(Q39876274)

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A hierarchical cascade activated by non-canonical Notch signaling and the mTOR-Rictor complex regulates neglect-induced death in mammalian cells

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scholarly article

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Europe PubMed Central

PubMed publication ID

15 September 2017

A hierarchical cascade activated by non-canonical Notch signaling and the mTOR-Rictor complex regulates neglect-induced death in mammalian cells (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

author name string

L R Perumalsamy

1

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

M Nagala

2

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

P Banerjee

3

1 reference

Europe PubMed Central

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15 September 2017

A Sarin

4

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15 September 2017

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publication date

6 March 2009

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Europe PubMed Central

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15 September 2017

Cell Death & Differentiation

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15 September 2017

16

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Europe PubMed Central

PubMed publication ID

15 September 2017

6

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Europe PubMed Central

PubMed publication ID

15 September 2017

879-889

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Europe PubMed Central

PubMed publication ID

15 September 2017

https://scigraph.springernature.com/pub.10.1038/cdd.2009.20

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The biochemistry of apoptosis

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Notch signaling: from the outside in

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Notch signaling: cell fate control and signal integration in development

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Notch signalling during peripheral T-cell activation and differentiation

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Evidence for a role for notch signaling in the cytokine-dependent survival of activated T cells

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Survival signaling by Notch1: mammalian target of rapamycin (mTOR)-dependent inhibition of p53

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The Anti-apoptotic Effect of Notch-1 Requires p56 -dependent, Akt/PKB-mediated Signaling in T Cells

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Reciprocal regulation of Notch and PI3K/Akt signalling in T-ALL cells In Vitro

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Notch promotes survival of pre-T cells at the beta-selection checkpoint by regulating cellular metabolism

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Protein kinase B/Akt at a glance

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Cytokine stimulation promotes glucose uptake via phosphatidylinositol-3 kinase/Akt regulation of Glut1 activity and trafficking

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Mitochondrial hexokinases, novel mediators of the antiapoptotic effects of growth factors and Akt.

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PKB and the mitochondria: AKTing on apoptosis

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TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling

1 reference

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Upstream and downstream of mTOR

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Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex

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mSin1 is necessary for Akt/PKB phosphorylation, and its isoforms define three distinct mTORC2s

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mTORC2 Caught in a SINful Akt.

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A ligand-induced extracellular cleavage regulates gamma-secretase-like proteolytic activation of Notch1

1 reference

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Notch signalling regulates stem cell numbers in vitro and in vivo

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mTOR.RICTOR is the Ser473 kinase for Akt/protein kinase B in 3T3-L1 adipocytes

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Ablation in mice of the mTORC components raptor, rictor, or mLST8 reveals that mTORC2 is required for signaling to Akt-FOXO and PKCalpha, but not S6K1

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SIN1/MIP1 maintains rictor-mTOR complex integrity and regulates Akt phosphorylation and substrate specificity

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Multiallelic disruption of the rictor gene in mice reveals that mTOR complex 2 is essential for fetal growth and viability

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Identification of Sin1 as an essential TORC2 component required for complex formation and kinase activity

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Multiple phosphoinositide 3-kinase-dependent steps in activation of protein kinase B

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Notch1 augments NF-kappaB activity by facilitating its nuclear retention

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Neoplastic transformation by Notch requires nuclear localization

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Crossing paths with Notch in the hyper-network

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Growing roles for the mTOR pathway

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TOR signaling in growth and metabolism

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Mechanism of activation of protein kinase B by insulin and IGF-1

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Molecular mechanism for the regulation of protein kinase B/Akt by hydrophobic motif phosphorylation

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The two TORCs and Akt.

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CSL-independent Notch signalling: a checkpoint in cell fate decisions during development?

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Canonical notch signaling is dispensable for the maintenance of adult hematopoietic stem cells

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EGFP-tagged core and linker histones diffuse via distinct mechanisms within living cells

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Identifiers

10.1038/CDD.2009.20

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 September 2017

ResearchGate publication ID

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