Kaneko-Ishino T - Search Results

1

No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients.

Kobayashi S, Uemura H, Kohda T, Nagai T, Chinen Y, Naritomi K, Kinoshita EI, Ohashi H, Imaizumi K, Tsukahara M, Sugio Y, Tonoki H, Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, Kaneko-Ishino T, Ishino F. Kobayashi S, et al. Am J Med Genet. 2001 Dec 1;104(3):225-31. Am J Med Genet. 2001. PMID: 11754049

2

Fate of haploid parthenogenetic cells in mouse chimeras during development.

Ito M, Kaneko-Ishino T, Ishino F, Matsuhashi M, Yokoyama M, Katsuki M. Ito M, et al. J Exp Zool. 1991 Feb;257(2):178-83. doi: 10.1002/jez.1402570206. J Exp Zool. 1991. PMID: 1990050

3

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization.

Kaneko-Ishino T, Kuroiwa Y, Miyoshi N, Kohda T, Suzuki R, Yokoyama M, Viville S, Barton SC, Ishino F, Surani MA. Kaneko-Ishino T, et al. Nat Genet. 1995 Sep;11(1):52-9. doi: 10.1038/ng0995-52. Nat Genet. 1995. PMID: 7550314

4

Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein.

Kuroiwa Y, Kaneko-Ishino T, Kagitani F, Kohda T, Li LL, Tada M, Suzuki R, Yokoyama M, Shiroishi T, Wakana S, Barton SC, Ishino F, Surani MA. Kuroiwa Y, et al. Nat Genet. 1996 Feb;12(2):186-90. doi: 10.1038/ng0296-186. Nat Genet. 1996. PMID: 8563758

5

Human PEG1/MEST, an imprinted gene on chromosome 7.

Kobayashi S, Kohda T, Miyoshi N, Kuroiwa Y, Aisaka K, Tsutsumi O, Kaneko-Ishino T, Ishino F. Kobayashi S, et al. Hum Mol Genet. 1997 May;6(5):781-6. doi: 10.1093/hmg/6.5.781. Hum Mol Genet. 1997. PMID: 9158153

6

Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse.

Kagitani F, Kuroiwa Y, Wakana S, Shiroishi T, Miyoshi N, Kobayashi S, Nishida M, Kohda T, Kaneko-Ishino T, Ishino F. Kagitani F, et al. Nucleic Acids Res. 1997 Sep 1;25(17):3428-32. doi: 10.1093/nar/25.17.3428. Nucleic Acids Res. 1997. PMID: 9254699 Free PMC article.

7

Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene.

Miyoshi N, Kuroiwa Y, Kohda T, Shitara H, Yonekawa H, Kawabe T, Hasegawa H, Barton SC, Surani MA, Kaneko-Ishino T, Ishino F. Miyoshi N, et al. Proc Natl Acad Sci U S A. 1998 Feb 3;95(3):1102-7. doi: 10.1073/pnas.95.3.1102. Proc Natl Acad Sci U S A. 1998. PMID: 9448292 Free PMC article.

8

Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis.

Obata Y, Kaneko-Ishino T, Koide T, Takai Y, Ueda T, Domeki I, Shiroishi T, Ishino F, Kono T. Obata Y, et al. Development. 1998 Apr;125(8):1553-60. doi: 10.1242/dev.125.8.1553. Development. 1998. PMID: 9502736

9

Expression and imprinting status of human PEG8/IGF2AS, a paternally expressed antisense transcript from the IGF2 locus, in Wilms' tumors.

Okutsu T, Kuroiwa Y, Kagitani F, Kai M, Aisaka K, Tsutsumi O, Kaneko Y, Yokomori K, Surani MA, Kohda T, Kaneko-Ishino T, Ishino F. Okutsu T, et al. J Biochem. 2000 Mar;127(3):475-83. doi: 10.1093/oxfordjournals.jbchem.a022630. J Biochem. 2000. PMID: 10731720 Free article.

10

Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.

Miyoshi N, Wagatsuma H, Wakana S, Shiroishi T, Nomura M, Aisaka K, Kohda T, Surani MA, Kaneko-Ishino T, Ishino F. Miyoshi N, et al. Genes Cells. 2000 Mar;5(3):211-20. doi: 10.1046/j.1365-2443.2000.00320.x. Genes Cells. 2000. PMID: 10759892 Free article.

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