PMC Links for Gene (Select 105259599) - PMC

Result Filters

Links from Gene

Items: 1 to 20 of 55

<< First< Prev

Page of 3

Select item 47172101.

(Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome

Alessandro Mussa, Silvia Russo, Agostina De Crescenzo, Andrea Freschi, Luciano Calzari, Silvia Maitz, Marina Macchiaiolo, Cristina Molinatto, Giuseppina Baldassarre, Milena Mariani, Luigi Tarani, Maria Francesca Bedeschi, Donatella Milani, Daniela Melis, Andrea Bartuli, Maria Vittoria Cubellis, Angelo Selicorni, Margherita Cirillo Silengo, Lidia Larizza, Andrea Riccio, Giovanni Battista Ferrero

Eur J Hum Genet. 2016 Feb; 24(2): 183–190. Published online 2015 Apr 22. doi: 10.1038/ejhg.2015.88

PMCID:: PMC4717210

Article PDF–1.4M

Select item 46228572.

Novel DNA methylation profiles associated with key gene regulation and transcription pathways in blood and placenta of growth-restricted neonates

Sara L Hillman, Sarah Finer, Melissa C Smart, Chris Mathews, Robert Lowe, Vardhman K Rakyan, Graham A Hitman, David J Williams

Epigenetics. 2015 Jan; 10(1): 50–61. Published online 2015 Jan 23. doi: 10.4161/15592294.2014.989741

PMCID:: PMC4622857

Article PDF–374K

Select item 45685683.

Genome-wide methylation analysis in Silver-Russell syndrome patients

AR Prickett, M Ishida, S Böhm, JM Frost, W Puszyk, S Abu-Amero, P Stanier, R Schulz, GE Moore, RJ Oakey

Hum Genet. Author manuscript; available in PMC 2015 Sep 14.

Published in final edited form as: Hum Genet. 2015 Mar; 134(3): 317–332. Published online 2015 Jan 7. doi: 10.1007/s00439-014-1526-1

PMCID:: PMC4568568

Article PDF–1.1M

Select item 45600704.

Breast cancer risk and imprinting methylation in blood

Kristina Harrison, Gwen Hoad, Paula Scott, Louise Simpson, Graham W. Horgan, Elizabeth Smyth, Steven D. Heys, Paul Haggarty

Clin Epigenetics. 2015; 7(1): 92. Published online 2015 Sep 4. doi: 10.1186/s13148-015-0125-x

PMCID:: PMC4560070

Article PDF–637K

Select item 45011725.

A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome

Salah Azzi, Jennifer Salem, Nathalie Thibaud, Sandra Chantot-Bastaraud, Eli Lieber, Irène Netchine, Madeleine D Harbison

J Med Genet. 2015 Jul; 52(7): 446–453. Published online 2015 May 7. doi: 10.1136/jmedgenet-2014-102979

PMCID:: PMC4501172

Article PDF–1.3M

Select item 44378456.

Aberrant methylation of imprinted genes is associated with negative hormone receptor status in invasive breast cancer

Timothy M Barrow, Ludovic Barault, Rachel E Ellsworth, Holly R Harris, Alexandra M Binder, Allyson L Valente, Craig D Shriver, Karin B Michels

Int J Cancer. Author manuscript; available in PMC 2016 Aug 1.

Published in final edited form as: Int J Cancer. 2015 Aug 1; 137(3): 537–547. Published online 2015 Jan 21. doi: 10.1002/ijc.29419

PMCID:: PMC4437845

Article PDF–1.6M

Select item 43543907.

Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: a South African Fetal Alcohol Syndrome cohort study

Matshane L. Masemola, Lize van der Merwe, Zané Lombard, Denis Viljoen, Michèle Ramsay

Front Genet. 2015; 6: 85. Published online 2015 Mar 10. doi: 10.3389/fgene.2015.00085

PMCID:: PMC4354390

Article PDF–3.0M

Select item 43181848.

Decreased expression of cell proliferation-related genes in clonally derived skin fibroblasts from children with Silver-Russell syndrome is independent of the degree of 11p15 ICR1 hypomethylation

Doreen Heckmann, Christina Urban, Karin Weber, Kai Kannenberg, Gerhard Binder

Clin Epigenetics. 2015; 7(1): 5. Published online 2015 Jan 22. doi: 10.1186/s13148-014-0038-0

PMCID:: PMC4318184

Article PDF–1.0M

Select item 40653459.

Silver–Russell Syndrome Due to Paternal H19/IGF2 Hypomethylation in a Twin Girl Born After In Vitro Fertilization

Guido Cocchi, Concetta Marsico, Anita Cosentino, Chiara Spadoni, Alessandro Rocca, Agostina De Crescenzo, Andrea Riccio

Am J Med Genet A. 2013 Oct; 161(10): 2652–2655. Published online 2013 Aug 16. doi: 10.1002/ajmg.a.36145

PMCID:: PMC4065345

Article PDF–87K

Select item 406426410.

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects

Abdulla Ibrahim, Gail Kirby, Carol Hardy, Renuka P Dias, Louise Tee, Derek Lim, Jonathan Berg, Fiona MacDonald, Peter Nightingale, Eamonn R Maher

Clin Epigenetics. 2014; 6(1): 11. Published online 2014 Jun 4. doi: 10.1186/1868-7083-6-11

PMCID:: PMC4064264

Article PDF–741K

Select item 389168611.

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Mariarosaria Calvello, Silvia Tabano, Patrizia Colapietro, Silvia Maitz, Alessandra Pansa, Claudia Augello, Faustina Lalatta, Barbara Gentilin, Filippo Spreafico, Luciano Calzari, Daniela Perotti, Lidia Larizza, Silvia Russo, Angelo Selicorni, Silvia M Sirchia, Monica Miozzo

Epigenetics. 2013 Oct 1; 8(10): 1053–1060. Published online 2013 Aug 5. doi: 10.4161/epi.25812

PMCID:: PMC3891686

Article PDF–1.5M

Select item 387885412.

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

Louise Tee, Derek HK Lim, Renuka P Dias, Marie-Odile Baudement, Amy A Slater, Gail Kirby, Tom Hancocks, Helen Stewart, Carol Hardy, Fiona Macdonald, Eamonn R Maher

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

PMCID:: PMC3878854

Article PDF–781K

Select item 383108213.

Evidence for anticipation in Beckwith–Wiedemann syndrome

Siren Berland, Mia Appelbäck, Ove Bruland, Jasmin Beygo, Karin Buiting, Deborah J G Mackay, I Karen Temple, Gunnar Houge

Eur J Hum Genet. 2013 Dec; 21(12): 1344–1348. Published online 2013 Apr 10. doi: 10.1038/ejhg.2013.71

PMCID:: PMC3831082

Article PDF–852K

Select item 368132314.

Relaxed imprinting of IGF2 in peripheral blood cells of patients with a history of prostate cancer

Djeda Belharazem, Matthias Kirchner, Franziska Geissler, Peter Bugert, Martin Spahn, Burkhard Kneitz, Hubertus Riedmiller, Christian Sauer, Stefan Küffer, Lutz Trojan, Christian Bolenz, Maurice Stephan Michel, Alexander Marx, Philipp Ströbel

Endocr Connect. 2012 Nov 1; 1(2): 87–94. Published online 2012 Oct 24. doi: 10.1530/EC-12-0054

PMCID:: PMC3681323

Article PDF–224K

Select item 356700315.

Leukocyte DNA as Surrogate for the Evaluation of Imprinted Loci Methylation in Mammary Tissue DNA

Ludovic Barault, Rachel E. Ellsworth, Holly R. Harris, Allyson L. Valente, Craig D. Shriver, Karin B. Michels

PLoS One. 2013; 8(2): e55896. Published online 2013 Feb 7. doi: 10.1371/journal.pone.0055896

PMCID:: PMC3567003

Article PDF–332K

Select item 352398316.

IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome

Kai Kannenberg, Karin Weber, Cathrin Binder, Christina Urban, Hans-Joachim Kirschner, Gerhard Binder

Clin Epigenetics. 2012; 4(1): 15. Published online 2012 Sep 18. doi: 10.1186/1868-7083-4-15

PMCID:: PMC3523983

Article PDF–567K

Select item 351420317.

Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age

Rinki Murphy, Deborah Mackay, Ed A Mitchell

BMC Med Genet. 2012; 13: 99. Published online 2012 Nov 1. doi: 10.1186/1471-2350-13-99

PMCID:: PMC3514203

Article PDF–801K

Select item 350774218.

DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults

Rae-Chi Huang, John C Galati, Sally Burrows, Lawrence J Beilin, Xin Li, Craig E Pennell, JAM van Eekelen, Trevor A Mori, Leon A Adams, Jeffrey M Craig

Clin Epigenetics. 2012; 4(1): 21. Published online 2012 Nov 13. doi: 10.1186/1868-7083-4-21