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Items: 1 to 20 of 102

1.

Mosaic analysis with double markers reveals cell-type-specific paternal growth dominance.

Hippenmeyer S, Johnson RL, Luo L.

Cell Rep. 2013 Mar 28;3(3):960-7. doi: 10.1016/j.celrep.2013.02.002. Epub 2013 Feb 28.

2.

Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith-Wiedemann syndrome and ovarian steroid cell tumour.

Gogiel M, Begemann M, Spengler S, Soellner L, Göretzlehner U, Eggermann T, Strobl-Wildemann G.

Eur J Hum Genet. 2013 Jul;21(7):788-91. doi: 10.1038/ejhg.2012.259. Epub 2012 Nov 28.

3.

Mosaic paternal genome-wide uniparental isodisomy with down syndrome.

Darcy D, Atwal PS, Angell C, Gadi I, Wallerstein R.

Am J Med Genet A. 2015 Oct;167A(10):2463-9. doi: 10.1002/ajmg.a.37187. Epub 2015 Jul 29.

PMID:
26219535
4.

Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes.

Feil R, Walter J, Allen ND, Reik W.

Development. 1994 Oct;120(10):2933-43.

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.

PMID:
9722161
6.

Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques.

Romanelli V, Meneses HN, Fernández L, Martínez-Glez V, Gracia-Bouthelier R, F Fraga M, Guillén E, Nevado J, Gean E, Martorell L, Marfil VE, García-Miñaur S, Lapunzina P.

Eur J Hum Genet. 2011 Apr;19(4):416-21. doi: 10.1038/ejhg.2010.236. Epub 2011 Jan 19.

7.

Mosaicism for genome-wide paternal uniparental disomy with features of multiple imprinting disorders: diagnostic and management issues.

Inbar-Feigenberg M, Choufani S, Cytrynbaum C, Chen YA, Steele L, Shuman C, Ray PN, Weksberg R.

Am J Med Genet A. 2013 Jan;161A(1):13-20. doi: 10.1002/ajmg.a.35651. Epub 2012 Dec 13.

PMID:
23239666
9.

Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14.

Ogata T, Kagami M, Ferguson-Smith AC.

Epigenetics. 2008 Jul-Aug;3(4):181-7. Epub 2008 Jul 2. Review.

PMID:
18698157
10.

Interactions between imprinting effects in the mouse.

Cattanach BM, Beechey CV, Peters J.

Genetics. 2004 Sep;168(1):397-413.

11.

Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?

Smith A.

Acta Genet Med Gemellol (Roma). 1996;45(1-2):179-89. Review.

PMID:
8872029
12.

Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.

Hannula-Jouppi K, Muurinen M, Lipsanen-Nyman M, Reinius LE, Ezer S, Greco D, Kere J.

Epigenetics. 2014 Mar;9(3):351-65. doi: 10.4161/epi.27160. Epub 2013 Nov 18.

13.

Genome-wide androgenetic mosaicism.

Johnson JP, Waterson J, Schwanke C, Schoof J.

Clin Genet. 2014 Mar;85(3):282-5. doi: 10.1111/cge.12146. Epub 2013 Apr 23.

PMID:
23509941
14.

Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies.

Yong PJ, Marion SA, Barrett IJ, Kalousek DK, Robinson WP.

Am J Med Genet. 2002 Oct 1;112(2):123-32.

PMID:
12244544
15.

Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.

Cooper WN, Curley R, Macdonald F, Maher ER.

Genomics. 2007 May;89(5):613-7. Epub 2007 Mar 6.

16.

Rapid detection of methylation change at H19 in human imprinting disorders using methylation-sensitive high-resolution melting.

Wojdacz TK, Dobrovic A, Algar EM.

Hum Mutat. 2008 Oct;29(10):1255-60. doi: 10.1002/humu.20779.

PMID:
18473334
17.

Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction.

Tabano S, Colapietro P, Cetin I, Grati FR, Zanutto S, Mandò C, Antonazzo P, Pileri P, Rossella F, Larizza L, Sirchia SM, Miozzo M.

Epigenetics. 2010 May 16;5(4):313-24. Epub 2010 May 28.

PMID:
20418667
18.
19.
20.

[Genomic imprinting and problem of parthenogenesis in mammals].

Platonov ES.

Ontogenez. 2005 Jul-Aug;36(4):300-9. Review. Russian.

PMID:
16208941

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