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Aiko Sato-Otsubo

Showing results (1-10 of 71) with videos related to

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Seminars in Oncology|February 1, 2012
Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?Aiko Sato-Otsubo, Masashi Sanada, Seishi Ogawa
Pediatrics International : Official Journal of the Japan Pediatric Society|January 19, 2021
Copy number alteration analysis for neuroblastoma using droplet digital polymerase chain reactionYuko Ishii, Aiko Sato-Otsubo, Junko Takita, et al.
Genes, Chromosomes & Cancer|February 4, 2012
Contribution of germline mutations to PARK2 gene inactivation in lung adenocarcinomaReika Iwakawa, Hirokazu Okayama, Takashi Kohno, et al.
Leukemia Research|November 11, 2011
Older patients with normal karyotype acute myeloid leukemia have a higher rate of genomic changes compared to young patients as determined by SNP array analysisMaya Koren-Michowitz, Aiko Sato-Otsubo, Arnon Nagler, et al.
Investigative Ophthalmology & Visual Science|June 30, 2015
Genome-Wide Analysis of Ocular Adnexal Lymphoproliferative Disorders Using High-Resolution Single Nucleotide Polymorphism ArrayHiroki Takahashi, Yoshihiko Usui, Shunichiro Ueda, et al.
Pediatric Blood & Cancer|November 1, 2021
Genomic analysis of two rare cases of pediatric Ph-positive T-ALLAiko Sato-Otsubo, Tomoo Osumi, Masanori Yoshida, et al.
International Journal of Hematology|June 25, 2025
Inborn errors of immunity-associated gene variants in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosisKenichi Sakamoto, Shutaro Inoue, Aiko Sato-Otsubo, et al.
Haematologica|June 13, 2012
Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO 'MDS-U' designationKohei Hosokawa, Takamasa Katagiri, Naomi Sugimori, et al.
International Journal of Oncology|May 28, 2013
Genetic differences between Asian and Caucasian chronic lymphocytic leukemiaNorihiko Kawamata, Chimene Moreilhon, Takayuki Saitoh, et al.
Blood|December 6, 2011
CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML)Norio Shiba, Daisuke Hasegawa, Myoung-ja Park, et al.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Seminars in Oncology|February 1, 2012
Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?Aiko Sato-Otsubo, Masashi Sanada, Seishi Ogawa
Pediatrics International : Official Journal of the Japan Pediatric Society|January 19, 2021
Copy number alteration analysis for neuroblastoma using droplet digital polymerase chain reactionYuko Ishii, Aiko Sato-Otsubo, Junko Takita, et al.
Genes, Chromosomes & Cancer|February 4, 2012
Contribution of germline mutations to PARK2 gene inactivation in lung adenocarcinomaReika Iwakawa, Hirokazu Okayama, Takashi Kohno, et al.
Leukemia Research|November 11, 2011
Older patients with normal karyotype acute myeloid leukemia have a higher rate of genomic changes compared to young patients as determined by SNP array analysisMaya Koren-Michowitz, Aiko Sato-Otsubo, Arnon Nagler, et al.
Investigative Ophthalmology & Visual Science|June 30, 2015
Genome-Wide Analysis of Ocular Adnexal Lymphoproliferative Disorders Using High-Resolution Single Nucleotide Polymorphism ArrayHiroki Takahashi, Yoshihiko Usui, Shunichiro Ueda, et al.
Pediatric Blood & Cancer|November 1, 2021
Genomic analysis of two rare cases of pediatric Ph-positive T-ALLAiko Sato-Otsubo, Tomoo Osumi, Masanori Yoshida, et al.
International Journal of Hematology|June 25, 2025
Inborn errors of immunity-associated gene variants in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosisKenichi Sakamoto, Shutaro Inoue, Aiko Sato-Otsubo, et al.
Haematologica|June 13, 2012
Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO 'MDS-U' designationKohei Hosokawa, Takamasa Katagiri, Naomi Sugimori, et al.
International Journal of Oncology|May 28, 2013
Genetic differences between Asian and Caucasian chronic lymphocytic leukemiaNorihiko Kawamata, Chimene Moreilhon, Takayuki Saitoh, et al.
Blood|December 6, 2011
CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML)Norio Shiba, Daisuke Hasegawa, Myoung-ja Park, et al.
Pageof 8