Skeletal development: insights from targeting the mouse genome (Q35204518)

7 August 2017

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title

Skeletal development: insights from targeting the mouse genome (English)

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7 August 2017

William A Horton

1

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7 August 2017

language of work or name

English

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publication date

1 August 2003

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7 August 2017

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7 August 2017

volume

362

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7 August 2017

issue

9383

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7 August 2017

page(s)

560-569

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Initial sequencing and analysis of the human genome

7 August 2017

cites work

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7 January 2021

The Sequence of the Human Genome

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7 January 2021

Molecular genetic basis of the human chondrodysplasias

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7 January 2021

Gene targeting in the mouse

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7 January 2021

Mouse models for human disease

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7 January 2021

Generating mice with targeted mutations

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7 January 2021

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7 January 2021

Somatic expression of herpes thymidine kinase in mice following injection of a fusion gene into eggs

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7 January 2021

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7 January 2021

Production of transgenic mice

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7 January 2021

Target practice in transgenics

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7 January 2021

An Alu element from the K18 gene confers position-independent expression in transgenic mice

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7 January 2021

Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes

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7 January 2021

Detection of targeted GFP-Hox gene fusions during mouse embryogenesis

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7 January 2021

The color of mice: in the light of GFP-variant reporters

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7 January 2021

Targeting genes for self-excision in the germ line

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7 January 2021

Cre recombinase: The universal reagent for genome tailoring

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7 January 2021

Toward a molecular understanding of skeletal development

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7 January 2021

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7 January 2021

All for one and one for all: condensations and the initiation of skeletal development

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

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7 January 2021

Cellular interactions and signaling in cartilage development

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7 January 2021

The membranous skeleton: the role of cell condensations in vertebrate skeletogenesis

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7 January 2021

Derivation of the mammalian skull vault

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7 January 2021

Development of the clavicles in birds and mammals

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7 January 2021

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

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7 January 2021

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

1 reference

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7 January 2021

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

1 reference

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7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

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7 January 2021

The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation

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7 January 2021

Genetics of craniofacial development and malformation

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7 January 2021

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

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7 January 2021

A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Regulatory mechanisms in the pathways of cartilage and bone formation

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7 January 2021

Sox9 is required for cartilage formation

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7 January 2021

L-Sox5, Sox6 and Sox9 control essential steps of the chondrocyte differentiation pathway

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7 January 2021

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

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7 January 2021

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

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7 January 2021

Spatiotemporal pattern of type X collagen gene expression and collagen deposition in embryonic chick vertebrae undergoing endochondral ossification

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7 January 2021

VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation

1 reference

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7 January 2021

Maturational disturbance of chondrocytes in Cbfa1-deficient mice

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7 January 2021

HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo

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7 January 2021

Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein

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7 January 2021

Bone formation via cartilage models: the "borderline" chondrocyte

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7 January 2021

Mechanism of longitudinal bone growth and its regulation by growth plate chondrocytes

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7 January 2021

Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia

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7 January 2021

Reduced amounts of cartilage collagen fibrils and growth plate anomalies in transgenic mice harboring a glycine-to-cysteine mutation in the mouse type II procollagen alpha 1-chain gene

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7 January 2021

Chondrodysplasia in transgenic mice harboring a 15-amino acid deletion in the triple helical domain of pro alpha 1(II) collagen chain

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7 January 2021

Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral bone

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Collagen II is essential for the removal of the notochord and the formation of intervertebral discs

1 reference

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7 January 2021

Collagens and collagen-related diseases

1 reference

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7 January 2021

Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Indian hedgehog couples chondrogenesis to osteogenesis in endochondral bone development

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

A constitutively active mutant PTH-PTHrP receptor in Jansen-type metaphyseal chondrodysplasia

1 reference

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7 January 2021

Vertebrate Hedgehog signalling modulated by induction of a Hedgehog-binding protein

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7 January 2021

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.

1 reference

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7 January 2021

Fibroblast growth factor receptor 3 is a negative regulator of bone growth

1 reference

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7 January 2021

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Gly369Cys mutation in mouse FGFR3 causes achondroplasia by affecting both chondrogenesis and osteogenesis

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Skeletal dysplasia and defective chondrocyte differentiation by targeted overexpression of fibroblast growth factor 9 in transgenic mice.

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Activation of Stat1 by mutant fibroblast growth-factor receptor in thanatophoric dysplasia type II dwarfism

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Up-regulation of the chondrogenic Sox9 gene by fibroblast growth factors is mediated by the mitogen-activated protein kinase pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Phosphorylation of SOX9 by cyclic AMP-dependent protein kinase A enhances SOX9's ability to transactivate a Col2a1 chondrocyte-specific enhancer

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

MMP-9/gelatinase B is a key regulator of growth plate angiogenesis and apoptosis of hypertrophic chondrocytes

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https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Tissue specific regulation of VEGF expression during bone development requires Cbfa1/Runx2.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

TGF-beta latency: biological significance and mechanisms of activation

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7 January 2021

Growth plate chondrocytes store latent transforming growth factor (TGF)-beta 1 in their matrix through latent TGF-beta 1 binding protein-1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Activation of transforming growth factor beta in chondrocytes undergoing endochondral ossification

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

Dissociation between bone resorption and bone formation in osteopenic transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2914119-0

7 January 2021

The lac operator-repressor system is functional in the mouse

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7 January 2021

10.1016/S0140-6736(03)14119-0

Identifiers

DOI

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7 August 2017

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