(Q39201234)

9 September 2017

title

Single-stranded nucleic acids promote SAMHD1 complex formation (English)

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9 September 2017

10

Petra Schwille

1 reference

9 September 2017

9

Osvaldo Chara

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9 September 2017

11

Min Ae Lee-Kirsch

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9 September 2017

Victoria Tüngler

1

1 reference

9 September 2017

Wolfgang Staroske

2

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9 September 2017

Barbara Kind

3

1 reference

9 September 2017

Manuela Dobrick

4

1 reference

9 September 2017

Stefanie Kretschmer

5

1 reference

9 September 2017

Franziska Schmidt

6

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9 September 2017

Claudia Krug

7

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9 September 2017

Mike Lorenz

8

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9 September 2017

publication date

31 January 2013

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Journal of Molecular Medicine

9 September 2017

published in

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9 September 2017

volume

91

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9 September 2017

issue

6

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9 September 2017

page(s)

759-770

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HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

9 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Autosomal dominant inheritance of a heterozygous mutation in SAMHD1 causing familial chilblain lupus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Visualizing protein-RNA interactions inside cells by fluorescence resonance energy transfer

21 January 2018

1 reference

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Dual-color fluorescence cross-correlation spectroscopy for multicomponent diffusional analysis in solution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Fluorescence cross-correlation spectroscopy in living cells

21 January 2018

1 reference

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Factors affecting the quantification of biomolecular interactions by fluorescence cross-correlation spectroscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Quantitative comparison of different fluorescent protein couples for fast FRET-FLIM acquisition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Aicardi-Goutieres syndrome gene and HIV-1 restriction factor SAMHD1 is a dGTP-regulated deoxynucleotide triphosphohydrolase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Toll-like receptors in systemic autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

SAMHD1 is a nucleic-acid binding protein that is mislocalized due to aicardi-goutières syndrome-associated mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

HIV/simian immunodeficiency virus (SIV) accessory virulence factor Vpx loads the host cell restriction factor SAMHD1 onto the E3 ubiquitin ligase complex CRL4DCAF1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Evolutionary and functional analyses of the interaction between the myeloid restriction factor SAMHD1 and the lentiviral Vpx protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

The ability of primate lentiviruses to degrade the monocyte restriction factor SAMHD1 preceded the birth of the viral accessory protein Vpx.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Role of SAMHD1 nuclear localization in restriction of HIV-1 and SIVmac

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

A novel DCAF1-binding motif required for Vpx-mediated degradation of nuclear SAMHD1 and Vpr-induced G2 arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Natural DNA precursor pool asymmetry and base sequence context as determinants of replication fidelity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Effects of biological DNA precursor pool asymmetry upon accuracy of DNA replication in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

PCNA directs type 2 RNase H activity on DNA replication and repair substrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Genome instability due to ribonucleotide incorporation into DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

How p53 binds DNA as a tetramer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Structural Synergy and Molecular Crosstalk between Bacterial Helicase Loaders and Replication Initiators

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Homomeric ring assemblies of eukaryotic Sm proteins have affinity for both RNA and DNA. Crystal structure of an oligomeric complex of yeast SmF

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Trex1 prevents cell-intrinsic initiation of autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

DNA precursor metabolism and genomic stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Contribution of SAM and HD domains to retroviral restriction mediated by human SAMHD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-013-0995-3

Aicardi-Goutières syndrome and systemic lupus erythematosus (SLE) in a 12-year-old boy with SAMHD1 mutations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23371319

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00109-013-0995-3

1 reference

9 September 2017

1 reference