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Similar articles for PubMed (Select 22802932)


Pairing of homologous regions in the mouse genome is associated with transcription but not imprinting status.

Krueger C, King MR, Krueger F, Branco MR, Osborne CS, Niakan KK, Higgins MJ, Reik W.

PLoS One. 2012;7(7):e38983. doi: 10.1371/journal.pone.0038983. Epub 2012 Jul 3.


Telomeric NAP1L4 and OSBPL5 of the KCNQ1 cluster, and the DECORIN gene are not imprinted in human trophoblast stem cells.

Frost JM, Udayashankar R, Moore HD, Moore GE.

PLoS One. 2010 Jul 14;5(7):e11595. doi: 10.1371/journal.pone.0011595.


Parental origin of chromosomes influences crossover activity within the Kcnq1 transcriptionally imprinted domain of Mus musculus.

Ng SH, Madeira R, Parvanov ED, Petros LM, Petkov PM, Paigen K.

BMC Mol Biol. 2009 May 13;10:43. doi: 10.1186/1471-2199-10-43.


Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.

Umlauf D, Goto Y, Cao R, Cerqueira F, Wagschal A, Zhang Y, Feil R.

Nat Genet. 2004 Dec;36(12):1296-300. Epub 2004 Oct 31.


Preferential S-phase pairing of the imprinted region on distal mouse chromosome 7.

Riesselmann L, Haaf T.

Cytogenet Cell Genet. 1999;86(1):39-42.


Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines.

Kim KP, Thurston A, Mummery C, Ward-van Oostwaard D, Priddle H, Allegrucci C, Denning C, Young L.

Genome Res. 2007 Dec;17(12):1731-42. Epub 2007 Nov 7.


The Kcnq1ot1 long non-coding RNA affects chromatin conformation and expression of Kcnq1, but does not regulate its imprinting in the developing heart.

Korostowski L, Sedlak N, Engel N.

PLoS Genet. 2012 Sep;8(9):e1002956. doi: 10.1371/journal.pgen.1002956. Epub 2012 Sep 20.


At least ten genes define the imprinted Dlk1-Dio3 cluster on mouse chromosome 12qF1.

Hagan JP, O'Neill BL, Stewart CL, Kozlov SV, Croce CM.

PLoS One. 2009;4(2):e4352. doi: 10.1371/journal.pone.0004352. Epub 2009 Feb 5.


Imprinting of the mouse Igf2r gene depends on an intronic CpG island.

Wutz A, Barlow DP.

Mol Cell Endocrinol. 1998 May 25;140(1-2):9-14. Review.


Imprinting at the mouse Ins2 locus: evidence for cis- and trans-allelic interactions.

Duvillié B, Bucchini D, Tang T, Jami J, Pàldi A.

Genomics. 1998 Jan 1;47(1):52-7.


Domain-specific response of imprinted genes to reduced DNMT1.

Weaver JR, Sarkisian G, Krapp C, Mager J, Mann MR, Bartolomei MS.

Mol Cell Biol. 2010 Aug;30(16):3916-28. doi: 10.1128/MCB.01278-09. Epub 2010 Jun 14.


ES cell differentiation system recapitulates the establishment of imprinted gene expression in a cell-type-specific manner.

Kohama C, Kato H, Numata K, Hirose M, Takemasa T, Ogura A, Kiyosawa H.

Hum Mol Genet. 2012 Mar 15;21(6):1391-401. doi: 10.1093/hmg/ddr577. Epub 2011 Dec 9.


Limited evolutionary conservation of imprinting in the human placenta.

Monk D, Arnaud P, Apostolidou S, Hills FA, Kelsey G, Stanier P, Feil R, Moore GE.

Proc Natl Acad Sci U S A. 2006 Apr 25;103(17):6623-8. Epub 2006 Apr 13.


Evidence that homologous X-chromosome pairing requires transcription and Ctcf protein.

Xu N, Donohoe ME, Silva SS, Lee JT.

Nat Genet. 2007 Nov;39(11):1390-6. Epub 2007 Oct 21.


Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center.

Xin Z, Tachibana M, Guggiari M, Heard E, Shinkai Y, Wagstaff J.

J Biol Chem. 2003 Apr 25;278(17):14996-5000. Epub 2003 Feb 13.


Evolution of the CDKN1C-KCNQ1 imprinted domain.

Ager EI, Pask AJ, Gehring HM, Shaw G, Renfree MB.

BMC Evol Biol. 2008 May 29;8:163. doi: 10.1186/1471-2148-8-163.

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