(Q36861283)

16 August 2017

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title

Animal models of osteogenesis imperfecta and related syndromes (English)

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16 August 2017

main subject

osteogenesis imperfecta

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author name string

Agnès S Kamoun-Goldrat

series ordinal

1

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16 August 2017

Martine F Le Merrer

series ordinal

2

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16 August 2017

language of work or name

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25 June 2007

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Journal of Bone and Mineral Metabolism

16 August 2017

published in

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16 August 2017

volume

25

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16 August 2017

issue

4

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16 August 2017

page(s)

211-218

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https://scigraph.springernature.com/pub.10.1007/s00774-007-0750-3

16 August 2017

exact match

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cites work

Life expectancy in osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1007%2FS00774-007-0750-3

Age- and genotype-dependence of bone material properties in the osteogenesis imperfecta murine model (oim).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00774-007-0750-3

Myocardial mechanics and collagen structure in the osteogenesis imperfecta murine (oim).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00774-007-0750-3

Alendronate affects long bone length and growth plate morphology in the oim mouse model for Osteogenesis Imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00774-007-0750-3

Alendronate treatment for infants with osteogenesis imperfecta: demonstration of efficacy in a mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00774-007-0750-3

An ultrastructural, microanalytical, and spectroscopic study of bone from a transgenic mouse with a COL1.A1 pro-alpha-1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00774-007-0750-3

Lethal osteogenesis imperfecta and skin fragility in newborn New Zealand Romney lambs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00774-007-0750-3

Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease

21 January 2018

1 reference

12 December 2020

Heterozygous oim mice exhibit a mild form of osteogenesis imperfecta

1 reference

12 December 2020

Introduction of the human pro alpha 1(I) collagen gene into pro alpha 1(I)-deficient Mov-13 mouse cells leads to formation of functional mouse-human hybrid type I collagen

1 reference

12 December 2020

Brittle IV mouse model for osteogenesis imperfecta IV demonstrates postpubertal adaptations to improve whole bone strength

1 reference

12 December 2020

Canine COL1A2 mutation resulting in C-terminal truncation of pro-alpha2(I) and severe osteogenesis imperfecta

1 reference

12 December 2020

Bone fragility in a kitten: an osteogenesis imperfecta-like syndrome.

1 reference

12 December 2020

Osteogenesis imperfecta murine: interaction between type I collagen homotrimers

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12 December 2020

Mechanisms of Wnt signaling in development

1 reference

12 December 2020

A single amino acid substitution (D1441Y) in the carboxyl-terminal propeptide of the proalpha1(I) chain of type I collagen results in a lethal variant of osteogenesis imperfecta with features of dense bone diseases

1 reference

12 December 2020

Insertion of retrovirus into the first intron of alpha 1(I) collagen gene to embryonic lethal mutation in mice

1 reference

12 December 2020

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12 December 2020

Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect.

1 reference

12 December 2020

Growth hormone injections improve bone quality in a mouse model of osteogenesis imperfecta.

1 reference

12 December 2020

Clinical signs and diagnosis of osteogenesis imperfecta in three dogs

1 reference

12 December 2020

Mineral changes in a transgenic mouse model for osteogenesis imperfecta

1 reference

12 December 2020

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

1 reference

12 December 2020

Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta

1 reference

12 December 2020

Fragilitas ossium: a new autosomal recessive mutation in the mouse

1 reference

12 December 2020

Embryonic lethal mutation in mice induced by retrovirus insertion into the alpha 1(I) collagen gene.

1 reference

12 December 2020

Collagen from the osteogenesis imperfecta mouse model (oim) shows reduced resistance against tensile stress

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12 December 2020

Low-density lipoprotein receptor-related protein 5 (LRP5) is essential for normal cholesterol metabolism and glucose-induced insulin secretion

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12 December 2020

Osteogenesis imperfecta in 2 collie litter siblings

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12 December 2020

Phenotypic variability and incomplete penetrance of spontaneous fractures in an inbred strain of transgenic mice expressing a mutated collagen gene (COL1A1)

1 reference

12 December 2020

Wnt-14 plays a pivotal role in inducing synovial joint formation in the developing appendicular skeleton

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12 December 2020

Alpha 2(I) collagen deficient oim mice have altered biomechanical integrity, collagen content, and collagen crosslinking of their thoracic aorta.

1 reference

12 December 2020

Two bovine models of osteogenesis imperfecta exhibit decreased apatite crystal size

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12 December 2020

Osteogenesis imperfecta

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12 December 2020

Osteogenesis imperfecta. Human, dog, cat, fox. Comparative analysis of the ultrastructural aspects

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12 December 2020

Radiographic analysis of zebrafish skeletal defects

1 reference

12 December 2020

Retrovirally transduced bone marrow stromal cells isolated from a mouse model of human osteogenesis imperfecta (oim) persist in bone and retain the ability to form cartilage and bone after extended passaging

1 reference

12 December 2020

Bone mineralization in an osteogenesis imperfecta mouse model studied by small-angle x-ray scattering

1 reference

12 December 2020

Structure, stability and interactions of type I collagen with GLY349-CYS substitution in alpha 1(I) chain in a murine Osteogenesis Imperfecta model

1 reference

12 December 2020

Properties of collagen in OIM mouse tissues

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12 December 2020

Congenital blindness and osteoporosis-pseudoglioma syndrome.

