848212 | ||
MEF2C loss-of-function mutation contributes to congenital heart defects | Q43466893 | ||
heart of glass regulates the concentric growth of the heart in zebrafish. | Q44696937 | ||
A mutation in zebrafish hmgcr1b reveals a role for isoprenoids in vertebrate heart-tube formation | Q44811336 | ||
Growth of the developing mouse heart: an interactive qualitative and quantitative 3D atlas. | Q45913620 | ||
The right ventricle, outflow tract, and ventricular septum comprise a restricted expression domain within the secondary/anterior heart field | Q46196456 | ||
Mef2 and the skeletal muscle differentiation program. | Q46258408 | ||
Mef2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development | Q46350581 | ||
Ligament versus bone cell identity in the zebrafish hyoid skeleton is regulated by mef2ca. | Q46436159 | ||
Three zebrafish MEF2 genes delineate somitic and cardiac muscle development in wild-type and mutant embryos | Q47073138 | ||
Mutation of weak atrium/atrial myosin heavy chain disrupts atrial function and influences ventricular morphogenesis in zebrafish | Q47073414 | ||
Dependence of cardiac trabeculation on neuregulin signaling and blood flow in zebrafish | Q47073947 | ||
Mef2cb regulates late myocardial cell addition from a second heart field-like population of progenitors in zebrafish | Q47074114 | ||
Right ventricular myocardium derives from the anterior heart field | Q47290410 | ||
Unique developmental trajectories and genetic regulation of ventricular and outflow tract progenitors in the zebrafish second heart field. | Q47614504 | ||
The clonal origin of myocardial cells in different regions of the embryonic mouse heart | Q47640178 | ||
A new tinman-related gene, nkx2.7, anticipates the expression of nkx2.5 and nkx2.3 in zebrafish heart and pharyngeal endoderm | Q48056707 | ||
Differential expression of two tropoelastin genes in zebrafish | Q48083395 | ||
nkx genes establish SHF cardiomyocyte progenitors at the arterial pole and pattern the venous pole through Isl1 repression. | Q48183264 | ||
P577 | publication date | 2020-11-24 | |
P1433 | published in | Developmental Biology | Q3025402 |
P1476 | title | Mef2c factors are required for early but not late addition of cardiomyocytes to the ventricle |