Barton SC - Search Results

1

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. Among authors: barton sc. 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.

2

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: barton sc. Nat Genet. 1995 Sep;11(1):52-9. doi: 10.1038/ng0995-52. Nat Genet. 1995. PMID: 7550314

3

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: barton sc. Nat Genet. 1996 Feb;12(2):186-90. doi: 10.1038/ng0296-186. Nat Genet. 1996. PMID: 8563758

4

Influence of sex chromosome constitution on the genomic imprinting of germ cells.

Durcova-Hills G, Hajkova P, Sullivan S, Barton S, Surani MA, McLaren A. Durcova-Hills G, et al. Proc Natl Acad Sci U S A. 2006 Jul 25;103(30):11184-8. doi: 10.1073/pnas.0602621103. Epub 2006 Jul 17. Proc Natl Acad Sci U S A. 2006. PMID: 16847261 Free PMC article.

5

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: barton sc. Nat Genet. 1998 Oct;20(2):163-9. doi: 10.1038/2464. Nat Genet. 1998. PMID: 9771709

6

A silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice.

Brenton JD, Drewell RA, Viville S, Hilton KJ, Barton SC, Ainscough JF, Surani MA. Brenton JD, et al. Among authors: barton sc. Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9242-7. doi: 10.1073/pnas.96.16.9242. Proc Natl Acad Sci U S A. 1999. PMID: 10430927 Free PMC article.

7

A human p57(KIP2) transgene is not activated by passage through the maternal mouse germline.

John RM, Hodges M, Little P, Barton SC, Surani MA. John RM, et al. Among authors: barton sc. Hum Mol Genet. 1999 Nov;8(12):2211-9. doi: 10.1093/hmg/8.12.2211. Hum Mol Genet. 1999. PMID: 10545601

8

A skeletal muscle-specific mouse Igf2 repressor lies 40 kb downstream of the gene.

Ainscough JF, John RM, Barton SC, Surani MA. Ainscough JF, et al. Among authors: barton sc. Development. 2000 Sep;127(18):3923-30. doi: 10.1242/dev.127.18.3923. Development. 2000. PMID: 10952890

9

Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome.

John RM, Ainscough JF, Barton SC, Surani MA. John RM, et al. Among authors: barton sc. Hum Mol Genet. 2001 Jul 15;10(15):1601-9. doi: 10.1093/hmg/10.15.1601. Hum Mol Genet. 2001. PMID: 11468278

10

Cdkn1c (p57Kip2) is the major regulator of embryonic growth within its imprinted domain on mouse distal chromosome 7.

Andrews SC, Wood MD, Tunster SJ, Barton SC, Surani MA, John RM. Andrews SC, et al. Among authors: barton sc. BMC Dev Biol. 2007 May 21;7:53. doi: 10.1186/1471-213X-7-53. BMC Dev Biol. 2007. PMID: 17517131 Free PMC article.

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