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Showing results (351-360 of 541) with videos related to

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The Journal of Allergy and Clinical Immunology|February 14, 2013
Common variable immunodeficiency as the initial presentation of dyskeratosis congenitaEric J Allenspach, Cristian Bellodi, David Jeong, et al.
Blood|March 21, 2012
Ubiquitous high-level gene expression in hematopoietic lineages provides effective lentiviral gene therapy of murine Wiskott-Aldrich syndromeAlexander Astrakhan, Blythe D Sather, Byoung Y Ryu, et al.
Blood|February 24, 2016
Targeted gene editing restores regulated CD40L function in X-linked hyper-IgM syndromeNicholas Hubbard, David Hagin, Karen Sommer, et al.
Clinical Immunology (Orlando, Fla.)|March 10, 2001
Immunologic reconstitution following bone marrow transplantation for X-linked hyper IgM syndromeJ E Duplantier, K Seyama, N K Day, et al.
Journal of Human Genetics|July 15, 2011
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genesTakashi Arai, Meina Zhao, Hirokazu Kanegane, et al.
Biochemistry|February 7, 1995
Structural basis for pleckstrin homology domain mutations in X-linked agammaglobulinemiaM Vihinen, M J Zvelebil, Q Zhu, et al.
Journal of Clinical Immunology|January 19, 2006
Health-related quality of life and treatment satisfaction in North American patients with primary immunedeficiency diseases receiving subcutaneous IgG self-infusions at homeUwe Nicolay, Peter Kiessling, Melvin Berger, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 15, 1997
Bispecific monoclonal antibody complexes bound to primate erythrocyte complement receptor 1 facilitate virus clearance in a monkey modelR P Taylor, W M Sutherland, E N Martin, et al.
Journal of Hepatology|September 1, 1994
Hepatitis C virus transmission by intravenous immunoglobulinP L Yap, F McOmish, A D Webster, et al.
Journal of Medical Genetics|January 5, 2002
Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)I Kobayashi, R Shiari, M Yamada, et al.
Pageof 55

Showing results (351-360 of 541) with videos related to

Sort By:
Pageof 55
The Journal of Allergy and Clinical Immunology|February 14, 2013
Common variable immunodeficiency as the initial presentation of dyskeratosis congenitaEric J Allenspach, Cristian Bellodi, David Jeong, et al.
Blood|March 21, 2012
Ubiquitous high-level gene expression in hematopoietic lineages provides effective lentiviral gene therapy of murine Wiskott-Aldrich syndromeAlexander Astrakhan, Blythe D Sather, Byoung Y Ryu, et al.
Blood|February 24, 2016
Targeted gene editing restores regulated CD40L function in X-linked hyper-IgM syndromeNicholas Hubbard, David Hagin, Karen Sommer, et al.
Clinical Immunology (Orlando, Fla.)|March 10, 2001
Immunologic reconstitution following bone marrow transplantation for X-linked hyper IgM syndromeJ E Duplantier, K Seyama, N K Day, et al.
Journal of Human Genetics|July 15, 2011
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genesTakashi Arai, Meina Zhao, Hirokazu Kanegane, et al.
Biochemistry|February 7, 1995
Structural basis for pleckstrin homology domain mutations in X-linked agammaglobulinemiaM Vihinen, M J Zvelebil, Q Zhu, et al.
Journal of Clinical Immunology|January 19, 2006
Health-related quality of life and treatment satisfaction in North American patients with primary immunedeficiency diseases receiving subcutaneous IgG self-infusions at homeUwe Nicolay, Peter Kiessling, Melvin Berger, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 15, 1997
Bispecific monoclonal antibody complexes bound to primate erythrocyte complement receptor 1 facilitate virus clearance in a monkey modelR P Taylor, W M Sutherland, E N Martin, et al.
Journal of Hepatology|September 1, 1994
Hepatitis C virus transmission by intravenous immunoglobulinP L Yap, F McOmish, A D Webster, et al.
Journal of Medical Genetics|January 5, 2002
Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)I Kobayashi, R Shiari, M Yamada, et al.
Pageof 55