(Q47736443)

English

Deficiency of somatic hypermutation of immunoglobulin G transcripts is a better predictor of severe respiratory tract infections than lack of memory B cells in common variable immunodeficiency

scientific article published in July 2005

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Deficiency of somatic hypermutation of immunoglobulin G transcripts is a better predictor of severe respiratory tract infections than lack of memory B cells in common variable immunodeficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

1 reference

based on heuristic

inferred from title

Torben Barington

7

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

4

object named as

Henrik Permin

0 references

author name string

Lone Schejbel

1

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Hanne Marquart

2

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Vagn Andersen

3

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Henrik Permin

4

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Pernille Andersen

5

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Arne Svejgaard

6

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

publication date

1 July 2005

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

number of pages

12

1 reference

based on heuristic

inferred from page(s)

Journal of Clinical Immunology

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

25

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

4

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

392-403

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Impaired antibody affinity maturation process characterizes a subset of patients with common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-005-5034-X

21 January 2018

Human memory B cells transferred by allogenic bone marrow transplantation contribute significantly to the antibody repertoire of the recipient

1 reference

https://api.crossref.org/works/10.1007%2FS10875-005-5034-X

21 January 2018

Identification of a subset of common variable immunodeficiency patients with impaired B-cell protein tyrosine phosphorylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective surface expression of attractin on T cells in patients with common variable immunodeficiency (CVID)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bias in somatic hypermutation of human VH genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delineation of selective influences shaping the mutated expressed human Ig heavy chain repertoire

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced interleukin-2 (IL-2) production in common variable immunodeficiency is due to a primary abnormality of CD4+ T cell differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective CD2 T cell pathway activation in common variable immunodeficiency (CVID)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discriminating intrinsic and antigen-selected mutational hotspots in immunoglobulin V genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency: clinical and immunological features of 248 patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of thymic output in common variable immunodeficiency patients by evaluation of T cell receptor excision circles

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the heavy chain repertoire of human peripheral B cells using single-cell polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A reporter gene to analyse the hypermutation of immunoglobulin genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

B cell co-receptors regulating T cell-dependent antibody production in common variable immunodeficiency: CD27 pathway defects identify subsets of severely immuno-compromised patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of functional human splenic memory B cells by expression of CD148 and CD27.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human immunoglobulin (Ig)M+IgD+ peripheral blood B cells expressing the CD27 cell surface antigen carry somatically mutated variable region genes: CD27 as a general marker for somatically mutated (memory) B cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary immunodeficiency disorders: antibody deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired up-regulation of CD70 and CD86 in naive (CD27-) B cells from patients with common variable immunodeficiency (CVID).

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immune deficiency: respiratory manifestations, pulmonary function and high-resolution CT scan findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maintenance of serological memory by polyclonal activation of human memory B cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-frequency representation of a single VH gene in the expressed human B cell repertoire

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ICOS deficiency in patients with common variable immunodeficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of memory B cells in patients with common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk among patients with IgA deficiency or common variable immunodeficiency and their relatives: a combined Danish and Swedish study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the human VH gene repertoire. Differential effects of selection and somatic hypermutation on human peripheral CD5(+)/IgM+ and CD5(-)/IgM+ B cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modifying the sequence of an immunoglobulin V-gene alters the resulting pattern of hypermutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human heavy chain Ig V region gene repertoire is biased at all stages of B cell ontogeny, including early pre-B cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germinal center reaction.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible role of IL-2 deficiency for hypogammaglobulinaemia in patients with common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic findings in 95 Finnish patients with common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lymphomas of mucosal-associated lymphoid tissue in common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of CD19(hi)CD21(lo/neg) B cells in common variable immunodeficiency (CVID) patients with autoimmune cytopenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypogammaglobulinaemia: cumulative experience in 49 patients in a tertiary care institution.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of specific antibody response in common variable immunodeficiency (CVID) associated with failure in production of antigen-specific memory T cells. MRC Immunodeficiency Group.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Study of the B cell memory compartment in common variable immunodeficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Respiratory disorders in common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Representation of rearranged VH gene segments in the human adult antibody repertoire

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective recruitment and activation of ZAP-70 in common variable immunodeficiency patients with T cell defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defect of lck in a patient with common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency is associated with defective functions of dendritic cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classification of patients with common variable immunodeficiency by B cell secretion of IgM and IgG in response to anti-IgM and interleukin-2

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting regional mutability in antibody V genes based solely on di- and trinucleotide sequence composition

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

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/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of somatic hypermutation of the antibody light chain is associated with increased frequency of severe respiratory tract infection in common variable immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/16133996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10875-005-5034-X

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 February 2018

http://europepmc.org/abstract/MED/16133996

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q47736443&oldid=2208798589"