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Items: 8


Allele-specific splicing effects on DKKL1 and ZNF419 transcripts in HeLa cells.

Martin G, Selcuklu SD, Schouest K, Nembaware V, McKeown PC, Seoighe C, Spillane C.

Gene. 2017 Jan 20;598:107-112. doi: 10.1016/j.gene.2016.11.004. Epub 2016 Nov 5.


Proceedings of a Sickle Cell Disease Ontology workshop - Towards the first comprehensive ontology for Sickle Cell Disease.

Mulder N, Nembaware V, Adekile A, Anie KA, Inusa B, Brown B, Campbell A, Chinenere F, Chunda-Liyoka C, Derebail VK, Geard A, Ghedira K, Hamilton CM, Hanchard NA, Haendel M, Huggins W, Ibrahim M, Jupp S, Kamga KK, Knight-Madden J, Lopez-Sall P, Mbiyavanga M, Munube D, Nirenberg D, Nnodu O, Ofori-Acquah SF, Ohene-Frempong K, Opap KB, Panji S, Park M, Pule G, Royal C, Sangeda R, Tayo B, Treadwell M, Tshilolo L, Wonkam A.

Appl Transl Genom. 2016 Mar 15;9:23-9. doi: 10.1016/j.atg.2016.03.005. eCollection 2016 Jun.


Investigation into the use of short message services to expand uptake of human immunodeficiency virus testing, and whether content and dosage have impact.

de Tolly K, Skinner D, Nembaware V, Benjamin P.

Telemed J E Health. 2012 Jan-Feb;18(1):18-23. doi: 10.1089/tmj.2011.0058. Epub 2011 Dec 8.


Genome-wide survey of allele-specific splicing in humans.

Nembaware V, Lupindo B, Schouest K, Spillane C, Scheffler K, Seoighe C.

BMC Genomics. 2008 Jun 2;9:265. doi: 10.1186/1471-2164-9-265.


Maximum likelihood inference of imprinting and allele-specific expression from EST data.

Seoighe C, Nembaware V, Scheffler K.

Bioinformatics. 2006 Dec 15;22(24):3032-9. Epub 2006 Oct 11.


Allele-specific transcript isoforms in human.

Nembaware V, Wolfe KH, Bettoni F, Kelso J, Seoighe C.

FEBS Lett. 2004 Nov 5;577(1-2):233-8.


Impact of the presence of paralogs on sequence divergence in a set of mouse-human orthologs.

Nembaware V, Crum K, Kelso J, Seoighe C.

Genome Res. 2002 Sep;12(9):1370-6.

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