O Parolini|M E Conley - JoVE Visualize

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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.

Cell|January 29, 1993

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemiaS Tsukada, D C Saffran, D J Rawlings, 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.

Oncogene|August 19, 2007

Diacylglycerol kinase-alpha phosphorylation by Src on Y335 is required for activation, membrane recruitment and Hgf-induced cell motilityG Baldanzi, S Cutrupi, F Chianale, et al.

Annals of Hematology|September 12, 2002

Analysis of SH2D1A mutations in patients with severe Epstein-Barr virus infections, Burkitt's lymphoma, and Hodgkin's lymphomaO Parolini, B Kagerbauer, I Simonitsch-Klupp, et al.

Toxicology and Applied Pharmacology|November 16, 2004

Target-specific action of organochlorine compounds in reproductive and nonreproductive tissues of estrogen-reporter male miceR Villa, E Bonetti, M L Penza, et al.

British Journal of Haematology|June 20, 1998

Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.

Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:

Pageof 12

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.

Cell|January 29, 1993

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemiaS Tsukada, D C Saffran, D J Rawlings, 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.

Oncogene|August 19, 2007

Diacylglycerol kinase-alpha phosphorylation by Src on Y335 is required for activation, membrane recruitment and Hgf-induced cell motilityG Baldanzi, S Cutrupi, F Chianale, et al.

Annals of Hematology|September 12, 2002

Analysis of SH2D1A mutations in patients with severe Epstein-Barr virus infections, Burkitt's lymphoma, and Hodgkin's lymphomaO Parolini, B Kagerbauer, I Simonitsch-Klupp, et al.

Toxicology and Applied Pharmacology|November 16, 2004

Target-specific action of organochlorine compounds in reproductive and nonreproductive tissues of estrogen-reporter male miceR Villa, E Bonetti, M L Penza, et al.

British Journal of Haematology|June 20, 1998

Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.

Pageof 12