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SMAD proteins control DROSHA-mediated microRNA maturation
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
title
SMAD proteins control DROSHA-mediated microRNA maturation
(English)
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
main subject
SMAD protein
0 references
microRNA
0 references
SMAD family member 3
1 reference
stated in
GOA release 2020-03-11
DEAD-box helicase 5
1 reference
stated in
GOA release 2020-03-11
SMAD family member 5
1 reference
stated in
GOA release 2020-03-11
Drosha ribonuclease III
1 reference
stated in
GOA release 2020-03-11
SMAD family member 1
1 reference
stated in
GOA release 2020-03-11
SMAD family member 2
1 reference
stated in
GOA release 2020-03-11
transforming growth factor beta 1
1 reference
stated in
GOA release 2020-03-11
Programmed cell death 4
1 reference
stated in
GOA release 2020-03-11
bone morphogenetic protein 4
1 reference
stated in
GOA release 2020-03-11
primary miRNA binding
1 reference
stated in
GOA release 2020-03-11
author name string
Brandi N. Davis
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
Aaron C. Hilyard
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
Giorgio Lagna
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
Akiko Hata
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
language of work or name
English
0 references
publication date
3 July 2008
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
published in
Nature
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
volume
454
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
page(s)
56–61
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stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
issue
7200
1 reference
stated in
PubMed
PubMed ID
18548003
retrieved
14 March 2017
cites work
Programmed cell death 4 (PDCD4) is an important functional target of the microRNA miR-21 in breast cancer cells
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DEAD-box RNA helicase subunits of the Drosha complex are required for processing of rRNA and a subset of microRNAs
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Smad transcription factors
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PubMed Central
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The Drosha-DGCR8 complex in primary microRNA processing
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16 March 2017
Functional interaction between Smad, CREB binding protein, and p68 RNA helicase
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16 March 2017
The nuclear RNase III Drosha initiates microRNA processing
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Crystal structure of a Smad MH1 domain bound to DNA: insights on DNA binding in TGF-beta signaling
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The TGF-beta family mediator Smad1 is phosphorylated directly and activated functionally by the BMP receptor kinase
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16 March 2017
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MicroRNA-21 (miR-21) post-transcriptionally downregulates tumor suppressor Pdcd4 and stimulates invasion, intravasation and metastasis in colorectal cancer
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3 June 2018
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3 June 2018
Interleukin-6 dependent survival of multiple myeloma cells involves the Stat3-mediated induction of microRNA-21 through a highly conserved enhancer
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3 June 2018
MicroRNA expression signature and antisense-mediated depletion reveal an essential role of MicroRNA in vascular neointimal lesion formation
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A developmental view of microRNA function
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Smad4 dependency defines two classes of transforming growth factor {beta} (TGF-{beta}) target genes and distinguishes TGF-{beta}-induced epithelial-mesenchymal transition from its antiproliferative and migratory responses
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Roles of bone morphogenetic protein type I receptors and Smad proteins in osteoblast and chondroblast differentiation.
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3 June 2018
Regulation of differentiation of vascular smooth muscle cells
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3 June 2018
A novel regulatory mechanism of the bone morphogenetic protein (BMP) signaling pathway involving the carboxyl-terminal tail domain of BMP type II receptor
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26 November 2018
The multifunctional RNA-binding protein hnRNP A1 is required for processing of miR-18a
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18548003
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/NATURE07086
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
938724
Dimensions Publication ID
1032756706
0 references
OpenCitations bibliographic resource ID
938724
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
938724
PMCID
2653422
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
938724
PubMed ID
18548003
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
938724
ResearchGate publication ID
5309228
0 references
Springer Nature article ID
10.1038/nature07086
0 references
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