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Cited In for PubMed (Select 10958646)


A pathway from chromosome transfer to engineering resulting in human and mouse artificial chromosomes for a variety of applications to bio-medical challenges.

Oshimura M, Uno N, Kazuki Y, Katoh M, Inoue T.

Chromosome Res. 2015 Feb;23(1):111-33. doi: 10.1007/s10577-014-9459-z.


Association between long non-coding RNA and human rare diseases (Review).

He JH, Han ZP, Li YG.

Biomed Rep. 2014 Jan;2(1):19-23. Epub 2013 Oct 31.


Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology.

Tee L, Lim DH, Dias RP, Baudement MO, Slater AA, Kirby G, Hancocks T, Stewart H, Hardy C, Macdonald F, Maher ER.

Clin Epigenetics. 2013 Dec 10;5(1):23. doi: 10.1186/1868-7083-5-23.


Large offspring syndrome: a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann.

Chen Z, Robbins KM, Wells KD, Rivera RM.

Epigenetics. 2013 Jun;8(6):591-601. doi: 10.4161/epi.24655. Epub 2013 May 10.


Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p.

Gurrieri F, Zollino M, Oliva A, Pascali V, Orteschi D, Pietrobono R, Camporeale A, Coll Vidal M, Partemi S, Brugada R, Bellocci F, Neri G.

Eur J Hum Genet. 2013 Sep;21(9):965-9. doi: 10.1038/ejhg.2012.280. Epub 2013 Mar 20.


MyoD regulates p57kip2 expression by interacting with a distant cis-element and modifying a higher order chromatin structure.

Busanello A, Battistelli C, Carbone M, Mostocotto C, Maione R.

Nucleic Acids Res. 2012 Sep 1;40(17):8266-75. Epub 2012 Jun 26.


Long non-coding RNAs: versatile master regulators of gene expression and crucial players in cancer.

Nie L, Wu HJ, Hsu JM, Chang SS, Labaff AM, Li CW, Wang Y, Hsu JL, Hung MC.

Am J Transl Res. 2012;4(2):127-50. Epub 2012 Apr 8.


An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C.

Algar E, Dagar V, Sebaj M, Pachter N.

PLoS One. 2011;6(12):e29034. doi: 10.1371/journal.pone.0029034. Epub 2011 Dec 19.


Depletion of Kcnq1ot1 non-coding RNA does not affect imprinting maintenance in stem cells.

Golding MC, Magri LS, Zhang L, Lalone SA, Higgins MJ, Mann MR.

Development. 2011 Sep;138(17):3667-78. doi: 10.1242/dev.057778. Epub 2011 Jul 20.


Regulatory long non-coding RNAs and neuronal disorders.

Kohtz JD, Berghoff EG.

Physiol Behav. 2010 Jun 1;100(3):250-4. doi: 10.1016/j.physbeh.2010.01.015. Epub 2010 Jan 25.


Identification of a region of the DNMT1 methyltransferase that regulates the maintenance of genomic imprints.

Borowczyk E, Mohan KN, D'Aiuto L, Cirio MC, Chaillet JR.

Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20806-11. doi: 10.1073/pnas.0905668106. Epub 2009 Nov 18.


Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.

Zhou H, Brockington M, Jungbluth H, Monk D, Stanier P, Sewry CA, Moore GE, Muntoni F.

Am J Hum Genet. 2006 Nov;79(5):859-68. Epub 2006 Sep 21.


The silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals.

Tufarelli C.

Philos Trans R Soc Lond B Biol Sci. 2006 Jan 29;361(1465):67-79. Review.


Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome.

Diaz-Meyer N, Yang Y, Sait SN, Maher ER, Higgins MJ.

J Med Genet. 2005 Aug;42(8):648-55.


Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans.

Landers M, Calciano MA, Colosi D, Glatt-Deeley H, Wagstaff J, Lalande M.

Nucleic Acids Res. 2005 Jul 18;33(13):3976-84. Print 2005.


ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.

Arima T, Kamikihara T, Hayashida T, Kato K, Inoue T, Shirayoshi Y, Oshimura M, Soejima H, Mukai T, Wake N.

Nucleic Acids Res. 2005 May 11;33(8):2650-60. Print 2005.


Evolution of the Beckwith-Wiedemann syndrome region in vertebrates.

Paulsen M, Khare T, Burgard C, Tierling S, Walter J.

Genome Res. 2005 Jan;15(1):146-53. Epub 2004 Dec 8.


Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region.

Yokomine T, Shirohzu H, Purbowasito W, Toyoda A, Iwama H, Ikeo K, Hori T, Mizuno S, Tsudzuki M, Matsuda Y, Hattori M, Sakaki Y, Sasaki H.

Genome Res. 2005 Jan;15(1):154-65. Epub 2004 Dec 8.


Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.

Niemitz EL, DeBaun MR, Fallon J, Murakami K, Kugoh H, Oshimura M, Feinberg AP.

Am J Hum Genet. 2004 Nov;75(5):844-9. Epub 2004 Sep 15.

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