scholarly article | Q13442814 |
P50 | author | Katelynn M Mannix | Q86189940 |
P2093 | author name string | Andrew M Hudson | |
Lynn Cooley | |||
P2860 | cites work | K33-Linked Polyubiquitination of Coronin 7 by Cul3-KLHL20 Ubiquitin E3 Ligase Regulates Protein Trafficking | Q24295450 |
Structure of the Keap1:Nrf2 interface provides mechanistic insight into Nrf2 signaling | Q24298930 | ||
Ubiquitination of Keap1, a BTB-Kelch substrate adaptor protein for Cul3, targets Keap1 for degradation by a proteasome-independent pathway | Q24306215 | ||
The Cullin 3 substrate adaptor KLHL20 mediates DAPK ubiquitination to control interferon responses | Q24306576 | ||
A Cul3-based E3 ligase removes Aurora B from mitotic chromosomes, regulating mitotic progression and completion of cytokinesis in human cells | Q24307672 | ||
Cullin mediates degradation of RhoA through evolutionarily conserved BTB adaptors to control actin cytoskeleton structure and cell movement | Q24318748 | ||
Regulation of WASH-dependent actin polymerization and protein trafficking by ubiquitination | Q24321352 | ||
Adaptor protein self-assembly drives the control of a cullin-RING ubiquitin ligase | Q24336527 | ||
The Cul3-KLHL21 E3 ubiquitin ligase targets aurora B to midzone microtubules in anaphase and is required for cytokinesis | Q24336860 | ||
Sequence and domain organization of scruin, an actin-cross-linking protein in the acrosomal process of Limulus sperm | Q24672920 | ||
Sequence and structural analysis of BTB domain proteins | Q24812693 | ||
Building and remodelling Cullin-RING E3 ubiquitin ligases | Q27027816 | ||
Structures of SPOP-Substrate Complexes: Insights into Molecular Architectures of BTB-Cul3 Ubiquitin Ligases | Q27657740 | ||
Structural Basis for Cul3 Protein Assembly with the BTB-Kelch Family of E3 Ubiquitin Ligases | Q27675990 | ||
Structural and biochemical characterization of the KLHL3–WNK kinase interaction important in blood pressure regulation | Q27682289 | ||
A proteolytic pathway that recognizes ubiquitin as a degradation signal | Q27932607 | ||
Sgt1p and Skp1p modulate the assembly and turnover of CBF3 complexes required for proper kinetochore function | Q27935235 | ||
Function and regulation of cullin-RING ubiquitin ligases | Q28131707 | ||
Regulation of cell polarity and protrusion formation by targeting RhoA for degradation | Q28189565 | ||
VHL loss causes spindle misorientation and chromosome instability. | Q39822734 | ||
Looking at oogenesis | Q40501183 | ||
BTB proteins are substrate-specific adaptors in an SCF-like modular ubiquitin ligase containing CUL-3. | Q40633677 | ||
Regulating the Yeast Kinetochore by Ubiquitin-Dependent Degradation and Skp1p-Mediated Phosphorylation | Q41077870 | ||
Gal4 in the Drosophila female germline | Q42465549 | ||
The BTB protein MEL-26 promotes cytokinesis in C. elegans by a CUL-3-independent mechanism. | Q46708967 | ||
The BTB protein MEL-26 is a substrate-specific adaptor of the CUL-3 ubiquitin-ligase. | Q47069071 | ||
Neddylation and deneddylation regulate Cul1 and Cul3 protein accumulation. | Q47070899 | ||
Orbit/Mast, the CLASP orthologue of Drosophila, is required for asymmetric stem cell and cystocyte divisions and development of the polarised microtubule network that interconnects oocyte and nurse cells during oogenesis. | Q47070935 | ||
Importin-alpha 2 is critically required for the assembly of ring canals during Drosophila oogenesis | Q47071576 | ||
Drosophila filamin encoded by the cheerio locus is a component of ovarian ring canals | Q47072260 | ||
The osmolarity of adult Drosophila hemolymph and its effect on oocyte-nurse cell electrical polarity | Q49119222 | ||
What Determines the Specificity and Outcomes of Ubiquitin Signaling? | Q57206327 | ||
Short-lived green fluorescent proteins for quantifying ubiquitin/proteasome-dependent proteolysis in living cells | Q61788079 | ||
Ubiquitination and degradation of the substrate recognition subunits of SCF ubiquitin-protein ligases | Q77652490 | ||
pVHL: a multipurpose adaptor protein | Q81470388 | ||
Polyubiquitin chains: polymeric protein signals | Q28294396 | ||
A subset of dynamic actin rearrangements in Drosophila requires the Arp2/3 complex | Q28756055 | ||
Recognition and processing of ubiquitin-protein conjugates by the proteasome | Q29547616 | ||
SCF and Cullin/Ring H2-based ubiquitin ligases | Q29547637 | ||
Structural basis for defects of Keap1 activity provoked by its point mutations in lung cancer | Q29616499 | ||
Isolation of mutations in the Drosophila homologues of the human Neurofibromatosis 2 and yeast CDC42 genes using a simple and efficient reverse-genetic method. | Q30498647 | ||
Drosophila Kelch functions with Cullin-3 to organize the ring canal actin cytoskeleton | Q33616443 | ||
