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Ryoji Hanada

Showing results (31-40 of 86) with videos related to

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[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|May 14, 2013
[The feasibility of Erwinia asparaginase for pediatric patients who developed an allergic reaction to E.coli asparaginase during treatment of acute lymphoblastic leukemia]Hiroyoshi Takahashi, Katsuyoshi Koh, Motohiro Kato, et al.
Blood|November 18, 2005
KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study GroupAkira Shimada, Tomohiko Taki, Ken Tabuchi, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|January 16, 2013
[Unrelated cord blood transplantation in a child with very severe aplastic anemia]Naoko Yasui, Katsuyoshi Koh, Myoung-Ja Park, et al.
Pediatric Blood & Cancer|September 1, 2007
Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study GroupAkira Shimada, Tomohiko Taki, Ken Tabuchi, et al.
Blood|July 20, 2002
Risk factors for evolution of acquired aplastic anemia into myelodysplastic syndrome and acute myeloid leukemia after immunosuppressive therapy in childrenSeiji Kojima, Akira Ohara, Masahiro Tsuchida, et al.
Cancer Research|January 26, 2002
SEPTIN6, a human homologue to mouse Septin6, is fused to MLL in infant acute myeloid leukemia with complex chromosomal abnormalities involving 11q23 and Xq24Ryoichi Ono, Tomohiko Taki, Takeshi Taketani, et al.
Genes, Chromosomes & Cancer|April 22, 2004
Gene expression profiling and identification of novel prognostic marker genes in neuroblastomaJunko Takita, Masami Ishii, Shuichi Tsutsumi, et al.
Blood|September 25, 2003
FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidyTakeshi Taketani, Tomohiko Taki, Kanji Sugita, et al.
Genes, Chromosomes & Cancer|July 23, 2003
AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignanciesTakeshi Taketani, Tomohiko Taki, Junko Takita, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|June 7, 2019
[Successful management of acute chest syndrome in a patient with sickle cell disease]Yasuo Kubota, Yuki Arakawa, Kentaro Watanabe, et al.
Pageof 9

Showing results (31-40 of 86) with videos related to

Sort By:
Pageof 9
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|May 14, 2013
[The feasibility of Erwinia asparaginase for pediatric patients who developed an allergic reaction to E.coli asparaginase during treatment of acute lymphoblastic leukemia]Hiroyoshi Takahashi, Katsuyoshi Koh, Motohiro Kato, et al.
Blood|November 18, 2005
KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study GroupAkira Shimada, Tomohiko Taki, Ken Tabuchi, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|January 16, 2013
[Unrelated cord blood transplantation in a child with very severe aplastic anemia]Naoko Yasui, Katsuyoshi Koh, Myoung-Ja Park, et al.
Pediatric Blood & Cancer|September 1, 2007
Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study GroupAkira Shimada, Tomohiko Taki, Ken Tabuchi, et al.
Blood|July 20, 2002
Risk factors for evolution of acquired aplastic anemia into myelodysplastic syndrome and acute myeloid leukemia after immunosuppressive therapy in childrenSeiji Kojima, Akira Ohara, Masahiro Tsuchida, et al.
Cancer Research|January 26, 2002
SEPTIN6, a human homologue to mouse Septin6, is fused to MLL in infant acute myeloid leukemia with complex chromosomal abnormalities involving 11q23 and Xq24Ryoichi Ono, Tomohiko Taki, Takeshi Taketani, et al.
Genes, Chromosomes & Cancer|April 22, 2004
Gene expression profiling and identification of novel prognostic marker genes in neuroblastomaJunko Takita, Masami Ishii, Shuichi Tsutsumi, et al.
Blood|September 25, 2003
FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidyTakeshi Taketani, Tomohiko Taki, Kanji Sugita, et al.
Genes, Chromosomes & Cancer|July 23, 2003
AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignanciesTakeshi Taketani, Tomohiko Taki, Junko Takita, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|June 7, 2019
[Successful management of acute chest syndrome in a patient with sickle cell disease]Yasuo Kubota, Yuki Arakawa, Kentaro Watanabe, et al.
Pageof 9