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Cellular Immunology
|
October 1, 1995
Severe combined immunodeficiency with absence of peripheral blood CD8+ T cells due to ZAP-70 deficiency
M E Elder, T J Hope, T G Parslow, et al.
Science (New York, N.Y.)
|
June 10, 1994
Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase
M E Elder, D Lin, J Clever, et al.
The Journal of Allergy and Clinical Immunology
|
November 7, 1999
Cytokine profile of a long-term pediatric HIV survivor with hyper-IgE syndrome and a normal CD4 T-cell count
C M Seroogy, D W Wara, M H Bluth, et al.
Science (New York, N.Y.)
|
June 10, 1994
ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency
A C Chan, T A Kadlecek, M E Elder, et al.
American Journal of Human Genetics
|
November 15, 2000
A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)
J Zonana, M E Elder, L C Schneider, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Cellular Immunology
|
October 1, 1995
Severe combined immunodeficiency with absence of peripheral blood CD8+ T cells due to ZAP-70 deficiency
M E Elder, T J Hope, T G Parslow, et al.
Science (New York, N.Y.)
|
June 10, 1994
Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase
M E Elder, D Lin, J Clever, et al.
The Journal of Allergy and Clinical Immunology
|
November 7, 1999
Cytokine profile of a long-term pediatric HIV survivor with hyper-IgE syndrome and a normal CD4 T-cell count
C M Seroogy, D W Wara, M H Bluth, et al.
Science (New York, N.Y.)
|
June 10, 1994
ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency
A C Chan, T A Kadlecek, M E Elder, et al.
American Journal of Human Genetics
|
November 15, 2000
A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)
J Zonana, M E Elder, L C Schneider, et al.
Page
of 2