Skip to search formSkip to main contentSkip to account menu

CRTAP gene

Known as: LEPREL3, P3H5, CARTILAGE-ASSOCIATED PROTEIN 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Identification of a Candidate Mutation in the COL1A2 Gene of a Chow Chow With Osteogenesis Imperfecta
Osteogenesis imperfecta (OI) is a genetic disease that occurs in humans and animals. Individuals with OI exhibit signs of extreme… 
2016
2016
Investigação de mutações nos genes LEPRE1, CRTAP, PPIB, FKBP10, SERPINH1 e SERPINF1 causadoras da osteogênese imperfeita recessiva
2015
2015
Correction: Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta
Review
2013
Review
2013
Osteogenesis Imperfecta, an Ever‐Expanding Conundrum
Osteogenesis imperfecta (OI), or brittle bone disease, a rare heritable connective tissue disorder, was described more than a… 
2013
2013
Osteogenesis imperfecta: Bench to bedside
2012
2012
세포외 매트릭스와 연관되는, 피부 색소 반점의 분자 지표
본 발명은 유전자 TGFBR2, TGFBI, BMP2, SMAD3, THBS2, TGFBR3, SEMA5A, SMAD7, SOSTDC1, FRAS1, LEPREL1, MATN2, DST, PLOD2, ITGA2, COL6A3… 
2012
2012
Osteogenesis imperfecta type VIII: A case report
2011
2011
A new culprit in osteogenesis imperfecta
Osteogenesis imperfecta (OI) is a heterogeneous group of heritable disorders affecting bone and connective tissue. It is most… 
2000
2000
cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP)
We have recently isolated and characterized cDNA clones coding for a novel developmentally regulated avian and mouse embryo… 
1999
1999
cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)