Methods for studying oogenesis | Q33723700 | ||
Rotation and asymmetry of the mitotic spindle direct asymmetric cell division in the developing central nervous system. | Q33885616 | ||
Formation of the Drosophila ovarian ring canal inner rim depends on cheerio | Q33969705 | ||
kelch encodes a component of intercellular bridges in Drosophila egg chambers | Q34061810 | ||
A genome-scale shRNA resource for transgenic RNAi in Drosophila | Q34175440 | ||
VHL, the story of a tumour suppressor gene | Q34455226 | ||
Regulation of microtubule stability by the von Hippel-Lindau tumour suppressor protein pVHL. | Q34530199 | ||
The dominant temperature-sensitive lethal DTS7 of Drosophila melanogaster encodes an altered 20S proteasome beta-type subunit. | Q34606007 | ||
Construction of transgenic Drosophila by using the site-specific integrase from phage phiC31 | Q34644225 | ||
Crystal structure of KLHL3 in complex with Cullin3 | Q34661978 | ||
Quantitative image analysis identifies pVHL as a key regulator of microtubule dynamic instability | Q35005618 | ||
Phosphoinositide regulation of the actin cytoskeleton | Q35019759 | ||
The E3 ubiquitin ligase specificity subunit ASB2α targets filamins for proteasomal degradation by interacting with the filamin actin-binding domain | Q35112298 | ||
The F-box protein Skp2 is a ubiquitylation target of a Cul1-based core ubiquitin ligase complex: evidence for a role of Cul1 in the suppression of Skp2 expression in quiescent fibroblasts | Q35116922 | ||
Ubiquitin and transcription: The SCF/Met4 pathway, a (protein-) complex issue | Q35146031 | ||
Ubiquitin-dependent degradation of multiple F-box proteins by an autocatalytic mechanism | Q35596995 | ||
Control of nonmuscle myosins by phosphorylation | Q35671081 | ||
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities | Q35754537 | ||
Drosophila Kelch Is an Oligomeric Ring Canal Actin Organizer | Q36267663 | ||
Filamin is required for ring canal assembly and actin organization during Drosophila oogenesis | Q36316648 | ||
Drosophila Kelch regulates actin organization via Src64-dependent tyrosine phosphorylation | Q36325815 | ||
Identification of an essential gene, l(3)73Ai, with a dominant temperature-sensitive lethal allele, encoding a Drosophila proteasome subunit | Q36556898 | ||
Exploiting position effects and the gypsy retrovirus insulator to engineer precisely expressed transgenes | Q36580731 | ||
Phylogenetic, structural and functional relationships between WD- and Kelch-repeat proteins | Q37299802 | ||
Duplicated proteasome subunit genes in Drosophila and their roles in spermatogenesis | Q37412265 | ||
Ubiquitination of E3 ligases: self-regulation of the ubiquitin system via proteolytic and non-proteolytic mechanisms | Q37849576 | ||
Gastrulation: Making and Shaping Germ Layers | Q38026928 | ||
Signaling mechanisms and functional roles of cofilin phosphorylation and dephosphorylation | Q38059941 | ||
Stability of homologue of Slimb F-box protein is regulated by availability of its substrate | Q38346254 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cytoskeleton | Q154626 |
Drosophila | Q312154 | ||
P1104 | number of pages | 15 | |
P304 | page(s) | 1117-1131 | |
P577 | publication date | 2015-09-16 | |
P1433 | published in | Genetics | Q3100575 |
P1476 | title | Actin Cytoskeletal Organization in Drosophila Germline Ring Canals Depends on Kelch Function in a Cullin-RING E3 Ligase | |
P478 | volume | 201 |
Q44533045 | A screen for E3 ubiquitination ligases that genetically interact with the adaptor protein Cindr during Drosophila eye patterning |
Q38927009 | Broad-complex, tramtrack, and bric-à-brac (BTB) proteins: Critical regulators of development |
Q47284253 | Cullin 3-Based Ubiquitin Ligases as Master Regulators of Mammalian Cell Differentiation. |
Q64970946 | Cullin-3 dependent deregulation of ACTN1 represents a new pathogenic mechanism in nemaline myopathy. |
Q46504619 | Drosophila glob1 is required for the maintenance of cytoskeletal integrity during oogenesis |
Q37151366 | Oncogenic transformation of Drosophila somatic cells induces a functional piRNA pathway |
Q46300798 | Stay Connected: A Germ Cell Strategy |
Q50186703 | Subcellular Specialization and Organelle Behavior in Germ Cells |
Q90595758 | Targeted substrate degradation by Kelch controls the actin cytoskeleton during ring canal expansion |
Q54110383 | The Misshapen kinase regulates the size and stability of the germline ring canals in the Drosophila egg chamber |
Q90118062 | Transcriptomic and computational analysis identified LPA metabolism, KLHL14 and KCNE3 as novel regulators of Epithelial-Mesenchymal Transition |
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