(Q24317049)

4

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author name string

Hongying Zhang

2

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Haining Wang

3

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Toshiyuki Miyashita

5

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Haian Fu

Experimental Cell Research

6

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language of work or name

English

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publication date

1 April 2004

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published in

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volume

294

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issue

2

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page(s)

581-91

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cites work

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Molecular cloning and characterization of a novel protein kinase with a catalytic domain homologous to mitogen-activated protein kinase kinase kinase

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Induction of apoptosis by ASK1, a mammalian MAPKKK that activates SAPK/JNK and p38 signaling pathways

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Execution of Apoptosis Signal-regulating Kinase 1 (ASK1)-induced Apoptosis by the Mitochondria-dependent Caspase Activation

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ASK1 mediates apoptotic cell death induced by genotoxic stress.

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ASK1 is required for sustained activations of JNK/p38 MAP kinases and apoptosis

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Activation of apoptosis signal-regulating kinase 1 by the stress-induced activating phosphorylation of pre-formed oligomer

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Akt phosphorylates and negatively regulates apoptosis signal-regulating kinase 1

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Suppression of apoptosis signal-regulating kinase 1-induced cell death by 14-3-3 proteins

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ASK1 is essential for JNK/SAPK activation by TRAF2

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Role of glutaredoxin in metabolic oxidative stress. Glutaredoxin as a sensor of oxidative stress mediated by H2O2.

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Interaction of 14-3-3 with signaling proteins is mediated by the recognition of phosphoserine

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The structural basis for 14-3-3:phosphopeptide binding specificity

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14-3-3 proteins: regulation of subcellular localization by molecular interference

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14-3-3 proteins block apoptosis and differentially regulate MAPK cascades

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Functional conservation of 14-3-3 isoforms in inhibiting bad-induced apoptosis

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Raf-1 kinase and exoenzyme S interact with 14-3-3zeta through a common site involving lysine 49.

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Cdi1, a human G1 and S phase protein phosphatase that associates with Cdk2

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Raf-1 promotes cell survival by antagonizing apoptosis signal-regulating kinase 1 through a MEK-ERK independent mechanism

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Serine phosphorylation of death agonist BAD in response to survival factor results in binding to 14-3-3 not BCL-X(L)

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Mitotic and G2 checkpoint control: regulation of 14-3-3 protein binding by phosphorylation of Cdc25C on serine-216

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A novel heterodimerization domain, CRM1, and 14-3-3 control subcellular localization of the MondoA-Mlx heterocomplex.

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14-3-3Sigma is required to prevent mitotic catastrophe after DNA damage

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Regulation of histone deacetylase 4 and 5 and transcriptional activity by 14-3-3-dependent cellular localization

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Integration of calcium and cyclic AMP signaling pathways by 14-3-3

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Involvement of 14-3-3 proteins in nuclear localization of telomerase

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Exit of major histocompatibility complex class II-invariant chain p35 complexes from the endoplasmic reticulum is modulated by phosphorylation

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Forward transport. 14-3-3 binding overcomes retention in endoplasmic reticulum by dibasic signals

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ASK1 is essential for endoplasmic reticulum stress-induced neuronal cell death triggered by expanded polyglutamine repeats

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Analysis of endoplasmic reticulum trafficking signals by combinatorial screening in mammalian cells

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Type 1 insulin-like growth factor receptor (IGF-IR) signaling inhibits apoptosis signal-regulating kinase 1 (ASK1)

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Thioredoxin promotes ASK1 ubiquitination and degradation to inhibit ASK1-mediated apoptosis in a redox activity-independent manner

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Interaction of ALG-2 with ASK1 influences ASK1 localization and subsequent JNK activation

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