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M E Conley

Showing results (61-70 of 116) with videos related to

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Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 13, 2004
Quantitative effects of palivizumab and donor-derived T cells on chronic respiratory syncytial virus infection, lung disease, and fusion glycoprotein amino acid sequences in a patient before and after bone marrow transplantationC M El Saleeby, J Suzich, M E Conley, et al.
The Journal of Allergy and Clinical Immunology|October 1, 1987
Recurrent infections and staphylococcal liver abscess in a child with C1r deficiencyB Z Garty, M E Conley, S D Douglas, et al.
American Journal of Human Genetics|May 1, 1989
X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysisJ M Puck, R L Nussbaum, D L Smead, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1980
Differentiation of human B cells expressing the IgA subclasses as demonstrated by monoclonal hybridoma antibodiesM E Conley, J F Kearney, A R Lawton, et al.
Clinical Immunology (Orlando, Fla.)|October 21, 1999
Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1M E Conley, L Rapalus, E C Boylin, et al.
Clinical Immunology (Orlando, Fla.)|December 1, 2001
Analysis of SWAP-70 as a candidate gene for non-X-linked hyper IgM syndrome and common variable immunodeficiencyL Rapalus, Y Minegishi, A Lavoie, et al.
Immunological Reviews|February 24, 2001
Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouseM E Conley, J Rohrer, L Rapalus, et al.
Clinical Immunology and Immunopathology|June 1, 1990
X chromosome inactivation patterns in obligate carriers of X-linked lymphoproliferative syndromeM E Conley, J L Sullivan, J A Neidich, et al.
The Journal of Pediatrics|July 1, 1996
Wiskott-Aldrich syndrome in a family with Fanconi anemiaJ Rohrer, R C Ribeiro, A D Auerbach, et al.
Clinical Genetics|January 26, 2007
A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X-linked gene WASA K Dobbs, T Yang, D M Farmer, et al.
Pageof 12

Showing results (61-70 of 116) with videos related to

Sort By:
Pageof 12
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 13, 2004
Quantitative effects of palivizumab and donor-derived T cells on chronic respiratory syncytial virus infection, lung disease, and fusion glycoprotein amino acid sequences in a patient before and after bone marrow transplantationC M El Saleeby, J Suzich, M E Conley, et al.
The Journal of Allergy and Clinical Immunology|October 1, 1987
Recurrent infections and staphylococcal liver abscess in a child with C1r deficiencyB Z Garty, M E Conley, S D Douglas, et al.
American Journal of Human Genetics|May 1, 1989
X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysisJ M Puck, R L Nussbaum, D L Smead, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1980
Differentiation of human B cells expressing the IgA subclasses as demonstrated by monoclonal hybridoma antibodiesM E Conley, J F Kearney, A R Lawton, et al.
Clinical Immunology (Orlando, Fla.)|October 21, 1999
Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene lambda 5/14.1M E Conley, L Rapalus, E C Boylin, et al.
Clinical Immunology (Orlando, Fla.)|December 1, 2001
Analysis of SWAP-70 as a candidate gene for non-X-linked hyper IgM syndrome and common variable immunodeficiencyL Rapalus, Y Minegishi, A Lavoie, et al.
Immunological Reviews|February 24, 2001
Defects in early B-cell development: comparing the consequences of abnormalities in pre-BCR signaling in the human and the mouseM E Conley, J Rohrer, L Rapalus, et al.
Clinical Immunology and Immunopathology|June 1, 1990
X chromosome inactivation patterns in obligate carriers of X-linked lymphoproliferative syndromeM E Conley, J L Sullivan, J A Neidich, et al.
The Journal of Pediatrics|July 1, 1996
Wiskott-Aldrich syndrome in a family with Fanconi anemiaJ Rohrer, R C Ribeiro, A D Auerbach, et al.
Clinical Genetics|January 26, 2007
A possible bichromatid mutation in a male gamete giving rise to a female mosaic for two different mutations in the X-linked gene WASA K Dobbs, T Yang, D M Farmer, et al.
Pageof 12