SNORD107 gene

Known as: HBII-436, SNORD107, small nucleolar RNA, C/D box 107 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2001-2014
0120012014

Papers overview

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2015
2015
Obesity is accompanied by hyperphagia in several classical genetic obesity-related syndromes that are rare, including Prader… (More)
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2014
2014
Prader-Willi Syndrome (PWS) is a neurogenetic disorder caused by the deletion of imprinted genes on the paternally inherited… (More)
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Review
2009
Review
2009
To increase our understanding of imprinted genes in swine, we carried out a comprehensive analysis of this gene family using two… (More)
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2007
2007
AbstractPrader-Willi syndrome (PWS) is a neurodevelopmental disorder associated with abnormalities of chromosome 15q11q13. The… (More)
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Highly Cited
2001
Highly Cited
2001
The imprinted domain on human chromosome 15 consists of two oppositely imprinted gene clusters, which are under the coordinated… (More)
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