scholarly article | Q13442814 |
P50 | author | Ernest G Heimsath | Q82839061 |
P2093 | author name string | John A Hammer | |
Richard E Cheney | |||
Mirna Mustapha | |||
Yang-In Yim | |||
P2860 | cites work | A reexamination of the role of microfilaments in neurulation in the chick embryo | Q68282109 |
In vivo evidence for short- and long-range cell communication in cranial neural crest cells | Q81018759 | ||
Ena/VASP Is Required for neuritogenesis in the developing cortex | Q81565765 | ||
Neural tube defects | Q87405864 | ||
Myosin-X is a molecular motor that functions in filopodia formation | Q24299253 | ||
Structural basis of cargo recognition by the myosin-X MyTH4-FERM domain | Q24305586 | ||
Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice | Q24555217 | ||
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia | Q24568070 | ||
Globally optimal stitching of tiled 3D microscopic image acquisitions | Q24643398 | ||
Describing the Prevalence of Neural Tube Defects Worldwide: A Systematic Literature Review | Q26750401 | ||
Myosin-X and disease | Q26825835 | ||
Direct Microtubule-Binding by Myosin-10 Orients Centrosomes toward Retraction Fibers and Subcortical Actin Clouds | Q27314555 | ||
The myosin X motor is optimized for movement on actin bundles | Q27333243 | ||
Antiparallel coiled-coil-mediated dimerization of myosin X | Q27673659 | ||
Structural basis of the myosin X PH1N-PH2-PH1C tandem as a specific and acute cellular PI(3,4,5)P3 sensor | Q27674679 | ||
Myosin X is a downstream effector of PI(3)K during phagocytosis | Q28114999 | ||
Myosin X regulates netrin receptors and functions in axonal path-finding | Q28506167 | ||
Repulsive guidance molecule (RGM) gene function is required for neural tube closure but not retinal topography in the mouse visual system | Q28506752 | ||
Myo10 in brain: developmental regulation, identification of a headless isoform and dynamics in neurons | Q28507574 | ||
Syndactyly and preaxial synpolydactyly in the single Sfrp2 deleted mutant mice | Q28508599 | ||
An essential role for frizzled 5 in mammalian ocular development | Q28511042 | ||
WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature | Q28511517 | ||
A type VII myosin encoded by the mouse deafness gene shaker-1 | Q28512902 | ||
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells | Q28513409 | ||
Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction | Q28569812 | ||
Novel myosin heavy chain encoded by murine dilute coat colour locus | Q28590446 | ||
A mutation in Rab27a causes the vesicle transport defects observed in ashen mice | Q28594384 | ||
VEGF guides angiogenic sprouting utilizing endothelial tip cell filopodia | Q29617501 | ||
Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice | Q30459515 | ||
Integrin-mediated adhesion orients the spindle parallel to the substratum in an EB1- and myosin X-dependent manner | Q30479119 | ||
The motor activity of myosin-X promotes actin fiber convergence at the cell periphery to initiate filopodia formation. | Q30480576 | ||
Myosin-10 and actin filaments are essential for mitotic spindle function | Q30482632 | ||
Fascin1 is dispensable for mouse development but is favorable for neonatal survival | Q30490009 | ||
Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle | Q30493544 | ||
The motor protein myosin-X transports VE-cadherin along filopodia to allow the formation of early endothelial cell-cell contacts. | Q30493646 | ||
Headless Myo10 is a regulator of microtubule stability during neuronal development. | Q50577636 | ||
Kinked tail mutation results in notochord defects in heterozygotes and distal visceral endoderm defects in homozygotes. | Q51923489 | ||
Neogenin and RGMa control neural tube closure and neuroepithelial morphology by regulating cell polarity. | Q51946032 | ||
Role of BMP-2 and OP-1 (BMP-7) in programmed cell death and skeletogenesis during chick limb development. | Q52195974 | ||
A microtubule-binding myosin required for nuclear anchoring and spindle assembly. | Q52560093 | ||
PtdIns(3,4,5)P₃ is a regulator of myosin-X localization and filopodia formation. | Q52604153 | ||
Phospholipid-dependent regulation of the motor activity of myosin X. | Q52612413 | ||
The predicted coiled-coil domain of myosin 10 forms a novel elongated domain that lengthens the head. | Q52857621 | ||
Proper closure of the optic fissure requires ephrin A5-EphB2-JNK signaling. | Q52886264 | ||
Filopodia are dispensable for endothelial tip cell guidance. | Q53089715 | ||
Melanin transfer in human skin cells is mediated by filopodia--a model for homotypic and heterotypic lysosome-related organelle transfer. | Q54426509 | ||
How filopodia pull: what we know about the mechanics and dynamics of filopodia. | Q38130179 | ||
Specific Myosins Control Actin Organization, Cell Morphology, and Migration in Prostate Cancer Cells | Q38811650 | ||
MyTH4-FERM myosins in the assembly and maintenance of actin-based protrusions | Q39005661 | ||
Different gene knockout/transgenic mouse models manifesting persistent fetal vasculature: Are integrins to blame for this pathological condition? | Q39063261 | ||
Developmental regression of hyaloid vasculature is triggered by neurons | Q39668079 | ||
Coordination by Cdc42 of Actin, Contractility, and Adhesion for Melanoblast Movement in Mouse Skin | Q40317118 | ||
