(Q34322258)

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Depletion of physiological levels of the human TID1 protein renders cancer cell lines resistant to apoptosis mediated by multiple exogenous stimuli

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Europe PubMed Central

PubMed publication ID

1 August 2017

Depletion of physiological levels of the human TID1 protein renders cancer cell lines resistant to apoptosis mediated by multiple exogenous stimuli (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Kirsten M Edwards

1

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Europe PubMed Central

PubMed publication ID

1 August 2017

Karl Münger

2

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Europe PubMed Central

PubMed publication ID

1 August 2017

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publication date

1 November 2004

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Europe PubMed Central

PubMed publication ID

1 August 2017

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Europe PubMed Central

PubMed publication ID

1 August 2017

23

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Europe PubMed Central

PubMed publication ID

1 August 2017

52

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

8419-8431

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Death and survival: viral regulation of TNF signaling pathways

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Understanding human cancer using Drosophila: Tid47, a cytosolic product of the DnaJ-like tumor suppressor gene l2Tid, is a novel molecular partner of patched related to skin cancer

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HTLV-1 Tax-associated hTid-1, a human DnaJ protein, is a repressor of Ikappa B kinase beta subunit

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Bax and Bak independently promote cytochrome C release from mitochondria

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Bid-induced conformational change of Bax is responsible for mitochondrial cytochrome c release during apoptosis

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The human DnaJ protein, hTid-1, enhances binding of a multimer of the herpes simplex virus type 1 UL9 protein to oris, an origin of viral DNA replication

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Caspase cleaved BID targets mitochondria and is required for cytochrome c release, while BCL-XL prevents this release but not tumor necrosis factor-R1/Fas death

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Control of folding and membrane translocation by binding of the chaperone DnaJ to nascent polypeptides

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Mechanism of regulation of hsp70 chaperones by DnaJ cochaperones

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hTid-1, a human DnaJ protein, modulates the interferon signaling pathway

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A DNA vector-based RNAi technology to suppress gene expression in mammalian cells

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Tumor necrosis factor-alpha induces Bax-Bak interaction and apoptosis, which is inhibited by adenovirus E1B 19K

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TID1, a human homolog of the Drosophila tumor suppressor l(2)tid, encodes two mitochondrial modulators of apoptosis with opposing functions

1 reference

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A mouse homologue of the Drosophila tumor suppressor l(2)tid gene defines a novel Ras GTPase-activating protein (RasGAP)-binding protein

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Bax and Bak can localize to the endoplasmic reticulum to initiate apoptosis

1 reference

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21 January 2018

Signalling pathways of the TNF superfamily: a double-edged sword

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7 January 2021

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The Hsp70 and Hsp60 chaperone machines

1 reference

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Human T cell leukemia virus type 1 Tax associates with a molecular chaperone complex containing hTid-1 and Hsp70

1 reference

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DnaJ-like proteins: molecular chaperones and specific regulators of Hsp70.

1 reference

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Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition

1 reference

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Bid induces the oligomerization and insertion of Bax into the outer mitochondrial membrane

1 reference

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Oxidants, oxidative stress and the biology of ageing

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Expression of BAX in cell nucleus after experimentally induced apoptosis revealed by immunogold and embedment-free electron microscopy

1 reference

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Molecular chaperones in cellular protein folding

1 reference

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Bcl-2 functions in an antioxidant pathway to prevent apoptosis

1 reference

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Molecular chaperones: How J domains turn on Hsp70s

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Tumor necrosis factor (TNF) receptor type 1 (p55) is a main mediator for TNF-alpha-induced skin inflammation

1 reference

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Mitochondrial localization and temporal expression of the Drosophila melanogaster DnaJ homologous tumor suppressor Tid50.

1 reference

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Tumor suppression in Drosophila is causally related to the function of the lethal(2) tumorous imaginal discs gene, a dnaJ homolog

1 reference

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Genetic, cytogenetic and developmental analysis of the Drosophila melanogaster tumor suppressor gene lethal(2)tumorous imaginal discs (1(2)tid)

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Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis

1 reference

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Bid, a Bcl2 interacting protein, mediates cytochrome c release from mitochondria in response to activation of cell surface death receptors

1 reference

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7 January 2021

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BCL-2-related protein expression in apoptosis: oxidative stress versus serum deprivation in PC12 cells

1 reference

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The Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis

1 reference

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J proteins catalytically activate Hsp70 molecules to trap a wide range of peptide sequences

1 reference

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7 January 2021

based on heuristic

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Bax-mediated Ca2+ mobilization promotes cytochrome c release during apoptosis

1 reference

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based on heuristic

inferred from DOI database lookup

Bax and Bak promote apoptosis by modulating endoplasmic reticular and mitochondrial Ca2+ stores

1 reference

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The protein import machinery of the mitochondrial inner membrane

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Isolation and characterization of a novel gene, hRFI, preferentially expressed in esophageal cancer

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BAX and BAK regulation of endoplasmic reticulum Ca2+: a control point for apoptosis

1 reference

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TID1, a mammalian homologue of the drosophila tumor suppressor lethal(2) tumorous imaginal discs, regulates activation-induced cell death in Th2 cells

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A novel domain within the 55 kd TNF receptor signals cell death

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Identification of DIABLO, a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins

1 reference

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BID: a novel BH3 domain-only death agonist

1 reference

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Proapoptotic BAX and BAK: a requisite gateway to mitochondrial dysfunction and death

1 reference

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Genomic organization and expression of the human tumorous imaginal disc (TID1) gene

1 reference

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10.1038/SJ.ONC.1207732

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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