| scholarly article | Q13442814 |
| P2093 | author name string | Robert S Krauss | |
| Giselle A Joseph | |||
| Aviva J Goel | |||
| P2860 | cites work | Neural tube and notochord promote in vitro myogenesis in single somite explants. | Q51128231 |
| Sonic hedgehog controls epaxial muscle determination through Myf5 activation. | Q52174934 | ||
| Combinatorial signaling by Sonic hedgehog and Wnt family members induces myogenic bHLH gene expression in the somite. | Q52204666 | ||
| Combinatorial signals from the neural tube, floor plate and notochord induce myogenic bHLH gene expression in the somite. | Q52209854 | ||
| SNS: Adhesive properties, localization requirements and ectodomain dependence in S2 cells and embryonic myoblasts. | Q52652934 | ||
| Evolutionary conservation in myoblast fusion. | Q52680178 | ||
| Myogenesis in paraxial mesoderm: preferential induction by dorsal neural tube and by cells expressing Wnt-1 | Q70953088 | ||
| Notch3 Null Mutation in Mice Causes Muscle Hyperplasia by Repetitive Muscle Regeneration | Q85226461 | ||
| CDO: An Oncogene-, Serum-, and Anchorage-regulated Member of the Ig/Fibronectin Type III Repeat Family | Q24316104 | ||
| The cell adhesion molecule M-cadherin is not essential for muscle development and regeneration | Q24537537 | ||
| Proteinuria and perinatal lethality in mice lacking NEPH1, a novel protein with homology to NEPHRIN | Q24550913 | ||
| p38 and extracellular signal-regulated kinases regulate the myogenic program at multiple steps | Q24554203 | ||
| Netrins and neogenin promote myotube formation | Q24676178 | ||
| Junctional adhesion molecule, a novel member of the immunoglobulin superfamily that distributes at intercellular junctions and modulates monocyte transmigration | Q24682572 | ||
| Promyogenic members of the Ig and cadherin families associate to positively regulate differentiation | Q24683397 | ||
| Tissue-specific stem cells: lessons from the skeletal muscle satellite cell | Q26825719 | ||
| Ephrin-A3 promotes and maintains slow muscle fiber identity during postnatal development and reinnervation. | Q27310123 | ||
| Mechanisms of myoblast fusion during muscle development | Q28081230 | ||
| Intrinsic and extrinsic mechanisms regulating satellite cell function | Q28084614 | ||
| Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting | Q28085606 | ||
| Development of the vertebrate neuromuscular junction | Q28141504 | ||
| Neural crest regulates myogenesis through the transient activation of NOTCH | Q28237632 | ||
| FOXO3 promotes quiescence in adult muscle stem cells during the process of self-renewal | Q28238543 | ||
| N-cadherin/catenin complex as a master regulator of intercalated disc function | Q28238884 | ||
| A role for the Myoblast city homologues Dock1 and Dock5 and the adaptor proteins Crk and Crk-like in zebrafish myoblast fusion | Q28239021 | ||
| Developmental defects in mouse embryos lacking N-cadherin | Q28302581 | ||
| TGF-β-activated kinase 1 (TAK1) and apoptosis signal-regulating kinase 1 (ASK1) interact with the promyogenic receptor Cdo to promote myogenic differentiation via activation of p38MAPK pathway | Q28504736 | ||
| Regulation of vertebrate myotome development by the p38 MAP kinase-MEF2 signaling pathway | Q28505919 | ||
| A role for nephrin, a renal protein, in vertebrate skeletal muscle cell fusion | Q28507874 | ||
| Maintenance of muscle stem-cell quiescence by microRNA-489 | Q28509431 | ||
| Premature myogenic differentiation and depletion of progenitor cells cause severe muscle hypotrophy in Delta1 mutants | Q28509714 | ||
| Cdo functions at multiple points in the Sonic Hedgehog pathway, and Cdo-deficient mice accurately model human holoprosencephaly | Q28512829 | ||
| Colonization of the satellite cell niche by skeletal muscle progenitor cells depends on Notch signals | Q28513392 | ||
| Myomaker is essential for muscle regeneration | Q28585754 | ||
| Myomaker is a membrane activator of myoblast fusion and muscle formation | Q28586981 | ||
| Kirrel3 is required for the coalescence of vomeronasal sensory neuron axons into glomeruli and for male-male aggression | Q28587878 | ||
| The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death | Q28588477 | ||
| Spermatid differentiation requires the assembly of a cell polarity complex downstream of junctional adhesion molecule-C | Q28589240 | ||
| Positive regulation of myogenic bHLH factors and skeletal muscle development by the cell surface receptor CDO | Q28590654 | ||
