Reik W - Search Results

1

Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans.

Petry CJ, Ong KK, Barratt BJ, Wingate D, Cordell HJ, Ring SM, Pembrey ME, Reik W, Todd JA, Dunger DB; ALSPAC Study Team. Petry CJ, et al. Among authors: reik w. BMC Genet. 2005 May 10;6:22. doi: 10.1186/1471-2156-6-22. BMC Genet. 2005. PMID: 15885138 Free PMC article.

2

Raised late pregnancy glucose concentrations in mice carrying pups with targeted disruption of H19delta13.

Petry CJ, Evans ML, Wingate DL, Ong KK, Reik W, Constância M, Dunger DB. Petry CJ, et al. Among authors: reik w. Diabetes. 2010 Jan;59(1):282-6. doi: 10.2337/db09-0757. Epub 2009 Sep 30. Diabetes. 2010. PMID: 19794064 Free PMC article.

3

Increased placental glucose transport rates in pregnant mice carrying fetuses with targeted disruption of their placental-specific Igf2 transcripts are not associated with raised circulating glucose concentrations.

Petry CJ, Evans ML, Wingate DL, Ong KK, Reik W, Constância M, Dunger DB. Petry CJ, et al. Among authors: reik w. Exp Diabetes Res. 2011;2011:171376. doi: 10.1155/2011/171376. Epub 2011 Feb 8. Exp Diabetes Res. 2011. PMID: 21331382 Free PMC article.

4

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

Joyce JA, Lam WK, Catchpoole DJ, Jenks P, Reik W, Maher ER, Schofield PN. Joyce JA, et al. Among authors: reik w. Hum Mol Genet. 1997 Sep;6(9):1543-8. doi: 10.1093/hmg/6.9.1543. Hum Mol Genet. 1997. PMID: 9285792

5

Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops.

Murrell A, Heeson S, Reik W. Murrell A, et al. Among authors: reik w. Nat Genet. 2004 Aug;36(8):889-93. doi: 10.1038/ng1402. Epub 2004 Jul 25. Nat Genet. 2004. PMID: 15273689

6

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Catchpoole D, Lam WW, Valler D, Temple IK, Joyce JA, Reik W, Schofield PN, Maher ER. Catchpoole D, et al. Among authors: reik w. J Med Genet. 1997 May;34(5):353-9. doi: 10.1136/jmg.34.5.353. J Med Genet. 1997. PMID: 9152830 Free PMC article.

7

Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.

Constância M, Dean W, Lopes S, Moore T, Kelsey G, Reik W. Constância M, et al. Among authors: reik w. Nat Genet. 2000 Oct;26(2):203-6. doi: 10.1038/79930. Nat Genet. 2000. PMID: 11017078

8

Cohesin is required for higher-order chromatin conformation at the imprinted IGF2-H19 locus.

Nativio R, Wendt KS, Ito Y, Huddleston JE, Uribe-Lewis S, Woodfine K, Krueger C, Reik W, Peters JM, Murrell A. Nativio R, et al. Among authors: reik w. PLoS Genet. 2009 Nov;5(11):e1000739. doi: 10.1371/journal.pgen.1000739. Epub 2009 Nov 26. PLoS Genet. 2009. PMID: 19956766 Free PMC article.

9

Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA.

Cerrato F, Dean W, Davies K, Kagotani K, Mitsuya K, Okumura K, Riccio A, Reik W. Cerrato F, et al. Among authors: reik w. Hum Mol Genet. 2003 Dec 1;12(23):3123-32. doi: 10.1093/hmg/ddg338. Epub 2003 Oct 7. Hum Mol Genet. 2003. PMID: 14532328

10

Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians.

Smits G, Mungall AJ, Griffiths-Jones S, Smith P, Beury D, Matthews L, Rogers J, Pask AJ, Shaw G, VandeBerg JL, McCarrey JR; SAVOIR Consortium; Renfree MB, Reik W, Dunham I. Smits G, et al. Among authors: reik w. Nat Genet. 2008 Aug;40(8):971-6. doi: 10.1038/ng.168. Epub 2008 Jun 29. Nat Genet. 2008. PMID: 18587395

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