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Article

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

14 Jun 2009

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Share to Inflammasome and immune disorders
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Share to Systemic Lupus Erythematosus Research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19525956
DOI: 10.1038/ng.373

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Related research

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Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune responsePMID 19525956Read ↗

Aicardi-Goutières Syndrome caused by SAMHD1 mutation: Pathogenesis and Beyond.Semantic proximity Read ↗

A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi–Goutiéres syndrome associated with mtDNA deletionsSemantic proximity Read ↗

SAMHD1 Mutations Are Also Responsible for Aicardi-Goutières in the Cree Population.Semantic proximity Read ↗

Aicardi-Goutières Syndrome Is Caused by IFIH1 MutationsSemantic proximity Read ↗

SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damageSemantic proximity Read ↗

Aicardi–Goutieres syndrome: from patients to genes and beyondSemantic proximity Read ↗

SAMHD1 Functions and Human Diseases.Semantic proximity Read ↗

MicroRNA-181 contributes to downregulation of SAMHD1 expression in CD4+ T-cells derived from Sèzary syndrome patientsSemantic proximity Read ↗

Familial chilblain lupus in a child with heterozygous mutation in SAMHD1 and normal interferon signature.Semantic proximity Read ↗

Aicardi-Goutières syndrome: A monogenic type I interferonopathy.Semantic proximity Read ↗

Cerebral vasculopathy is a common feature in Aicardi–Goutières syndrome associated with <i>SAMHD1</i> mutationsSemantic proximity Read ↗

One mutation, divergent journeys: expanding the clinical spectrum of homozygous SAMHD1 deficiency in childhood.Semantic proximity Read ↗

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