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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1988 | 1 |
1991 | 1 |
1992 | 1 |
2006 | 1 |
2024 | 0 |
PubMed (cited) for id: 610163
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Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency.
N Engl J Med. 2006 May 4;354(18):1913-21. doi: 10.1056/NEJMoa053750.
N Engl J Med. 2006.
PMID: 16672702
Free article.
Familial defect in the surface expression of the T-cell receptor-CD3 complex.
Alarcon B, Regueiro JR, Arnaiz-Villena A, Terhorst C.
Alarcon B, et al.
N Engl J Med. 1988 Nov 3;319(18):1203-8. doi: 10.1056/NEJM198811033191806.
N Engl J Med. 1988.
PMID: 3262828
No abstract available.
Item in Clipboard
Biochemical basis of a novel T lymphocyte receptor immunodeficiency by immunohistochemistry. A possible CD3 gamma abnormality.
Arnaiz-Villena A, Perez-Aciego P, Ballestin C, Sotelo T, Perez-Seoane C, Martin-Villa JM, Regueiro JR.
Arnaiz-Villena A, et al.
Lab Invest. 1991 May;64(5):675-81.
Lab Invest. 1991.
PMID: 1709425
Item in Clipboard
Brief report: primary immunodeficiency caused by mutations in the gene encoding the CD3-gamma subunit of the T-lymphocyte receptor.
Arnaiz-Villena A, Timon M, Corell A, Perez-Aciego P, Martin-Villa JM, Regueiro JR.
Arnaiz-Villena A, et al.
N Engl J Med. 1992 Aug 20;327(8):529-33. doi: 10.1056/NEJM199208203270805.
N Engl J Med. 1992.
PMID: 1635567
Free article.
No abstract available.
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