(Q53815954)

English

Low bone mass and high material bone density in two patients with Loeys-Dietz syndrome caused by transforming growth factor beta receptor 2 mutations.

scientific article

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Low bone mass and high material bone density in two patients with Loeys-Dietz syndrome caused by transforming growth factor beta receptor 2 mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Loeys-Dietz syndrome

1 reference

based on heuristic

inferred from title

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Klaus Klaushofer

7

object named as

Klaus Klaushofer

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

author name string

I Mouna Ben Amor

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Francis H Glorieux

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Gilles Chabot

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Marc Tischkowitz

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Paul Roschger

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

publication date

1 March 2012

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Journal of Bone and Mineral Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

27

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

713-718

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22095581%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Aneurysm syndromes caused by mutations in the TGF-beta receptor

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Musculoskeletal findings of Loeys-Dietz syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Mechanism of activation of the TGF-beta receptor

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Quantitative analysis of TGFBR2 mutations in Marfan-syndrome-related disorders suggests a correlation between phenotypic severity and Smad signaling activity.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Pharmacologic inhibition of the TGF-beta type I receptor kinase has anabolic and anti-catabolic effects on bone

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

TGF-beta regulates the mechanical properties and composition of bone matrix

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Normative data for iliac bone histomorphometry in growing children.

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Bone histomorphometry: standardization of nomenclature, symbols, and units. Report of the ASBMR Histomorphometry Nomenclature Committee

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Normative data on mineralization density distribution in iliac bone biopsies of children, adolescents and young adults

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Two-dimensional echocardiographic aortic root dimensions in normal children and adults

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Increased expression of TGF-beta 2 in osteoblasts results in an osteoporosis-like phenotype

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome

1 reference

https://api.crossref.org/works/10.1002%2FJBMR.1470

21 January 2018

Identifiers

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=Q53815954&oldid=1503514282"