Primary T-cell immunodeficiencies
Copyright policy )Primary T-cell immunodeficiencies
The phenotypes of many primary T-cell immunodeficiencies have been described, including diseases associated with defective T-cell differentiation and/or activation. Recently, genotypes have been defined for some of them, such as X-linked severe combined immunodeficiency and CD3 deficiencies (or hyper IgM syndrome). Phenotype/genotype correlation studies open a fruitful way to a better understanding of primary T-cell immunodeficiencies.
X Chromosome, CD3 Complex, DNA Repair, Adenosine Deaminase, Genetic Linkage, T-Lymphocytes, Histocompatibility Antigens Class II, Immunologic Deficiency Syndromes, Lymphocyte Activation, Wiskott-Aldrich Syndrome, DiGeorge Syndrome, Humans, Severe Combined Immunodeficiency
X Chromosome, CD3 Complex, DNA Repair, Adenosine Deaminase, Genetic Linkage, T-Lymphocytes, Histocompatibility Antigens Class II, Immunologic Deficiency Syndromes, Lymphocyte Activation, Wiskott-Aldrich Syndrome, DiGeorge Syndrome, Humans, Severe Combined Immunodeficiency
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).40 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Average influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
Citations provided by BIP!Popularity provided by BIP!