scholarly article | Q13442814 |
P356 | DOI | 10.1534/GENETICS.112.143727 |
P8608 | Fatcat ID | release_ytqd2uxvmfdutb7gavzlnh4yk4 |
P932 | PMC publication ID | 3522167 |
P698 | PubMed publication ID | 22887819 |
P2093 | author name string | Diane G Morton | |
Kenneth J Kemphues | |||
Wendy A Hoose | |||
P2860 | cites work | Complexes between the LKB1 tumor suppressor, STRAD alpha/beta and MO25 alpha/beta are upstream kinases in the AMP-activated protein kinase cascade | Q21245891 |
MO25alpha/beta interact with STRADalpha/beta enhancing their ability to bind, activate and localize LKB1 in the cytoplasm | Q24296287 | ||
Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRAD | Q24305094 | ||
The genetics of Caenorhabditis elegans | Q24533408 | ||
Heat-shock protein 90 and Cdc37 interact with LKB1 and regulate its stability | Q24535623 | ||
WormBase: a comprehensive resource for nematode research | Q24642944 | ||
The Pfam protein families database | Q24644670 | ||
SMART 6: recent updates and new developments | Q24655795 | ||
Functional and phylogenetic analysis of the ubiquitylation system in Caenorhabditis elegans: ubiquitin-conjugating enzymes, ubiquitin-activating enzymes, and ubiquitin-like proteins | Q24802049 | ||
Basic local alignment search tool | Q25938991 | ||
Systematic functional analysis of the Caenorhabditis elegans genome using RNAi | Q27860839 | ||
Ubc9p is the conjugating enzyme for the ubiquitin-like protein Smt3p | Q27930030 | ||
Microtubules induce self-organization of polarized PAR domains in Caenorhabditis elegans zygotes | Q28116344 | ||
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome | Q28119198 | ||
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase | Q28258611 | ||
C. elegans PAR proteins function by mobilizing and stabilizing asymmetrically localized protein complexes | Q28265914 | ||
Cortical and cytoplasmic flow polarity in early embryonic cells of Caenorhabditis elegans | Q28270015 | ||
Proteasome-independent functions of ubiquitin in endocytosis and signaling | Q28282959 | ||
par-1, a gene required for establishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed | Q28301842 | ||
New member of the Snf1/AMPK kinase family, Melk, is expressed in the mouse egg and preimplantation embryo | Q28506665 | ||
Expression of Melk, a new protein kinase, during early mouse development | Q28511671 | ||
LKB1 and SAD kinases define a pathway required for the polarization of cortical neurons | Q28591764 | ||
Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library | Q28770084 | ||
P bodies and the control of mRNA translation and degradation | Q29547253 | ||
Specific interference by ingested dsRNA | Q29617516 | ||
Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans | Q29618535 | ||
Stabilization of cell polarity by the C. elegans RING protein PAR-2. | Q30478491 | ||
SUMO regulates the assembly and function of a cytoplasmic intermediate filament protein in C. elegans | Q30492693 | ||
Symmetry breaking and polarization of the C. elegans zygote by the polarity protein PAR-2 | Q30494245 | ||
Extracellular control of PAR protein localization during asymmetric cell division in the C. elegans embryo | Q30496455 | ||
The C. elegans homolog of Drosophila Lethal giant larvae functions redundantly with PAR-2 to maintain polarity in the early embryo | Q30497313 | ||
The SAD-1 kinase regulates presynaptic vesicle clustering and axon termination | Q31965163 | ||
SUMO, ubiquitin's mysterious cousin | Q33939449 | ||
par-4, a gene required for cytoplasmic localization and determination of specific cell types in Caenorhabditis elegans embryogenesis | Q33959251 | ||
Control of cleavage spindle orientation in Caenorhabditis elegans: the role of the genes par-2 and par-3. | Q33964428 | ||
Cell polarity in eggs and epithelia: parallels and diversity | Q34118022 | ||
The C. elegans par-4 gene encodes a putative serine-threonine kinase required for establishing embryonic asymmetry | Q34507504 | ||
LKB1-dependent signaling pathways | Q34535140 | ||
Stability of the Peutz-Jeghers syndrome kinase LKB1 requires its binding to the molecular chaperones Hsp90/Cdc37. | Q34543848 | ||
Processing bodies and germ granules are distinct RNA granules that interact in C. elegans embryos | Q47069466 | ||
Asymmetrically distributed PAR-3 protein contributes to cell polarity and spindle alignment in early C. elegans embryos | Q47069501 | ||
