R J Levinsky|K Tiedeman - JoVE Visualize

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Lancet (London, England)|July 8, 1995

Gene transfer to primary chronic granulomatous disease monocytesA J Thrasher, C M Casimir, C Kinnon, et al.

The Journal of Experimental Medicine|August 1, 1995

The protein product of the c-cbl protooncogene is phosphorylated after B cell receptor stimulation and binds the SH3 domain of Bruton's tyrosine kinaseG O Cory, R C Lovering, S Hinshelwood, et al.

Archives of Disease in Childhood|April 1, 1985

Treatment of respiratory papillomatosis with adenine arabinosideW A Hendrickse, B C Irwin, R J Levinsky, et al.

Blood|October 15, 1994

p22-phox-deficient chronic granulomatous disease: reconstitution by retrovirus-mediated expression and identification of a biosynthetic intermediate of gp91-phoxC D Porter, M H Parkar, A J Verhoeven, et al.

Human Genetics|December 1, 1994

Physical mapping in the region of the Bruton's tyrosine kinase and alpha-galactosidase A gene loci in proximal Xq22A K Sweatman, L A Bradley, R C Lovering, et al.

Clinical Science (London, England : 1979)|December 1, 1983

Importance of platelet-free preparations for evaluating lymphocyte nucleotide levels in inherited or acquired immunodeficiency syndromesA Goday, H A Simmonds, D R Webster, et al.

Immunology Letters|May 1, 1992

Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populationsR J Lipscombe, Y L Lau, R J Levinsky, et al.

Human Genetics|October 1, 1995

Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysisP A Clark, T Lester, S Genet, et al.

Lancet (London, England)|June 29, 1991

Molecular basis of opsonic defect in immunodeficient childrenM Sumiya, M Super, P Tabona, et al.

Clinical and Experimental Immunology|December 1, 1987

Heterogeneity of biochemical, clinical and immunological parameters in severe combined immunodeficiency due to adenosine deaminase deficiencyG Morgan, R J Levinsky, K Hugh-Jones, et al.

Pageof 14

Showing results (91-100 of 132) with videos related to

Sort By:

Pageof 14

Lancet (London, England)|July 8, 1995

Gene transfer to primary chronic granulomatous disease monocytesA J Thrasher, C M Casimir, C Kinnon, et al.

The Journal of Experimental Medicine|August 1, 1995

The protein product of the c-cbl protooncogene is phosphorylated after B cell receptor stimulation and binds the SH3 domain of Bruton's tyrosine kinaseG O Cory, R C Lovering, S Hinshelwood, et al.

Archives of Disease in Childhood|April 1, 1985

Treatment of respiratory papillomatosis with adenine arabinosideW A Hendrickse, B C Irwin, R J Levinsky, et al.

Blood|October 15, 1994

p22-phox-deficient chronic granulomatous disease: reconstitution by retrovirus-mediated expression and identification of a biosynthetic intermediate of gp91-phoxC D Porter, M H Parkar, A J Verhoeven, et al.

Human Genetics|December 1, 1994

Physical mapping in the region of the Bruton's tyrosine kinase and alpha-galactosidase A gene loci in proximal Xq22A K Sweatman, L A Bradley, R C Lovering, et al.

Clinical Science (London, England : 1979)|December 1, 1983

Importance of platelet-free preparations for evaluating lymphocyte nucleotide levels in inherited or acquired immunodeficiency syndromesA Goday, H A Simmonds, D R Webster, et al.

Immunology Letters|May 1, 1992

Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populationsR J Lipscombe, Y L Lau, R J Levinsky, et al.

Human Genetics|October 1, 1995

Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysisP A Clark, T Lester, S Genet, et al.

Lancet (London, England)|June 29, 1991

Molecular basis of opsonic defect in immunodeficient childrenM Sumiya, M Super, P Tabona, et al.

Clinical and Experimental Immunology|December 1, 1987

Heterogeneity of biochemical, clinical and immunological parameters in severe combined immunodeficiency due to adenosine deaminase deficiencyG Morgan, R J Levinsky, K Hugh-Jones, et al.

Pageof 14