CRTAP gene

Known as: LEPREL3, P3H5, CARTILAGE-ASSOCIATED PROTEIN 
 

Topic mentions per year

Topic mentions per year

1991-2015
012319912015

Papers overview

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2016
2016
Osteogenesis imperfecta (OI) is a set of clinically and genetically heterogeneous disorders with autosomal dominant, recessive… (More)
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2015
2015
In 1987, Cole and Carpenter reported two unrelated infants with multiple fractures and deformities of bone, with a skeletal… (More)
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2015
2015
Osteogenesis imperfecta (OI) is a spectrum of genetic disorders with decreased bone density and bone fragility. Most of the cases… (More)
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2015
2015
Isovalency rationalizes fundamental chemical properties of elements in the same group, but often fails to account for differences… (More)
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2014
2014
Members of the Leprecan family of proteins include enzymes, prolyl 3-hydroxylase 1 (P3h1), P3h2, and P3h3, and nonenzymatic… (More)
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2014
2014
Osteogenesis imperfecta (OI) is a hereditary bone disease characterized by decreased bone density and multiple fractures, usually… (More)
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2013
2009
2009
Osteogenesis Imperfecta (OI) is a human syndrome characterized by exquisitely fragile bones due to osteoporosis. The majority of… (More)
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Highly Cited
2007
Highly Cited
2007
Alternative pre-mRNA splicing increases proteomic diversity and provides a potential mechanism underlying both phenotypic… (More)
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Highly Cited
2006
Highly Cited
2006
Prolyl hydroxylation is a critical posttranslational modification that affects structure, function, and turnover of target… (More)
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