Novel and recurrent mutations in WISP3 and an atypical phenotype. (Q53501344)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25988854%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

title

Novel and recurrent mutations in WISP3 and an atypical phenotype (English)

1 reference

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Gandham SriLakshmi Bhavani

8 March 2020

author

1

1 reference

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8 March 2020

Hitesh Shah

2

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8 March 2020

Hitesh Shah

3

1 reference

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8 March 2020

Shubha R Phadke

8

1 reference

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8 March 2020

Madhulika Kabra

10

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8 March 2020

author name string

Ashwin B Dalal

4

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8 March 2020

Anju Shukla

5

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8 March 2020

Sumita Danda

6

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8 March 2020

Shagun Aggarwal

7

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8 March 2020

Neerja Gupta

9

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8 March 2020

Kalpana Gowrishankar

11

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8 March 2020

Anju Gupta

12

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8 March 2020

Meenakshi Bhat

13

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8 March 2020

Ratna D Puri

14

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8 March 2020

Sunita Bijarnia-Mahay

15

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8 March 2020

Sheela Nampoothiri

16

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8 March 2020

Kavitha M Mohanasundaram

17

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8 March 2020

S Rajeswari

18

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8 March 2020

Akhil M Kulkarni

19

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8 March 2020

Muralidhar L Kulkarni

20

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8 March 2020

Prajnya Ranganath

21

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8 March 2020

A Radha Ramadevi

22

1 reference

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8 March 2020

Sankar V Hariharan

23

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8 March 2020

Katta Mohan Girisha

24

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8 March 2020

language of work or name

English

0 references

publication date

18 May 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25988854%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics

8 March 2020

published in

1 reference

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8 March 2020

volume

167A

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8 March 2020

page(s)

2481-2484

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8 March 2020

issue

10

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

8 March 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37164

The CCN family of proteins: structure-function relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37164

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37164

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37164

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37164

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37164