Sanada M - Search Results

1

Smap1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia.

Kon S, Minegishi N, Tanabe K, Watanabe T, Funaki T, Wong WF, Sakamoto D, Higuchi Y, Kiyonari H, Asano K, Iwakura Y, Fukumoto M, Osato M, Sanada M, Ogawa S, Nakamura T, Satake M. Kon S, et al. Among authors: sanada m. J Clin Invest. 2013 Mar;123(3):1123-37. doi: 10.1172/JCI63711. Epub 2013 Feb 22. J Clin Invest. 2013. PMID: 23434593 Free PMC article.

2

Identification of a SRC-like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation.

Hosoya N, Qiao Y, Hangaishi A, Wang L, Nannya Y, Sanada M, Kurokawa M, Chiba S, Hirai H, Ogawa S. Hosoya N, et al. Among authors: sanada m. Genes Chromosomes Cancer. 2005 Mar;42(3):269-79. doi: 10.1002/gcc.20147. Genes Chromosomes Cancer. 2005. PMID: 15611931

3

Gain-of-function c-CBL mutations associated with uniparental disomy of 11q in myeloid neoplasms.

Ogawa S, Sanada M, Shih LY, Suzuki T, Otsu M, Nakauchi H, Koeffler HP. Ogawa S, et al. Among authors: sanada m. Cell Cycle. 2010 Mar 15;9(6):1051-6. doi: 10.4161/cc.9.6.11034. Epub 2010 Mar 15. Cell Cycle. 2010. PMID: 20237427 Free PMC article. Review.

4

Deregulated intracellular signaling by mutated c-CBL in myeloid neoplasms.

Ogawa S, Shih LY, Suzuki T, Otsu M, Nakauchi H, Koeffler HP, Sanada M. Ogawa S, et al. Among authors: sanada m. Clin Cancer Res. 2010 Aug 1;16(15):3825-31. doi: 10.1158/1078-0432.CCR-09-2341. Epub 2010 Jun 14. Clin Cancer Res. 2010. PMID: 20547695 Review.

5

Oncogenic mutations of ALK in neuroblastoma.

Ogawa S, Takita J, Sanada M, Hayashi Y. Ogawa S, et al. Among authors: sanada m. Cancer Sci. 2011 Feb;102(2):302-8. doi: 10.1111/j.1349-7006.2010.01825.x. Cancer Sci. 2011. PMID: 21205076 Free PMC article. Review.

6

A high occurrence of acquisition and/or expansion of C-CBL mutant clones in the progression of high-risk myelodysplastic syndrome to acute myeloid leukemia.

Kao HW, Sanada M, Liang DC, Lai CL, Lee EH, Kuo MC, Lin TL, Shih YS, Wu JH, Huang CF, Ogawa S, Shih LY. Kao HW, et al. Among authors: sanada m. Neoplasia. 2011 Nov;13(11):1035-42. doi: 10.1593/neo.111192. Neoplasia. 2011. PMID: 22131879 Free PMC article.

7

Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?

Sato-Otsubo A, Sanada M, Ogawa S. Sato-Otsubo A, et al. Among authors: sanada m. Semin Oncol. 2012 Feb;39(1):13-25. doi: 10.1053/j.seminoncol.2011.11.010. Semin Oncol. 2012. PMID: 22289488 Review.

8

Genome-wide analysis of myelodysplastic syndromes.

Sanada M, Ogawa S. Sanada M, et al. Curr Pharm Des. 2012;18(22):3163-9. doi: 10.2174/1381612811209023163. Curr Pharm Des. 2012. PMID: 22571694 Review.

9

[IDH1/2 gene mutations in myelodysplastic syndromes].

Yoshida K, Sanada M, Ogawa S. Yoshida K, et al. Among authors: sanada m. Rinsho Ketsueki. 2012 Apr;53(4):391-5. Rinsho Ketsueki. 2012. PMID: 22687971 Review. Japanese. No abstract available.

10

Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO 'MDS-U' designation.

Hosokawa K, Katagiri T, Sugimori N, Ishiyama K, Sasaki Y, Seiki Y, Sato-Otsubo A, Sanada M, Ogawa S, Nakao S. Hosokawa K, et al. Among authors: sanada m. Haematologica. 2012 Dec;97(12):1845-9. doi: 10.3324/haematol.2011.061127. Epub 2012 Jun 11. Haematologica. 2012. PMID: 22689682 Free PMC article.

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