(Q38025995)

English

The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals

scientific article published on 12 July 2012

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

27 August 2017

The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals (English)

1 reference

Europe PubMed Central

27 August 2017

Andrea Superti-Furga

28

object named as

Andrea Superti-Furga

0 references

object named as

Geert Mortier

16

0 references

Valérie Cormier-Daire

object named as

Valerie Cormier-Daire

8

0 references

object named as

Sheila Unger

23

0 references

7

object named as

Rolando Cimaz

1 reference

Europe PubMed Central

27 August 2017

19

object named as

Ewa Obersztyn

1 reference

Europe PubMed Central

27 August 2017

29

object named as

Luisa Bonafé

1 reference

Europe PubMed Central

27 August 2017

author name string

Nuria Garcia Segarra

1

1 reference

Europe PubMed Central

27 August 2017

Laureane Mittaz

2

1 reference

Europe PubMed Central

27 August 2017

Ana Belinda Campos-Xavier

3

1 reference

Europe PubMed Central

27 August 2017

Cynthia F Bartels

4

1 reference

Europe PubMed Central

27 August 2017

Beyhan Tuysuz

5

1 reference

Europe PubMed Central

27 August 2017

Yasemin Alanay

6

1 reference

Europe PubMed Central

27 August 2017

Maja Di Rocco

9

1 reference

Europe PubMed Central

27 August 2017

Hans-Christoph Duba

10

1 reference

Europe PubMed Central

27 August 2017

Nursel H Elcioglu

11

1 reference

Europe PubMed Central

27 August 2017

Francesca Forzano

12

1 reference

Europe PubMed Central

27 August 2017

Toni Hospach

13

1 reference

Europe PubMed Central

27 August 2017

Esra Kilic

14

1 reference

Europe PubMed Central

27 August 2017

Jasmin B Kuemmerle-Deschner

15

1 reference

Europe PubMed Central

27 August 2017

Sonja Mrusek

17

1 reference

Europe PubMed Central

27 August 2017

Sheela Nampoothiri

18

1 reference

Europe PubMed Central

27 August 2017

Richard M Pauli

20

1 reference

Europe PubMed Central

27 August 2017

Angelo Selicorni

21

1 reference

Europe PubMed Central

27 August 2017

Romano Tenconi

22

1 reference

Europe PubMed Central

27 August 2017

G Eda Utine

24

1 reference

Europe PubMed Central

27 August 2017

Michael Wright

25

1 reference

Europe PubMed Central

27 August 2017

Bernhard Zabel

26

1 reference

Europe PubMed Central

27 August 2017

Matthew L Warman

27

1 reference

Europe PubMed Central

27 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

12 July 2012

1 reference

Europe PubMed Central

27 August 2017

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

1 reference

Europe PubMed Central

27 August 2017

160C

1 reference

Europe PubMed Central

27 August 2017

3

1 reference

Europe PubMed Central

27 August 2017

217-229

1 reference

Europe PubMed Central

27 August 2017

Dual regulation of metalloproteinase expression in chondrocytes by Wnt-1-inducible signaling pathway protein 3/CCN6.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Expression of WISPs and of their novel alternative variants in human hepatocellular carcinoma cells.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

WISP3 suppresses insulin-like growth factor signaling in human chondrocytes.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Progressive pseudorheumatoid dysplasia: report of a family and review

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Molecular differentiation between osteophytic and articular cartilage--clues for a transient and permanent chondrocyte phenotype

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Cyr61 and Fisp12 are both ECM-associated signaling molecules: activities, metabolism, and localization during development

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

The CCN family of angiogenic regulators: the integrin connection

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Potential role of WISP3 (CCN6) in regulating the accumulation of reactive oxygen species

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Normal growth and development in mice over-expressing the CCN family member WISP3

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

WISP genes are members of the connective tissue growth factor family that are up-regulated in wnt-1-transformed cells and aberrantly expressed in human colon tumors

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Nonsense-mediated decay of human HEXA mRNA.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

WISP3-dependent regulation of type II collagen and aggrecan production in chondrocytes

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Progressive pseudorheumatoid arthropathy of childhood (PPAC): a hereditary disorder simulating juvenile rheumatoid arthritis.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Molecular study ofWISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: Identification of two novel mutations, and description of a founder effect

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Progressive pseudorheumatoid dysplasia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31333

21 January 2018

Identifiers

10.1002/AJMG.C.31333

1 reference

Europe PubMed Central

27 August 2017

1 reference

Europe PubMed Central

27 August 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=Q38025995&oldid=2084484126"