MESTIT1 gene

Known as: MEST INTRONIC TRANSCRIPT 1, non-protein coding RNA 40, MESTIT1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2002-2017
01220022017

Papers overview

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2017
2017
Imprinted genes show parent-specific activity (functional haploidy), which makes them particularly vulnerable to epigenetic… (More)
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Review
2012
Review
2012
Die 2009 veröffentlichte Oxford-Klassifikation der IgA-Nephropathie beruht auf vier bioptisch zu beurteilenden histologischen… (More)
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2011
2011
Phenotypic variation within populations is a crucial factor in evolution and is mainly thought to be driven by heritable changes… (More)
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Highly Cited
2010
Highly Cited
2010
Aberrant imprinting in spermatozoa in a subset of infertile men has been postulated to be a risk factor for congenital diseases… (More)
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2010
2010
Several methods to improve the parton-shower description of hard processes by an injection of matrix-element-based information… (More)
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2009
2009
The concept of multiple partonic interactions in hadronic events is vital for the understanding of both minimum-bias and… (More)
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Review
2008
Review
2008
Modelling multiple partonic interactions in hadronic events is vital for understanding minimum-bias physics, as well as the… (More)
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2003
2003
Silver-Russell syndrome 1 2 is a malformation syndrome characterised by a severe reduction in weight and length at birth, short… (More)
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2003
2003
Imprinted gene(s) on human chromosome 7q32-qter have been postulated to be involved in intrauterine growth restriction associated… (More)
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2002
2002
Imprinted gene(s) on human chromosome 7 are thought to be involved in Russell-Silver syndrome (RSS), based on the fact that… (More)
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