Takita J - Search Results

1

Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.

Shiba N, Yoshida K, Shiraishi Y, Okuno Y, Yamato G, Hara Y, Nagata Y, Chiba K, Tanaka H, Terui K, Kato M, Park MJ, Ohki K, Shimada A, Takita J, Tomizawa D, Kudo K, Arakawa H, Adachi S, Taga T, Tawa A, Ito E, Horibe K, Sanada M, Miyano S, Ogawa S, Hayashi Y. Shiba N, et al. Among authors: takita j. Br J Haematol. 2016 Nov;175(3):476-489. doi: 10.1111/bjh.14247. Epub 2016 Jul 29. Br J Haematol. 2016. PMID: 27470916 Free article.

2

Deletion map of chromosome 9 and p16 (CDKN2A) gene alterations in neuroblastoma.

Takita J, Hayashi Y, Kohno T, Yamaguchi N, Hanada R, Yamamoto K, Yokota J. Takita J, et al. Cancer Res. 1997 Mar 1;57(5):907-12. Cancer Res. 1997. PMID: 9041193

3

Alterations of the tumour suppressor gene DCC in neuroblastoma.

Kong XT, Choi SH, Inoue A, Takita J, Yokota J, Hanada R, Yamamoto K, Bessho F, Yanagisawa M, Hayashi Y. Kong XT, et al. Among authors: takita j. Eur J Cancer. 1997 Oct;33(12):1962-5. doi: 10.1016/s0959-8049(97)00209-8. Eur J Cancer. 1997. PMID: 9516833

4

Loss of heterozygosity in neuroblastomas--an overview.

Takita J, Hayashi Y, Yokota J. Takita J, et al. Eur J Cancer. 1997 Oct;33(12):1971-3. doi: 10.1016/s0959-8049(97)00292-x. Eur J Cancer. 1997. PMID: 9516835 Review.

5

Alterations of the PPP1R3 gene in hematological malignancies.

Inoue K, Kohno T, Takakura S, Morishita K, Takita J, Hayashi Y, Mizoguchi H, Yokota J. Inoue K, et al. Among authors: takita j. Int J Oncol. 2000 Oct;17(4):717-21. doi: 10.3892/ijo.17.4.717. Int J Oncol. 2000. PMID: 10995882

6

Lack of aberrations of the BMP4, BMP2, and PTX1 genes in a patient with pituitary hypoplasia, os odontoideum, renal dysplasia, and right leg anomalies.

Goto M, Takita J, Hashimoto N, Tateshita F, Toyoji H, Kato H, Egi S, Hayashi Y. Goto M, et al. Among authors: takita j. Int J Mol Med. 2002 Sep;10(3):293-7. Int J Mol Med. 2002. PMID: 12165803

7

The kinesin superfamily protein Rab6KIFL is not involved in the pathophysiology of Charcot-Marie-Tooth disease type 4C.

Nagura M, Nagao Y, Takita J, Igarashi T, LeGuern E, Hayashi Y. Nagura M, et al. Among authors: takita j. Int J Mol Med. 2003 Jan;11(1):45-7. Int J Mol Med. 2003. PMID: 12469216

8

A family of episodic ataxia type 2: no evidence of genetic linkage to the CACNA1A gene.

Hirose H, Arayama T, Takita J, Igarashi T, Hayashi Y, Nagao Y. Hirose H, et al. Among authors: takita j. Int J Mol Med. 2003 Feb;11(2):187-9. Int J Mol Med. 2003. PMID: 12525875

9

AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.

Taketani T, Taki T, Takita J, Tsuchida M, Hanada R, Hongo T, Kaneko T, Manabe A, Ida K, Hayashi Y. Taketani T, et al. Among authors: takita j. Genes Chromosomes Cancer. 2003 Sep;38(1):1-7. doi: 10.1002/gcc.10246. Genes Chromosomes Cancer. 2003. PMID: 12874780

10

Genomic structure and mutational analysis of the human KIF1Balpha gene located at 1p36.2 in neuroblastoma.

Chen YY, Takita J, Chen YZ, Yang HW, Hanada R, Yamamoto K, Hayashi Y. Chen YY, et al. Among authors: takita j. Int J Oncol. 2003 Sep;23(3):737-44. Int J Oncol. 2003. PMID: 12888911

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