Defective expression of p56lck in an infant with severe combined immunodeficiency.
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Diagnosis of severe combined immunodeficiencyGenetics of SCIDGenetics of inflammatory bowel disease from multifactorial to monogenic formsAutoimmunity in primary T-cell immunodeficiencies.Downregulation of p56(lck) tyrosine kinase activity in T cells of squirrel monkeys (Saimiri sciureus) correlates with the nontransforming and apathogenic properties of herpesvirus saimiri in its natural hostSevere combined immunodeficiency--molecular pathogenesis and diagnosis.Combined immunodeficiency evolving into predominant CD4+ lymphopenia caused by somatic chimerism in JAK3Progress towards the development of SH2 domain inhibitors.Molecular aspects of primary immunodeficiencies: lessons from cytokine and other signaling pathways.A mutation in the human Uncoordinated 119 gene impairs TCR signaling and is associated with CD4 lymphopenia.PBMC transcriptome profiles identifies potential candidate genes and functional networks controlling the innate and the adaptive immune response to PRRSV vaccine in Pietrain pigPartial defects of T-cell development associated with poor T-cell function.The genetic basis of severe combined immunodeficiency and its variants.T cell Receptor Signal Transduction in T lymphocytes.Predictive Model of Lymphocyte-Specific Protein Tyrosine Kinase (LCK) AutoregulationDivide, Conquer, and Sense: CD8+CD28- T Cells in Perspective.FOXN1 deficient nude severe combined immunodeficiency.Update on lymphocyte specific kinase inhibitors: a patent survey.Consequences of a mutation in the UNC119 gene for T cell function in idiopathic CD4 lymphopenia.Targeting kinases for the treatment of inflammatory diseases.New genetic discoveries and primary immune deficiencies.The role of membrane rafts in Lck transport, regulation and signalling in T-cells.Severe combined immunodeficiency--an update.Aberrant HS1 molecule in a patient with systemic lupus erythematosus.Binding is not enough: flexibility is needed for photocrosslinking of Lck kinase by benzophenone photoligands.Defective dendritic cell maturation in a child with nucleotide excision repair deficiency and CD4 lymphopenia.Laboratory technology for population-based screening for severe combined immunodeficiency in neonates: the winner is T-cell receptor excision circles.Atypical X-linked SCID phenotype associated with growth hormone hyporesponsiveness.Defective p56Lck activity in T cells from an adult patient with idiopathic CD4+ lymphocytopenia.Expanding genetics and phenotypic spectrum of epidermodysplasia verruciformis.
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P2860
Defective expression of p56lck in an infant with severe combined immunodeficiency.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 1998
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Defective expression of p56lck in an infant with severe combined immunodeficiency.
@en
Defective expression of p56lck in an infant with severe combined immunodeficiency.
@nl
type
label
Defective expression of p56lck in an infant with severe combined immunodeficiency.
@en
Defective expression of p56lck in an infant with severe combined immunodeficiency.
@nl
prefLabel
Defective expression of p56lck in an infant with severe combined immunodeficiency.
@en
Defective expression of p56lck in an infant with severe combined immunodeficiency.
@nl
P2093
P2860
P356
P1476
Defective expression of p56lck in an infant with severe combined immunodeficiency.
@en
P2093
B C Schutte
C Hollenback
F D Goldman
Z K Ballas
P2860
P304
P356
10.1172/JCI3205
P407
P577
1998-07-01T00:00:00Z