Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression
about
SAMHD1-deficient CD14+ cells from individuals with Aicardi-Goutières syndrome are highly susceptible to HIV-1 infectionStructural insight into dGTP-dependent activation of tetrameric SAMHD1 deoxynucleoside triphosphate triphosphohydrolaseA 4-year-old Amish boy with weakness, arthritis, rash, verbal delay, and failure to thriveSAMHD1 restricts HIV-1 infection in resting CD4(+) T cells.Mutations in CECR1 associated with a neutrophil signature in peripheral bloodModulation of LINE-1 and Alu/SVA retrotransposition by Aicardi-Goutières syndrome-related SAMHD1.Structural basis of allosteric activation of sterile α motif and histidine-aspartate domain-containing protein 1 (SAMHD1) by nucleoside triphosphates.Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndromeIntracellular nucleotide levels and the control of retroviral infections.SAMHD1: a novel antiviral factor in intrinsic immunity.Therapies in Aicardi-Goutières syndrome.SAMHD1's protein expression profile in humans.Aggressive CD8(+) epidermotropic cutaneous T-cell lymphoma associated with homozygous mutation in SAMHD1.MDA5-Associated Neuroinflammation and the Singleton-Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum.A SAMHD1 mutation associated with Aicardi-Goutières syndrome uncouples the ability of SAMHD1 to restrict HIV-1 from its ability to downmodulate type I interferon in humans.SAMHD1 Gene Mutations Are Associated with Cerebral Large-Artery Atherosclerosis.Cerebral vasculopathy is a common feature in Aicardi-Goutieres syndrome associated with SAMHD1 mutations.Reply to du Moulin et al.: Cerebral vasculopathy is a common hallmark in individuals with SAMHD1 mutations.LINE-1 Retrotransposons in Healthy and Diseased Human Brain.Dysregulation of the immune system in Aicardi-Goutières syndrome: another example in a TREX1-mutated patient.Aicardi-Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies.SAMHD1: Recurring roles in cell cycle, viral restriction, cancer, and innate immunity.Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.Atypical Aicardi-Goutieres syndrome: is the WRN locus a modifier?
P2860
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P2860
Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Cerebral arterial stenoses and ...... th altered cytokine expression
@ast
Cerebral arterial stenoses and ...... th altered cytokine expression
@en
Cerebral arterial stenoses and ...... th altered cytokine expression
@nl
type
label
Cerebral arterial stenoses and ...... th altered cytokine expression
@ast
Cerebral arterial stenoses and ...... th altered cytokine expression
@en
Cerebral arterial stenoses and ...... th altered cytokine expression
@nl
prefLabel
Cerebral arterial stenoses and ...... th altered cytokine expression
@ast
Cerebral arterial stenoses and ...... th altered cytokine expression
@en
Cerebral arterial stenoses and ...... th altered cytokine expression
@nl
P2093
P2860
P356
P1433
P1476
Cerebral arterial stenoses and ...... th altered cytokine expression
@en
P2093
Christel George
Frank Rutsch
Gerhard Kurlemann
Holger Thiele
Johannes Roth
Katarzyna Barczyk
Marcel du Moulin
Michael Frosch
Wolfram Schwindt
P2860
P304
P356
10.1002/HUMU.21357
P577
2010-11-01T00:00:00Z