| N-cadherin ligation, but not Sonic hedgehog binding, initiates Cdo-dependent p38alpha/beta MAPK signaling in skeletal myoblasts | Q28592379 | ||
| The Wnt/beta-catenin pathway regulates Gli-mediated Myf5 expression during somitogenesis | Q28594489 | ||
| p38-dependent phosphorylation of the mRNA decay-promoting factor KSRP controls the stability of select myogenic transcripts | Q28594660 | ||
| CDO, a robo-related cell surface protein that mediates myogenic differentiation | Q28646219 | ||
| Towards an integrated view of Wnt signaling in development | Q29615175 | ||
| Functional interdependence at the chromatin level between the MKK6/p38 and IGF1/PI3K/AKT pathways during muscle differentiation. | Q30439474 | ||
| Actin-propelled invasive membrane protrusions promote fusogenic protein engagement during cell-cell fusion | Q30539039 | ||
| The atypical Rac activator Dock180 (Dock1) regulates myoblast fusion in vivo | Q33372285 | ||
| Chromatin: the interface between extrinsic cues and the epigenetic regulation of muscle regeneration | Q33593168 | ||
| Evolution and development of distinct cell lineages derived from somites | Q33817693 | ||
| E47 phosphorylation by p38 MAPK promotes MyoD/E47 association and muscle-specific gene transcription | Q33930729 | ||
| Notch signaling: the core pathway and its posttranslational regulation | Q34017623 | ||
| Jamb and jamc are essential for vertebrate myocyte fusion | Q34105131 | ||
| p38 MAPK signaling regulates recruitment of Ash2L-containing methyltransferase complexes to specific genes during differentiation | Q34124906 | ||
| Regulation of promyogenic signal transduction by cell-cell contact and adhesion | Q34154815 | ||
| TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration. | Q34181742 | ||
| Overlapping roles and collective requirement for the coreceptors GAS1, CDO, and BOC in SHH pathway function | Q34191681 | ||
| Interaction between satellite cells and skeletal muscle fibers. | Q34248498 | ||
| The aged niche disrupts muscle stem cell quiescence. | Q34302715 | ||
| Membrane hyperpolarization triggers myogenin and myocyte enhancer factor-2 expression during human myoblast differentiation | Q34313596 | ||
| Skeletal muscle programming and re-programming | Q34350083 | ||
| An invasive podosome-like structure promotes fusion pore formation during myoblast fusion. | Q34368627 | ||
| Close encounters: regulation of vertebrate skeletal myogenesis by cell-cell contact. | Q34422334 | ||
| The circuitry of a master switch: Myod and the regulation of skeletal muscle gene transcription | Q34650621 | ||
| Inducible depletion of satellite cells in adult, sedentary mice impairs muscle regenerative capacity without affecting sarcopenia | Q34892571 | ||
| Cadherin-based cell adhesion in neuromuscular development | Q35034036 | ||
| Putative "stemness" gene jam-B is not required for maintenance of stem cell state in embryonic, neural, or hematopoietic stem cells. | Q35071195 | ||
| Regulation of dorsal somitic cell fates: BMPs and Noggin control the timing and pattern of myogenic regulator expression | Q35189860 | ||
| Sculpting chromatin beyond the double helix: epigenetic control of skeletal myogenesis. | Q35212612 | ||
| Nuclear signaling from cadherin adhesion complexes | Q35539061 | ||
| Cdo suppresses canonical Wnt signalling via interaction with Lrp6 thereby promoting neuronal differentiation | Q35545497 | ||
| RBP-J (Rbpsuh) is essential to maintain muscle progenitor cells and to generate satellite cells | Q35670105 | ||
| Myoblast fusion: lessons from flies and mice | Q35691569 | ||
| Hesr1 and Hesr3 are essential to generate undifferentiated quiescent satellite cells and to maintain satellite cell numbers. | Q35693118 | ||
| Phosphorylation of Stim1 at serine 575 via netrin-2/Cdo-activated ERK1/2 is critical for the promyogenic function of Stim1 | Q35861824 | ||
| Cdo Regulates Surface Expression of Kir2.1 K+ Channel in Myoblast Differentiation | Q36068353 | ||
| The actin regulator N-WASp is required for muscle-cell fusion in mice | Q36094269 | ||
| Activation of p38alpha/beta MAPK in myogenesis via binding of the scaffold protein JLP to the cell surface protein Cdo. | Q36118993 | ||
| Fusion competence of myoblasts rendered genetically null for N-cadherin in culture | Q36268144 | ||
| Kin of IRRE-like Protein 2 Is a Phosphorylated Glycoprotein That Regulates Basal Insulin Secretion. | Q36283499 | ||
| Group I PAKs function downstream of Rac to promote podosome invasion during myoblast fusion in vivo | Q36289093 | ||
| Human myoblast fusion requires expression of functional inward rectifier Kir2.1 channels | Q36366011 | ||
| Tissue organization by cadherin adhesion molecules: dynamic molecular and cellular mechanisms of morphogenetic regulation | Q36567245 | ||
| Structure-function analysis of myomaker domains required for myoblast fusion | Q36646542 | ||
| A Cdo-Bnip-2-Cdc42 signaling pathway regulates p38alpha/beta MAPK activity and myogenic differentiation | Q36817884 | ||
| Cellular heterogeneity during vertebrate skeletal muscle development | Q36870830 | ||
| Cytoplasmic NOTCH and membrane-derived β-catenin link cell fate choice to epithelial-mesenchymal transition during myogenesis | Q37029486 | ||
| Eph receptor signaling and ephrins | Q37122330 | ||
| The small G-proteins Rac1 and Cdc42 are essential for myoblast fusion in the mouse | Q37193382 | ||
| Neogenin regulates skeletal myofiber size and focal adhesion kinase and extracellular signal-regulated kinase activities in vivo and in vitro | Q37448278 | ||
| Skeletal muscle fiber type: using insights from muscle developmental biology to dissect targets for susceptibility and resistance to muscle disease | Q37529679 | ||
| Fiber types in mammalian skeletal muscles | Q37947567 | ||
| Signaling mechanisms in mammalian myoblast fusion | Q38101240 | ||
| Molecular and cellular regulation of skeletal myogenesis | Q38253502 | ||
| A critical requirement for notch signaling in maintenance of the quiescent skeletal muscle stem cell state | Q38330434 | ||
| Muscle stem cells on the edge | Q38550063 | ||
| Group I Paks Promote Skeletal Myoblast Differentiation In Vivo and In Vitro | Q38727502 | ||
| p38 pathway targets SWI-SNF chromatin-remodeling complex to muscle-specific loci | Q40543190 | ||
| Muscle stem cells contribute to myofibres in sedentary adult mice | Q40789586 | ||
| An NF-κB--EphrinA5-Dependent Communication between NG2(+) Interstitial Cells and Myoblasts Promotes Muscle Growth in Neonates. | Q40970642 | ||
| E-cadherin cytoplasmic domain inhibits cell surface localization of endogenous cadherins and fusion of C2C12 myoblasts | Q41824969 | ||
| Notch signaling is necessary to maintain quiescence in adult muscle stem cells | Q42217084 | ||
| Differential effects of N-cadherin-mediated adhesion on the development of myotomal waves | Q42490916 | ||
| A conserved molecular pathway mediates myoblast fusion in insects and vertebrates | Q47073444 | ||
| Myomaker mediates fusion of fast myocytes in zebrafish embryos | Q47073524 | ||
| P-cadherin is a direct PAX3-FOXO1A target involved in alveolar rhabdomyosarcoma aggressiveness. | Q47606306 | ||
| Differential activation of Myf5 and MyoD by different Wnts in explants of mouse paraxial mesoderm and the later activation of myogenesis in the absence of Myf5. | Q51094486 | ||
| P433 | issue | 2 | |
| P577 | publication date | 2017-01-06 | |
| P1433 | published in | Cold Spring Harbor Perspectives in Biology | Q3927509 |
| P1476 | title | Keep Your Friends Close: Cell-Cell Contact and Skeletal Myogenesis | |
| P478 | volume | 9 |
| Q33112265 | Control of muscle formation by the fusogenic micropeptide myomixer. |
| Q89994249 | Downregulation of POFUT1 Impairs Secondary Myogenic Fusion Through a Reduced NFATc2/IL-4 Signaling Pathway |
| Q92112216 | EphA7 promotes myogenic differentiation via cell-cell contact |
| Q93363137 | Genetic Mutations in jamb, jamc, and myomaker Revealed Different Roles on Myoblast Fusion and Muscle Growth |
| Q90570276 | Glucose Uptake and Insulin Response in Tissue-engineered Human Skeletal Muscle |
| Q55284543 | HDAC4 regulates satellite cell proliferation and differentiation by targeting P21 and Sharp1 genes. |
| Q90099860 | Multiplexed RNAscope and immunofluorescence on whole-mount skeletal myofibers and their associated stem cells |
| Q57025433 | Muscle Satellite Cell Cross-Talk with a Vascular Niche Maintains Quiescence via VEGF and Notch Signaling |
| Q90914096 | Muscle tissue engineering in fibrous gelatin: implications for meat analogs |
| Q48131580 | Myoblast fusion confusion: the resolution begins. |
| Q89963027 | Stable Knockdown of Genes Encoding Extracellular Matrix Proteins in the C2C12 Myoblast Cell Line Using Small-Hairpin (sh)RNA |
| Q59806119 | The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression |
| Q91106459 | Zfp422 promotes skeletal muscle differentiation by regulating EphA7 to induce appropriate myoblast apoptosis |
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