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M E Conley

Showing results (91-100 of 116) with videos related to

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Clinical and Experimental Immunology|February 5, 2008
A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical diseaseM E Conley, D M Farmer, A K Dobbs, et al.
Molecular Immunology|April 1, 1986
Monoclonal antibodies against isotypic and isoallotypic determinants of human IgA1 and IgA2: fine specificities and binding propertiesD L Delacroix, J Van Snick, J P Vaerman, et al.
Lancet (London, England)|September 4, 1993
Correction of Duncan's syndrome by allogeneic bone marrow transplantationL L Williams, C M Rooney, M E Conley, et al.
Pediatric Blood & Cancer|April 17, 2013
Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasmsJ T Sandlund, S A Shurtleff, M Onciu, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|May 8, 2001
A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafnessD Richter, M E Conley, J Rohrer, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 1, 1996
CD38 signal transduction in human B cell precursors. Rapid induction of tyrosine phosphorylation, activation of syk tyrosine kinase, and phosphorylation of phospholipase C-gamma and phosphatidylinositol 3-kinaseO Silvennoinen, H Nishigaki, A Kitanaka, et al.
Science (New York, N.Y.)|December 3, 1999
An essential role for BLNK in human B cell developmentY Minegishi, J Rohrer, E Coustan-Smith, et al.
Human Mutation|April 29, 1999
Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemiaM Vihinen, S P Kwan, T Lester, et al.
The New England Journal of Medicine|May 26, 1994
Brief report: a point mutation in the SH2 domain of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemiaD C Saffran, O Parolini, M E Fitch-Hilgenberg, et al.
Human Mutation|April 13, 1999
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. OnlineF X Arrendondo-Vega, I Santisteban, L D Notarangelo, et al.
Pageof 12

Showing results (91-100 of 116) with videos related to

Sort By:
Pageof 12
Clinical and Experimental Immunology|February 5, 2008
A minimally hypomorphic mutation in Btk resulting in reduced B cell numbers but no clinical diseaseM E Conley, D M Farmer, A K Dobbs, et al.
Molecular Immunology|April 1, 1986
Monoclonal antibodies against isotypic and isoallotypic determinants of human IgA1 and IgA2: fine specificities and binding propertiesD L Delacroix, J Van Snick, J P Vaerman, et al.
Lancet (London, England)|September 4, 1993
Correction of Duncan's syndrome by allogeneic bone marrow transplantationL L Williams, C M Rooney, M E Conley, et al.
Pediatric Blood & Cancer|April 17, 2013
Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasmsJ T Sandlund, S A Shurtleff, M Onciu, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|May 8, 2001
A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafnessD Richter, M E Conley, J Rohrer, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 1, 1996
CD38 signal transduction in human B cell precursors. Rapid induction of tyrosine phosphorylation, activation of syk tyrosine kinase, and phosphorylation of phospholipase C-gamma and phosphatidylinositol 3-kinaseO Silvennoinen, H Nishigaki, A Kitanaka, et al.
Science (New York, N.Y.)|December 3, 1999
An essential role for BLNK in human B cell developmentY Minegishi, J Rohrer, E Coustan-Smith, et al.
Human Mutation|April 29, 1999
Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemiaM Vihinen, S P Kwan, T Lester, et al.
The New England Journal of Medicine|May 26, 1994
Brief report: a point mutation in the SH2 domain of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemiaD C Saffran, O Parolini, M E Fitch-Hilgenberg, et al.
Human Mutation|April 13, 1999
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. OnlineF X Arrendondo-Vega, I Santisteban, L D Notarangelo, et al.
Pageof 12