Deregulated type I IFN response in TREX1-associated familial chilblain lupus (Q44067890)

29 November 2017

title

Deregulated type I IFN response in TREX1-associated familial chilblain lupus (English)

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29 November 2017

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6

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8 June 2020

Rayk Behrendt

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8 June 2020

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Min Ae Lee-Kirsch

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8 June 2020

author name string

Katrin Peschke

1

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8 June 2020

Franziska Friebe

2

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8 June 2020

Nick Zimmermann

3

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8 June 2020

Tom Wahlicht

4

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8 June 2020

Tina Schumann

5

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8 June 2020

Nicole Berndt

7

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8 June 2020

Hella Luksch

8

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8 June 2020

Axel Roers

11

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8 June 2020

Claudia Günther

12

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8 June 2020

language of work or name

English

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publication date

22 November 2013

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Journal of Investigative Dermatology

29 November 2017

published in

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8 June 2020

volume

134

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8 June 2020

issue

5

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8 June 2020

page(s)

1456-1459

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Trex1 prevents cell-intrinsic initiation of autoimmunity

8 June 2020

cites work

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12 December 2020

Aicardi-Goutières syndrome: a model disease for systemic autoimmunity

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12 December 2020

A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

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12 December 2020

Enhanced type I interferon signalling promotes Th1-biased inflammation in cutaneous lupus erythematosus

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12 December 2020

Gene-targeted mice lacking the Trex1 (DNase III) 3'-->5' DNA exonuclease develop inflammatory myocarditis

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12 December 2020

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

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12 December 2020

Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p.

1 reference

12 December 2020

Excision of 3' termini by the Trex1 and TREX2 3'-->5' exonucleases. Characterization of the recombinant proteins

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

Familial chilblain lupus--a monogenic form of cutaneous lupus erythematosus due to a heterozygous mutation in TREX1.

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

Identifiers

DOI

10.1038/JID.2013.496

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8 June 2020

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