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Genetics. Mysterious ribosomopathies
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
title
Genetics. Mysterious ribosomopathies
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
author
Susan Baserga
series ordinal
2
object named as
Susan J Baserga
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
author name string
Kathleen L McCann
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
language of work or name
English
0 references
publication date
1 August 2013
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
published in
Science
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
volume
341
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
page(s)
849-850
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
issue
6148
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
cites work
The emerging importance of ribosomal dysfunction in the pathogenesis of hematologic disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
A ribosome-specialized translation initiation pathway is required for cap-dependent translation of vesicular stomatitis virus mRNAs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
NOL11, implicated in the pathogenesis of North American Indian childhood cirrhosis, is required for pre-rRNA transcription and processing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Ribosomal biogenesis genes play an essential and p53-independent role in zebrafish pancreas development
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Ribosomal deficiencies in Diamond-Blackfan anemia impair translation of transcripts essential for differentiation of murine and human erythroblasts
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Non-Diamond Blackfan anemia disorders of ribosome function: Shwachman Diamond syndrome and 5q- syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
When ribosomes go bad: diseases of ribosome biogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Disruption of the nucleolus mediates stabilization of p53 in response to DNA damage and other stresses
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3893057
retrieved
6 July 2018
Identifiers
DOI
10.1126/SCIENCE.1244156
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
Fatcat ID
release_toppvkjy3fau5konhe777khmo4
1 reference
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Fatcat
reference URL
https://api.fatcat.wiki/v0/release/toppvkjy3fau5konhe777khmo4
retrieved
24 November 2022
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mapped directly with Wikidata item
PMCID
3893057
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
PubMed ID
23970686
1 reference
stated in
Europe PubMed Central
PubMed ID
23970686
retrieved
1 August 2017
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