(Q73763993)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Transcriptional mechanisms in osteoblast differentiation and bone formation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

Kazuhisa Nakashima

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Benoit de Crombrugghe

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 August 2003

1 reference

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6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

458-466

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

8

1 reference

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Toward a molecular understanding of skeletal development

6 November 2019

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Leptin inhibits bone formation through a hypothalamic relay: a central control of bone mass

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7 January 2021

Leptin regulates bone formation via the sympathetic nervous system

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7 January 2021

Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis.

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7 January 2021

Molecular basis of tissue-specific gene expression mediated by the runt domain transcription factor PEBP2/CBF.

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7 January 2021

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

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7 January 2021

Causal relationship between the loss of RUNX3 expression and gastric cancer

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7 January 2021

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

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7 January 2021

Maturational disturbance of chondrocytes in Cbfa1-deficient mice

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7 January 2021

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

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7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

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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

Core-binding factor beta interacts with Runx2 and is required for skeletal development

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7 January 2021

Cbfbeta interacts with Runx2 and has a critical role in bone development

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7 January 2021

The core-binding factor beta subunit is required for bone formation and hematopoietic maturation

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7 January 2021

Continuous expression of Cbfa1 in nonhypertrophic chondrocytes uncovers its ability to induce hypertrophic chondrocyte differentiation and partially rescues Cbfa1-deficient mice

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7 January 2021

Skeletal malformations caused by overexpression of Cbfa1 or its dominant negative form in chondrocytes

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7 January 2021

Overexpression of Cbfa1 in osteoblasts inhibits osteoblast maturation and causes osteopenia with multiple fractures

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7 January 2021

High bone resorption in adult aging transgenic mice overexpressing cbfa1/runx2 in cells of the osteoblastic lineage

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7 January 2021

Subnuclear targeting of Runx/Cbfa/AML factors is essential for tissue-specific differentiation during embryonic development

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7 January 2021

A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia

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7 January 2021

Fibroblast growth factor 2 induction of the osteocalcin gene requires MAPK activity and phosphorylation of the osteoblast transcription factor, Cbfa1/Runx2.

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7 January 2021

Inhibition of osteoblast-specific transcription factor Cbfa1 by the cAMP pathway in osteoblastic cells. Ubiquitin/proteasome-dependent regulation.

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7 January 2021

Serine phosphorylation of RUNX2 with novel potential functions as negative regulatory mechanisms

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7 January 2021

Two domains unique to osteoblast-specific transcription factor Osf2/Cbfa1 contribute to its transactivation function and its inability to heterodimerize with Cbfbeta

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7 January 2021

The mammalian basic helix loop helix protein HES-1 binds to and modulates the transactivating function of the runt-related factor Cbfa1

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7 January 2021

The retinoblastoma protein acts as a transcriptional coactivator required for osteogenic differentiation

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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

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

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7 January 2021

The osteoblast-specific transcription factor Cbfa1 contributes to the expression of osteoprotegerin, a potent inhibitor of osteoclast differentiation and function

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7 January 2021

Chondrogenic cell differentiation from membrane bone periostea

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7 January 2021

The genetic transformation of bone biology

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7 January 2021

Differentiation of muscle, fat, cartilage, and bone from progenitor cells present in a bone-derived clonal cell population: effect of dexamethasone

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7 January 2021

The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6

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7 January 2021

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

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7 January 2021

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

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7 January 2021

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

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7 January 2021

rDlx, a novel distal-less-like homeoprotein is expressed in developing cartilages and discrete neuronal tissues

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7 January 2021

Dlx5 and Dlx6: an evolutionary conserved pair of murine homeobox genes expressed in the embryonic skeleton

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7 January 2021

Cloning and characterization of two members of the vertebrate Dlx gene family

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7 January 2021

The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development

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7 January 2021

Specification of jaw subdivisions by Dlx genes

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7 January 2021

A BMP-inducible gene, dlx5, regulates osteoblast differentiation and mesoderm induction

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7 January 2021

Overexpression of Dlx5 in chicken calvarial cells accelerates osteoblastic differentiation

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7 January 2021

Dermo-1: a novel twist-related bHLH protein expressed in the developing dermis

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7 January 2021

twist is required in head mesenchyme for cranial neural tube morphogenesis

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7 January 2021

Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

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7 January 2021

Mutations of the TWIST gene in the Saethre-Chotzen syndrome

1 reference

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7 January 2021

The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome

1 reference

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7 January 2021

Increased bone formation and decreased osteocalcin expression induced by reduced Twist dosage in Saethre-Chotzen syndrome

1 reference

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7 January 2021

Overexpression of DeltaFosB transcription factor(s) increases bone formation and inhibits adipogenesis.

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7 January 2021

Increased bone formation and osteosclerosis in mice overexpressing the transcription factor Fra-1

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7 January 2021

Transcription factor Sp3 is essential for post-natal survival and late tooth development

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7 January 2021

Impaired ossification in mice lacking the transcription factor Sp3.

1 reference

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7 January 2021

10.1016/S0168-9525(03)00176-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12902164%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference