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P3H2 gene

Known as: LEPRECAN-LIKE 1, LEPREL1, PROLYL 3-HYDROXYLASE 2 
National Institutes of Health

Papers overview

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2017
2017
High myopia (HM) is a leading cause of mid-way blindness with a high heritability in East Asia. Although only a few disease genes… Expand
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2015
2015
Abstract Purpose: To uncover the homozygous recessive gene mutation underlying familial lens subluxation and/or juvenile lens… Expand
Highly Cited
2014
Highly Cited
2014
PURPOSE To evaluate variants in the LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 genes in 298 unrelated patients with early… Expand
2014
2014
High myopia is a severe visual impairment which can increase the risk of retinal degeneration, subretinal hemorrhage, choroidal… Expand
2011
2011
The fibrillar collagen types I, II, and V/XI have recently been shown to have partially 3-hydroxylated proline (3Hyp) residues at… Expand
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Highly Cited
2011
Highly Cited
2011
Autosomal-recessive high-grade axial myopia was diagnosed in Bedouin Israeli consanguineous kindred. Some affected individuals… Expand
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2009
2009
Expression of P3H2 (Leprel1) and P3H3 (Leprel2) but not P3H1 (Leprecan) is down-regulated in breast cancer by aberrant CpG… Expand
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Highly Cited
2008
Highly Cited
2008
The single 3-hydroxyproline residue in the collagen I polypeptides is essential for proper fibril formation and bone development… Expand
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Highly Cited
2004
Highly Cited
2004
The collagen prolyl hydroxylases are enzymes that are required for proper collagen biosynthesis, folding, and assembly. They… Expand
2001
2001
Anecdotal evidence suggests that multilinguals' ability to learn languages increases the more languages they know; experimental… Expand