(Q28275605)

Elizabeth Whittaker

46

0 references

Tracy Briggs

Tracy A Briggs

10

0 references

Mary A O'Connell

Mary A O'Connell

52

0 references

Gillian I. Rice

Gillian I Rice

1

0 references

Simon C Lovell

Simon C Lovell

53

0 references

Adeline Vanderver

Adeline Vanderver

42

0 references

Elisa Fazzi

Elisa Fazzi

22

0 references

Jean-Pierre Lin

Jean-Pierre S-M Lin

27

0 references

Yanick J. Crow

Yanick J Crow

54

0 references

Roberta Battini

Roberta Battini

13

0 references

Enrico Bertini

Enrico Bertini

14

0 references

Tiong Y Tan

Tiong Y Tan

0 references

Arvid Heiberg

24

Arvid Heiberg

0 references

Carlos A Bacino

12

Carlos A Bacino

0 references

Corinne De Laet

18

Corinne De Laet

0 references

Àngels García-Cazorla

23

Angels Garcia-Cazorla

0 references

Magnhild Rasmussen

35

Magnhild Rasmussen

0 references

Evangeline Wassmer

45

Evangeline Wassmer

0 references

Isabelle Desguerre

21

Isabelle Desguerre

0 references

Pascale de Lonlay

19

Pascale de Lonlay

0 references

William G van der Merwe

41

William G van der Merwe

0 references

Simona Orcesi

33

Simona Orcesi

0 references

Emma Wakeling

44

Emma L Wakeling

0 references

Gabriella M A Forte

3

Gabriella M A Forte

0 references

Marcin Szynkiewicz

6

Marcin Szynkiewicz

0 references

Ivana Olivieri

32

Ivana Olivieri

0 references

Flore Rozenberg

37

Flore Rozenberg

0 references

Grace Vassallo

43

Grace Vassallo

0 references

author name string

Niamh M Mannion

4

0 references

Sam M Greenwood

5

0 references

Jonathan E Dickerson

7

0 references

Sanjeev S Bhaskar

8

0 references

Massimiliano Zampini

9

0 references

Emma M Jenkinson

11

0 references

Paul A Brogan

15

0 references

Louise A Brueton

16

0 references

Marialuisa Carpanelli

17

0 references

Mireia del Toro

20

0 references

Masakazu Kawaguchi

25

0 references

Ram Kumar

26

0 references

Charles M Lourenco

28

0 references

Alison M Male

29

0 references

Wilson Marques

30

0 references

Cyril Mignot

31

0 references

Prab Prabhakar

34

0 references

Robert A Robinson

36

0 references

Johanna L Schmidt

38

0 references

Katharina Steindl

39

0 references

John H Livingston

47

0 references

Pierre Lebon

48

0 references

Tamio Suzuki

49

0 references

Paul J McLaughlin

50

0 references

Liam P Keegan

SAMHD1 restricts the replication of human immunodeficiency virus type 1 by depleting the intracellular pool of deoxynucleoside triphosphates

51

0 references

language of work or name

English

0 references

publication date

November 2012

0 references

published in

Nature Genetics

0 references

volume

44

0 references

page(s)

1243-8

0 references

issue

11

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Vpx relieves inhibition of HIV-1 infection of macrophages mediated by the SAMHD1 protein

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

SAMHD1 is the dendritic- and myeloid-cell-specific HIV-1 restriction factor counteracted by Vpx

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

The Solution Structure of the ADAR2 dsRBM-RNA Complex Reveals a Sequence-Specific Readout of the Minor Groove

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

KING (Kinemage, Next Generation): a versatile interactive molecular and scientific visualization program

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Editing independent effects of ADARs on the miRNA/siRNA pathways

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Trex1 prevents cell-intrinsic initiation of autoimmunity

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Clinical and molecular phenotype of Aicardi-Goutieres syndrome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Clustal W and Clustal X version 2.0

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Inositol hexakisphosphate is bound in the ADAR2 core and required for RNA editing

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

ADAR1 RNA deaminase limits short interfering RNA efficacy in mammalian cells

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Widespread A-to-I RNA editing of Alu-containing mRNAs in the human transcriptome

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Requirement of dimerization for RNA editing activity of adenosine deaminases acting on RNA

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Crystal structure of the Zalpha domain of the human editing enzyme ADAR1 bound to left-handed Z-DNA

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Human RNA-specific adenosine deaminase ADAR1 transcripts possess alternative exon 1 structures that initiate from different promoters, one constitutively active and the other interferon inducible

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

A Z-DNA binding domain present in the human editing enzyme, double-stranded RNA adenosine deaminase

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Comparative protein modelling by satisfaction of spatial restraints

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

The penultimate rotamer library

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Asparagine and glutamine: using hydrogen atom contacts in the choice of side-chain amide orientation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Systematic identification of abundant A-to-I editing sites in the human transcriptome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Autoimmunity initiates in nonhematopoietic cells and progresses via lymphocytes in an interferon-dependent autoimmune disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

An autoimmune disease prevented by anti-retroviral drugs

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Competition between ADAR and RNAi pathways for an extensive class of RNA targets

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Automated genome-wide visual profiling of cellular proteins involved in HIV infection

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

RNA editing by mammalian ADARs

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Development of Potential Pharmacodynamic and Diagnostic Markers for Anti-IFN-α Monoclonal Antibody Trials in Systemic Lupus Erythematosus

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

ADAR editing in double-stranded UTRs and other noncoding RNA sequences

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Aicardi-Goutières syndrome: an important Mendelian mimic of congenital infection

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

A survey of RNA editing in human brain

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Widespread RNA editing of embedded alu elements in the human transcriptome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

An ADAR that edits transcripts encoding ion channel subunits functions as a dimer.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Visualizing and quantifying molecular goodness-of-fit: small-probe contact dots with explicit hydrogen atoms

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Double-stranded RNAs containing multiple IU pairs are sufficient to suppress interferon induction and apoptosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Type I interferonopathies: a novel set of inborn errors of immunity

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi-Goutières syndrome

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Chilblains as a Diagnostic Sign of Aicardi-Goutières Syndrome

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Dyschromatosis symmetrica hereditaria associated with neurological disorders

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Crystal structure of Staphylococcus aureus tRNA adenosine deaminase TadA in complex with RNA.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4154508

Patients with systemic lupus erythematosus, myositis, rheumatoid arthritis and scleroderma share activation of a common type I interferon pathway

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23001123

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The penultimate rotamer library

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2414

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.2414

1 reference

Dimensions Publication ID

1035891

1000086415

0 references

1035891

1 reference

1 reference

1 reference