Engineered transient and stable overexpression of translation factors eIF3i and eIF3c in CHOK1 and HEK293 cells gives enhanced cell growth associated with increased c-Myc expression and increased recombinant protein synthesis (Q89729270)

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scientific article published on 13 February 2020

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English	Engineered transient and stable overexpression of translation factors eIF3i and eIF3c in CHOK1 and HEK293 cells gives enhanced cell growth associated with increased c-Myc expression and increased recombinant protein synthesis	scientific article published on 13 February 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32061967 AND SRC:MED&resulttype=core&format=json

8 April 2020

Engineered transient and stable overexpression of translation factors eIF3i and eIF3c in CHOK1 and HEK293 cells gives enhanced cell growth associated with increased c-Myc expression and increased recombinant protein synthesis (English)

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8 April 2020

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8 April 2020

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Anne Roobol

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8 April 2020

Joanne Roobol

2

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8 April 2020

Matthew E Smith

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8 April 2020

Martin J Carden

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8 April 2020

John W B Hershey

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8 April 2020

C Mark Smales

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8 April 2020

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13 February 2020

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8 April 2020

Metabolic Engineering

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8 April 2020

59

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8 April 2020

98-105

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8 April 2020

Carcinoma-associated eIF3i overexpression facilitates mTOR-dependent growth transformation

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Biological insights into the expression of translation initiation factors from recombinant CHOK1SV cell lines and their relationship to enhanced productivity.

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Hepatitis-C-virus-like internal ribosome entry sites displace eIF3 to gain access to the 40S subunit

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mTORC1 signalling and eIF4E/4E-BP1 translation initiation factor stoichiometry influence recombinant protein productivity from GS-CHOK1 cells.

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Reconstitution reveals the functional core of mammalian eIF3

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Architecture of human translation initiation factor 3.

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The chaperonin CCT interacts with and mediates the correct folding and activity of three subunits of translation initiation factor eIF3: b, i and h.

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