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Noriko Satake, MD

Title(s)Associate Professor, General Pediatrics
SchoolUniversity of California, Davis
Phone916-734-2781
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Yoshida S, Duong C, Oestergaard M, Fazio M, Chen C, Peralta R, Guo S, Seth PP, Li Y, Beckett L, Nitin N, Satake N. MXD3 antisense oligonucleotide with superparamagnetic iron oxide nanoparticles: A new targeted approach for neuroblastoma. Nanomedicine. 2019 Nov 26; 24:102127. PMID: 31783139.
      View in: PubMed
    2. Duong C, Yoshida S, Chen C, Barisone G, Diaz E, Li Y, Beckett L, Chung J, Antony R, Nolta J, Nitin N, Satake N. Novel targeted therapy for neuroblastoma: silencing the MXD3 gene using siRNA. Pediatr Res. 2017 Sep; 82(3):527-535. PMID: 28419087.
      View in: PubMed
    3. Yoshida S, Tuscano E, Duong C, Chung J, Li Y, Beckett L, Tuscano JM, Satake N. Efficacy of an anti-CD22 antibody-monomethyl auristatin E conjugate in a preclinical xenograft model of precursor B-cell acute lymphoblastic leukemia. Leuk Lymphoma. 2017 05; 58(5):1254-1257. PMID: 27701909.
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    4. Barisone GA, Satake N, Lewis C, Duong C, Chen C, Lam KS, Nolta J, D?az E. Loss of MXD3 induces apoptosis of Reh human precursor B acute lymphoblastic leukemia cells. Blood Cells Mol Dis. 2015 Apr; 54(4):329-35. PMID: 25554682.
      View in: PubMed
    5. Satake N, Duong C, Chen C, Barisone GA, Diaz E, Tuscano J, Rocke DM, Nolta J, Nitin N. Targeted therapy with MXD3 siRNA, anti-CD22 antibody and nanoparticles for precursor B-cell acute lymphoblastic leukaemia. Br J Haematol. 2014 Nov; 167(4):487-99. PMID: 25196579.
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    6. Kim Y, Schulz VP, Satake N, Gruber TA, Teixeira AM, Halene S, Gallagher PG, Krause DS. Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia. Leukemia. 2014 Apr; 28(4):945-8. PMID: 24157583.
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    7. Liu R, Mao Z, Matthews DL, Li CS, Chan JW, Satake N. Novel single-cell functional analysis of red blood cells using laser tweezers Raman spectroscopy: application for sickle cell disease. Exp Hematol. 2013 Jul; 41(7):656-661.e1. PMID: 23537725.
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    8. Kato J, Satake N, O'Donnell RT, Abuhay M, Lewis C, Tuscano JM. Efficacy of a CD22-targeted antibody-saporin conjugate in a xenograft model of precursor-B cell acute lymphoblastic leukemia. Leuk Res. 2013 Jan; 37(1):83-8. PMID: 23040543.
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    9. Thampi S, Salmi D, Imashuku S, Ducore J, Satake N. Thrombotic thrombocytopenic purpura in a child with systemic lupus erythematosus. J Pediatr Hematol Oncol. 2011 Apr; 33(3):221-3. PMID: 21336165.
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    10. Salmi D, Patel C, Imashuku S, Shimada H, Satake N. Neuroblastoma of unknown primary site with periorbital bone metastasis in a child. Pediatr Blood Cancer. 2010 Aug; 55(2):361-3. PMID: 20582979.
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    11. Marsh RA, Satake N, Biroschak J, Jacobs T, Johnson J, Jordan MB, Bleesing JJ, Filipovich AH, Zhang K. STX11 mutations and clinical phenotypes of familial hemophagocytic lymphohistiocytosis in North America. Pediatr Blood Cancer. 2010 Jul 15; 55(1):134-40. PMID: 20486178.
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    12. Salmi D, Bhat A, Corman L, Raff G, Satake N. Diagnostic challenges in native valve fungal endocarditis producing a massive septic pulmonary embolus. Nihon Ishinkin Gakkai Zasshi. 2010; 51(4):207-10. PMID: 21060214.
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    13. Kimura Y, Sumiyoshi M, Samukawa K, Satake N, Sakanaka M. Facilitating action of asiaticoside at low doses on burn wound repair and its mechanism. Eur J Pharmacol. 2008 Apr 28; 584(2-3):415-23. PMID: 18353310.
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    14. Zheng Y, Rozengurt N, Ryazantsev S, Kohn DB, Satake N, Neufeld EF. Treatment of the mouse model of mucopolysaccharidosis I with retrovirally transduced bone marrow. Mol Genet Metab. 2003 Aug; 79(4):233-44. PMID: 12948739.
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    15. Skelton D, Satake N, Kohn DB. The enhanced green fluorescent protein (eGFP) is minimally immunogenic in C57BL/6 mice. Gene Ther. 2001 Dec; 8(23):1813-4. PMID: 11803402.
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    16. Anderson CP, Seeger RC, Satake N, Monforte-Munoz HL, Keshelava N, Bailey HH, Reynolds CP. Buthionine sulfoximine and myeloablative concentrations of melphalan overcome resistance in a melphalan-resistant neuroblastoma cell line. J Pediatr Hematol Oncol. 2001 Nov; 23(8):500-5. PMID: 11878777.
