scholarly article | Q13442814 |
P50 | author | Richard Cheney | Q42703433 |
P2093 | author name string | Cam Patterson | |
Rongqin Ren | |||
Xinchun Pi | |||
Chunlian Zhang | |||
Martin Moser | |||
Aparna B Bohil | |||
Melinda Divito | |||
Russell Kelley | |||
P2860 | cites work | TGF-beta signal transduction | Q22003891 |
Myosin-X is a molecular motor that functions in filopodia formation | Q24299253 | ||
A new direct-viewing chemotaxis chamber | Q28240876 | ||
BMP receptor 1b is required for axon guidance and cell survival in the developing retina | Q28507158 | ||
Myo10 in brain: developmental regulation, identification of a headless isoform and dynamics in neurons | Q28507574 | ||
Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development | Q28513337 | ||
VEGF guides angiogenic sprouting utilizing endothelial tip cell filopodia | Q29617501 | ||
The molecular biology of axon guidance | Q29617857 | ||
Myosin-X is an unconventional myosin that undergoes intrafilopodial motility. | Q34115035 | ||
Vasculogenesis and angiogenesis as mechanisms of vascular network formation, growth and remodeling | Q34178814 | ||
Myosin-X provides a motor-based link between integrins and the cytoskeleton. | Q34322246 | ||
Dependence of Drosophila wing imaginal disc cytonemes on Decapentaplegic | Q34452981 | ||
Overview of bone morphogenetic proteins | Q34805680 | ||
Controlling cell fate by bone morphogenetic protein receptors. | Q35600636 | ||
Gene expression profiles identify a role for cyclooxygenase 2-dependent prostanoid generation in BMP6-induced angiogenic responses | Q35750952 | ||
Myosin-X: a molecular motor at the cell's fingertips | Q36248392 | ||
Regulators of Angiogenesis | Q36653534 | ||
The actin cytoskeleton. | Q38213614 | ||
Bone morphogenetic protein 2 (BMP-2) and induction of tumor angiogenesis | Q40379049 | ||
Bone morphogenetic proteins stimulate angiogenesis through osteoblast-derived vascular endothelial growth factor A. | Q40744204 | ||
Exogenously regulated stem cell-mediated gene therapy for bone regeneration. | Q40810215 | ||
Bone morphogenetic proteins in development | Q41100028 | ||
Early vascularization of the embryonic cerebral cortex: Golgi and electron microscopic studies | Q42437025 | ||
Stimulation of Id1 expression by bone morphogenetic protein is sufficient and necessary for bone morphogenetic protein-induced activation of endothelial cells | Q44187496 | ||
The formation of capillary basement membranes during internal vascularization of the rat's cerebral cortex | Q51107938 | ||
Angiogenesis defects and mesenchymal apoptosis in mice lacking SMAD5. | Q52178715 | ||
Growth/Differentiation Factor-5 Induces Angiogenesisin Vivo | Q57267086 | ||
A family of angiogenic peptides | Q59071772 | ||
Intussusceptive microvascular growth in a human colon adenocarcinoma xenograft: a novel mechanism of tumor angiogenesis | Q71459931 | ||
Effect of colchicine on remote phases of growing capillaries in the brain | Q76486824 | ||
BMK1/ERK5 is a novel regulator of angiogenesis by destabilizing hypoxia inducible factor 1alpha | Q81724557 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 14 | |
P304 | page(s) | 1569-1582 | |
P577 | publication date | 2007-12-24 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | Sequential roles for myosin-X in BMP6-dependent filopodial extension, migration, and activation of BMP receptors | |
P478 | volume | 179 |
Q33840016 | Actin, microtubules, and vimentin intermediate filaments cooperate for elongation of invadopodia |
Q38945280 | Alk2/ACVR1 and Alk3/BMPR1A Provide Essential Function for Bone Morphogenetic Protein-Induced Retinal Angiogenesis |
Q30494552 | An unconventional myosin required for cell polarization and chemotaxis |
Q35023249 | BMP-2 induces versican and hyaluronan that contribute to post-EMT AV cushion cell migration |
Q35067319 | BMPR1B up-regulation via a miRNA binding site variation defines endometriosis susceptibility and CA125 levels |
Q36445238 | Bmper inhibits endothelial expression of inflammatory adhesion molecules and protects against atherosclerosis. |
Q37947050 | Bone Morphogenetic Protein functions as a context-dependent angiogenic cue in vertebrates |
Q33719268 | Bone morphogenetic protein 2 signaling negatively modulates lymphatic development in vertebrate embryos |
Q35250759 | Bone morphogenetic protein endothelial cell precursor-derived regulator regulates retinal angiogenesis in vivo in a mouse model of oxygen-induced retinopathy |
Q44507684 | Both Myosin-10 isoforms are required for radial neuronal migration in the developing cerebral cortex |
Q37043917 | CXCL12/CXCR4 signaling and other recruitment and homing pathways in fracture repair |
Q27666969 | Cargo recognition mechanism of myosin X revealed by the structure of its tail MyTH4-FERM tandem in complex with the DCC P3 domain |
Q45093732 | Cloning, characterization, and promoter analysis of mouse Myo10 gene |
Q30514794 | Differential regulation of myosin X movements by its cargos, DCC and neogenin. |
