SAMHD1 is a nucleic-acid binding protein that is mislocalized due to aicardi-goutières syndrome-associated mutations (Q24310328)

GOA release 2020-03-11

RNA binding

1 reference

GOA release 2020-03-11

author

Giulio Superti-Furga

6

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Tilmann Bürckstümmer

7

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Gillian I. Rice

object named as

Gillian I Rice

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Yanick J. Crow

object named as

Yanick J Crow

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Keiryn L Bennett

4

object named as

Keiryn L Bennett

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author name string

Adriana Goncalves

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Evren Karayel

The HD domain defines a new superfamily of metal-dependent phosphohydrolases

2

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language of work or name

English

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publication date

July 2012

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published in

Human Mutation

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volume

33

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page(s)

1116-22

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issue

7

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cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22087

The RNA-binding SAM domain of Smaug defines a new family of post-transcriptional regulators

21 January 2018

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An autoimmune disease prevented by anti-retroviral drugs

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An orthogonal proteomic-genomic screen identifies AIM2 as a cytoplasmic DNA sensor for the inflammasome

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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Aicardi-Goutieres syndrome and related phenotypes: linking nucleic acid metabolism with autoimmunity

21 January 2018

1 reference

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Familial Aicardi-Goutières syndrome due toSAMHD1mutations is associated with chronic arthropathy and contractures

21 January 2018

1 reference

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HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

21 January 2018

1 reference

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Adenovirus infection triggers a rapid, MyD88-regulated transcriptome response critical to acute-phase and adaptive immune responses in vivo

21 January 2018

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Intracellular DNA recognition

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

21 January 2018

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The TLR-independent DNA recognition pathway in murine macrophages: Ligand features and molecular signature

21 January 2018

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SAM domains: uniform structure, diversity of function

21 January 2018

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Polymerization of the SAM domain of TEL in leukemogenesis and transcriptional repression

21 January 2018

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Structural organization of a Sex-comb-on-midleg/polyhomeotic copolymer

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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Identification of human homologue of mouse IFN-gamma induced protein from human dendritic cells

21 January 2018

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Dendritic cell-derived interferon-gamma-induced protein mediates tumor necrosis factor-alpha stimulation of human lung fibroblasts

21 January 2018

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Deoxyribonuclease IV: a new exonuclease from mammalian tissues

21 January 2018

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Shape-specific recognition in the structure of the Vts1p SAM domain with RNA.

21 January 2018

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IFIT1 is an antiviral protein that recognizes 5'-triphosphate RNA

21 January 2018

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

21 January 2018

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Virus infection switches TLR-3-positive human neurons to become strong producers of beta interferon

21 January 2018

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21 January 2018

The many faces of SAM

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Trex1 prevents cell-intrinsic initiation of autoimmunity

21 January 2018

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Trex1 exonuclease degrades ssDNA to prevent chronic checkpoint activation and autoimmune disease

21 January 2018

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Type I interferon in systemic lupus erythematosus.

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/HUMU.22087

1 reference

Consolidated OpenCitations Corpus – April 2017

1230313

1230313

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference