(Q38955663)

7 September 2017

1 reference

title

NLRP12 autoinflammatory disease: a Chinese case series and literature review (English)

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7 September 2017

Min Shen

1

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7 September 2017

Lin Tang

2

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7 September 2017

Xiaochun Shi

3

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7 September 2017

Xiaofeng Zeng

4

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7 September 2017

Qingping Yao

5

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7 September 2017

language of work or name

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16 September 2016

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7 September 2017

published in

Clinical Rheumatology

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7 September 2017

volume

36

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7 September 2017

issue

7

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7 September 2017

page(s)

1661-1667

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Update on genetics and pathogenesis of autoinflammatory diseases: the last 2 years

7 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Autoinflammatory disease reloaded: a clinical perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Mutations in NALP12 cause hereditary periodic fever syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

The fresco of autoinflammatory diseases from the pediatric perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

An international registry on autoinflammatory diseases: the Eurofever experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Altered cytokine profiles of mononuclear cells after stimulation in a patient with Blau syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Adult autoinflammatory disease frequency and our diagnostic experience in an adult autoinflammatory clinic

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Identification of a Novel NLRP12 Nonsense Mutation (Trp408X) in the Extremely Rare Disease FCAS by Exome Sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Clinical presentation and pathogenesis of cold-induced autoinflammatory disease in a family with recurrence of an NLRP12 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

The NLR gene family: a standard nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

The NACHT family - a new group of predicted NTPases implicated in apoptosis and MHC transcription activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Cutting edge: Monarch-1: a pyrin/nucleotide-binding domain/leucine-rich repeat protein that controls classical and nonclassical MHC class I genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

The CATERPILLER protein monarch-1 is an antagonist of toll-like receptor-, tumor necrosis factor alpha-, and Mycobacterium tuberculosis-induced pro-inflammatory signals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Monarch-1 suppresses non-canonical NF-kappaB activation and p52-dependent chemokine expression in monocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

Familial atypical cold urticaria: description of a new hereditary disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

CAPS--pathogenesis, presentation and treatment of an autoinflammatory disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10067-016-3410-Y

NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome.

21 January 2018

1 reference

12 December 2020

Rare NLRP12 variants associated with the NLRP12-autoinflammatory disorder phenotype: an Italian case series.

1 reference

12 December 2020

Role of interleukin-1β in NLRP12-associated autoinflammatory disorders and resistance to anti-interleukin-1 therapy

1 reference

12 December 2020

F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls

1 reference

12 December 2020

10.1007/S10067-016-3410-Y

Identifiers

DOI

1 reference

7 September 2017

1 reference