Q41993273 | Distinct signalling pathways regulate sprouting angiogenesis from the dorsal aorta and the axial vein |
Q38233800 | Diversity is in my veins: role of bone morphogenetic protein signaling during venous morphogenesis in zebrafish illustrates the heterogeneity within endothelial cells |
Q91334253 | Filopodia and focal adhesions: An integrated system driving branching morphogenesis in neuronal pathfinding and angiogenesis |
Q37326902 | GIT1 mediates VEGF-induced podosome formation in endothelial cells: critical role for PLCgamma |
Q50270865 | Gene profile of soluble growth factors involved in angiogenesis, in an adipose-derived stromal cell/endothelial cell co-culture, 3D gel model |
Q36127036 | Headless Myo10 is a negative regulator of full-length Myo10 and inhibits axon outgrowth in cortical neurons |
Q50577636 | Headless Myo10 is a regulator of microtubule stability during neuronal development. |
Q37339182 | Involvement of headless myosin X in the motility of immortalized gonadotropin-releasing hormone neuronal cells |
Q40244416 | LRP1 Regulates Retinal Angiogenesis by Inhibiting PARP-1 Activity and Endothelial Cell Proliferation |
Q39317513 | LRP1-dependent endocytic mechanism governs the signaling output of the bmp system in endothelial cells and in angiogenesis |
Q39067526 | Mechanism of pro-tumorigenic effect of BMP-6: neovascularization involving tumor-associated macrophages and IL-1a |
Q24610098 | MicroRNA miR-155 inhibits bone morphogenetic protein (BMP) signaling and BMP-mediated Epstein-Barr virus reactivation |
Q30572690 | Mutant p53-associated myosin-X upregulation promotes breast cancer invasion and metastasis. |
Q39005661 | MyTH4-FERM myosins in the assembly and maintenance of actin-based protrusions |
Q38930491 | Myo10 is required for neurogenic cell adhesion and migration |
Q36957296 | Myosin MyTH4-FERM structures highlight important principles of convergent evolution. |
Q37226406 | Myosin X and its motorless isoform differentially modulate dendritic spine development by regulating trafficking and retention of vasodilator-stimulated phosphoprotein |
Q89545561 | Myosin X is required for efficient melanoblast migration and melanoma initiation and metastasis |
Q35964174 | Myosin X regulates neuronal radial migration through interacting with N-cadherin |
Q30493830 | Myosin X regulates sealing zone patterning in osteoclasts through linkage of podosomes and microtubules |
Q34985570 | Myosin motor function: the ins and outs of actin-based membrane protrusions. |
Q87929283 | Myosin-Driven Intracellular Transport |
Q26825835 | Myosin-X and disease |
Q30513859 | Myosin-X functions in polarized epithelial cells |
Q30576361 | Myosin-X is critical for migratory ability of Xenopus cranial neural crest cells. |
Q30497957 | Myosin-X is required for cranial neural crest cell migration in Xenopus laevis |
Q47139973 | Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation. |
Q35576442 | Myosin-X: a MyTH-FERM myosin at the tips of filopodia |
Q60949857 | Myosins in Osteoclast Formation and Function |
Q37433692 | New insights into bone morphogenetic protein signaling: focus on angiogenesis |
Q34207052 | Non-muscle myosins in tumor progression, cancer cell invasion, and metastasis |
Q61444640 | Phenotypic analysis of Myo10 knockout (Myo10) mice lacking full-length (motorized) but not brain-specific headless myosin X |
Q54424215 | Prostaglandin E2 receptor subtype EP2- and EP4-regulated gene expression profiling in human ciliary smooth muscle cells. |
Q34271141 | PtdIns (3,4,5) P3 recruitment of Myo10 is essential for axon development |
Q42577163 | Reduction in endothelial tip cell filopodia corresponds to reduced intravitreous but not intraretinal vascularization in a model of ROP. |
Q41312017 | Regulation of Osteoclast Differentiation by Myosin X. |
Q42262102 | Role of bone morphogenetic proteins in sprouting angiogenesis: differential BMP receptor-dependent signaling pathways balance stalk vs. tip cell competence |
Q37153723 | SDF-1alpha stimulates JNK3 activity via eNOS-dependent nitrosylation of MKP7 to enhance endothelial migration |
Q30494681 | Single-molecule stepping and structural dynamics of myosin X. |
Q42098324 | Stalk cell phenotype depends on integration of Notch and Smad1/5 signaling cascades |
Q24305586 | Structural basis of cargo recognition by the myosin-X MyTH4-FERM domain |
Q27674679 | Structural basis of the myosin X PH1N-PH2-PH1C tandem as a specific and acute cellular PI(3,4,5)P3 sensor |
Q35819455 | TM4SF1: a tetraspanin-like protein necessary for nanopodia formation and endothelial cell migration |
Q30493646 | The motor protein myosin-X transports VE-cadherin along filopodia to allow the formation of early endothelial cell-cell contacts. |
Q38218507 | The role of BMPs in endothelial cell function and dysfunction |
Q37778482 | Vascular development: genetic mechanisms and links to vascular disease |
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