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    17. Anderson CP, Keshelava N, Satake N, Meek WH, Reynolds CP. Synergism of buthionine sulfoximine and melphalan against neuroblastoma cell lines derived after disease progression. Med Pediatr Oncol. 2000 Dec; 35(6):659-62. PMID: 11107141.
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    18. Satake N, Maseki N, Nishiyama M, Kobayashi H, Sakurai M, Inaba H, Katano N, Horikoshi Y, Eguchi H, Miyake M, Seto M, Kaneko Y. Chromosome abnormalities and MLL rearrangements in acute myeloid leukemia of infants. Leukemia. 1999 Jul; 13(7):1013-7. PMID: 10400416.
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    19. Stripecke R, Carmen Villacres M, Skelton D, Satake N, Halene S, Kohn D. Immune response to green fluorescent protein: implications for gene therapy. Gene Ther. 1999 Jul; 6(7):1305-12. PMID: 10455440.
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    20. Inaba H, Kawasaki H, Nakamura S, Yamamoto H, Kaneko Y, Satake N, Komada Y, Ito M, Sakurai M. Anaplastic large cell lymphoma associated with Sjögren's syndrome. Leuk Lymphoma. 1998 Dec; 32(1-2):183-8. PMID: 10037015.
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    21. Hinohara S, Satake N, Sekine K, Kaneko Y. Abnormalities of the FHIT transcripts in osteosarcoma and Ewing sarcoma. Jpn J Cancer Res. 1998 Sep; 89(9):887-94. PMID: 9818023.
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    22. Kobayashi H, Satake N, Maseki N, Sakurai M, Izumo T, Isobe M, Kaneko Y. Amplification of the TCL1 flanking region at 14q32.1 with no TCL1 gene transcription in a patient with peripheral T cell lymphoma. Leukemia. 1998 Jun; 12(6):970-1. PMID: 9639427.
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    23. Kobayashi H, Satake N, Kaneko Y. Detection of the Der (21)t(12;21) chromosome forming the TEL-AML1 fusion gene in childhood acute lymphoblastic leukemia. Leuk Lymphoma. 1997 Dec; 28(1-2):43-50. PMID: 9498702.
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    24. Satake N, Ishida Y, Otoh Y, Hinohara S, Kobayashi H, Sakashita A, Maseki N, Kaneko Y. Novel MLL-CBP fusion transcript in therapy-related chronic myelomonocytic leukemia with a t(11;16)(q23;p13) chromosome translocation. Genes Chromosomes Cancer. 1997 Sep; 20(1):60-3. PMID: 9290955.
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    25. Satake N, Sakashita A, Kobayashi H, Maseki N, Sakurai M, Kaneko Y. Minimal residual disease in acute monocytic leukemia patient with trisomy 11 and partial tandem duplication of MLL. Cancer Genet Cytogenet. 1997 Jul 01; 96(1):26-9. PMID: 9209466.
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    26. Satake N, Kobayashi H, Tsunematsu Y, Kawasaki H, Horikoshi Y, Koizumi S, Kaneko Y. Minimal residual disease with TEL-AML1 fusion transcript in childhood acute lymphoblastic leukaemia with t(12;21). Br J Haematol. 1997 Jun; 97(3):607-11. PMID: 9207408.
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    27. Kaneko Y, Kobayashi H, Handa M, Satake N, Maseki N. EWS-ERG fusion transcript produced by chromosomal insertion in a Ewing sarcoma. Genes Chromosomes Cancer. 1997 Mar; 18(3):228-31. PMID: 9071576.
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    28. Kobayashi H, Satake N, Maseki N, Sakashita A, Kaneko Y. The der(21)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia. Br J Haematol. 1996 Jul; 94(1):105-11. PMID: 8757516.
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    29. Satake N, Maseki N, Kozu T, Sakashita A, Kobayashi H, Sakurai M, Ohki M, Kaneko Y. Disappearance of AML1-MTG8(ETO) fusion transcript in acute myeloid leukaemia patients with t(8;21) in long-term remission. Br J Haematol. 1995 Dec; 91(4):892-8. PMID: 8547135.
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    30. Kubo S, Kishino T, Satake N, Okano M, Mikawa M, Ishikawa N. A neonatal case of hydranencephaly caused by atheromatous plaque obstruction of aortic arch: possible association with a congenital cytomegalovirus infection? J Perinatol. 1994 Nov-Dec; 14(6):483-6. PMID: 7876942.
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    31. Okano M, Kishiyama K, Satake N, Kubo S, Ishikawa N. A case of fulminant ecthyma gangrenosum associated with Pseudomonas aeruginosa infection in a patient with methylmalonic acidemia. Scand J Infect Dis. 1994; 26(1):107-8. PMID: 8191230.
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    32. Satake N, Nakanishi M, Okano M, Tomizawa K, Ishizaka A, Kojima K, Onodera M, Ariga T, Satake A, Sakiyama Y. A Japanese family of X-linked auto-immune enteropathy with haemolytic anaemia and polyendocrinopathy. Eur J Pediatr. 1993 Apr; 152(4):313-5. PMID: 8482279.
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