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I Dorval

Showing results (11-20 of 40) with videos related to

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Endocrinology|June 30, 1998
Expression of interferons-alpha and -gamma in testicular interstitial tissue and spermatogonia of the ratN Dejucq, M O Lienard, E Guillaume, et al.
Human Immunology|September 1, 1992
Requirements for lysis of activated T cells by class-II-restricted cytolytic T-lymphocytesA Eljaafari, I Dorval, D Zeliszewski, et al.
Clinical Chemistry|February 1, 1996
Rapid detection of the G1691A mutation of coagulation factor V by PCR-mediated site-directed mutagenesisC Guillerm, F Lellouche, L Darnige, et al.
Presse Medicale (Paris, France : 1983)|January 18, 1997
[Bone marrow aplasia and hepatitis G virus: what relation?]F Lellouche, G Le Bihan, I Plantin, et al.
Human Immunology|August 1, 1990
DR-restricted T-cell reactivities associated with the Dw19 specificity can be directed against the products of either locus DRB3 (DRw52c) or locus DRB1D Zeliszewski, J M Tiercy, I Dorval, et al.
Thrombosis and Haemostasis|November 3, 1998
Mesenteric venous thrombosis in two patients heterozygous for the 20210 A allele of the prothrombin geneL Darnige, P Jezequel, Z Amoura, et al.
Scandinavian Journal of Immunology|February 1, 1996
Sharing of four DR-beta sequence motifs between HLA-DRB1*1601 and DRB1*1101 correlates with frequent degenerate T-cell recognition of HA306-320 peptide complexed to these two moleculesD Zeliszewski, I Dorval, J J Golvano, et al.
Human Immunology|September 15, 1996
Binding of ALA-substituted analogs of HA306-320 to DR1101, DR1301, and DR0402 molecules: correlation of DR-peptide interactions with recognition by a single TCRD Zeliszewski, J J Golvano, P Gaudebout, et al.
Cellular Immunology|January 1, 1995
Contribution of p56lck to the upregulation of cytokine production and T cell proliferation by IL-2 in human CD3-stimulated T cell clonesA Eljaafari, I Dorval, M Soula, et al.
Atherosclerosis|February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patientsI Dorval, P Jezequel, C Dubourg, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Endocrinology|June 30, 1998
Expression of interferons-alpha and -gamma in testicular interstitial tissue and spermatogonia of the ratN Dejucq, M O Lienard, E Guillaume, et al.
Human Immunology|September 1, 1992
Requirements for lysis of activated T cells by class-II-restricted cytolytic T-lymphocytesA Eljaafari, I Dorval, D Zeliszewski, et al.
Clinical Chemistry|February 1, 1996
Rapid detection of the G1691A mutation of coagulation factor V by PCR-mediated site-directed mutagenesisC Guillerm, F Lellouche, L Darnige, et al.
Presse Medicale (Paris, France : 1983)|January 18, 1997
[Bone marrow aplasia and hepatitis G virus: what relation?]F Lellouche, G Le Bihan, I Plantin, et al.
Human Immunology|August 1, 1990
DR-restricted T-cell reactivities associated with the Dw19 specificity can be directed against the products of either locus DRB3 (DRw52c) or locus DRB1D Zeliszewski, J M Tiercy, I Dorval, et al.
Thrombosis and Haemostasis|November 3, 1998
Mesenteric venous thrombosis in two patients heterozygous for the 20210 A allele of the prothrombin geneL Darnige, P Jezequel, Z Amoura, et al.
Scandinavian Journal of Immunology|February 1, 1996
Sharing of four DR-beta sequence motifs between HLA-DRB1*1601 and DRB1*1101 correlates with frequent degenerate T-cell recognition of HA306-320 peptide complexed to these two moleculesD Zeliszewski, I Dorval, J J Golvano, et al.
Human Immunology|September 15, 1996
Binding of ALA-substituted analogs of HA306-320 to DR1101, DR1301, and DR0402 molecules: correlation of DR-peptide interactions with recognition by a single TCRD Zeliszewski, J J Golvano, P Gaudebout, et al.
Cellular Immunology|January 1, 1995
Contribution of p56lck to the upregulation of cytokine production and T cell proliferation by IL-2 in human CD3-stimulated T cell clonesA Eljaafari, I Dorval, M Soula, et al.
Atherosclerosis|February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patientsI Dorval, P Jezequel, C Dubourg, et al.
Pageof 4