(Q35883296)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22509093%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

title

NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome (English)

1 reference

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29 January 2020

author name string

Haotian Xiang

1

1 reference

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29 January 2020

Ting Zhang

2

1 reference

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29 January 2020

Mengping Chen

3

1 reference

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29 January 2020

Xiaomin Zhou

4

1 reference

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29 January 2020

Zhen Li

5

1 reference

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29 January 2020

Naihong Yan

6

1 reference

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29 January 2020

Shiguang Li

7

1 reference

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29 January 2020

Yu Han

8

1 reference

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29 January 2020

Qiyong Gong

9

1 reference

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29 January 2020

Xuyang Liu

10

1 reference

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29 January 2020

publication date

9 March 2012

1 reference

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29 January 2020

1 reference

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29 January 2020

volume

18

1 reference

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29 January 2020

page(s)

617-623

1 reference

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Sinus of valsalva aneurysm in Blau's syndrome

29 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Clinical and genetic aspects of Blau syndrome: a 25-year follow-up of one family and a literature review

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Primer: inflammasomes and interleukin 1beta in inflammatory disorders

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Nod-like receptors in innate immunity and inflammatory diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Role of Nods in bacterial infection

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Blau syndrome associated with a CARD15/NOD2 mutation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Altered host:pathogen interactions conferred by the Blau syndrome mutation of NOD2

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

A role for Erbin in the regulation of Nod2-dependent NF-kappaB signaling

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Ocular manifestations in Blau syndrome associated with a CARD15/Nod2 mutation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

NODs: intracellular proteins involved in inflammation and apoptosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

CARD15 mutations in Blau syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Blau syndrome of granulomatous arthritis, iritis, and skin rash: a new family and review of the literature

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Familial granulomatous synovitis, uveitis, and cranial neuropathies.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Mycobacterium paratuberculosis and autism: is this a trigger?

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Leg ulcers: a new symptom of Blau syndrome?

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

A new CARD15 mutation in Blau syndrome

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

CARD15 gene mutations in sarcoidosis.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Familial granulomatous arthritis, iritis, and rash

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3324354

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome

24 September 2018

1 reference

12 December 2020

Mutation screening of the CARD15 gene in sarcoidosis

1 reference

12 December 2020

Pediatric granulomatous arthritis: an international registry

1 reference

12 December 2020

Interstitial pneumonitis in Blau syndrome with documented mutation in CARD15

1 reference

12 December 2020

Investigation of NOD1/CARD4 variation in inflammatory bowel disease using a haplotype-tagging strategy

1 reference

12 December 2020

Central nervous system involvement in Blau syndrome: a new feature of the syndrome?

1 reference

12 December 2020

A novel mutation in the NOD2 gene associated with Blau syndrome: a Norwegian family with four affected members

1 reference

12 December 2020

Blau syndrome-associated mutations in exon 4 of the caspase activating recruitment domain 15 (CARD 15) gene are not found in ethnic Danes with sarcoidosis

1 reference

12 December 2020

1 reference

12 December 2020

NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis

1 reference

12 December 2020

Blau syndrome: a new kindred

1 reference

12 December 2020

Sarcoid arthritis in children

1 reference

12 December 2020

Autosomal dominant granulomatous arthritis, uveitis, skin rash, and synovial cysts

1 reference

12 December 2020

Liver involvement in familial granulomatous arthritis (Blau syndrome)

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22509093%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

PubMed publication ID

22509093

1 reference