Increased apoptosis of myoblasts in Drosophila model for the Walker-Warburg syndrome (Q33991629)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644630%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

title

Increased apoptosis of myoblasts in Drosophila model for the Walker-Warburg syndrome (English)

1 reference

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8 February 2020

0 references

0 references

1 reference

GOA release 2020-03-11

Rotated abdomen Dmel_CG6097

1 reference

GOA release 2020-03-11

author

Morio Ueyama

1

1 reference

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8 February 2020

author name string

Yoshihiro Akimoto

2

1 reference

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8 February 2020

Tomomi Ichimiya

3

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8 February 2020

Ryu Ueda

4

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8 February 2020

Hayato Kawakami

5

1 reference

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8 February 2020

Toshiro Aigaki

6

1 reference

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8 February 2020

Shoko Nishihara

7

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8 February 2020

language of work or name

English

0 references

publication date

13 July 2010

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8 February 2020

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8 February 2020

volume

5

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8 February 2020

issue

7

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8 February 2020

page(s)

e11557

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Creative Commons Attribution 4.0 International

8 February 2020

copyright license

start time

13 July 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality

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A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotype

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Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

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Muscular dystrophy into the new millennium

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Identifiers

DOI

10.1371/JOURNAL.PONE.0011557

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644630%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

0 references

1 reference

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8 February 2020

1 reference