(Q28578731)

English

Transforming growth factor-beta3 (Tgf-beta3) down-regulates Tgf-beta3 receptor type I (Tbetar-I) during rescue of cranial sutures from osseous obliteration

scientific journal article

In more languages

Statements

scholarly article

1 reference

PubMed publication ID

31 January 2017

Transforming growth factor-beta3 (Tgf-beta3) down-regulates Tgf-beta3 receptor type I (Tbetar-I) during rescue of cranial sutures from osseous obliteration (English)

1 reference

PubMed publication ID

31 January 2017

author name string

L. A. Opperman

1

1 reference

PubMed publication ID

31 January 2017

V. Galanis

2

1 reference

PubMed publication ID

31 January 2017

A. R. Williams

3

1 reference

PubMed publication ID

31 January 2017

K. Adab

4

1 reference

PubMed publication ID

31 January 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 February 2002

1 reference

PubMed publication ID

31 January 2017

Orthodontics & Craniofacial Research

1 reference

PubMed publication ID

31 January 2017

5

1 reference

PubMed publication ID

31 January 2017

1

1 reference

PubMed publication ID

31 January 2017

5–16

1 reference

PubMed publication ID

31 January 2017

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/10.1034/J.1600-0544.2002.01179.X

21 April 2017

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/10.1034/J.1600-0544.2002.01179.X

21 April 2017

Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras

1 reference

https://api.crossref.org/works/10.1034/J.1600-0544.2002.01179.X

21 April 2017

Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

1 reference

https://api.crossref.org/works/10.1034/J.1600-0544.2002.01179.X

21 April 2017

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

Cranial sutures as intramembranous bone growth sites

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

Rapid flux in transforming growth factor-beta receptors on bone cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

Incipient analysis of mesenchymal stem-cell-derived osteogenesis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

Expression and distribution of transforming growth factor-beta isoforms and their signaling receptors in growing human bone

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

Distribution and modulation of the cellular receptor for transforming growth factor-beta

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

Immunoreactive localization of transforming growth factor-beta type II receptor-positive cells in rat tibiae

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

CBFA1 Mutation Analysis and Functional Correlation with Phenotypic Variability in Cleidocranial Dysplasia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

21 January 2018

Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

TGF-beta 1, TGF-beta 2, and TGF-beta 3 exhibit distinct patterns of expression during cranial suture formation and obliteration in vivo and in vitro.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Studies in cranial suture biology: Part I. Increased immunoreactivity for TGF-beta isoforms (beta 1, beta 2, and beta 3) during rat cranial suture fusion

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Immunolocalization of transforming growth factor beta 1, beta 2, and beta 3 and insulin-like growth factor I in premature cranial suture fusion.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of high-affinity receptors for TGF-beta during rat cranial suture fusion

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cranial sutures require tissue interactions with dura mater to resist osseous obliteration in vitro.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the TWIST gene in the Saethre-Chotzen syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0544.2002.01179.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1034/J.1600-0544.2002.01179.X

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

PubMed publication ID

31 January 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28578731&oldid=1672707898"