Miyashita T - 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. Among authors: miyashita t. Discov Oncol. 2022 May 27;13(1):36. doi: 10.1007/s12672-022-00498-x. Discov Oncol. 2022. PMID: 35618979 Free PMC article.

2

Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in PTCH1.

Ikemoto Y, Miyashita T, Nasu M, Hatsuse H, Kajiwara K, Fujii K, Motojima T, Kokido I, Toyoda M, Umezawa A. Ikemoto Y, et al. Among authors: miyashita t. Aging (Albany NY). 2020 May 21;12(10):9935-9947. doi: 10.18632/aging.103258. Epub 2020 May 21. Aging (Albany NY). 2020. PMID: 32436863 Free PMC article.

3

Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndrome.

Suzuki M, Hatsuse H, Nagao K, Takayama Y, Kameyama K, Kabasawa Y, Omura K, Yoshida M, Fujii K, Miyashita T. Suzuki M, et al. Among authors: miyashita t. J Hum Genet. 2012 Jul;57(7):422-6. doi: 10.1038/jhg.2012.45. Epub 2012 May 10. J Hum Genet. 2012. PMID: 22572734

4

Heterozygous tandem duplication within the PTCH1 gene results in nevoid basal cell carcinoma syndrome.

Kosaki R, Nagao K, Kameyama K, Suzuki M, Fujii K, Miyashita T. Kosaki R, et al. Among authors: miyashita t. Am J Med Genet A. 2012 Jul;158A(7):1724-8. doi: 10.1002/ajmg.a.35412. Am J Med Genet A. 2012. PMID: 22711650

5

Downregulation of microRNA-431 by human interferon-β inhibits viability of medulloblastoma and glioblastoma cells via upregulation of SOCS6.

Tanaka T, Arai M, Jiang X, Sugaya S, Kanda T, Fujii K, Kita K, Sugita K, Imazeki F, Miyashita T, Kaneda A, Yokosuka O. Tanaka T, et al. Among authors: miyashita t. Int J Oncol. 2014 May;44(5):1685-90. doi: 10.3892/ijo.2014.2317. Epub 2014 Feb 28. Int J Oncol. 2014. PMID: 24584142

6

Gorlin syndrome (nevoid basal cell carcinoma syndrome): update and literature review.

Fujii K, Miyashita T. Fujii K, et al. Among authors: miyashita t. Pediatr Int. 2014 Oct;56(5):667-74. doi: 10.1111/ped.12461. Pediatr Int. 2014. PMID: 25131638 Review.

7

Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene.

Kato C, Fujii K, Arai Y, Hatsuse H, Nagao K, Takayama Y, Kameyama K, Fujii K, Miyashita T. Kato C, et al. Among authors: miyashita t. Fam Cancer. 2017 Jan;16(1):131-138. doi: 10.1007/s10689-016-9924-2. Fam Cancer. 2017. PMID: 27561271

8

Somatic mosaicism containing double mutations in PTCH1 revealed by generation of induced pluripotent stem cells from nevoid basal cell carcinoma syndrome.

Ikemoto Y, Takayama Y, Fujii K, Masuda M, Kato C, Hatsuse H, Fujitani K, Nagao K, Kameyama K, Ikehara H, Toyoda M, Umezawa A, Miyashita T. Ikemoto Y, et al. Among authors: miyashita t. J Med Genet. 2017 Aug;54(8):579-584. doi: 10.1136/jmedgenet-2016-104490. Epub 2017 Mar 31. J Med Genet. 2017. PMID: 28363938

9

Establishment of a Gorlin syndrome model from induced neural progenitor cells exhibiting constitutive GLI1 expression and high sensitivity to inhibition by smoothened (SMO).

Ikehara H, Fujii K, Miyashita T, Ikemoto Y, Nagamine M, Shimojo N, Umezawa A. Ikehara H, et al. Among authors: miyashita t. Lab Invest. 2020 Apr;100(4):657-664. doi: 10.1038/s41374-019-0346-2. Epub 2019 Nov 22. Lab Invest. 2020. PMID: 31758086 Free article.

10

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. Among authors: miyashita t. 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

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