Depletion of the co-chaperone CDC-37 reveals two modes of PAR-6 cortical association in C. elegans embryos | Q47069512 | ||
C. elegans STI-1, the homolog of Sti1/Hop, is involved in aging and stress response | Q47069557 | ||
Genetic requirements for PIE-1 localization and inhibition of gene expression in the embryonic germ lineage of Caenorhabditis elegans | Q47683015 | ||
Embryonic lethality caused by mutations in basement membrane collagen of C. elegans | Q48235123 | ||
Identification of a heat-shock pseudogene from Caenorhabditis elegans | Q48300028 | ||
Cell cycle regulation of pEg3, a new Xenopus protein kinase of the KIN1/PAR-1/MARK family. | Q48871311 | ||
Molecular chaperone complexes with antagonizing activities regulate stability and activity of the tumor suppressor LKB1. | Q51546346 | ||
Cell lineages and developmental defects of temperature-sensitive embryonic arrest mutants in Caenorhabditis elegans. | Q52298755 | ||
PLK-1 asymmetry contributes to asynchronous cell division of C. elegans embryos. | Q53495600 | ||
An analysis of the role of microfilaments in the establishment and maintenance of asymmetry in Caenorhabditis elegans zygotes | Q68123078 | ||
Identification of genes required for cytoplasmic localization in early C. elegans embryos | Q68273724 | ||
Asymmetric movements of cytoplasmic components in Caenorhabditis elegans zygotes | Q69227141 | ||
Parental effects and phenotypic characterization of mutations that affect early development in Caenorhabditis elegans | Q71183744 | ||
Generation of asymmetry and segregation of germ-line granules in early C. elegans embryos | Q71236703 | ||
Systematic, RNA-interference-mediated identification of mus-101 modifier genes in Caenorhabditis elegans | Q34572464 | ||
A genomewide screen for suppressors of par-2 uncovers potential regulators of PAR protein-dependent cell polarity in Caenorhabditis elegans | Q35038681 | ||
Overcoming redundancy: an RNAi enhancer screen for morphogenesis genes in Caenorhabditis elegans | Q35222713 | ||
par-2, a gene required for blastomere asymmetry in Caenorhabditis elegans, encodes zinc-finger and ATP-binding motifs | Q35553959 | ||
The Caenorhabditis elegans septin complex is nonpolar | Q35914622 | ||
Programmed elimination of cells by caspase-independent cell extrusion in C. elegans | Q36157242 | ||
Ubiquitylation and cell signaling | Q36251951 | ||
Characterization of alpha1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha1 and alpha2(IV) mutations on type IV collagen distribution | Q36262065 | ||
Immunofluorescence visualization of germ-line-specific cytoplasmic granules in embryos, larvae, and adults of Caenorhabditis elegans | Q36285245 | ||
The Caenorhabditis elegans vab-10 spectraplakin isoforms protect the epidermis against internal and external forces | Q36381451 | ||
PAR proteins direct asymmetry of the cell cycle regulators Polo-like kinase and Cdc25. | Q36491719 | ||
Acto-myosin reorganization and PAR polarity in C. elegans | Q36730900 | ||
MES-1, a protein required for unequal divisions of the germline in early C. elegans embryos, resembles receptor tyrosine kinases and is localized to the boundary between the germline and gut cells | Q36731904 | ||
Two conserved regulatory cytoplasmic poly(A) polymerases, GLD-4 and GLD-2, regulate meiotic progression in C. elegans | Q37152250 | ||
The art and design of genetic screens: RNA interference. | Q37180850 | ||
Using RNA interference to identify specific modifiers of a temperature-sensitive, embryonic-lethal mutation in the Caenorhabditis elegans ubiquitin-like Nedd8 protein modification pathway E1-activating gene rfl-1 | Q37310263 | ||
MAP kinase signaling antagonizes PAR-1 function during polarization of the early Caenorhabditis elegans embryo | Q37425052 | ||
Elaborating polarity: PAR proteins and the cytoskeleton | Q37838101 | ||
Role of LKB1-SAD/MARK pathway in neuronal polarization | Q37854547 | ||
The multifaceted roles of USP7: new therapeutic opportunities | Q37862125 | ||
The Ccr4--not complex | Q37949473 | ||
Pseudocleavage is dispensable for polarity and development in C. elegans embryos | Q38467112 | ||
PAR-2 is asymmetrically distributed and promotes association of P granules and PAR-1 with the cortex in C. elegans embryos | Q39758007 | ||
