scholarly article | Q13442814 |
P50 | author | David Pilgrim | Q43138583 |
P2093 | author name string | Anjon Audhya | |
Torah M Kachur | |||
P2860 | cites work | Dissection of the mammalian midbody proteome reveals conserved cytokinesis mechanisms. | Q24294556 |
Myosin II co-chaperone general cell UNC-45 overexpression is associated with ovarian cancer, rapid proliferation, and motility | Q24672758 | ||
Genome-wide RNAi of C. elegans using the hypersensitive rrf-3 strain reveals novel gene functions | Q24803805 | ||
Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans | Q27860867 | ||
Dissecting temporal and spatial control of cytokinesis with a myosin II Inhibitor | Q28183531 | ||
Cell Polarity and the Cytoskeleton in theCaenorhabditis ElegansZygote | Q28184418 | ||
Genome-wide RNAi screening in Caenorhabditis elegans | Q29617900 | ||
Reassessing the role and dynamics of nonmuscle myosin II during furrow formation in early Drosophila embryos | Q30506257 | ||
unc-45 gene of Caenorhabditis elegans encodes a muscle-specific tetratricopeptide repeat-containing protein | Q30658184 | ||
A homologue of the yeast SHE4 gene is essential for the transition between the syncytial and cellular stages during sexual reproduction of the fungus Podospora anserina | Q33888398 | ||
The Caenorhabditis elegans gonad: a test tube for cell and developmental biology | Q33924971 | ||
Two mammalian UNC-45 isoforms are related to distinct cytoskeletal and muscle-specific functions | Q34152511 | ||
The molecular requirements for cytokinesis | Q34404139 | ||
The UCS family of myosin chaperones | Q34925335 | ||
How one becomes many: blastoderm cellularization in Drosophila melanogaster | Q34974409 | ||
The nonmuscle myosin regulatory light chain gene mlc-4 is required for cytokinesis, anterior-posterior polarity, and body morphology during Caenorhabditis elegans embryogenesis | Q35506248 | ||
PAR proteins and the establishment of cell polarity during C. elegans development | Q36018009 | ||
Regulation of myosin II during cytokinesis in higher eukaryotes | Q36151437 | ||
Fluorescence visualization of the distribution of microfilaments in gonads and early embryos of the nematode Caenorhabditis elegans | Q36216689 | ||
Unc-45 mutations in Caenorhabditis elegans implicate a CRO1/She4p-like domain in myosin assembly | Q36256331 | ||
Myosin-II reorganization during mitosis is controlled temporally by its dephosphorylation and spatially by Mid1 in fission yeast | Q36322424 | ||
UCS protein Rng3p activates actin filament gliding by fission yeast myosin-II. | Q36322706 | ||
Myosin and the PAR proteins polarize microfilament-dependent forces that shape and position mitotic spindles in Caenorhabditis elegans | Q36323415 | ||
Caenorhabditis elegans UNC-45 is a component of muscle thick filaments and colocalizes with myosin heavy chain B, but not myosin heavy chain A | Q36326269 | ||
Acto-myosin reorganization and PAR polarity in C. elegans | Q36730900 | ||
A mitotic kinesin-like protein required for normal karyokinesis, myosin localization to the furrow, and cytokinesis in Dictyostelium | Q37621049 | ||
Myosin structure and function in cell motility | Q39683835 | ||
A non-muscle myosin required for embryonic polarity in Caenorhabditis elegans | Q39757928 | ||
Cortical flows powered by asymmetrical contraction transport PAR proteins to establish and maintain anterior-posterior polarity in the early C. elegans embryo | Q40483476 | ||
Chaperone-mediated folding and assembly of myosin in striated muscle | Q40601638 | ||
Folding of the striated muscle myosin motor domain | Q40719397 | ||
Role of the myosin assembly protein UNC-45 as a molecular chaperone for myosin | Q40754906 | ||
Polarization of the C. elegans zygote proceeds via distinct establishment and maintenance phases | Q42149368 | ||
A Formin Homology protein and a profilin are required for cytokinesis and Arp2/3-independent assembly of cortical microfilaments in C. elegans. | Q44259964 | ||
Distinct roles for two C. elegans anillins in the gonad and early embryo | Q44769074 | ||
Maternal UNC-45 is involved in cytokinesis and colocalizes with non-muscle myosin in the early Caenorhabditis elegans embryo | Q47068663 | ||
Gene clustering based on RNAi phenotypes of ovary-enriched genes in C. elegans | Q47068918 | ||
TheCaenorhabditis elegansnonmuscle myosin genesnmy-1andnmy-2function as redundant components of thelet-502/Rho-binding kinase andmel-11/myosin phosphatase pathway during embryonic morphogenesis | Q47069469 | ||
Asymmetrically distributed PAR-3 protein contributes to cell polarity and spindle alignment in early C. elegans embryos | Q47069501 | ||
The myosin co-chaperone UNC-45 is required for skeletal and cardiac muscle function in zebrafish | Q47073763 | ||
Temperature-sensitive mutation affecting myofilament assembly in Caenorhabditis elegans | Q47849134 | ||
A zebrafish unc-45-related gene expressed during muscle development | Q48285164 | ||
CYK-4/GAP provides a localized cue to initiate anteroposterior polarity upon fertilization. | Q53608548 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Caenorhabditis elegans | Q91703 |
P1104 | number of pages | 13 | |
P304 | page(s) | 287-299 | |
P577 | publication date | 2007-12-04 | |
P1433 | published in | Developmental Biology | Q3025402 |
P1476 | title | UNC-45 is required for NMY-2 contractile function in early embryonic polarity establishment and germline cellularization in C. elegans. | |
P478 | volume | 314 |
Q64106996 | A conserved morphogenetic mechanism for epidermal ensheathment of nociceptive sensory neurites |
Q30500031 | A high-resolution C. elegans essential gene network based on phenotypic profiling of a complex tissue |
Q34614173 | A secreted protein promotes cleavage furrow maturation during cytokinesis |
Q51635704 | ASSET: a robust algorithm for the automated segmentation and standardization of early Caenorhabditis elegans embryos. |
Q34727856 | Active torque generation by the actomyosin cell cortex drives left-right symmetry breaking |
Q50091958 | Actomyosin contractility regulators stabilize the cytoplasmic bridge between the two primordial germ cells during Caenorhabditis elegans embryogenesis |
Q35158993 | An extracellular matrix protein prevents cytokinesis failure and aneuploidy in the C. elegans germline |
Q50547684 | Antagonistic Behaviors of NMY-1 and NMY-2 Maintain Ring Channels in the C. elegans Gonad. |
Q41570390 | At the Start of the Sarcomere: A Previously Unrecognized Role for Myosin Chaperones and Associated Proteins during Early Myofibrillogenesis |
Q30583153 | C. elegans Anillin proteins regulate intercellular bridge stability and germline syncytial organization |
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Q34574189 | Drosophila UNC-45 accumulates in embryonic blastoderm and in muscles, and is essential for muscle myosin stability |
Q36290852 | Dual function of the UNC-45b chaperone with myosin and GATA4 in cardiac development |
Q34063804 | EHBP-1 functions with RAB-10 during endocytic recycling in Caenorhabditis elegans |
Q30510175 | GPI-anchor synthesis is indispensable for the germline development of the nematode Caenorhabditis elegans |
Q30491435 | In vivo roles for Arp2/3 in cortical actin organization during C. elegans gastrulation |
Q30497921 | Internalization of multiple cells during C. elegans gastrulation depends on common cytoskeletal mechanisms but different cell polarity and cell fate regulators |
Q31106786 | Lack of developmental redundancy between Unc45 proteins in zebrafish muscle development |
Q30513991 | Laminin is required to orient epithelial polarity in the C. elegans pharynx |
Q36344078 | Loss of function of myosin chaperones triggers Hsf1-mediated transcriptional response in skeletal muscle cells |
Q27321081 | Membrane invaginations reveal cortical sites that pull on mitotic spindles in one-cell C. elegans embryos |
Q28116344 | Microtubules induce self-organization of polarized PAR domains in Caenorhabditis elegans zygotes |
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Q43187716 | Myosin assembly, maintenance and degradation in muscle: Role of the chaperone UNC-45 in myosin thick filament dynamics |
Q26863588 | Myosin chaperones |
Q42167958 | PAR proteins regulate maintenance-phase myosin dynamics during Caenorhabditis elegans zygote polarization |
Q36245121 | Polarized Rac-dependent protrusions drive epithelial intercalation in the embryonic epidermis of C. elegans |
Q48217215 | Protease dead separase inhibits chromosome segregation and RAB-11 vesicle trafficking |
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Q34579574 | RNAi screening of human glycogene orthologs in the nematode Caenorhabditis elegans and the construction of the C. elegans glycogene database |
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Q47125851 | SID-1 Domains Important for dsRNA Import in Caenorhabditis elegans |
Q46009957 | Syndecan defines precise spindle orientation by modulating Wnt signaling in C. elegans. |
Q52580548 | The Caenorhabditis elegans gene ham-1 regulates daughter cell size asymmetry primarily in divisions that produce a small anterior daughter cell. |
Q27330328 | The UNC-45 chaperone is critical for establishing myosin-based myofibrillar organization and cardiac contractility in the Drosophila heart model |
Q34477894 | The UNC-45 myosin chaperone: from worms to flies to vertebrates. |
Q34356748 | The myosin chaperone UNC45B is involved in lens development and autosomal dominant juvenile cataract |
Q30509509 | Triggering a cell shape change by exploiting preexisting actomyosin contractions |
Q27305022 | Two distinct myosin II populations coordinate ovulatory contraction of the myoepithelial sheath in the Caenorhabditis elegans somatic gonad |
Q38285301 | UCS proteins: chaperones for myosin and co-chaperones for Hsp90. |
Q28586476 | Unc45 activates Hsp90-dependent folding of the myosin motor domain |
Q47074153 | Unc45b is essential for early myofibrillogenesis and costamere formation in zebrafish |
Q41461248 | aPKC Cycles between Functionally Distinct PAR Protein Assemblies to Drive Cell Polarity |