(Q40144366)

17 September 2017

title

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

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17 September 2017

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1

Min Ae Lee-Kirsch

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17 September 2017

9

Manfred Gahr

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17 September 2017

Dipanjan Chowdhury

2

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17 September 2017

Scott Harvey

3

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17 September 2017

Maoliang Gong

4

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17 September 2017

Lydia Senenko

5

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17 September 2017

Kerstin Engel

6

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17 September 2017

Christiane Pfeiffer

7

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17 September 2017

Thomas Hollis

8

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17 September 2017

Fred W Perrino

10

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17 September 2017

Judy Lieberman

11

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17 September 2017

Norbert Hubner

12

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17 September 2017

publication date

18 April 2007

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Journal of Molecular Medicine

17 September 2017

published in

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17 September 2017

volume

85

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17 September 2017

issue

5

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17 September 2017

page(s)

531-537

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https://scigraph.springernature.com/pub.10.1007/s00109-007-0199-9

17 September 2017

exact match

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cites work

Chronic polyarthritis caused by mammalian DNA that escapes from degradation in macrophages

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12 December 2020

Systemic Lupus Erythematosus or Aicardi-Goutières Syndrome?

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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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Cerebral thrombotic microangiopathy and antiphospholipid antibodies in Aicardi-Goutieres syndrome--report of two sisters.

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12 December 2020

Granzyme A activates an endoplasmic reticulum-associated caspase-independent nuclease to induce single-stranded DNA nicks

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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

Features of systemic lupus erythematosus in Dnase1-deficient mice

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12 December 2020

Mutation of DNASE1 in people with systemic lupus erythematosus

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12 December 2020

Chilblain lupus erythematosus is associated with antibodies to SSA/Ro

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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.

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12 December 2020

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

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12 December 2020

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

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12 December 2020

The lexicon of cutaneous lupus erythematosus--a review and personal perspective on the nomenclature and classification of the cutaneous manifestations of lupus erythematosus

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12 December 2020

Harveian Lectures on Lupus

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12 December 2020

Familial systemic lupus erythematosus and congenital infection-like syndrome

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12 December 2020

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

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12 December 2020

A human DNA editing enzyme homologous to the Escherichia coli DnaQ/MutD protein

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12 December 2020

Granzyme A induces caspase-independent mitochondrial damage, a required first step for apoptosis

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12 December 2020

Identification and expression of the TREX1 and TREX2 cDNA sequences encoding mammalian 3'-->5' exonucleases

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12 December 2020

The 1982 revised criteria for the classification of systemic lupus erythematosus

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12 December 2020

Phenotypic overlap between infantile systemic lupus erythematosus and Aicardi-Goutières syndrome.

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12 December 2020

Inherited and acquired death receptor defects in human Autoimmune Lymphoproliferative Syndrome

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12 December 2020

Encephalitis among Cree children in northern Quebec

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12 December 2020

Defective B cell tolerance checkpoints in systemic lupus erythematosus

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12 December 2020

The exonuclease TREX1 is in the SET complex and acts in concert with NM23-H1 to degrade DNA during granzyme A-mediated cell death

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12 December 2020

10.1007/S00109-007-0199-9

Identifiers

DOI

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17 September 2017

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