1 reference

12 December 2020

Transfer of proalpha2(I) cDNA into cells of a murine model of human Osteogenesis Imperfecta restores synthesis of type I collagen comprised of alpha1(I) and alpha2(I) heterotrimers in vitro and in vivo

1 reference

12 December 2020

A murine skeletal adaptation that significantly increases cortical bone mechanical properties. Implications for human skeletal fragility

1 reference

12 December 2020

Osteogenesis imperfecta with joint contractures: Bruck syndrome

1 reference

12 December 2020

A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse

1 reference

12 December 2020

Osteogenesis imperfecta in two litters of dachshunds.

1 reference

12 December 2020

Bone geometry and strength measurements in aging mice with the oim mutation

1 reference

12 December 2020

Genetic heterogeneity in osteogenesis imperfecta

1 reference

12 December 2020

A controlled study of the effects of alendronate in a growing mouse model of osteogenesis imperfecta

1 reference

12 December 2020

Perinatal lethal osteogenesis imperfecta in transgenic mice bearing an engineered mutant pro-alpha 1(I) collagen gene

1 reference

12 December 2020

The Material Basis for Reduced Mechanical Properties in oim Mice Bones

1 reference

12 December 2020

Novel collagen glomerulopathy in a homotrimeric type I collagen mouse (oim)

1 reference

12 December 2020

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

1 reference

12 December 2020

Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral

1 reference

12 December 2020

Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta

1 reference

12 December 2020

Mineralized tissue protein profiles in the Australian form of bovine osteogenesis imperfecta

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12 December 2020

Causes of death in osteogenesis imperfecta

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12 December 2020

Bone material elasticity in a murine model of osteogenesis imperfecta

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12 December 2020

Osteoporosis-pseudoglioma syndrome

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12 December 2020

Type V osteogenesis imperfecta: a new form of brittle bone disease

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12 December 2020

Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice.

1 reference

12 December 2020

The osteoporosis pseudoglioma syndrome

1 reference

12 December 2020

Sequence of normal canine COL1A1 cDNA and identification of a heterozygous alpha1(I) collagen Gly208Ala mutation in a severe case of canine osteogenesis imperfecta.

1 reference

12 December 2020

Heritable bone fragility, joint laxity and dysplastic dentin in Friesian calves: a bovine syndrome of osteogenesis imperfecta

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12 December 2020

Osteogenesis imperfecta in Holstein-Friesian calves.

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12 December 2020

Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragility

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12 December 2020

Osteoblastic cells express phospholipid receptors and phosphatases and proliferate in response to sphingosine-1-phosphate

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12 December 2020

Sexually dimorphic development of the mammalian reproductive tract requires Wnt-7a

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12 December 2020

The Formation of Triple-Helical Collagen Molecules from α1 or α2 Polypeptide Chains

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12 December 2020

Bone fragility, craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features: a newly recognized type of osteogenesis imperfecta

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12 December 2020

Fourier transform infrared imaging spectroscopy (FT-IRIS) of mineralization in bisphosphonate-treated oim/oim mice

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12 December 2020

Congenital osteogenesis imperfecta in Charollais cattle

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12 December 2020

A syndrome of osteogenesis imperfecta, microcephaly, and cataracts

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12 December 2020

Bone fragility in transgenic mice expressing a mutated gene for type I procollagen (COL1A1) parallels the age-dependent phenotype of human osteogenesis imperfecta

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12 December 2020

Germline integration of moloney murine leukemia virus at the Mov13 locus leads to recessive lethal mutation and early embryonic death.

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12 December 2020

Syndromes with congenital brittle bones

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12 December 2020

Female development in mammals is regulated by Wnt-4 signalling

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12 December 2020

Retrovirus-induced insertional mutation in Mov13 mice affects collagen I expression in a tissue-specific manner

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12 December 2020

Transgenic mouse model of the mild dominant form of osteogenesis imperfecta

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12 December 2020

Use of the Cre/lox recombination system to develop a non-lethal knock-in murine model for osteogenesis imperfecta with an alpha1(I) G349C substitution. Variability in phenotype in BrtlIV mice

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12 December 2020

Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta

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12 December 2020

Dental phenotype of the col1a2(oim) mutation: DI is present in both homozygotes and heterozygotes

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12 December 2020

Embryonic lethal mutation in mouse collagen I gene causes rupture of blood vessels and is associated with erythropoietic and mesenchymal cell death.

1 reference

12 December 2020

Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect.

1 reference

12 December 2020

10.1007/S00774-007-0750-3

Identifiers

DOI

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16 August 2017

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