Bartolomei MS - Search Results

1

Allele-specific RNA imaging shows that allelic imbalances can arise in tissues through transcriptional bursting.

Symmons O, Chang M, Mellis IA, Kalish JM, Park J, Suszták K, Bartolomei MS, Raj A. Symmons O, et al. Among authors: bartolomei ms. PLoS Genet. 2019 Jan 9;15(1):e1007874. doi: 10.1371/journal.pgen.1007874. eCollection 2019 Jan. PLoS Genet. 2019. PMID: 30625149 Free PMC article.

2

The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development.

Davis TL, Yang GJ, McCarrey JR, Bartolomei MS. Davis TL, et al. Among authors: bartolomei ms. Hum Mol Genet. 2000 Nov 22;9(19):2885-94. doi: 10.1093/hmg/9.19.2885. Hum Mol Genet. 2000. PMID: 11092765

3

Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3.

Reese KJ, Lin S, Verona RI, Schultz RM, Bartolomei MS. Reese KJ, et al. Among authors: bartolomei ms. PLoS Genet. 2007 Aug;3(8):e137. doi: 10.1371/journal.pgen.0030137. Epub 2007 Jun 29. PLoS Genet. 2007. PMID: 17708683 Free PMC article.

4

The transcriptional status but not the imprinting control region determines allele-specific histone modifications at the imprinted H19 locus.

Verona RI, Thorvaldsen JL, Reese KJ, Bartolomei MS. Verona RI, et al. Among authors: bartolomei ms. Mol Cell Biol. 2008 Jan;28(1):71-82. doi: 10.1128/MCB.01534-07. Epub 2007 Oct 29. Mol Cell Biol. 2008. PMID: 17967893 Free PMC article.

5

Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome.

Thorvaldsen JL, Krapp C, Willard HF, Bartolomei MS. Thorvaldsen JL, et al. Among authors: bartolomei ms. Genetics. 2012 Nov;192(3):1095-107. doi: 10.1534/genetics.112.144477. Epub 2012 Aug 10. Genetics. 2012. PMID: 22887817 Free PMC article.

6

Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy.

Kalish JM, Conlin LK, Bhatti TR, Dubbs HA, Harris MC, Izumi K, Mostoufi-Moab S, Mulchandani S, Saitta S, States LJ, Swarr DT, Wilkens AB, Zackai EH, Zelley K, Bartolomei MS, Nichols KE, Palladino AA, Spinner NB, Deardorff MA. Kalish JM, et al. Among authors: bartolomei ms. Am J Med Genet A. 2013 Aug;161A(8):1929-39. doi: 10.1002/ajmg.a.36045. Epub 2013 Jun 26. Am J Med Genet A. 2013. PMID: 23804593 Free PMC article.

7

Epigenetics and imprinting in human disease.

Kalish JM, Jiang C, Bartolomei MS. Kalish JM, et al. Among authors: bartolomei ms. Int J Dev Biol. 2014;58(2-4):291-8. doi: 10.1387/ijdb.140077mb. Int J Dev Biol. 2014. PMID: 25023695 Free article. Review.

8

Visualizing allele-specific expression in single cells reveals epigenetic mosaicism in an H19 loss-of-imprinting mutant.

Ginart P, Kalish JM, Jiang CL, Yu AC, Bartolomei MS, Raj A. Ginart P, et al. Among authors: bartolomei ms. Genes Dev. 2016 Mar 1;30(5):567-78. doi: 10.1101/gad.275958.115. Genes Dev. 2016. PMID: 26944681 Free PMC article.

9

A Hox-Embedded Long Noncoding RNA: Is It All Hot Air?

Selleri L, Bartolomei MS, Bickmore WA, He L, Stubbs L, Reik W, Barsh GS. Selleri L, et al. Among authors: bartolomei ms. PLoS Genet. 2016 Dec 15;12(12):e1006485. doi: 10.1371/journal.pgen.1006485. eCollection 2016 Dec. PLoS Genet. 2016. PMID: 27977680 Free PMC article. No abstract available.

10

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: bartolomei ms. 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.

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