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American Journal of Hematology|February 1, 1992
A female hemophilia A combined with hereditary coagulation factor XII deficiency: a case reportT Matsushita, J Takamatsu, K Kagami, et al.Blood|June 15, 1991
Genotype establishments for protein C deficiency by use of a DNA polymorphism in the geneK Yamamoto, M Tanimoto, T Matsushita, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|January 10, 1998
[Cord blood stem cell transplantation for infantile acute lymphoblastic leukemia after primary cytomegalovirus infection]K Goi, K Sugita, N Miyamoto, et al.Pediatric Research|February 25, 1998
Transient increase in CD45RO expression on T lymphocytes in infected newbornsT Tezuka, K Sugita, N Mizobe, et al.International Journal of Hematology|August 1, 1996
Analysis for heterozygosity of protein S mRNA: application to genetic screening and family studies in hereditary protein S deficiencyT Yamazaki, M Hamaguchi, J Takamatsu, et al.Leukemia|September 20, 2000
Expression of thrombopoietin receptor and its functional role in human B-precursor leukemia cells with 11q23 translocation or Philadelphia chromosomeK Iijima, K Sugita, T Inukai, et al.British Journal of Haematology|March 1, 1995
Expression of granulocyte colony-stimulating factor receptor on CD10-positive human B-cell precursorsT Inukai, K Sugita, K Iijima, et al.Blood|June 1, 1996
Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474T Yamazaki, A Katsumi, K Kagami, et al.Thrombosis and Haemostasis|January 1, 1997
Two distinct novel splice site mutations in a compound heterozygous patient with protein S deficiencyT Yamazaki, A Katsumi, Y Okamoto, et al.Leukemia|October 30, 2001
The JAK2 inhibitor AG490 predominantly abrogates the growth of human B-precursor leukemic cells with 11q23 translocation or Philadelphia chromosomeN Miyamoto, K Sugita, K Goi, et al.Pageof 4