A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss. (Q29347528)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27807076%20AND%20SRC:MED&resulttype=core&format=json

26 March 2020

title

A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27807076%20AND%20SRC:MED&resulttype=core&format=json

Protein O-glucosyltransferase 1

26 March 2020

main subject

1 reference

muscle tissue development

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Rumi Dmel_CG31152

1 reference

GOA release 2020-03-11

1 reference

Emilia Servián-Morilla

1

1 reference

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26 March 2020

Fabiola Mavillard

5

1 reference

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26 March 2020

Eloy Rivas

7

1 reference

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26 March 2020

Jose Luis Nieto-Gonzalez

8

1 reference

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26 March 2020

Macarena Cabrera Serrano

10

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26 March 2020

Xavier Suárez-Calvet

16

1 reference

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26 March 2020

Anne Bigot

18

1 reference

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26 March 2020

Eduard Gallardo

19

1 reference

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26 March 2020

Rafael Fernandez-Chacon

20

1 reference

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26 March 2020

Carmen Paradas

24

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26 March 2020

author name string

Hideyuki Takeuchi

2

1 reference

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26 March 2020

Tom V Lee

3

1 reference

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26 March 2020

Jordi Clarimon

4

1 reference

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26 March 2020

Estela Area-Gómez

6

1 reference

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26 March 2020

Maria C Rivero

9

1 reference

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26 March 2020

Leonardo Gómez-Sánchez

11

1 reference

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26 March 2020

Jose A Martínez-López

12

1 reference

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26 March 2020

Beatriz Estrada

13

1 reference

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26 March 2020

Celedonio Márquez

14

1 reference

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26 March 2020

Yolanda Morgado

15

1 reference

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26 March 2020

Guillermo Pita

17

1 reference

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26 March 2020

Michio Hirano

21

1 reference

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26 March 2020

Robert S Haltiwanger

22

1 reference

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26 March 2020

Hamed Jafar-Nejad

23

1 reference

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26 March 2020

publication date

2 November 2016

1 reference

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26 March 2020

number of pages

21

1 reference

inferred from page(s)

published in

EMBO Molecular Medicine

1 reference

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26 March 2020

volume

8

1 reference

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26 March 2020

page(s)

1289-1309

1 reference

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26 March 2020

issue

11

1 reference

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describes a project that uses

26 March 2020

ImageQuant

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC5090660/fullTextXML

inferred from PubMed Central ID database lookup

ImageJ

1 reference

11 June 2022

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inferred from PubMed Central ID database lookup

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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Mammalian Notch1 is modified with two unusual forms of O-linked glycosylation found on epidermal growth factor-like modules

3 June 2018

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3 June 2018

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1 reference

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MyoD converts primary dermal fibroblasts, chondroblasts, smooth muscle, and retinal pigmented epithelial cells into striated mononucleated myoblasts and multinucleated myotubes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090660

Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090660

Dystroglycanopathy muscles lacking functional glycosylation of alpha-dystroglycan retain regeneration capacity.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090660

Bidirectional Notch activation represses fusion competence in swarming adult Drosophila myoblasts.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090660

hCLP46 regulates U937 cell proliferation via Notch signaling pathway.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090660

The regulation of Notch signaling controls satellite cell activation and cell fate determination in postnatal myogenesis.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090660

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090660

A role for dystroglycan in basement membrane assembly

26 November 2018

1 reference

12 December 2020

Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy

1 reference

12 December 2020

A new trisaccharide sugar chain linked to a serine residue in bovine blood coagulation factors VII and IX

1 reference

12 December 2020

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

1 reference

12 December 2020

Brief report: Blockade of Notch signaling in muscle stem cells causes muscular dystrophic phenotype and impaired muscle regeneration

1 reference

12 December 2020

Identifiers

DOI

10.15252/EMMM.201505815

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27807076%20AND%20SRC:MED&resulttype=core&format=json

26 March 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27807076%20AND%20SRC:MED&resulttype=core&format=json

26 March 2020

2 references