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A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfectaER stress-mediated apoptosis in a new mouse model of osteogenesis imperfectaRapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strengthProlyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bonesThe zinc transporter SLC39A13/ZIP13 is required for connective tissue development; its involvement in BMP/TGF-beta signaling pathwaysExome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfectaCRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysisPhenotypic variability of osteogenesis imperfecta type V caused by an IFITM5 mutationCardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms.Mutations in SERPINF1 cause osteogenesis imperfecta type VIHomozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfectaMolecular and mesoscale mechanisms of osteogenesis imperfecta disease in collagen fibrilsCRTAP and LEPRE1 mutations in recessive osteogenesis imperfectaComprehensive Review of Adipose Stem Cells and Their Implication in Distraction Osteogenesis and Bone RegenerationBisphosphonate therapy in pediatric patientsOsteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessmentDifferential effects of collagen prolyl 3-hydroxylation on skeletal tissuesFragility of Bone Material Controlled by Internal InterfacesDesign, materials, and mechanobiology of biodegradable scaffolds for bone tissue engineeringVibration stimuli and the differentiation of musculoskeletal progenitor cells: Review of results in vitro and in vivoA cephalometric method to diagnosis the craniovertebral junction abnormalities in osteogenesis imperfecta patientsComparative appraisal of clodronate, aspirin and dexamethasone as agents reducing alendronate-induced inflammation in a murine modelCole-Carpenter syndrome is caused by a heterozygous missense mutation in P4HBBone and muscle: Interactions beyond mechanical.Nanotechnology in the regulation of stem cell behaviorThe management of osteoporosis in children.Mutational and structural characteristics of four novel heterozygous C-propeptide mutations in the proα1(I) collagen gene in Chinese osteogenesis imperfecta patients.The severity of Osteogenesis imperfecta and type I collagen pattern in human skin as determined by nonlinear microscopy: proof of principle of a diagnostic method.Increased susceptibility to microdamage in Brtl/+ mouse model for osteogenesis imperfecta.Hip Dysplasia in Children With Osteogenesis Imperfecta: Association With Collagen Type I C-Propeptide MutationsIdentification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta.The folding mechanism of collagen-like model peptides explored through detailed molecular simulations.Cardiovascular involvement in children with osteogenesis imperfecta.Managing the patient with osteogenesis imperfecta: a multidisciplinary approach.WHOLE-BODY VIBRATION EXERCISE IMPROVES FUNCTIONAL PARAMETERS IN PATIENTS WITH OSTEOGENESIS IMPERFECTA: A SYSTEMATIC REVIEW WITH A SUITABLE APPROACH.A normal reference of bone mineral density (BMD) measured by dual energy X-ray absorptiometry in healthy thai children and adolescents aged 5-18 years: a new reference for Southeast Asian PopulationsCRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VIIExcessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta.The ever-expanding conundrum of primary osteoporosis: aetiopathogenesis, diagnosis, and treatment.The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Osteogenesis imperfecta.
@ast
Osteogenesis imperfecta.
@en
Osteogenesis imperfecta.
@nl
type
label
Osteogenesis imperfecta.
@ast
Osteogenesis imperfecta.
@en
Osteogenesis imperfecta.
@nl
prefLabel
Osteogenesis imperfecta.
@ast
Osteogenesis imperfecta.
@en
Osteogenesis imperfecta.
@nl
P1433
P1476
Osteogenesis imperfecta.
@en
P2093
Francis H Glorieux
Frank Rauch
P304
P356
10.1016/S0140-6736(04)16051-0
P407
P577
2004-04-01T00:00:00Z