Ideraabdullah FY - Search Results

1

Tissue-specific insulator function at H19/Igf2 revealed by deletions at the imprinting control region.

Ideraabdullah FY, Thorvaldsen JL, Myers JA, Bartolomei MS. Ideraabdullah FY, et al. Hum Mol Genet. 2014 Dec 1;23(23):6246-59. doi: 10.1093/hmg/ddu344. Epub 2014 Jul 2. Hum Mol Genet. 2014. PMID: 24990148 Free PMC article.

2

The paternal gene of the DDK syndrome maps to the Schlafen gene cluster on mouse chromosome 11.

Bell TA, de la Casa-Esperón E, Doherty HE, Ideraabdullah F, Kim K, Wang Y, Lange LA, Wilhemsen K, Lange EM, Sapienza C, de Villena FP. Bell TA, et al. Genetics. 2006 Jan;172(1):411-23. doi: 10.1534/genetics.105.047118. Epub 2005 Sep 19. Genetics. 2006. PMID: 16172501 Free PMC article.

3

Genomic imprinting mechanisms in mammals.

Ideraabdullah FY, Vigneau S, Bartolomei MS. Ideraabdullah FY, et al. Mutat Res. 2008 Dec 1;647(1-2):77-85. doi: 10.1016/j.mrfmmm.2008.08.008. Epub 2008 Aug 20. Mutat Res. 2008. PMID: 18778719 Free PMC article. Review.

4

Novel cis-regulatory function in ICR-mediated imprinted repression of H19.

Ideraabdullah FY, Abramowitz LK, Thorvaldsen JL, Krapp C, Wen SC, Engel N, Bartolomei MS. Ideraabdullah FY, et al. Dev Biol. 2011 Jul 15;355(2):349-57. doi: 10.1016/j.ydbio.2011.04.036. Epub 2011 May 10. Dev Biol. 2011. PMID: 21600199 Free PMC article.

5

ZFP57: KAPturing DNA methylation at imprinted loci.

Ideraabdullah FY, Bartolomei MS. Ideraabdullah FY, et al. Mol Cell. 2011 Nov 4;44(3):341-2. doi: 10.1016/j.molcel.2011.10.008. Mol Cell. 2011. PMID: 22055179 Free article.

6

Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes.

Hur SK, Freschi A, Ideraabdullah F, Thorvaldsen JL, Luense LJ, Weller AH, Berger SL, Cerrato F, Riccio A, Bartolomei MS. Hur SK, et al. Proc Natl Acad Sci U S A. 2016 Sep 27;113(39):10938-43. doi: 10.1073/pnas.1603066113. Epub 2016 Sep 12. Proc Natl Acad Sci U S A. 2016. PMID: 27621468 Free PMC article.

7

Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.

Freschi A, Hur SK, Valente FM, Ideraabdullah FY, Sparago A, Gentile MT, Oneglia A, Di Nucci D, Colucci-D'Amato L, Thorvaldsen JL, Bartolomei MS, Riccio A, Cerrato F. Freschi A, et al. Among authors: ideraabdullah fy. PLoS Genet. 2018 Feb 22;14(2):e1007243. doi: 10.1371/journal.pgen.1007243. eCollection 2018 Feb. PLoS Genet. 2018. PMID: 29470501 Free PMC article.

8

Inference of putative cell-type-specific imprinted regulatory elements and genes during human neuronal differentiation.

Liang D, Aygün N, Matoba N, Ideraabdullah FY, Love MI, Stein JL. Liang D, et al. Among authors: ideraabdullah fy. Hum Mol Genet. 2023 Jan 13;32(3):402-416. doi: 10.1093/hmg/ddac207. Hum Mol Genet. 2023. PMID: 35994039 Free PMC article.

9

An assessment of molecular pathways of obesity susceptible to nutrient, toxicant and genetically induced epigenetic perturbation.

Xue J, Ideraabdullah FY. Xue J, et al. Among authors: ideraabdullah fy. J Nutr Biochem. 2016 Apr;30:1-13. doi: 10.1016/j.jnutbio.2015.09.002. Epub 2015 Oct 23. J Nutr Biochem. 2016. PMID: 27012616 Free PMC article. Review.

10

Maternal vitamin D depletion alters DNA methylation at imprinted loci in multiple generations.

Xue J, Schoenrock SA, Valdar W, Tarantino LM, Ideraabdullah FY. Xue J, et al. Among authors: ideraabdullah fy. Clin Epigenetics. 2016 Oct 12;8:107. doi: 10.1186/s13148-016-0276-4. eCollection 2016. Clin Epigenetics. 2016. PMID: 27777636 Free PMC article.

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