L A Rubin|D L Nelson - JoVE Visualize

Showing results (311-320 of 546) with videos related to

Pageof 55

Sort By:

The Journal of Pharmacology and Experimental Therapeutics|February 1, 1996

Pharmacologic characterization of the human 5-hydroxytryptamine2B receptor: evidence for species differencesD B Wainscott, V L Lucaites, J D Kursar, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 1, 1984

Antigen-stimulated human B cell clones are committed to the production of a single class of antibody in vitroR Yarchoan, R J Engler, L A Barrow, et al.

Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 22, 2014

Extending the model of Arabidopsis telomere length and composition across BrassicaceaeAndrew D L Nelson, Evan S Forsythe, Xiangchao Gan, et al.

Science (New York, N.Y.)|May 18, 1992

Triplet repeat mutations in human diseaseC T Caskey, A Pizzuti, Y H Fu, et al.

Annals of Internal Medicine|August 1, 1975

The pathogenesis of gluten-sensitive enteropathyW Strober, Z M Falchuk, G N Rogentine, et al.

Clinical and Experimental Immunology|July 1, 1988

Soluble Tac peptide is present in the urine of normal individuals and at elevated levels in patients with adult T cell leukaemia (ATL)L Marcon, M E Fritz, C C Kurman, et al.

Obesity Research|November 1, 1995

Molecular biology of serotonin receptorsM Baez, J D Kursar, L A Helton, et al.

Molecular Pharmacology|July 1, 1988

Molecular determinants for recognition of RU 24969 analogs at central 5-hydroxytryptamine recognition sites: use of a bilinear function and substituent volumes to describe steric fitE W Taylor, S S Nikam, G Lambert, et al.

Arthritis and Rheumatism|June 1, 1994

Serum levels of soluble interleukin-2 receptor. A marker of disease activity in localized sclerodermaY Uziel, B R Krafchik, B Feldman, et al.

Genomics|January 1, 1989

X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defectW L Greer, P C Kwong, M Peacocke, et al.

Pageof 55

Showing results (311-320 of 546) with videos related to

Sort By:

Pageof 55

The Journal of Pharmacology and Experimental Therapeutics|February 1, 1996

Pharmacologic characterization of the human 5-hydroxytryptamine2B receptor: evidence for species differencesD B Wainscott, V L Lucaites, J D Kursar, et al.

Journal of Immunology (Baltimore, Md. : 1950)|June 1, 1984

Antigen-stimulated human B cell clones are committed to the production of a single class of antibody in vitroR Yarchoan, R J Engler, L A Barrow, et al.

Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 22, 2014

Extending the model of Arabidopsis telomere length and composition across BrassicaceaeAndrew D L Nelson, Evan S Forsythe, Xiangchao Gan, et al.

Science (New York, N.Y.)|May 18, 1992

Triplet repeat mutations in human diseaseC T Caskey, A Pizzuti, Y H Fu, et al.

Annals of Internal Medicine|August 1, 1975

The pathogenesis of gluten-sensitive enteropathyW Strober, Z M Falchuk, G N Rogentine, et al.

Clinical and Experimental Immunology|July 1, 1988

Soluble Tac peptide is present in the urine of normal individuals and at elevated levels in patients with adult T cell leukaemia (ATL)L Marcon, M E Fritz, C C Kurman, et al.

Obesity Research|November 1, 1995

Molecular biology of serotonin receptorsM Baez, J D Kursar, L A Helton, et al.

Molecular Pharmacology|July 1, 1988

Molecular determinants for recognition of RU 24969 analogs at central 5-hydroxytryptamine recognition sites: use of a bilinear function and substituent volumes to describe steric fitE W Taylor, S S Nikam, G Lambert, et al.

Arthritis and Rheumatism|June 1, 1994

Serum levels of soluble interleukin-2 receptor. A marker of disease activity in localized sclerodermaY Uziel, B R Krafchik, B Feldman, et al.

Genomics|January 1, 1989

X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defectW L Greer, P C Kwong, M Peacocke, et al.

Pageof 55