Fukutin-related protein resides in the Golgi cisternae of skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction (Q21089946)

From Wikidata

Jump to navigation Jump to search

scientific article published in 2011

Language	Label	Description	Also known as
English	Fukutin-related protein resides in the Golgi cisternae of skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction	scientific article published in 2011

Statements

scholarly article

0 references

Fukutin-related protein resides in the Golgi cisternae of skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction (English)

0 references

Øivind Nilssen

7

author given names

Øivind

author last names

Nilssen

object named as

Øivind Nilssen

1 reference

PubMed publication ID

12 July 2022

Toril Fagerheim

3

author given names

Toril

author last names

Fagerheim

object named as

Toril Fagerheim

1 reference

PubMed publication ID

12 July 2022

4

author given names

Vigdis

author last names

Brox

object named as

Vigdis Brox

1 reference

PubMed publication ID

12 July 2022

author name string

Maisoon Alhamidi

1

author given names

Maisoon

author last names

Alhamidi

1 reference

PubMed publication ID

12 July 2022

Elisabeth Kjeldsen Buvang

2

author given names

Elisabeth

author last names

Kjeldsen Buvang

1 reference

PubMed publication ID

12 July 2022

Sigurd Lindal

5

author given names

Sigurd

author last names

Lindal

1 reference

PubMed publication ID

12 July 2022

Marijke Van Ghelue

6

author given names

Marijke

author last names

Van Ghelue

1 reference

PubMed publication ID

12 July 2022

language of work or name

0 references

publication date

2011

0 references

0 references

6

0 references

8

0 references

e22968

0 references

copyright license

Creative Commons Attribution 4.0 International

23 August 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Mutations alter secretion of fukutin-related protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Subcellular localization of fukutin and fukutin-related protein in muscle cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Toward a functional analysis of the yeast genome through exhaustive two-hybrid screens

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Functional requirements for fukutin-related protein in the Golgi apparatus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Localization of sarcoglycan, neuronal nitric oxide synthase, beta-dystroglycan, and dystrophin molecules in normal skeletal myofiber: triple immunogold labeling electron microscopy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Fukutin-related protein associates with the sarcolemmal dystrophin-glycoprotein complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Sub-cellular localisation of fukutin related protein in different cell lines and in the muscle of patients with MDC1C and LGMD2I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

19 March 2017

Membrane organization of the dystrophin-glycoprotein complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

7 April 2017

Golgi N-glycosyltransferases form both homo- and heterodimeric enzyme complexes in live cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

The genetic and molecular basis of muscular dystrophy: roles of cell-matrix linkage in the pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Mechanisms of disease: congenital muscular dystrophies-glycosylation takes center stage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Dystroglycan: from biosynthesis to pathogenesis of human disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

The roles of enzyme localisation and complex formation in glycan assembly within the Golgi apparatus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Organization of Golgi glycosyltransferases in membranes: complexity via complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Protein glycosylation in disease: new insights into the congenital muscular dystrophies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Structural and functional features of glycosyltransferases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Dystroglycan inside and out.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Ras-Raf interaction: two-hybrid analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

12 September 2017

Fukutin-related protein localizes to the Golgi apparatus and mutations lead to mislocalization in muscle in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

27 September 2017

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3160285

30 May 2018

Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022968

21 January 2018

How do nematodes transfer phosphorylcholine to carbohydrates?

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022968

21 January 2018

Fukutin-related protein mutations that cause congenital muscular dystrophy result in ER-retention of the mutant protein in cultured cells.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022968

21 January 2018

Mutated fukutin-related protein (FKRP) localises as wild type in differentiated muscle cells.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022968

21 January 2018

Different glycosyltransferases are differentially processed for secretion, dimerization, and autoglycosylation.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022968

21 January 2018

Co-localization of dystrophin and beta-dystroglycan demonstrated in en face view by double immunogold labeling of freeze-fractured skeletal muscle

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022968

21 January 2018

Targeting of proteins to the Golgi apparatus

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022968

21 January 2018

Application of cryoultramicrotomy to immunocytochemistry

1 reference

https://pubmed.ncbi.nlm.nih.gov/21886772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein disulfide isomerase and newly synthesized procollagen chains form higher-order structures in the lumen of the endoplasmic reticulum

1 reference

https://pubmed.ncbi.nlm.nih.gov/21886772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fukutin protein family--predicted enzymes modifying cell-surface molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/21886772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The organization of the Golgi complex and microtubules in skeletal muscle is fiber type-dependent.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21886772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

1 reference

https://pubmed.ncbi.nlm.nih.gov/21886772

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0022968

0 references

2011PLoSO...622968A

0 references

release_nslr2zn67zbr3bnxfbpksnm55y

0 references

PMC publication ID

0 references

PubMed publication ID

0 references

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=Q21089946&oldid=2252190266"