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[Related PubMed/MEDLINE]
Total Number of Papers: 23
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| Abbreviation |
: P3H1 |
| Long Form |
: prolyl 3-hydroxylase 1 |
|
| No. |
Year |
Title |
Co-occurring Abbreviation |
| 1 |
2022 |
Discovery of Novel Circulating Immune Complexes in Lupus Nephritis Using Immunoproteomics. |
AI, AUC, CI, HC, ICx, LN, MEF2C, PHACTR4, RGS12, scRNA Seq, UBC |
| 2 |
2022 |
Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive P3H1 Pathogenic Variant. |
COL1A1, OI, P3H1-CRTAP-CyPB |
| 3 |
2020 |
Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype. |
CRTAP, ER |
| 4 |
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 |
| 5 |
2016 |
Bone matrix hypermineralization in prolyl-3 hydroxylase 1 deficient mice. |
--- |
| 6 |
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 |
| 7 |
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 |
| 8 |
2013 |
Collagen prolyl 3-hydroxylation: a major role for a minor post-translational modification? |
3-Hyp |
| 9 |
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 |
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