A Search Service for Abbreviation / Long Form

■ Related PubMed/MEDLINE Info.

[Related PubMed/MEDLINE]
Total Number of Papers: 23
[Display Entries]
[Entries Per Page]
 per page
Page Control
Page: of
Abbreviation : P3H1
Long Form : prolyl 3-hydroxylase 1
No. Year Title Co-occurring Abbreviation
2022 Discovery of Novel Circulating Immune Complexes in Lupus Nephritis Using Immunoproteomics. AI, AUC, CI, HC, ICx, LN, MEF2C, PHACTR4, RGS12, scRNA Seq, UBC
2022 Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive P3H1 Pathogenic Variant. COL1A1, OI, P3H1-CRTAP-CyPB
2020 Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype. CRTAP, ER
2019 Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate. 4-PBA, CRTAP, ER, OI, p-PERK
2016 Bone matrix hypermineralization in prolyl-3 hydroxylase 1 deficient mice. ---
2014 Osteogenesis imperfecta due to mutations in non-collagenous genes: lessons in the biology of bone formation. BMP-1, CRTAP, CypB, FKBP65, HSP47, IFITM, OASIS, PEDF, TRIC-B, WNT1
2013 An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1cartilage-associated proteincyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro. CypB, PDI
2013 Collagen prolyl 3-hydroxylation: a major role for a minor post-translational modification? 3-Hyp
2013 Posttranslational modifications in type I collagen from different tissues extracted from wild type and prolyl 3-hydroxylase 1 null mice. ---
10  2013 Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis. ER
11  2012 A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfecta. CRTAP, ER, OI
12  2012 Prolyl 3-hydroxylase-1 null mice exhibit hearing impairment and abnormal morphology of the middle ear bone joints. ABRs, micro-CT, OI
13  2011 Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. CRTAP, CypB, OI
14  2011 Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes. CRTAP, CypB, LEPRE1, OI, P4H1, PDI, PPIB, RER
15  2011 Severe osteogenesis imperfecta caused by a small in-frame deletion in CRTAP. CRTAP, OI
16  2010 Generalized connective tissue disease in Crtap-/- mouse. CypB
17  2010 Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding. CRTAP, CypB, PPIB
18  2010 Prolyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bones. CRTAP, OI
19  2009 Biochemical characterization of the prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B complex. CRTAP, CypB
20  2009 CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis. CRTAP, OI
21  2009 PPIB mutations cause severe osteogenesis imperfecta. CRTAP, OI
22  2008 Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation. aa, AD, CypB, OI
23  2007 Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone development. CRTAP, CypB