The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations - Wikidata - awgldk - TriplyDB

The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

http://www.wikidata.org/entity/Q33847609

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Activation of Wnt Signaling by Mechanical Loading Is Impaired in the Bone of Old Mice Relevance of Wnt signaling for osteoanabolic therapy.Value of rare low bone mass diseases for osteoporosis genetics.Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations Genetic Approaches To Identifying Novel Osteoporosis Drug Targets.Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis Pharmacological and biological therapeutic strategies for osteogenesis imperfecta.Wnt signaling and cellular metabolism in osteoblasts.Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3.Wntless spatially regulates bone development through β-catenin-dependent and independent mechanisms.Wnt/β-catenin signaling during early vertebrate neural development.Skeletal Characteristics of WNT1 Osteoporosis in Children and Young Adults.The brains of the bones: how osteocytes use WNT1 to control bone formation.Correlations Between Bone Mechanical Properties and Bone Composition Parameters in Mouse Models of Dominant and Recessive Osteogenesis Imperfecta and the Response to Anti-TGF-β Treatment.Genetic causes and mechanisms of Osteogenesis Imperfecta.

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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

http://www.wikidata.org/entity/Q33847609

description

2014 nî lūn-bûn

@nan

2014 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի մարտին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

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Human Molecular Genetics

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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations

@en

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Annie M Abraham

http://www.w3.org/2001/XMLSchema#string

Brendan H Lee

http://www.w3.org/2001/XMLSchema#string

Hao Ding

http://www.w3.org/2001/XMLSchema#string

Kyu Sang Joeng

http://www.w3.org/2001/XMLSchema#string

Ming-Ming Jiang

http://www.w3.org/2001/XMLSchema#string

Terry K Bertin

http://www.w3.org/2001/XMLSchema#string

Xiaohong Bi

http://www.w3.org/2001/XMLSchema#string

Yi-Chien Lee

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Yuqing Chen

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P2860

Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding

Mutations in WNT1 cause different forms of bone fragility

A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait

Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta

Lrp5 functions in bone to regulate bone mass

Mutations in SERPINF1 cause osteogenesis imperfecta type VI

Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta

High bone mass in mice expressing a mutant LRP5 gene

P304

4035-4042

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scholarly article

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10.1093/HMG/DDU117

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15

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23

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Catherine Ambrose

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2014-03-14T00:00:00Z

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260842703

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24634143

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P921

osteogenesis imperfecta

P932

4082367

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