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Journal of Neonatal Nursing, ISSN 1355-1841, 12/2012, Volume 18, Issue 6, pp. 217 - 220
Osteogenesis imperfecta is a genetic bone disorder that requires a multi-disciplinary healthcare team to achieve optimal patient outcomes. It is most... 
Genetic | Imperfecta | Bone | Osteogenesis | Osteogenesis imperfecta
Journal Article
Cell Cycle, ISSN 1538-4101, 07/2007, Volume 6, Issue 14, pp. 1675 - 1681
Prolyl 3-hydroxylase 1 (P3H1), cartilage-associated protein (CRTAP) and cyclophilin B (CyPB) form a complex in the endoplasmic reticulum which is responsible... 
Binding | Proteins | Landes | Calcium | Bioscience | Biology | Cell | Cycle | Cancer | Organogenesis | Cartilage-associated protein | Osteogenesis imperfecta type VII | Cyclophilin B | Leprecan | Osteogenesis imperfecta type VIII | Recessive bone dysplasia | Type I collagen | Prolyl 3-hydroxylase 1 | cyclophilin B | type I collagen | TRIPLE-HELIX FORMATION | I COLLAGEN | osteogenesis imperfecta type VIII | leprecan | CELL BIOLOGY | recessive bone dysplasia | CYCLOPHILIN-B | prolyl 3-hydroxylase 1 | cartilage-associated protein | CIS-TRANS-ISOMERASE | DISEASE | osteogenesis imperfecta type VII | OSTEOGENESIS IMPERFECTA | MEMBRANE-ASSOCIATED PROTEOGLYCAN | TETRATRICOPEPTIDE REPEAT | CDNA CLONING | Bone and Bones - pathology | Membrane Glycoproteins - metabolism | Osteogenesis Imperfecta - metabolism | Bone Development - physiology | Humans | Extracellular Matrix - metabolism | Molecular Sequence Data | Osteogenesis Imperfecta - genetics | Cyclophilins - metabolism | Extracellular Matrix - chemistry | Multiprotein Complexes - metabolism | Collagen Type I - genetics | Peptidylprolyl Isomerase - metabolism | Peptidylprolyl Isomerase - genetics | Extracellular Matrix Proteins - metabolism | Bone and Bones - cytology | Amino Acid Sequence | Bone and Bones - physiology | Collagen Type I - metabolism | Hydroxylation | Extracellular Matrix Proteins - genetics | Proteoglycans - metabolism | Cyclophilins - genetics | Membrane Glycoproteins - genetics | Sequence Alignment | Animals | Proteoglycans - genetics
Journal Article
Pediatric Anesthesia, ISSN 1155-5645, 09/2018, Volume 28, Issue 9, pp. 817 - 818
Osteogenesis imperfecta is a heterogeneous genetic disorder characterized by bone fragility, with disease ranging from mild fractures to death in utero. We... 
congenital | brittle bone disease | general anesthesia | autosomal recessive | orthopedic surgery | perioperative care | ANESTHESIOLOGY | PEDIATRICS | Osteogenesis imperfecta | Orthopedic surgery | Scoliosis | Analysis | Central nervous system agents | Neurophysiology
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2009, Volume 53, Issue 1, pp. 1 - 5
Journal Article
Disease models & mechanisms, ISSN 1754-8403, 06/2019, Volume 12, Issue 6, p. dmm038521
Osteogenesis imperfecta (OI) types VII, VIII and IX, caused by recessive mutations in cartilage-associated protein ( ), prolyl-3-hydroxylase 1 ( ) and... 
Chemical chaperone | PROTEIN | 4-PBA | RECESSIVE OSTEOGENESIS IMPERFECTA | PHENOTYPE | AUTOPHAGY | PATHOLOGY | DEFICIENCY | Endoplasmic reticulum stress | Unfolded protein response | CELL BIOLOGY | CYCLOPHILIN-B | 3-HYDROXYLATION | MOUSE MODEL | Osteogenesis imperfecta | MUTATIONS | LETHAL | 311
Journal Article
SPINE, ISSN 0362-2436, 08/2019, Volume 44, Issue 15, pp. 1057 - 1063
STUDY DESIGN.Retrospective clinical study of individuals with osteogenesis imperfecta (OI). OBJECTIVE.To assess the relationship between severity of scoliosis... 
IDIOPATHIC SCOLIOSIS | scoliosis | pulmonary insufficiency | LUNG-FUNCTION | CLASSIFICATION | DISORDERS | restrictive lung disease | PULMONARY HYPOPLASIA | RELIABILITY | osteogenesis imperfecta | CLINICAL NEUROLOGY | type I collagenopathy | SPINAL DEFORMITIES | reduced pulmonary function | HEALTH SURVEY SF-36 | QUALITY-OF-LIFE | ORTHOPEDICS | RESPIRATORY-FAILURE
Journal Article
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 6, p. e1004465
Journal Article