IFITM5 gene

Known as: IFITM5, INTERFERON-INDUCED TRANSMEMBRANE PROTEIN 5, interferon induced transmembrane protein 5 
 

Topic mentions per year

Topic mentions per year

2010-2018
024620102018

Papers overview

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2017
2017
The adenosine A2A receptor (A2AR) has long been implicated in cardiovascular disorders. As more selective A2AR ligands are being… (More)
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2014
2014
The IFITM5 gene has recently been found to be mutated in patients with autosomal dominant osteogenesis imperfecta (OI) type V… (More)
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2014
2014
Osteogenesis imperfecta (OI) is a hereditary connective tissue disorder characterized by a wide range of skeletal symptoms. Most… (More)
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2014
2014
Osteogenesis imperfecta (OI) types V and VI are caused, respectively, by a unique dominant mutation in IFITM5, encoding BRIL, a… (More)
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2014
2014
Interferon-induced transmembrane protein 5 (IFITM5) is an osteoblast-specific membrane protein that plays an important role in… (More)
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2013
2013
Osteogenesis imperfecta (OI) is typically caused by mutations in type 1 collagen genes, but in recent years new recessive and… (More)
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2013
2013
BACKGROUND Osteogenesis imperfecta (OI) type V is an autosomal dominant bone fragility disorder that we had described a decade… (More)
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2013
2013
Recently, one of the interferon-induced transmembrane (IFITM) family proteins, IFITM3, has become an important target for the… (More)
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2013
2013
BACKGROUND BRIL is a bone-specific membrane protein that is involved in osteogenesis imperfecta type V. RESULTS Bril… (More)
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2012
2012
Interferon induced transmembrane protein 5 (IFITM5) has been recognized as an osteoblast differentiation factor. Its regulation… (More)
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