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Molecular Human Reproduction|June 8, 2004
Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failureB Bodega, C Porta, P G Crosignani, et al.Acta Haematologica|January 1, 1997
Thrombotic complications in acute promyelocytic leukemia during all-trans-retinoic acid therapyE M Pogliani, F Rossini, I Casaroli, et al.Journal of Immunology (Baltimore, Md. : 1950)|April 1, 1983
Acquisition of deoxyguanosine resistance by TPA-induced T lymphoid linesN Sacchi, G Fiorini, P Plevani, et al.Mutagenesis|July 1, 1996
dCTP misincorporation in a Chinese hamster mutator phenotype: the role of GGA genetic contextG Rainaldi, R Meneveri, L Mariani, et al.Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|April 25, 2000
Defibrotide in recurrent thrombotic thrombocytopenic purpuraE M Pogliani, P Perseghin, M Parma, et al.Acta Haematologica|January 1, 1987
Translocation of oncogene c-sis from chromosome 22 to chromosome 17 in a human myelogenous leukemia cell lineP Tripputi, L A Cannizzaro, J Kuo, et al.Allergologia Et Immunopathologia|May 1, 1991
Lymphocyte subsets in patients with idiopathic thrombocytopenic purpura during high-dose gamma globulin therapyE M Pogliani, A Della Volpe, I Casaroli, et al.Genomics|June 13, 2006
The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolutionB Bodega, M F Cardone, M Rocchi, et al.Journal of Biotechnology|July 9, 1998
In vitro selection of HIV-1 TAR variants by the Tat proteinA Marozzi, R Meneveri, M Giacca, et al.Human Genetics|August 14, 2001
The structure of duplications on human acrocentric chromosome short arms derived by the analysis of 15pI Piccini, L Ballarati, C Bassi, et al.Pageof 9