Arginylation-dependent neural crest cell migration is essential for mouse development
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The N-end rule pathwayFactors controlling cardiac neural crest cell migrationSmall molecule inhibitors of arginyltransferase regulate arginylation-dependent protein degradation, cell motility, and angiogenesisArginylation of myosin heavy chain regulates skeletal muscle strengthProtein arginylation, a global biological regulator that targets actin cytoskeleton and the muscleThe N-end rule pathway and regulation by proteolysisArginyltransferase is an ATP-independent self-regulating enzyme that forms distinct functional complexes in vivo.Arginylation regulates purine nucleotide biosynthesis by enhancing the activity of phosphoribosyl pyrophosphate synthaseOsteoblasts Have a Neural Origin in Heterotopic Ossification.Arginylation-dependent regulation of a proteolytic product of talin is essential for cell-cell adhesion.Characterization of arginylation branch of N-end rule pathway in G-protein-mediated proliferation and signaling of cardiomyocytesA novel spiroindoline targets cell cycle and migration via modulation of microtubule cytoskeleton.Post-translational modification and regulation of actin.Posttranslational arginylation enzyme Ate1 affects DNA mutagenesis by regulating stress responseLoss of ATE1-mediated arginylation leads to impaired platelet myosin phosphorylation, clot retraction, and in vivo thrombosis formation.Posttranslational arginylation as a global biological regulator.Post-translational protein arginylation in the normal nervous system and in neurodegeneration.Arginylation regulates myofibrils to maintain heart function and prevent dilated cardiomyopathy.The N-end rule pathway is mediated by a complex of the RING-type Ubr1 and HECT-type Ufd4 ubiquitin ligases.Protein arginylation targets alpha synuclein, facilitates normal brain health, and prevents neurodegenerationProtein arginylation regulates cellular stress response by stabilizing HSP70 and HSP40 transcripts.Analyzing N-terminal Arginylation through the Use of Peptide Arrays and Degradation Assays.Arginyltransferase ATE1 is targeted to the neuronal growth cones and regulates neurite outgrowth during brain development.Arginyltransferase suppresses cell tumorigenic potential and inversely correlates with metastases in human cancers.Talin is cut out for intercellular adhesion.Rapid and dynamic arginylation of the leading edge β- actin is required for cell migration.
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P2860
Arginylation-dependent neural crest cell migration is essential for mouse development
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2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Arginylation-dependent neural crest cell migration is essential for mouse development
@ast
Arginylation-dependent neural crest cell migration is essential for mouse development
@en
Arginylation-dependent neural crest cell migration is essential for mouse development
@nl
type
label
Arginylation-dependent neural crest cell migration is essential for mouse development
@ast
Arginylation-dependent neural crest cell migration is essential for mouse development
@en
Arginylation-dependent neural crest cell migration is essential for mouse development
@nl
prefLabel
Arginylation-dependent neural crest cell migration is essential for mouse development
@ast
Arginylation-dependent neural crest cell migration is essential for mouse development
@en
Arginylation-dependent neural crest cell migration is essential for mouse development
@nl
P2093
P2860
P3181
P1433
P1476
Arginylation-dependent neural crest cell migration is essential for mouse development
@en
P2093
Anna Kashina
Caiying Guo
Fangliang Zhang
Junling Wang
N Adrian Leu
Ralph Bunte
Satoshi Kurosaka
Sougata Saha
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1000878
P407
P577
2010-03-01T00:00:00Z