(Q39288511)

English

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

scientific article published on 23 April 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

1 reference

based on heuristic

inferred from title

Abdelhamid Barakat

4

object named as

Abdelhamid Barakat

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

author name string

Hamid Naamane

1

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

Ouafaa El Maataoui

2

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

Fatima Ailal

3

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

Siham Bennani

5

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

Jilali Najib

6

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

Mohammed Hassar

7

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

Rachid Saile

8

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

Ahmed Aziz Bousfiha

9

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

publication date

23 April 2010

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

169

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

1069-1074

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

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

1 reference

https://api.crossref.org/works/10.1007%2FS00431-010-1179-6

21 January 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://api.crossref.org/works/10.1007%2FS00431-010-1179-6

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00431-010-1179-6

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

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/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Primary immunodeficiency in Tunisia: study of 152 cases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consanguinity and public health in Morocco

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical course of patients with major histocompatibility complex class II deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of MHC class II genes: lessons from a disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

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/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined immunodeficiency with abnormal expression of MHC class II genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of an MHC class II deficiency patient reveals a novel mutation in the RFX5 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assembly, transport, and function of MHC class II molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consanguinity and public health. Algerian study

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20414676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-010-1179-6

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 September 2017

ResearchGate publication ID

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