(Q42378170)

English

Clinical, immunological and genetic features in eleven Algerian patients with major histocompatibility complex class II expression deficiency

scientific article published on 3 August 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Clinical, immunological and genetic features in eleven Algerian patients with major histocompatibility complex class II expression deficiency (English)

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

0 references

author name string

Réda Djidjik

1

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Nesrine Messaoudani

2

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Azzedine Tahiat

3

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Yanis Meddour

4

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Samia Chaib

5

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Aziz Atek

6

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Mohammed Elmokhtar Khiari

7

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Nafissa Keltoum Benhalla

8

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Leila Smati

9

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Abdelatif Bensenouci

10

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Mourad Baghriche

11

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Mohammed Ghaffor

12

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

publication date

3 August 2012

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Allergy, Asthma & Clinical Immunology

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

8

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

1

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

14

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

copyright license

Creative Commons Attribution 2.0 Generic

3 August 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

Classification of primary immunodeficiency diseases by the International Union of Immunological Societies (IUIS) Expert Committee on Primary Immunodeficiency 2011.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Regulation of MHC class II expression, a unique regulatory system identified by the study of a primary immunodeficiency disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Lymphocyte subsets in healthy children from birth through 18 years of age: the Pediatric AIDS Clinical Trials Group P1009 study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Splicing defect in RFXANK results in a moderate combined immunodeficiency and long-duration clinical course

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Mutation in the class II trans-activator leading to a mild immunodeficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Analysis of ankyrin repeats reveals how a single point mutation in RFXANK results in bare lymphocyte syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHC class II deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Clinical course of patients with major histocompatibility complex class II deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

CIITA is a transcriptional coactivator that is recruited to MHC class II promoters by multiple synergistic interactions with an enhanceosome complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Novel mutations within the RFX-B gene and partial rescue of MHC and related genes through exogenous class II transactivator in RFX-B-deficient cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Genetic and molecular definition of complementation group D in MHC class II deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Regulation of MHC class II expression by interferon-gamma mediated by the transactivator gene CIITA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Two complementation groups account for most cases of inherited MHC class II deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Consanguinity and public health. Algerian study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Congenital immunodeficiencies associated with absence of HLA class II antigens on lymphocytes result from distinct mutations in trans-acting factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Combined immunodeficiency with abnormal expression of MHC class II genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

Combined immunodeficiency with defective expression in major histocompatibility complex class II genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

28 May 2018

[Primary immunodeficiency in Tunisia: study of 152 cases]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

16 August 2018

Consanguinity and public health in Morocco

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3511802

16 August 2018

Primary immunodeficiency diseases. Report of an IUIS Scientific Committee. International Union of Immunological Societies

1 reference

https://pubmed.ncbi.nlm.nih.gov/22863278

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22863278

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Primary immunologic deficiency by deficiency of HLA class II antigens: nine new Tunisian cases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/22863278

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1710-1492-8-14

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

28 October 2017

ResearchGate publication ID

0 references

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