Hayashi Y - Search Results

1

Frequent inactivation of A20 in B-cell lymphomas.

Kato M, Sanada M, Kato I, Sato Y, Takita J, Takeuchi K, Niwa A, Chen Y, Nakazaki K, Nomoto J, Asakura Y, Muto S, Tamura A, Iio M, Akatsuka Y, Hayashi Y, Mori H, Igarashi T, Kurokawa M, Chiba S, Mori S, Ishikawa Y, Okamoto K, Tobinai K, Nakagama H, Nakahata T, Yoshino T, Kobayashi Y, Ogawa S. Kato M, et al. Among authors: hayashi y. Nature. 2009 Jun 4;459(7247):712-6. doi: 10.1038/nature07969. Epub 2009 May 3. Nature. 2009. PMID: 19412163

2

Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors.

Uno K, Takita J, Yokomori K, Tanaka Y, Ohta S, Shimada H, Gilles FH, Sugita K, Abe S, Sako M, Hashizume K, Hayashi Y. Uno K, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2002 May;34(1):33-41. doi: 10.1002/gcc.10052. Genes Chromosomes Cancer. 2002. PMID: 11921280

3

The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9.

Taketani T, Taki T, Ono R, Kobayashi Y, Ida K, Hayashi Y. Taketani T, et al. Among authors: hayashi y. Genes Chromosomes Cancer. 2002 Aug;34(4):437-43. doi: 10.1002/gcc.10077. Genes Chromosomes Cancer. 2002. PMID: 12112533

4

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: hayashi y. Int J Mol Med. 2002 Sep;10(3):293-7. Int J Mol Med. 2002. PMID: 12165803

5

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: hayashi y. Int J Mol Med. 2003 Jan;11(1):45-7. Int J Mol Med. 2003. PMID: 12469216

6

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: hayashi y. Int J Mol Med. 2003 Feb;11(2):187-9. Int J Mol Med. 2003. PMID: 12525875

7

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: hayashi y. Genes Chromosomes Cancer. 2003 Sep;38(1):1-7. doi: 10.1002/gcc.10246. Genes Chromosomes Cancer. 2003. PMID: 12874780

8

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: hayashi y. Int J Oncol. 2003 Sep;23(3):737-44. Int J Oncol. 2003. PMID: 12888911

9

Aberrations of p16INK4A, p14ARF and p15INK4B genes in pediatric solid tumors.

Obana K, Yang HW, Piao HY, Taki T, Hashizume K, Hanada R, Yamamoto K, Tanaka Y, Toyoda Y, Takita J, Tsuchida Y, Hayashi Y. Obana K, et al. Among authors: hayashi y. Int J Oncol. 2003 Oct;23(4):1151-7. Int J Oncol. 2003. PMID: 12963998

10

Promoter-specific repression of hepatocyte nuclear factor (HNF)-1 beta and HNF-1 alpha transcriptional activity by an HNF-1 beta missense mutant associated with Type 5 maturity-onset diabetes of the young with hepatic and biliary manifestations.

Kitanaka S, Miki Y, Hayashi Y, Igarashi T. Kitanaka S, et al. Among authors: hayashi y. J Clin Endocrinol Metab. 2004 Mar;89(3):1369-78. doi: 10.1210/jc.2003-031308. J Clin Endocrinol Metab. 2004. PMID: 15001636

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