(Q28279175)

English

NFKB2 mutation in common variable immunodeficiency and isolated adrenocorticotropic hormone deficiency: A case report and review of literature

scientific article

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scholarly article

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15 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

17 November 2019

20 November 2019

28 November 2019

11 December 2019

19 December 2019

22 December 2019

6 November 2020

21 June 2021

31 July 2022

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NFKB2 mutation in common variable immunodeficiency and isolated adrenocorticotropic hormone deficiency: A case report and review of literature (English)

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adrenocorticotropic hormone deficiency

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common variable immunodeficiency

13 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

17 November 2019

20 November 2019

28 November 2019

11 December 2019

19 December 2019

22 December 2019

6 November 2020

endocrine system disease

14 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

17 November 2019

20 November 2019

28 November 2019

11 December 2019

19 December 2019

22 December 2019

6 November 2020

21 June 2021

genetic disease

12 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

17 November 2019

20 November 2019

28 November 2019

11 December 2019

19 December 2019

22 December 2019

13 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

17 November 2019

20 November 2019

28 November 2019

11 December 2019

19 December 2019

22 December 2019

6 November 2020

1 reference

2 August 2019

genetic variation

1 reference

14 September 2019

1 reference

17 November 2019

1 reference

20 November 2019

transport protein

1 reference

28 November 2019

DNA-binding protein

1 reference

11 December 2019

nerve tissue protein

1 reference

19 December 2019

nuclear protein

1 reference

19 December 2019

transcription factor

1 reference

22 December 2019

1 reference

6 November 2020

author name string

Chuan Shi

1

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Fen Wang

2

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Anli Tong

3

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Xiao-Qian Zhang

4

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Hong-Mei Song

5

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Zheng-Yin Liu

6

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Wei Lyu

7

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Yue-Hua Liu

8

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Wei-Bo Xia

9

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language of work or name

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publication date

October 2016

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1 October 2016

15 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

17 November 2019

20 November 2019

28 November 2019

11 December 2019

19 December 2019

22 December 2019

6 November 2020

21 June 2021

31 July 2022

15 references

24 March 2019

22 April 2019

20 June 2019

30 June 2019

2 August 2019

14 September 2019

17 November 2019

20 November 2019

28 November 2019

11 December 2019

19 December 2019

22 December 2019

6 November 2020

21 June 2021

31 July 2022

95

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40

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e5081

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copyright license

Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

15 references

Europe PubMed Central

24 March 2019

Europe PubMed Central

22 April 2019

Europe PubMed Central

20 June 2019

Europe PubMed Central

30 June 2019

Europe PubMed Central

2 August 2019

Europe PubMed Central

14 September 2019

Europe PubMed Central

17 November 2019

Europe PubMed Central

20 November 2019

Europe PubMed Central

28 November 2019

Europe PubMed Central

11 December 2019

Europe PubMed Central

19 December 2019

Europe PubMed Central

22 December 2019

Europe PubMed Central

6 November 2020

Europe PubMed Central

21 June 2021

Europe PubMed Central

31 July 2022

on focus list of Wikimedia project

0 references

Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

20 March 2017

Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

20 March 2017

Aire and T cell development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

20 March 2017

Introduction to NF-kappaB: players, pathways, perspectives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

20 March 2017

NF-kappaB-inducing kinase regulates the processing of NF-kappaB2 p100

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

20 March 2017

A highly conserved NF-κB-responsive enhancer is critical for thymic expression of Aire in mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

NF-κB in immunobiology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

Non-canonical NF-κB signaling pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

NKp30 ligation induces rapid activation of the canonical NF-kappaB pathway in NK cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

Isolated corticotrophin deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

NF-kappaB2 is required for the establishment of central tolerance through an Aire-dependent pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

Mechanism of processing of the NF-kappa B2 p100 precursor: identification of the specific polyubiquitin chain-anchoring lysine residue and analysis of the role of NEDD8-modification on the SCF(beta-TrCP) ubiquitin ligase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

A novel enhanced green fluorescent protein (EGFP)-K562 flow cytometric method for measuring natural killer (NK) cell cytotoxic activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

29 September 2017

[Application of measuring human peripheral NK cell activity with flow cytometry in diagnosis for hemophagocytic lymphohistiocytosis].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

2 June 2018

Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

27 November 2018

Combined immune deficiency in a patient with a novel NFKB2 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

27 November 2018

Novel NFKB2 mutation in early-onset CVID.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

27 November 2018

A novel mutation in the Nfkb2 gene generates an NF-kappa B2 "super repressor".

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

27 November 2018

beta-TrCP binding and processing of NF-kappaB2/p100 involve its phosphorylation at serines 866 and 870.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5059085

27 November 2018

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