PTB and TIAR binding to insulin mRNA 3'- and 5'UTRs; implications for insulin biosynthesis and messenger stability. - Wikidata - awgldk - TriplyDB

PTB and TIAR binding to insulin mRNA 3'- and 5'UTRs; implications for insulin biosynthesis and messenger stability.

PTB and TIAR binding to insulin mRNA 3'- and 5'UTRs; implications for insulin biosynthesis and messenger stability.

http://www.wikidata.org/entity/Q37280479

about

Stress and the nonsense-mediated RNA decay pathway.Trans-acting translational regulatory RNA binding proteins.

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PTB and TIAR binding to insulin mRNA 3'- and 5'UTRs; implications for insulin biosynthesis and messenger stability.

http://www.wikidata.org/entity/Q37280479

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 20 September 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

PTB and TIAR binding to insuli ...... hesis and messenger stability.

@en

PTB and TIAR binding to insuli ...... hesis and messenger stability.

@nl

type

label

PTB and TIAR binding to insuli ...... hesis and messenger stability.

@en

PTB and TIAR binding to insuli ...... hesis and messenger stability.

@nl

prefLabel

PTB and TIAR binding to insuli ...... hesis and messenger stability.

@en

PTB and TIAR binding to insuli ...... hesis and messenger stability.

@nl

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J.HELIYON.2016.E00159

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PTB and TIAR binding to insuli ...... hesis and messenger stability.

@en

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Christopher M Adams

http://www.w3.org/2001/XMLSchema#string

Nils Welsh

http://www.w3.org/2001/XMLSchema#string

Syrina Mehrabi

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P2860

Diverse RNA-binding proteins interact with functionally related sets of RNAs, suggesting an extensive regulatory system

High glucose suppresses human islet insulin biosynthesis by inducing miR-133a leading to decreased polypyrimidine tract binding protein-expression

Primary structure and binding activity of the hnRNP U protein: binding RNA through RGG box

Intronic CA-repeat and CA-rich elements: a new class of regulators of mammalian alternative splicing.

The RNA-binding protein TIAR is translocated from the nucleus to the cytoplasm during Fas-mediated apoptotic cell death

Herpes simplex virus 1 induces cytoplasmic accumulation of TIA-1/TIAR and both synthesis and cytoplasmic accumulation of tristetraprolin, two cellular proteins that bind and destabilize AU-rich RNAs

MicroRNAs regulate the expression of the alternative splicing factor nPTB during muscle development

Cytoplasmic foci are sites of mRNA decay in human cells

Heterogeneous nuclear ribonucleoprotein L interacts with the 3' border of the internal ribosomal entry site of hepatitis C virus

The proximal region of the 3'-untranslated region of cyclooxygenase-2 is recognized by a multimeric protein complex containing HuR, TIA-1, TIAR, and the heterogeneous nuclear ribonucleoprotein U

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e00159

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scholarly article

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10.1016/J.HELIYON.2016.E00159

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9

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