Morrison H - Search Results

1

Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animals.

Cowell IG, Aucott R, Mahadevaiah SK, Burgoyne PS, Huskisson N, Bongiorni S, Prantera G, Fanti L, Pimpinelli S, Wu R, Gilbert DM, Shi W, Fundele R, Morrison H, Jeppesen P, Singh PB. Cowell IG, et al. Among authors: morrison h. Chromosoma. 2002 Mar;111(1):22-36. doi: 10.1007/s00412-002-0182-8. Chromosoma. 2002. PMID: 12068920

2

Allele-specific underacetylation of histone H4 downstream from promoters is associated with X-inactivation in human cells.

Morrison H, Jeppesen P. Morrison H, et al. Chromosome Res. 2002;10(7):579-95. doi: 10.1023/a:1020966719605. Chromosome Res. 2002. PMID: 12498347

3

Epigenetic control of mammalian centromere protein binding: does DNA methylation have a role?

Mitchell AR, Jeppesen P, Nicol L, Morrison H, Kipling D. Mitchell AR, et al. Among authors: morrison h. J Cell Sci. 1996 Sep;109 ( Pt 9):2199-206. doi: 10.1242/jcs.109.9.2199. J Cell Sci. 1996. PMID: 8886971

4

Analysis of loss of inactive X chromosomes in interphase cells.

Surrallés J, Jeppesen P, Morrison H, Natarajan AT. Surrallés J, et al. Among authors: morrison h. Am J Hum Genet. 1996 Nov;59(5):1091-6. Am J Hum Genet. 1996. PMID: 8900238 Free PMC article.

5

Low-copy-number human transgene is recognized as an X inactivation center in mouse ES cells, but fails to induce cis-inactivation in chimeric mice.

Migeon BR, Winter H, Kazi E, Chowdhury AK, Hughes A, Haisley-Royster C, Morrison H, Jeppesen P. Migeon BR, et al. Among authors: morrison h. Genomics. 2001 Jan 15;71(2):156-62. doi: 10.1006/geno.2000.6421. Genomics. 2001. PMID: 11161809

6

Human X inactivation center induces random X chromosome inactivation in male transgenic mice.

Migeon BR, Kazi E, Haisley-Royster C, Hu J, Reeves R, Call L, Lawler A, Moore CS, Morrison H, Jeppesen P. Migeon BR, et al. Among authors: morrison h. Genomics. 1999 Jul 15;59(2):113-21. doi: 10.1006/geno.1999.5861. Genomics. 1999. PMID: 10409422 Free article.

7

Coronary Artery Formation Is Driven by Localized Expression of R-spondin3.

Da Silva F, Rocha AS, Motamedi FJ, Massa F, Basboga C, Morrison H, Wagner KD, Schedl A. Da Silva F, et al. Among authors: morrison h. Cell Rep. 2017 Aug 22;20(8):1745-1754. doi: 10.1016/j.celrep.2017.08.004. Cell Rep. 2017. PMID: 28834739 Free article.

8

FRA2A is a CGG repeat expansion associated with silencing of AFF3.

Metsu S, Rooms L, Rainger J, Taylor MS, Bengani H, Wilson DI, Chilamakuri CS, Morrison H, Vandeweyer G, Reyniers E, Douglas E, Thompson G, Haan E, Gecz J, Fitzpatrick DR, Kooy RF. Metsu S, et al. Among authors: morrison h. PLoS Genet. 2014 Apr 24;10(4):e1004242. doi: 10.1371/journal.pgen.1004242. eCollection 2014 Apr. PLoS Genet. 2014. PMID: 24763282 Free PMC article.

9

The podocyte protein nephrin is required for cardiac vessel formation.

Wagner N, Morrison H, Pagnotta S, Michiels JF, Schwab Y, Tryggvason K, Schedl A, Wagner KD. Wagner N, et al. Among authors: morrison h. Hum Mol Genet. 2011 Jun 1;20(11):2182-94. doi: 10.1093/hmg/ddr106. Epub 2011 Mar 14. Hum Mol Genet. 2011. PMID: 21402589

10

ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy.

Handley MT, Reddy K, Wills J, Rosser E, Kamath A, Halachev M, Falkous G, Williams D, Cox P, Meynert A, Raymond ES, Morrison H, Brown S, Allan E, Aligianis I, Jackson AP, Ramsahoye BH, von Kriegsheim A, Taylor RW, Finch AJ, FitzPatrick DR. Handley MT, et al. Among authors: morrison h. PLoS Genet. 2019 Mar 11;15(3):e1007605. doi: 10.1371/journal.pgen.1007605. eCollection 2019 Mar. PLoS Genet. 2019. PMID: 30856165 Free PMC article.

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