ISPD gene

Known as: notch1-induced protein, Nip, IspD 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2018
02420082018

Papers overview

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2017
2017
Congenital muscular dystrophies (CMDs) are clinically and genetically heterogeneous conditions; some fatal in the first few years… (More)
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Review
2016
Review
2016
Department of Medicine and Therapeutics,1 Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong; University of… (More)
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2015
2015
As resistance to current therapies spreads, novel antimalarials are urgently needed. In this work, we examine the potential for… (More)
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2015
2015
A unique, unsolved O-mannosyl glycan on α-dystroglycan is essential for its interaction with protein ligands in the extracellular… (More)
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2015
2015
Within the group of muscular dystrophies, dystroglycanopathies represent an important subgroup of recessively inherited disorders… (More)
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2015
2015
Walker-Warburg syndrome (WWS) is a rare form of autosomal recessive, congenital muscular dystrophy that is associated with brain… (More)
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2014
2014
CRISPR/Cas9 technology is a highly promising genome editing tool in the mouse, potentially overcoming the costs and time required… (More)
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2013
2013
Dystroglycanopathies are a clinically and genetically diverse group of recessively inherited conditions ranging from the most… (More)
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2013
2013
Walker-Warburg syndrome (WWS) is a severe muscular dystrophy with eye and brain malformations. On a molecular level, WWS is a… (More)
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2008
2008
We study a natural and potentially devastating attack against BitTorrent, namely, attacking the initial seed in a torrent’s early… (More)
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