The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations (Q33847609)

29 July 2017

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

1 reference

29 July 2017

osteogenesis imperfecta

0 references

author

Catherine Ambrose

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

author name string

Kyu Sang Joeng

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Yi-Chien Lee

2

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10 June 2020

Ming-Ming Jiang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Terry K Bertin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Yuqing Chen

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Annie M Abraham

6

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Hao Ding

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

Xiaohong Bi

8

1 reference

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10 June 2020

Brendan H Lee

10

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10 June 2020

publication date

14 March 2014

1 reference

29 July 2017

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

volume

23

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10 June 2020

issue

15

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10 June 2020

page(s)

4035-4042

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

Prostate cancer metastases alter bone mineral and matrix composition independent of effects on bone architecture in mice--a quantitative study using microCT and Raman spectroscopy

10 June 2020

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5 July 2018

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WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta

5 July 2018

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WNT1 mutations in families affected by moderately severe and progressive recessive osteogenesis imperfecta

5 July 2018

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Mutations in WNT1 cause different forms of bone fragility

5 July 2018

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WNT signaling in bone homeostasis and disease: from human mutations to treatments

5 July 2018

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Sclerostin antibody inhibits skeletal deterioration due to reduced mechanical loading

5 July 2018

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5 July 2018

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Lrp5 and Lrp6 redundantly control skeletal development in the mouse embryo

5 July 2018

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Mutations in SERPINF1 cause osteogenesis imperfecta type VI

5 July 2018

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New perspectives on osteogenesis imperfecta

5 July 2018

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Lrp5 functions in bone to regulate bone mass

5 July 2018

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

5 July 2018

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Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled study.

5 July 2018

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Raman and mechanical properties correlate at whole bone- and tissue-levels in a genetic mouse model

5 July 2018

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Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome

5 July 2018

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Single-dose, placebo-controlled, randomized study of AMG 785, a sclerostin monoclonal antibody

5 July 2018

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

5 July 2018

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Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding

5 July 2018

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A serotonin-dependent mechanism explains the leptin regulation of bone mass, appetite, and energy expenditure

5 July 2018

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Osteogenesis imperfecta: recent findings shed new light on this once well-understood condition.

5 July 2018

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CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta

5 July 2018

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

5 July 2018

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Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta

5 July 2018

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CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta

5 July 2018

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Lrp5-independent activation of Wnt signaling by lithium chloride increases bone formation and bone mass in mice

5 July 2018

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Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation

5 July 2018

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5 July 2018

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5 July 2018

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Skeletal effects and functional outcome with olpadronate in children with osteogenesis imperfecta: a 2-year randomised placebo-controlled study

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Cbfa1-independent decrease in osteoblast proliferation, osteopenia, and persistent embryonic eye vascularization in mice deficient in Lrp5, a Wnt coreceptor

5 July 2018

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

5 July 2018

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5 July 2018

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Reduced secretion of structurally abnormal type I procollagen in a form of osteogenesis imperfecta

5 July 2018

1 reference

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Perinatal lethal osteogenesis imperfecta (OI type II): a biochemically heterogeneous disorder usually due to new mutations in the genes for type I collagen

5 July 2018

1 reference

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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4082367

Swaying is a mutant allele of the proto-oncogene Wnt-1

5 July 2018

1 reference

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The midbrain-hindbrain phenotype of Wnt-1-/Wnt-1- mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum.

5 July 2018

1 reference

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Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta.

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDU117

Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDU117

Sclerostin mediates bone response to mechanical unloading through antagonizing Wnt/beta-catenin signaling.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDU117

Synthesis and processing of a type I procollagen containing shortened pro-alpha 1(I) chains by fibroblasts from a patient with osteogenesis imperfecta

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4082367

Safety and efficacy of a 1-year treatment with zoledronic acid compared with pamidronate in children with osteogenesis imperfecta

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24634143

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations in WNT1 are a cause of osteogenesis imperfecta

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24634143

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDU117

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24634143%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference

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