Hosoda F - Search Results

1

Integrated genetic and epigenetic analysis of myxofibrosarcoma.

Ogura K, Hosoda F, Arai Y, Nakamura H, Hama N, Totoki Y, Yoshida A, Nagai M, Kato M, Arakawa E, Mukai W, Rokutan H, Kawai A, Tanaka S, Shibata T. Ogura K, et al. Among authors: hosoda f. Nat Commun. 2018 Jul 17;9(1):2765. doi: 10.1038/s41467-018-03891-9. Nat Commun. 2018. PMID: 30018380 Free PMC article.

2

A NotI restriction map of the entire long arm of human chromosome 21.

Ichikawa H, Hosoda F, Arai Y, Shimizu K, Ohira M, Ohki M. Ichikawa H, et al. Among authors: hosoda f. Nat Genet. 1993 Aug;4(4):361-6. doi: 10.1038/ng0893-361. Nat Genet. 1993. PMID: 8401583

3

A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3.

Arai Y, Hosoda F, Nakayama K, Ohki M. Arai Y, et al. Among authors: hosoda f. Genomics. 1996 Jul 1;35(1):196-206. doi: 10.1006/geno.1996.0339. Genomics. 1996. PMID: 8661121

4

The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene, DDX10.

Arai Y, Hosoda F, Kobayashi H, Arai K, Hayashi Y, Kamada N, Kaneko Y, Ohki M. Arai Y, et al. Among authors: hosoda f. Blood. 1997 Jun 1;89(11):3936-44. Blood. 1997. PMID: 9166830 Free article.

5

Inversion of chromosome 11 inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: identification of a P1 clone spanning the 11q22 breakpoint.

Kobayashi H, Arai Y, Hosoda F, Maseki N, Hayashi Y, Eguchi H, Ohki M, Kaneko Y. Kobayashi H, et al. Among authors: hosoda f. Genes Chromosomes Cancer. 1997 Jul;19(3):150-5. Genes Chromosomes Cancer. 1997. PMID: 9218995

6

Fusion of MOZ and p300 histone acetyltransferases in acute monocytic leukemia with a t(8;22)(p11;q13) chromosome translocation.

Kitabayashi I, Aikawa Y, Yokoyama A, Hosoda F, Nagai M, Kakazu N, Abe T, Ohki M. Kitabayashi I, et al. Among authors: hosoda f. Leukemia. 2001 Jan;15(1):89-94. doi: 10.1038/sj.leu.2401983. Leukemia. 2001. PMID: 11243405

7

Genetic profile of hepatocellular carcinoma revealed by array-based comparative genomic hybridization: identification of genetic indicators to predict patient outcome.

Katoh H, Shibata T, Kokubu A, Ojima H, Loukopoulos P, Kanai Y, Kosuge T, Fukayama M, Kondo T, Sakamoto M, Hosoda F, Ohki M, Imoto I, Inazawa J, Hirohashi S. Katoh H, et al. Among authors: hosoda f. J Hepatol. 2005 Nov;43(5):863-74. doi: 10.1016/j.jhep.2005.05.033. Epub 2005 Jul 5. J Hepatol. 2005. PMID: 16139920

8

Genetic classification of lung adenocarcinoma based on array-based comparative genomic hybridization analysis: its association with clinicopathologic features.

Shibata T, Uryu S, Kokubu A, Hosoda F, Ohki M, Sakiyama T, Matsuno Y, Tsuchiya R, Kanai Y, Kondo T, Imoto I, Inazawa J, Hirohashi S. Shibata T, et al. Among authors: hosoda f. Clin Cancer Res. 2005 Sep 1;11(17):6177-85. doi: 10.1158/1078-0432.CCR-05-0293. Clin Cancer Res. 2005. PMID: 16144918

9

Array-based comparative genomic hybridization analysis of high-grade neuroendocrine tumors of the lung.

Peng WX, Shibata T, Katoh H, Kokubu A, Matsuno Y, Asamura H, Tsuchiya R, Kanai Y, Hosoda F, Sakiyama T, Ohki M, Imoto I, Inazawa J, Hirohashi S. Peng WX, et al. Among authors: hosoda f. Cancer Sci. 2005 Oct;96(10):661-7. doi: 10.1111/j.1349-7006.2005.00092.x. Cancer Sci. 2005. PMID: 16232197 Free PMC article.

10

Frequent silencing of the candidate tumor suppressor PCDH20 by epigenetic mechanism in non-small-cell lung cancers.

Imoto I, Izumi H, Yokoi S, Hosoda H, Shibata T, Hosoda F, Ohki M, Hirohashi S, Inazawa J. Imoto I, et al. Among authors: hosoda f, hosoda h. Cancer Res. 2006 May 1;66(9):4617-26. doi: 10.1158/0008-5472.CAN-05-4437. Cancer Res. 2006. PMID: 16651412

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