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S P Kwan

Showing results (11-20 of 26) with videos related to

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The Journal of Clinical Investigation|February 1, 1986
Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphismS P Kwan, L Kunkel, G Bruns, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 1995
Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease geneS P Kwan, T L Hagemann, B E Radtke, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1980
Immunoglobulin V/J recombination is accompanied by deletion of joining site and variable region segmentsJ G Seidman, M M Nau, B Norman, et al.
Genomics|May 1, 1994
Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23T Hagemann, R Surosky, A P Monaco, et al.
The New England Journal of Medicine|February 13, 1986
Evidence for a defect in "switch" T cells in patients with immunodeficiency and hyperimmunoglobulinemia ML Mayer, S P Kwan, C Thompson, et al.
Nucleic Acids Research|January 1, 1996
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)M Vihinen, T Iwata, C Kinnon, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1981
Recombination events that activate, diversify, and delete immunoglobulin genesP Leder, E E Max, J G Seidman, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 1, 1997
Variable expression of WASP in B cell lines of Wiskott-Aldrich syndrome patientsE Remold-O'Donnell, J Cooley, A Shcherbina, 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.
Genomics|February 1, 1990
Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locusS P Kwan, J Terwilliger, R Parmley, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Investigation|February 1, 1986
Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphismS P Kwan, L Kunkel, G Bruns, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 1995
Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease geneS P Kwan, T L Hagemann, B E Radtke, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1980
Immunoglobulin V/J recombination is accompanied by deletion of joining site and variable region segmentsJ G Seidman, M M Nau, B Norman, et al.
Genomics|May 1, 1994
Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23T Hagemann, R Surosky, A P Monaco, et al.
The New England Journal of Medicine|February 13, 1986
Evidence for a defect in "switch" T cells in patients with immunodeficiency and hyperimmunoglobulinemia ML Mayer, S P Kwan, C Thompson, et al.
Nucleic Acids Research|January 1, 1996
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)M Vihinen, T Iwata, C Kinnon, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1981
Recombination events that activate, diversify, and delete immunoglobulin genesP Leder, E E Max, J G Seidman, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 1, 1997
Variable expression of WASP in B cell lines of Wiskott-Aldrich syndrome patientsE Remold-O'Donnell, J Cooley, A Shcherbina, 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.
Genomics|February 1, 1990
Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locusS P Kwan, J Terwilliger, R Parmley, et al.
Pageof 3