(Q34272909)

1 August 2017

Mutations in CECR1 associated with a neutrophil signature in peripheral blood (English)

1 reference

Sophie Collardeau-Frachon

1 August 2017

12

Sophie Collardeau-Frachon

1 reference

1 August 2017

Paul R Kasher

7

0 references

Julie Demaret

Julie Demaret

10

0 references

Alexandre Belot

Alexandre Belot

1

0 references

Yanick J. Crow

Yanick J Crow

18

0 references

Anne-Laure Mathieu

Anne-Laure Mathieu

8

0 references

Thierry Walzer

Thierry Walzer

15

0 references

Laurent Derex

14

Laurent Derex

1 reference

1 August 2017

4

Jean-Christophe Lega

1 reference

1 August 2017

17

Isabelle Durieu

1 reference

1 August 2017

Evangeline Wassmer

2

1 reference

1 August 2017

Marinka Twilt

3

1 reference

1 August 2017

Leo Ah Zeef

5

1 reference

1 August 2017

Anthony Oojageer

6

1 reference

1 August 2017

Christophe Malcus

9

1 reference

1 August 2017

Nicole Fabien

11

1 reference

1 August 2017

Laura Mechtouff

13

1 reference

1 August 2017

Gillian I Rice

16

1 reference

1 August 2017

24 September 2014

1 reference

Pediatric Rheumatology Online Journal

1 August 2017

1 reference

1 August 2017

12

1 reference

1 August 2017

44

1 reference

describes a project that uses

1 August 2017

DESeq2

DESeq

1 reference

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

exact match

https://scigraph.springernature.com/pub.10.1186/1546-0096-12-44

0 references

cites work

Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Early-onset stroke and vasculopathy associated with mutations in ADA2

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

β2 integrin-mediated cell-cell contact transfers active myeloperoxidase from neutrophils to endothelial cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Purinergic signaling during inflammation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Cerebral vasculopathy is a common feature in Aicardi-Goutieres syndrome associated with SAMHD1 mutations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Differential expression analysis for sequence count data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Clinical and molecular phenotype of Aicardi-Goutieres syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Endothelial catabolism of extracellular adenosine during hypoxia: the role of surface adenosine deaminase and CD26

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

The adenosine/neutrophil paradox resolved: human neutrophils possess both A1 and A2 receptors that promote chemotaxis and inhibit O2 generation, respectively

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4181355

Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1546-0096-12-44

Novel adenosine deaminase 2 mutations in a child with a fatal vasculopathy

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25278816

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1546-0096-12-44

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference

1 August 2017

1 reference