Nagao K - Search Results

1

PTCH1-null induced pluripotent stem cells exclusively differentiate into immature ectodermal cells with large areas of medulloblastoma-like tissue.

Nagao K, Kato C, Ikemoto Y, Motojima T, Fujii K, Umezawa A, Miyashita T. Nagao K, et al. Discov Oncol. 2022 May 27;13(1):36. doi: 10.1007/s12672-022-00498-x. Discov Oncol. 2022. PMID: 35618979 Free PMC article.

2

Intracellular aggregate formation of dentatorubral-pallidoluysian atrophy (DRPLA) protein with the extended polyglutamine.

Miyashita T, Nagao K, Ohmi K, Yanagisawa H, Okamura-Oho Y, Yamada M. Miyashita T, et al. Among authors: nagao k. Biochem Biophys Res Commun. 1998 Aug 10;249(1):96-102. doi: 10.1006/bbrc.1998.9096. Biochem Biophys Res Commun. 1998. PMID: 9705838

3

Investigation of glucocorticoid-induced apoptotic pathway: processing of caspase-6 but not caspase-3.

Miyashita T, Nagao K, Krajewski S, Salvesen GS, Reed JC, Inoue T, Yamada M. Miyashita T, et al. Among authors: nagao k. Cell Death Differ. 1998 Dec;5(12):1034-41. doi: 10.1038/sj.cdd.4400442. Cell Death Differ. 1998. PMID: 9894610

4

Dentatorubral-pallidoluysian atrophy protein is phosphorylated by c-Jun NH2-terminal kinase.

Okamura-Oho Y, Miyashita T, Nagao K, Shima S, Ogata Y, Katada T, Nishina H, Yamada M. Okamura-Oho Y, et al. Among authors: nagao k. Hum Mol Genet. 2003 Jul 1;12(13):1535-42. doi: 10.1093/hmg/ddg168. Hum Mol Genet. 2003. PMID: 12812981

5

Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes.

Nagao K, Fujii K, Yamada M, Miyashita T. Nagao K, et al. J Hum Genet. 2004;49(2):97-101. doi: 10.1007/s10038-003-0117-0. Epub 2004 Jan 21. J Hum Genet. 2004. PMID: 14735326

6

Identification and characterization of multiple isoforms of a murine and human tumor suppressor, patched, having distinct first exons.

Nagao K, Toyoda M, Takeuchi-Inoue K, Fujii K, Yamada M, Miyashita T. Nagao K, et al. Genomics. 2005 Apr;85(4):462-71. doi: 10.1016/j.ygeno.2004.11.014. Genomics. 2005. PMID: 15780749

7

Frequent occurrence of protein isoforms with or without a single amino acid residue by subtle alternative splicing: the case of Gln in DRPLA affects subcellular localization of the products.

Tadokoro K, Yamazaki-Inoue M, Tachibana M, Fujishiro M, Nagao K, Toyoda M, Ozaki M, Ono M, Miki N, Miyashita T, Yamada M. Tadokoro K, et al. Among authors: nagao k. J Hum Genet. 2005;50(8):382-394. doi: 10.1007/s10038-005-0261-9. Epub 2005 Aug 10. J Hum Genet. 2005. PMID: 16091834

8

Detecting tissue-specific alternative splicing and disease-associated aberrant splicing of the PTCH gene with exon junction microarrays.

Nagao K, Togawa N, Fujii K, Uchikawa H, Kohno Y, Yamada M, Miyashita T. Nagao K, et al. Hum Mol Genet. 2005 Nov 15;14(22):3379-88. doi: 10.1093/hmg/ddi369. Epub 2005 Oct 3. Hum Mol Genet. 2005. PMID: 16203740

9

Brain- and heart-specific Patched-1 containing exon 12b is a dominant negative isoform and is expressed in medulloblastomas.

Uchikawa H, Toyoda M, Nagao K, Miyauchi H, Nishikawa R, Fujii K, Kohno Y, Yamada M, Miyashita T. Uchikawa H, et al. Among authors: nagao k. Biochem Biophys Res Commun. 2006 Oct 13;349(1):277-83. doi: 10.1016/j.bbrc.2006.08.046. Epub 2006 Aug 17. Biochem Biophys Res Commun. 2006. PMID: 16934747

10

U7 snRNA-mediated correction of aberrant splicing caused by activation of cryptic splice sites.

Uchikawa H, Fujii K, Kohno Y, Katsumata N, Nagao K, Yamada M, Miyashita T. Uchikawa H, et al. Among authors: nagao k. J Hum Genet. 2007;52(11):891-897. doi: 10.1007/s10038-007-0192-8. Epub 2007 Sep 13. J Hum Genet. 2007. PMID: 17851636

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