(Q33305715)

25 July 2017

Alternative polyadenylation signals and promoters act in concert to control tissue-specific expression of the Opitz Syndrome gene MID1. (English)

1 reference

25 July 2017

Jennifer Winter

1

1 reference

25 July 2017

Melanie Kunath

2

1 reference

25 July 2017

Stefan Roepcke

3

1 reference

25 July 2017

Sven Krause

4

1 reference

25 July 2017

Rainer Schneider

5

1 reference

25 July 2017

Susann Schweiger

6

1 reference

25 July 2017

15 November 2007

1 reference

25 July 2017

BMC Molecular Biology

1 reference

25 July 2017

8

1 reference

25 July 2017

105

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2199-8-105

25 July 2017

0 references

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An interaction between U2AF 65 and CF I(m) links the splicing and 3' end processing machineries

21 June 2018

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Conservation of alternative polyadenylation patterns in mammalian genes

21 June 2018

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Genome-wide analysis of mammalian promoter architecture and evolution

21 June 2018

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Regulation of gene expression by alternative untranslated regions

21 June 2018

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Regulating gene expression through RNA nuclear retention

21 June 2018

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A large-scale analysis of mRNA polyadenylation of human and mouse genes

21 June 2018

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New perspectives on connecting messenger RNA 3' end formation to transcription

21 June 2018

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Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing

21 June 2018

1 reference

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Identification of a target RNA motif for RNA-binding protein HuR.

21 June 2018

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Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome

21 June 2018

1 reference

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AU-rich element-mediated translational control: complexity and multiple activities of trans-activating factors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

Widely spaced alternative promoters, conserved between human and rodent, control expression of the Opitz syndrome gene MID1

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

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21 June 2018

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A history of poly A sequences: from formation to factors to function

21 June 2018

1 reference

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An extensive network of coupling among gene expression machines

21 June 2018

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SRm160 splicing coactivator promotes transcript 3'-end cleavage

21 June 2018

1 reference

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MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation

21 June 2018

1 reference

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A complex containing CstF-64 and the SL2 snRNP connects mRNA 3' end formation and trans-splicing in C. elegans operons.

21 June 2018

1 reference

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Translational control by CPEB: a means to the end

21 June 2018

1 reference

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21 June 2018

HuR and mRNA stability

1 reference

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mRNA stability in eukaryotes

21 June 2018

1 reference

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The Opitz syndrome gene product, MID1, associates with microtubules

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

Further analysis of cytoplasmic polyadenylation in Xenopus embryos and identification of embryonic cytoplasmic polyadenylation element-binding proteins

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

Molecular biology: RNA lost in translation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248598

31 October 2018

Identifiers

DOI

10.1186/1471-2199-8-105

1 reference

25 July 2017

1 reference

25 July 2017

1 reference