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International Journal of Hematology|June 1, 1995
Band 4.2 Komatsu: 523 GAT-->TAT (175 Asp-->Tyr) in exon 4 of the band 4.2 gene associated with total deficiency of band 4.2, hemolytic anemia with ovalostomatocytosis and marked disruption of the cytoskeletal networkA Kanzaki, Y Yawata, A Yawata, et al.Oncogene|July 1, 1992
Gene rearrangement and overexpression of PRAD1 in lymphoid malignancy with t(11;14)(q13;q32) translocationM Seto, K Yamamoto, S Iida, et al.Blood|April 1, 1992
An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)E E Bouhassira, R S Schwartz, Y Yawata, et al.British Journal of Haematology|March 1, 1997
Granulocyte-colony stimulating factor-induced proliferation of primary adult T-cell leukaemia cellsK Matsushita, N Arima, H Ohtsubo, et al.British Journal of Haematology|September 12, 1998
Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near-normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiencyT Inoue, A Kanzaki, M Kaku, et al.British Journal of Haematology|December 24, 1997
Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosisA Kanzaki, S Hayette, L Morlé, et al.British Journal of Haematology|September 13, 2001
Cell cycle analysis and expression of cell cycle regulator genes in myeloma cells overexpressing cyclin D1K Yata, Y Sadahira, T Otsuki, et al.Leukemia & Lymphoma|November 8, 2001
Establishment of CD7+ human myeloma sister cell lines, KMS-21-PE and KMS-21-BM, carrying t(11;14) and t(8;14)T Otsuki, H Wada, N Nakazawa, et al.The Journal of Clinical Investigation|April 15, 1996
Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutationM Inaba, A Yawata, I Koshino, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|March 1, 1996
[Five cases of hereditary high red cell membrane phosphatidylcholine hemolytic anemia in three families]M Wakita, T Matsui, M Tsuzuki, et al.Pageof 10