Kayashima T - Search Results

1

The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting.

Yamada T, Kayashima T, Yamasaki K, Ohta T, Yoshiura Ki, Matsumoto N, Fujimoto S, Niikawa N, Kishino T. Yamada T, et al. Among authors: kayashima t. Gene. 2002 Apr 17;288(1-2):57-63. doi: 10.1016/s0378-1119(02)00428-6. Gene. 2002. PMID: 12034494

2

The novel imprinted carboxypeptidase A4 gene ( CPA4) in the 7q32 imprinting domain.

Kayashima T, Yamasaki K, Yamada T, Sakai H, Miwa N, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Kanetake H, Ishino F, Niikawa N, Kishino T. Kayashima T, et al. Hum Genet. 2003 Mar;112(3):220-6. doi: 10.1007/s00439-002-0891-3. Epub 2003 Jan 28. Hum Genet. 2003. PMID: 12552318

3

Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting.

Kayashima T, Yamasaki K, Joh K, Yamada T, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Mukai T, Niikawa N, Kishino T. Kayashima T, et al. Genomics. 2003 Jun;81(6):644-7. doi: 10.1016/s0888-7543(03)00077-6. Genomics. 2003. PMID: 12782135

4

Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32.

Yamada T, Mitsuya K, Kayashima T, Yamasaki K, Ohta T, Yoshiura K, Matsumoto N, Yamada H, Minakami H, Oshimura M, Niikawa N, Kishino T. Yamada T, et al. Among authors: kayashima t. Genomics. 2004 Mar;83(3):402-12. doi: 10.1016/j.ygeno.2003.08.016. Genomics. 2004. PMID: 14962666

5

Neuron-specific relaxation of Igf2r imprinting is associated with neuron-specific histone modifications and lack of its antisense transcript Air.

Yamasaki Y, Kayashima T, Soejima H, Kinoshita A, Yoshiura K, Matsumoto N, Ohta T, Urano T, Masuzaki H, Ishimaru T, Mukai T, Niikawa N, Kishino T. Yamasaki Y, et al. Among authors: kayashima t. Hum Mol Genet. 2005 Sep 1;14(17):2511-20. doi: 10.1093/hmg/ddi255. Epub 2005 Jul 21. Hum Mol Genet. 2005. PMID: 16037066

6

On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?

Kayashima T, Ohta T, Niikawa N, Kishino T. Kayashima T, et al. J Hum Genet. 2003;48(9):492-493. doi: 10.1007/s10038-003-0061-z. Epub 2003 Sep 4. J Hum Genet. 2003. PMID: 12955587 No abstract available.

7

Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10.

Yamasaki-Ishizaki Y, Kayashima T, Mapendano CK, Soejima H, Ohta T, Masuzaki H, Kinoshita A, Urano T, Yoshiura K, Matsumoto N, Ishimaru T, Mukai T, Niikawa N, Kishino T. Yamasaki-Ishizaki Y, et al. Among authors: kayashima t. Mol Cell Biol. 2007 Jan;27(2):732-42. doi: 10.1128/MCB.01329-06. Epub 2006 Nov 13. Mol Cell Biol. 2007. PMID: 17101788 Free PMC article.

8

Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE).

Kayashima T, Matsuo H, Satoh A, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Niikawa N, Kishino T. Kayashima T, et al. J Hum Genet. 2002;47(2):77-9. doi: 10.1007/s100380200004. J Hum Genet. 2002. PMID: 11916006

9

Maternal isodisomy for 14q21-q24 in a man with diabetes mellitus.

Kayashima T, Katahira M, Harada N, Miwa N, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Nakamura Y, Kajii T, Niikawa N, Kishino T. Kayashima T, et al. Am J Med Genet. 2002 Jul 22;111(1):38-42. doi: 10.1002/ajmg.10511. Am J Med Genet. 2002. PMID: 12124731

10

[Cohen syndrome].

Kayashima T, Niikawa N. Kayashima T, et al. Ryoikibetsu Shokogun Shirizu. 2001;(36):477-8. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596442 Review. Japanese. No abstract available.

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