Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency
about
Severe combined immunodeficiencies (SCID)AIRE deficiency in thymus of 2 patients with Omenn syndrome.Autosomal SCID caused by a point mutation in the N-terminus of Jak3: mapping of the Jak3-receptor interaction domain.Complex effects of naturally occurring mutations in the JAK3 pseudokinase domain: evidence for interactions between the kinase and pseudokinase domains.Immunodeficiency due to a unique protracted developmental delay in the B-cell lineageMolecular aspects of primary immunodeficiencies: lessons from cytokine and other signaling pathways.Severe papillomavirus infection progressing to metastatic squamous cell carcinoma in bone marrow-transplanted X-linked SCID dogsIdentification of Gene Networks for Residual Feed Intake in Angus Cattle Using Genomic Prediction and RNA-seq.Variable phenotypic expression of mutations in genes of the immune system.Interleukin 7 independent development of human B cells.Severe combined immunodeficiences: new and old scenarios.The Janus Kinase (JAK) FERM and SH2 Domains: Bringing Specificity to JAK-Receptor Interactions.An interleukin-2 receptor gamma chain mutation with normal thymus morphology.Clinical characteristics and genetic profiles of 44 patients with severe combined immunodeficiency (SCID): report from Shanghai, China (2004-2011).Genesis of progressive T-cell deficiency owing to a single missense mutation in the common gamma chain gene.Epigenetic Maintenance of Acquired Gene Expression Programs during Memory CD8 T Cell Homeostasis.Trisomy 4 pter-q12 and monosomy of chromosome 13 pter-q12 in a male with deficiency of all blood lymphocyte populations.Reduced memory B-cell populations in boys with B-cell dysfunction after bone marrow transplantation for X-linked severe combined immunodeficiency.Molecular assessment of thymus capabilities in the evaluation of T-cell immunodeficiency.
P2860
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P2860
Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency
description
1995 nî lūn-bûn
@nan
1995 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի մարտին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@ast
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@en
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@nl
type
label
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@ast
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@en
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@nl
prefLabel
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@ast
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@en
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@nl
P2093
P2860
P3181
P356
P1476
Missense mutation in exon 7 of ...... nked combined immunodeficiency
@en
P2093
A S Goldman
E G Brooks
F C Schmalstieg
H E Rudloff
R M Denney
W J Leonard
P2860
P304
P3181
P356
10.1172/JCI117765
P407
P577
1995-03-01T00:00:00Z