(Q28207468)

Silvia Fernández de Mattos

2

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René H. Medema

René H Medema

8

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Jan J. Brosens

Jan J Brosens

4

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Eric W-F Lam

Eric W-F Lam

10

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Andrew Sunters

1

Andrew Sunters

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Georgia Zoumpoulidou

5

Georgia Zoumpoulidou

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author name string

Marie Stahl

3

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Catherine A Saunders

6

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Paul J Coffer

7

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R Charles Coombes

Journal of Biological Chemistry

9

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language of work or name

English

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publication date

12 December 2003

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published in

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volume

278

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issue

50

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page(s)

49795-805

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cites work

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FOXO transcription factors as regulators of immune homeostasis: molecules to die for?

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Inactivation of the forkhead transcription factor FoxO3 is essential for PKB-mediated survival of hematopoietic progenitor cells by kit ligand

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Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor

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Phosphorylation of serine 256 by protein kinase B disrupts transactivation by FKHR and mediates effects of insulin on insulin-like growth factor-binding protein-1 promoter activity through a conserved insulin response sequence

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Protein kinase B/Akt-mediated phosphorylation promotes nuclear exclusion of the winged helix transcription factor FKHR1

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AFX-like Forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1

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Forkhead transcription factor FKHR-L1 modulates cytokine-dependent transcriptional regulation of p27(KIP1).

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Expression of the pro-apoptotic Bcl-2 family member Bim is regulated by the forkhead transcription factor FKHR-L1

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FOXO transcription factors directly activate bim gene expression and promote apoptosis in sympathetic neurons

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Ligand-dependent interaction of estrogen receptor-alpha with members of the forkhead transcription factor family

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The PTEN/MMAC1/TEP tumor suppressor gene decreases cell growth and induces apoptosis and anoikis in breast cancer cells

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Transforming growth factor-beta 2 is a transcriptional target for Akt/protein kinase B via forkhead transcription factor

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Nitric oxide suppression triggers apoptosis through the FKHRL1 (FOXO3A)/ROCK kinase pathway in human breast carcinoma cells

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Dominant-negative c-Jun promotes neuronal survival by reducing BIM expression and inhibiting mitochondrial cytochrome c release

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The proapoptotic activity of the Bcl-2 family member Bim is regulated by interaction with the dynein motor complex

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JNK-mediated BIM phosphorylation potentiates BAX-dependent apoptosis

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JNK phosphorylation of Bim-related members of the Bcl2 family induces Bax-dependent apoptosis

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BH3-only proteins that bind pro-survival Bcl-2 family members fail to induce apoptosis in the absence of Bax and Bak

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Activation of ERK1/2 by deltaRaf-1:ER* represses Bim expression independently of the JNK or PI3K pathways

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Forkhead transcription factors contribute to execution of the mitotic programme in mammals

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DNA repair pathway stimulated by the forkhead transcription factor FOXO3a through the Gadd45 protein

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Bcl-2/bcl-xL bispecific antisense treatment sensitizes breast carcinoma cells to doxorubicin, paclitaxel and cyclophosphamide

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Potentiation of dexamethasone-, paclitaxel-, and Ad-p53-induced apoptosis by Bcl-2 antisense oligodeoxynucleotides in drug-resistant multiple myeloma cells.

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Forkhead transcription factor FOXO3a protects quiescent cells from oxidative stress

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FOXO forkhead transcription factors induce G(2)-M checkpoint in response to oxidative stress

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Cell cycle inhibition by FoxO forkhead transcription factors involves downregulation of cyclin D.

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Molecular genetics of life span in C. elegans: how much does it teach us?

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The cyclin dependent kinase inhibitor p27 and its prognostic role in breast cancer.

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The proapoptotic BH3-only protein bim is expressed in hematopoietic, epithelial, neuronal, and germ cells

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Proapoptotic Bcl-2 relative Bim required for certain apoptotic responses, leukocyte homeostasis, and to preclude autoimmunity

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BCR signals target p27Kip1 and cyclin D2 via the PI3-K signalling pathway to mediate cell cycle arrest and apoptosis of WEHI 231 B cells

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Identifiers

DOI

10.1074/JBC.M309523200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

14527951

1 reference

Consolidated OpenCitations Corpus – April 2017