Transcription factors in bone: developmental and pathological aspects (Q34735288)

4 August 2017

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title

Transcription factors in bone: developmental and pathological aspects (English)

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4 August 2017

Xiangli Yang

1

1 reference

PubMed ID

12114114

4 August 2017

Gerard Karsenty

series ordinal

2

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PubMed ID

12114114

4 August 2017

language of work or name

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1 July 2002

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Trends in Molecular Medicine

4 August 2017

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4 August 2017

8

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4 August 2017

340-345

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4 August 2017

7

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In vitro chondrogenesis in human chondrodysplasias

4 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Expression patterns of matrix genes during human skeletal development.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

SOX9 directly regulates the type-II collagen gene

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Sox9 is required for cartilage formation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

The transcription factors L-Sox5 and Sox6 are essential for cartilage formation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

FGF signaling inhibits chondrocyte proliferation and regulates bone development through the STAT-1 pathway

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

The transcription factor NF-ATc is essential for cardiac valve formation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

The nuclear factor of activated T cells (NFAT) transcription factor NFATp (NFATc2) is a repressor of chondrogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Cbfa1 is a positive regulatory factor in chondrocyte maturation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

The genetic transformation of bone biology

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Characterization of a novel KRAB/C2H2 zinc finger transcription factor involved in bone development.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Characterization of Osf1, an osteoblast-specific transcription factor binding to a critical cis-acting element in the mouse Osteocalcin promoters

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Chondrodysplasia and neurological abnormalities in ATF-2-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Human c-fos oncogene mapped within chromosomal region 14q21----q31

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Osteopetrosis in mice lacking haematopoietic transcription factor PU.1.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

SHOX haploinsufficiency and overdosage: impact of gonadal function status.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Requirement of transcription factor PU.1 in the development of multiple hematopoietic lineages.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Osteoblasts are target cells for transformation in c-fos transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Bone and haematopoietic defects in mice lacking c-fos

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Fra-1 replaces c-Fos-dependent functions in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Fosl1 is a transcriptional target of c-Fos during osteoclast differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Effects of NF-kappaB1 (p50) targeted gene disruption on ionizing radiation-induced NF-kappaB activation and TNFalpha, IL-1alpha, IL-1beta and IL-6 mRNA expression in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Nuclear factor (NF)-kappa B2 (p100/p52) is required for normal splenic microarchitecture and B cell-mediated immune responses

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Linking osteopetrosis and pycnodysostosis: regulation of cathepsin K expression by the microphthalmia transcription factor family

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Paralogous Hox genes: function and regulation

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

twist is required in head mesenchyme for cranial neural tube morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

The eye and skeletal effects of two mutant alleles at the microphthalmia locus of Mus musculus

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2802%2902340-7

7 January 2021

10.1016/S1471-4914(02)02340-7

Identifiers

DOI

1 reference

4 August 2017

1 reference

PubMed ID

12114114