LKB1/STRAD promotes axon initiation during neuronal polarization. | Q40136806 | ||
Cortical flows powered by asymmetrical contraction transport PAR proteins to establish and maintain anterior-posterior polarity in the early C. elegans embryo | Q40483476 | ||
Mutations in ooc-5 and ooc-3 disrupt oocyte formation and the reestablishment of asymmetric PAR protein localization in two-cell Caenorhabditis elegans embryos | Q41699806 | ||
Polarization of the C. elegans zygote proceeds via distinct establishment and maintenance phases | Q42149368 | ||
The Caenorhabditis elegans par-5 gene encodes a 14-3-3 protein required for cellular asymmetry in the early embryo | Q43849657 | ||
SRC-1 and Wnt signaling act together to specify endoderm and to control cleavage orientation in early C. elegans embryos | Q44057731 | ||
PAR-1 is required for morphogenesis of the Caenorhabditis elegans vulva | Q44254664 | ||
The C. elegans MELK ortholog PIG-1 regulates cell size asymmetry and daughter cell fate in asymmetric neuroblast divisions. | Q44846511 | ||
MEX-5 asymmetry in one-cell C. elegans embryos requires PAR-4- and PAR-1-dependent phosphorylation. | Q45211998 | ||
LGL can partition the cortex of one-cell Caenorhabditis elegans embryos into two domains | Q45401297 | ||
OOC-3, a novel putative transmembrane protein required for establishment of cortical domains and spindle orientation in the P(1) blastomere of C. elegans embryos | Q47068753 | ||
PAR-6 is a conserved PDZ domain-containing protein that colocalizes with PAR-3 in Caenorhabditis elegans embryos. | Q47068779 | ||
C. elegans STRADalpha and SAD cooperatively regulate neuronal polarity and synaptic organization | Q47068978 | ||
par-6, a gene involved in the establishment of asymmetry in early C. elegans embryos, mediates the asymmetric localization of PAR-3. | Q47068999 | ||
C. elegans PAR-3 and PAR-6 are required for apicobasal asymmetries associated with cell adhesion and gastrulation. | Q47069009 | ||
Neuronal polarity is regulated by a direct interaction between a scaffolding protein, Neurabin, and a presynaptic SAD-1 kinase in Caenorhabditis elegans | Q47069032 | ||
CRT-1/calreticulin and the E3 ligase EEL-1/HUWE1 control hemidesmosome maturation in C. elegans development. | Q47069038 | ||
The non-canonical Hop protein from Caenorhabditis elegans exerts essential functions and forms binary complexes with either Hsc70 or Hsp90. | Q47069319 | ||
Differential requirements for STRAD in LKB1-dependent functions in C. elegans. | Q47069379 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Caenorhabditis elegans | Q91703 |
P1104 | number of pages | 14 | |
P304 | page(s) | 929-942 | |
P577 | publication date | 2012-08-10 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | A genome-wide RNAi screen for enhancers of par mutants reveals new contributors to early embryonic polarity in Caenorhabditis elegans | |
P478 | volume | 192 |
Q54210803 | 'Goldilocks' suppressor screen identifies web of polarity regulators. |
Q35621410 | A Synthetic Lethal Screen Identifies a Role for Lin-44/Wnt in C. elegans Embryogenesis |
Q36643905 | Caenorhabditis elegans PIG-1/MELK acts in a conserved PAR-4/LKB1 polarity pathway to promote asymmetric neuroblast divisions |
Q57980365 | Cell Polarity in One-Cell C. elegans Embryos: Ensuring an Accurate and Precise Spatial Axis During Development |
Q27329642 | Deubiquitylation machinery is required for embryonic polarity in Caenorhabditis elegans |
Q43491720 | LET-99 functions in the astral furrowing pathway, where it is required for myosin enrichment in the contractile ring |
Q33973337 | Noncanonical cell death in the nematode Caenorhabditis elegans |
Q27309993 | PAR-4 and anillin regulate myosin to coordinate spindle and furrow position during asymmetric division. |
Q99568699 | PIG-1 MELK-dependent phosphorylation of nonmuscle myosin II promotes apoptosis through CES-1 Snail partitioning |
Q39242272 | Size Matters: How C. elegans Asymmetric Divisions Regulate Apoptosis |
Q26860998 | The PAR network: redundancy and robustness in a symmetry-breaking system |
Q91433684 | The kinases PIG-1 and PAR-1 act in redundant pathways to regulate asymmetric division in the EMS blastomere of C. elegans |
Q38161449 | Wnt-signaling and planar cell polarity genes regulate axon guidance along the anteroposterior axis in C. elegans |
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