(Q40271553)

19 September 2017

Genes required for B cell development (English)

1 reference

19 September 2017

Mary Ellen Conley

1

1 reference

PMC publication ID

281652

19 September 2017

language of work or name

English

0 references

publication date

1 December 2003

1 reference

Journal of Clinical Investigation

19 September 2017

1 reference

19 September 2017

112

1 reference

19 September 2017

11

1 reference

19 September 2017

1636-1638

1 reference

A congenital mutation of the novel gene LRRC8 causes agammaglobulinemia in humans

19 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

B-cell commitment: deciding on the players

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Clinical and molecular analysis of patients with defects in micro heavy chain gene.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouse

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

An essential role for BLNK in human B cell development

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Mutations in Igalpha (CD79a) result in a complete block in B-cell development

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Mutations in btk in patients with presumed X-linked agammaglobulinemia

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Mutations in the human lambda5/14.1 gene result in B cell deficiency and agammaglobulinemia

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Early B-cell development in the mouse: insights from mutations introduced by gene targeting

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Clonal selection and learning in the antibody system

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Microphthalmia, facial anomalies, microcephaly, thumb and hallux hypoplasia, and agammaglobulinemia

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

A syndrome involving intrauterine growth retardation, microcephaly, cerebellar hypoplasia, B lymphocyte deficiency, and progressive pancytopenia

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Expression of Bruton's agammaglobulinemia tyrosine kinase gene, BTK, is selectively down-regulated in T lymphocytes and plasma cells.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Phenotypic features and proliferative activity of B cell progenitors in X-linked agammaglobulinemia

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Growth failure, intracranial calcifications, acquired pancytopenia, and unusual humoral immunodeficiency: a genetic syndrome?

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

A role for Bruton's tyrosine kinase (Btk) in platelet activation by collagen.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Expression of Bruton's tyrosine kinase protein within the B cell lineage

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=281652

Hypogammaglobulinemia and reduced numbers of B-cells in children with myelodysplastic syndrome

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14660738

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical findings leading to the diagnosis of X-linked agammaglobulinemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14660738

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic basis of abnormal B cell development

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/14660738

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI20408

1 reference

19 September 2017

1 reference

PMC publication ID

281652

19 September 2017

PubMed publication ID

14660738

1 reference

PMC publication ID

281652