Ishino F - Search Results

1

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.

Lefebvre L, Viville S, Barton SC, Ishino F, Keverne EB, Surani MA. Lefebvre L, et al. Among authors: ishino f. Nat Genet. 1998 Oct;20(2):163-9. doi: 10.1038/2464. Nat Genet. 1998. PMID: 9771709

2

Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

Li L, Keverne EB, Aparicio SA, Ishino F, Barton SC, Surani MA. Li L, et al. Among authors: ishino f. Science. 1999 Apr 9;284(5412):330-3. doi: 10.1126/science.284.5412.330. Science. 1999. PMID: 10195900

3

Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7.

Li LL, Szeto IY, Cattanach BM, Ishino F, Surani MA. Li LL, et al. Among authors: ishino f. Genomics. 2000 Feb 1;63(3):333-40. doi: 10.1006/geno.1999.6103. Genomics. 2000. PMID: 10704281

4

Genomic structure and parent-of-origin-specific methylation of Peg1.

Lefebvre L, Viville S, Barton SC, Ishino F, Surani MA. Lefebvre L, et al. Among authors: ishino f. Hum Mol Genet. 1997 Oct;6(11):1907-15. doi: 10.1093/hmg/6.11.1907. Hum Mol Genet. 1997. PMID: 9302270

5

Localisation of the imprinted gene neuronatin, Nnat, confirms and refines the location of a second imprinting region on mouse chromosome 2.

Williamson CM, Beechey CV, Ball ST, Dutton ER, Cattanach BM, Tease C, Ishino F, Peters J. Williamson CM, et al. Among authors: ishino f. Cytogenet Cell Genet. 1998;81(1):73-8. doi: 10.1159/000014992. Cytogenet Cell Genet. 1998. PMID: 9691180

6

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. Among authors: ishino f. Nat Genet. 1995 Sep;11(1):52-9. doi: 10.1038/ng0995-52. Nat Genet. 1995. PMID: 7550314

7

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. Among authors: ishino f. Am J Med Genet. 2001 Dec 1;104(3):225-31. Am J Med Genet. 2001. PMID: 11754049

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. Among authors: ishino f. Development. 1998 Apr;125(8):1553-60. doi: 10.1242/dev.125.8.1553. Development. 1998. PMID: 9502736

9

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. Among authors: ishino f. Nat Genet. 1996 Feb;12(2):186-90. doi: 10.1038/ng0296-186. Nat Genet. 1996. PMID: 8563758

10

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. Among authors: ishino f. Hum Mol Genet. 1997 May;6(5):781-6. doi: 10.1093/hmg/6.5.781. Hum Mol Genet. 1997. PMID: 9158153

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