Role of 5'- and 3'-untranslated regions of mRNAs in human diseases (Q34016479)

30 July 2017

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title

Role of 5'- and 3'-untranslated regions of mRNAs in human diseases (English)

1 reference

30 July 2017

Sangeeta Chatterjee

1

1 reference

PubMed ID

19275763

30 July 2017

Jayanta K Pal

series ordinal

2

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30 July 2017

1 May 2009

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30 July 2017

12

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based on heuristic

inferred from page(s)

published in

Biology of the Cell

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30 July 2017

101

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30 July 2017

251-262

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30 July 2017

5

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Clinical severity and thermodynamic effects of iron-responsive element mutations in hereditary hyperferritinemia-cataract syndrome

30 July 2017

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Inhibition of translation of transforming growth factor-beta 3 mRNA by its 5' untranslated region

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Enhanced translational efficiency of a novel transforming growth factor beta 3 mRNA in human breast cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Role of ferritin and ferroportin genes in unexplained hyperferritinaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Mutation in the PAX6 gene in twenty patients with aniridia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Missense mutations in the DNA-binding region and termination codon in PAX6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

A mutation in the c-myc-IRES leads to enhanced internal ribosome entry in multiple myeloma: a novel mechanism of oncogene de-regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

The 3' untranslated region of messenger RNA: A molecular 'hotspot' for pathology?

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Oncomirs - microRNAs with a role in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Members of the poly (rC) binding protein family stimulate the activity of the c-myc internal ribosome entry segment in vitro and in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

A usual frameshift and delayed termination codon mutation in keratin 5 causes a novel type of epidermolysis bullosa simplex with migratory circinate erythema.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Internal ribosome entry sites in eukaryotic mRNA molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Alpha-thalassaemia caused by a polyadenylation signal mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Analysis of a Charcot-Marie-Tooth disease mutation reveals an essential internal ribosome entry site element in the connexin-32 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Cap-dependent and cap-independent translation in eukaryotic systems

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Complex translational regulation of BACE1 involves upstream AUGs and stimulatory elements within the 5' untranslated region

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Upstream open reading frames as regulators of mRNA translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

IRP-1 Binding to Ferritin mRNA Prevents the Recruitment of the Small Ribosomal Subunit by the Cap-Binding Complex eIF4F

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Serotonin type 3 receptor genes: HTR3A, B, C, D, E.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

The implications of structured 5' untranslated regions on translation and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

In sickness and in health: the importance of translational regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Translation matters: protein synthesis defects in inherited disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

A somatic mutation in the 5'UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

MicroRNAs in disease and potential therapeutic applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

PTC124 targets genetic disorders caused by nonsense mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

The regulation of Foxp3 expression in regulatory CD4(+)CD25(+)T cells: multiple pathways on the road

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

Leaky scanning and reinitiation regulate BACE1 gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20080104

21 January 2018

Identifiers

DOI

10.1042/BC20080104

1 reference

30 July 2017

1 reference

PubMed ID

19275763