A mouse model for dominant collagen VI disorders: heterozygous deletion of Col6a3 Exon 16 (Q28505521)

24 January 2017

title

A mouse model for dominant collagen VI disorders: heterozygous deletion of Col6a3 Exon 16 (English)

1 reference

Collagen, type VI, alpha 6

24 January 2017

main subject

1 reference

Periostin, osteoblast specific factor

GOA release 2020-03-11

1 reference

Collagen, type VI, alpha 5

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

Te-Cheng Pan

1

1 reference

24 January 2017

Rui-Zhu Zhang

2

1 reference

24 January 2017

Machiko Arita

3

1 reference

24 January 2017

Sasha Bogdanovich

4

1 reference

24 January 2017

Sheila M. Adams

5

1 reference

24 January 2017

Sudheer Kumar Gara

6

1 reference

24 January 2017

Raimund Wagener

7

1 reference

24 January 2017

Tejvior S. Khurana

8

1 reference

24 January 2017

David E. Birk

9

1 reference

24 January 2017

Mon-Li Chu

10

1 reference

24 January 2017

language of work or name

English

0 references

publication date

11 April 2014

1 reference

Journal of Biological Chemistry

24 January 2017

published in

1 reference

24 January 2017

volume

289

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24 January 2017

issue

15

1 reference

24 January 2017

page(s)

10293–10307

1 reference

describes a project that uses

24 January 2017

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4036154/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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29 September 2017

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29 September 2017

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations

21 January 2018

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21 January 2018

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Effects on Collagen VI mRNA Stability and Microfibrillar Assembly of ThreeCOL6A2Mutations in Two Families with Ullrich Congenital Muscular Dystrophy

21 January 2018

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Variable penetrance of COL6A1 null mutations: Implications for prenatal diagnosis and genetic counselling in Ullrich congenital muscular dystrophy families

21 January 2018

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Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy

21 January 2018

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Ullrich congenital muscular dystrophy: Connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromes

21 January 2018

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Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan

21 January 2018

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21 January 2018

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