(Q35604712)

English

NLRP7, a nucleotide oligomerization domain-like receptor protein, is required for normal cytokine secretion and co-localizes with Golgi and the microtubule-organizing center

scientific article published on 24 October 2011

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scholarly article

1 reference

Europe PubMed Central

9 August 2017

NLRP7, a nucleotide oligomerization domain-like receptor protein, is required for normal cytokine secretion and co-localizes with Golgi and the microtubule-organizing center (English)

1 reference

Europe PubMed Central

9 August 2017

author name string

Christiane Messaed

1

1 reference

Europe PubMed Central

9 August 2017

Elie Akoury

2

1 reference

Europe PubMed Central

9 August 2017

Ugljesa Djuric

3

1 reference

Europe PubMed Central

9 August 2017

Jibin Zeng

4

1 reference

Europe PubMed Central

9 August 2017

Maya Saleh

5

1 reference

Europe PubMed Central

9 August 2017

Lucy Gilbert

6

1 reference

Europe PubMed Central

9 August 2017

Muhieddine Seoud

7

1 reference

Europe PubMed Central

9 August 2017

Salman Qureshi

8

1 reference

Europe PubMed Central

9 August 2017

Rima Slim

9

1 reference

Europe PubMed Central

9 August 2017

language of work or name

0 references

publication date

24 October 2011

1 reference

Europe PubMed Central

9 August 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

9 August 2017

286

1 reference

Europe PubMed Central

9 August 2017

50

1 reference

Europe PubMed Central

9 August 2017

43313-43323

1 reference

Europe PubMed Central

9 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3234874/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Gestational trophoblastic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Autoinflammatory disease reloaded: a clinical perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Functional consequences of a germline mutation in the leucine-rich repeat domain of NLRP3 identified in an atypical autoinflammatory disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Role of Filia, a maternal effect gene, in maintaining euploidy during cleavage-stage mouse embryogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

The infevers autoinflammatory mutation online registry: update with new genes and functions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Women heterozygous for NALP7/NLRP7 mutations are at risk for reproductive wastage: report of two novel mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Histone deacetylase inhibitors prevent exocytosis of interleukin-1beta-containing secretory lysosomes: role of microtubules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

PYPAF3, a PYRIN-containing APAF-1-like protein, is a feedback regulator of caspase-1-dependent interleukin-1beta secretion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Oncogenic role of NALP7 in testicular seminomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

NALP3 forms an IL-1beta-processing inflammasome with increased activity in Muckle-Wells autoinflammatory disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Epidemiology and aetiology of gestational trophoblastic diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

NALPs: a novel protein family involved in inflammation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Mater, a maternal effect gene required for early embryonic development in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Preimplantation diagnosis and recurrent hydatidiform mole

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Immunologic studies in patients with trophoblastic neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

12 July 2018

Homozygous NLRP7 mutations in a Moroccan woman with recurrent reproductive failure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.306191

21 January 2018

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.306191

21 January 2018

Genetic and epigenetic analysis of recurrent hydatidiform mole.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3234874

25 September 2018

Expression of NLRP7 (PYPAF3, NALP7) protein in endometrial cancer tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/22025618

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of NLRP7 mutations in French patients with recurrent hydatidiform mole

1 reference

https://pubmed.ncbi.nlm.nih.gov/22025618

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution

1 reference

https://pubmed.ncbi.nlm.nih.gov/22025618

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

1 reference

https://pubmed.ncbi.nlm.nih.gov/22025618

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunological status of trophoblastic neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22025618

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunological parameters in gestational trophoblastic neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22025618

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition (NLRP3 V198M mutation) for IL-1-mediated inflammation in a patient with Schnitzler syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22025618

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M111.306191

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

9 August 2017

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