Repulsive guidance molecule is a structural bridge between neogenin and bone morphogenetic protein | Q40979907 | ||
Persistent fetal vasculature (PFV): an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture | Q41645582 | ||
A novel form of motility in filopodia revealed by imaging myosin-X at the single-molecule level | Q41978648 | ||
Dynamic behaviors of the non-neural ectoderm during mammalian cranial neural tube closure. | Q42174995 | ||
Myosin-7b Promotes Distal Tip Localization of the Intermicrovillar Adhesion Complex | Q42365129 | ||
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. | Q42455765 | ||
Macrophages are required for cell death and tissue remodeling in the developing mouse eye. | Q42614151 | ||
Fascin 1 is dispensable for developmental and tumour angiogenesis | Q42906224 | ||
Filopodia are required for cortical neurite initiation. | Q46891046 | ||
Bone morphogenetic proteins differentially regulate pigmentation in human skin cells | Q47699993 | ||
Loop-tail phenotype in heterozygous mice and neural tube defects in homozygous mice result from a nonsense mutation in the Vangl2 gene | Q48189717 | ||
Teratogenicity of cytochalasin D in the mouse | Q48258523 | ||
Vascular defects and sensorineural deafness in a mouse model of Norrie disease. | Q48591907 | ||
Multiple roles of filopodial dynamics in particle capture and phagocytosis and phenotypes of Cdc42 and Myo10 deletion | Q48623666 | ||
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing | Q30494750 | ||
Myosin-X is required for cranial neural crest cell migration in Xenopus laevis | Q30497957 | ||
Fascin 1 is transiently expressed in mouse melanoblasts during development and promotes migration and proliferation | Q30570724 | ||
Mutant p53-associated myosin-X upregulation promotes breast cancer invasion and metastasis. | Q30572690 | ||
Myosin-X is critical for migratory ability of Xenopus cranial neural crest cells. | Q30576361 | ||
A Combination of Diffusion and Active Translocation Localizes Myosin 10 to the Filopodial Tip | Q30826156 | ||
Persistent hyperplastic primary vitreous. A clinicopathologic study of 62 cases and review of the literature | Q33544308 | ||
Actin, microtubules, and vimentin intermediate filaments cooperate for elongation of invadopodia | Q33840016 | ||
Myosin-X, a novel myosin with pleckstrin homology domains, associates with regions of dynamic actin. | Q33917620 | ||
Dynamic actin-based epithelial adhesion and cell matching during Drosophila dorsal closure. | Q33927041 | ||
Myosin-X is an unconventional myosin that undergoes intrafilopodial motility. | Q34115035 | ||
Filopodia are conduits for melanosome transfer to keratinocytes. | Q34118656 | ||
The Stepping Pattern of Myosin X Is Adapted for Processive Motility on Bundled Actin | Q34134758 | ||
Myosin-X provides a motor-based link between integrins and the cytoskeleton. | Q34322246 | ||
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. | Q34469642 | ||
Eyelid closure in embryogenesis is required for ocular adnexa development | Q34575826 | ||
Pathogenesis of persistent hyperplastic primary vitreous in mice lacking the arf tumor suppressor gene | Q35012702 | ||
Myosin-X: a MyTH-FERM myosin at the tips of filopodia | Q35576442 | ||
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders | Q35793513 | ||
SHIELD: an integrative gene expression database for inner ear research. | Q35885569 | ||
Mechanisms of tissue fusion during development. | Q35893613 | ||
Development and pathology of the hyaloid, choroidal and retinal vasculature. | Q35959824 | ||
Formation of persistent hyperplastic primary vitreous in ephrin-A5-/- mice | Q36103385 | ||
Headless Myo10 is a negative regulator of full-length Myo10 and inhibits axon outgrowth in cortical neurons | Q36127036 | ||
Sequential roles for myosin-X in BMP6-dependent filopodial extension, migration, and activation of BMP receptors | Q36639095 | ||
Development of the retinal vasculature | Q36745434 | ||
Mechanisms to suppress multipolar divisions in cancer cells with extra centrosomes | Q36843504 | ||
Myosin MyTH4-FERM structures highlight important principles of convergent evolution. | Q36957296 | ||
MyTH4-FERM myosins have an ancient and conserved role in filopod formation | Q37515120 | ||
Cytonemes as specialized signaling filopodia | Q37551588 | ||
High-throughput discovery of novel developmental phenotypes | Q37629635 | ||
Filopodia initiation: focus on the Arp2/3 complex and formins | Q37942763 | ||
Pleiotropic effects of coat colour-associated mutations in humans, mice and other mammals | Q38098789 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 17354 | |
P577 | publication date | 2017-12-11 | |
P1433 | published in | Scientific Reports | Q2261792 |
P1476 | title | Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation | |
P478 | volume | 7 |
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Q89545561 | Myosin X is required for efficient melanoblast migration and melanoma initiation and metastasis |
Q61444640 | Phenotypic analysis of Myo10 knockout (Myo10) mice lacking full-length (motorized) but not brain-specific headless myosin X |
Q58104023 | Roles for Ena/VASP proteins in FMNL3-mediated filopodial assembly |
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