(Q37572562)

21 August 2017

Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry (English)

1 reference

21 August 2017

0 references

0 references

2

Matthijs Raaben

1 reference

21 August 2017

9

Haluk Topaloglu

1 reference

21 August 2017

14

Hans van Bokhoven

1 reference

21 August 2017

Lucas T Jae

1

1 reference

21 August 2017

Moniek Riemersma

3

1 reference

21 August 2017

Ellen van Beusekom

4

1 reference

21 August 2017

Vincent A Blomen

5

1 reference

21 August 2017

Arno Velds

6

1 reference

21 August 2017

Ron M Kerkhoven

7

1 reference

21 August 2017

Jan E Carette

8

1 reference

21 August 2017

Peter Meinecke

10

1 reference

21 August 2017

Marja W Wessels

11

1 reference

21 August 2017

Dirk J Lefeber

12

1 reference

21 August 2017

Sean P Whelan

13

1 reference

21 August 2017

Thijn R Brummelkamp

15

1 reference

21 August 2017

language of work or name

English

0 references

publication date

21 March 2013

1 reference

21 August 2017

1 reference

21 August 2017

340

1 reference

21 August 2017

479-483

1 reference

21 August 2017

6131

1 reference

Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome.

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

TMEM165 deficiency causes a congenital disorder of glycosylation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

A transcription activator-like effector toolbox for genome engineering

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Ebola virus entry requires the cholesterol transporter Niemann-Pick C1

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Congenital hydrocephalus in genetically engineered mice

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Global gene disruption in human cells to assign genes to phenotypes by deep sequencing

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Haploid genetic screens in human cells identify host factors used by pathogens

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

A novel tandem reporter quantifies RNA polymerase II termination in mammalian cells

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Genome-wide detection and characterization of positive selection in human populations

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Lectin-resistant CHO glycosylation mutants

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Posttranslational modification of alpha-dystroglycan, the cellular receptor for arenaviruses, by the glycosyltransferase LARGE is critical for virus binding.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Expression cloning of the Golgi CMP-sialic acid transporter

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Efficient recovery of infectious vesicular stomatitis virus entirely from cDNA clones

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Dystroglycanopathies: coming into focus

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Enhanced laminin binding by alpha-dystroglycan after enzymatic deglycosylation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

A forward genetic strategy reveals destabilizing mutations in the Ebolavirus glycoprotein that alter its protease dependence during cell entry

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

Cancer gene discovery in solid tumours using transposon-based somatic mutagenesis in the mouse

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

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

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3919138

25 June 2018

Identifiers

DOI

10.1126/SCIENCE.1233675

1 reference

release_lc5d5pwajbefvnsuq3pwifjitq

21 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lc5d5pwajbefvnsuq3pwifjitq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

21 August 2017

1 reference