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Year Number of Results
2013 5
2014 3
2015 2
2020 0
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10 results
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Page 1
Braveheart, a long noncoding RNA required for cardiovascular lineage commitment.
Klattenhoff CA, Scheuermann JC, Surface LE, Bradley RK, Fields PA, Steinhauser ML, Ding H, Butty VL, Torrey L, Haas S, Abo R, Tabebordbar M, Lee RT, Burge CB, Boyer LA. Klattenhoff CA, et al. Cell. 2013 Jan 31;152(3):570-83. doi: 10.1016/j.cell.2013.01.003. Epub 2013 Jan 24. Cell. 2013. PMID: 23352431 Free PMC article.
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Li Y, Klena NT, Gabriel GC, Liu X, Kim AJ, Lemke K, Chen Y, Chatterjee B, Devine W, Damerla RR, Chang C, Yagi H, San Agustin JT, Thahir M, Anderton S, Lawhead C, Vescovi A, Pratt H, Morgan J, Haynes L, Smith CL, Eppig JT, Reinholdt L, Francis R, Leatherbury L, Ganapathiraju MK, Tobita K, Pazour GJ, Lo CW. Li Y, et al. Nature. 2015 May 28;521(7553):520-4. doi: 10.1038/nature14269. Epub 2015 Mar 25. Nature. 2015. PMID: 25807483 Free PMC article.
Optimization of genome engineering approaches with the CRISPR/Cas9 system.
Li K, Wang G, Andersen T, Zhou P, Pu WT. Li K, et al. PLoS One. 2014 Aug 28;9(8):e105779. doi: 10.1371/journal.pone.0105779. eCollection 2014. PLoS One. 2014. PMID: 25166277 Free PMC article.
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.
Guimier A, Gabriel GC, Bajolle F, Tsang M, Liu H, Noll A, Schwartz M, El Malti R, Smith LD, Klena NT, Jimenez G, Miller NA, Oufadem M, Moreau de Bellaing A, Yagi H, Saunders CJ, Baker CN, Di Filippo S, Peterson KA, Thiffault I, Bole-Feysot C, Cooley LD, Farrow EG, Masson C, Schoen P, Deleuze JF, Nitschké P, Lyonnet S, de Pontual L, Murray SA, Bonnet D, Kingsmore SF, Amiel J, Bouvagnet P, Lo CW, Gordon CT. Guimier A, et al. Nat Genet. 2015 Nov;47(11):1260-3. doi: 10.1038/ng.3376. Epub 2015 Oct 5. Nat Genet. 2015. PMID: 26437028 Free PMC article.
RNA-seq Data: Challenges in and Recommendations for Experimental Design and Analysis.
Williams AG, Thomas S, Wyman SK, Holloway AK. Williams AG, et al. Curr Protoc Hum Genet. 2014 Oct 1;83:11.13.1-20. doi: 10.1002/0471142905.hg1113s83. Curr Protoc Hum Genet. 2014. PMID: 25271838 Free PMC article.
Interrogating translational efficiency and lineage-specific transcriptomes using ribosome affinity purification.
Zhou P, Zhang Y, Ma Q, Gu F, Day DS, He A, Zhou B, Li J, Stevens SM, Romo D, Pu WT. Zhou P, et al. Proc Natl Acad Sci U S A. 2013 Sep 17;110(38):15395-400. doi: 10.1073/pnas.1304124110. Epub 2013 Sep 3. Proc Natl Acad Sci U S A. 2013. PMID: 24003143 Free PMC article.
Genome-wide analysis reveals the unique stem cell identity of human amniocytes.
Maguire CT, Demarest BL, Hill JT, Palmer JD, Brothman AR, Yost HJ, Condic ML. Maguire CT, et al. PLoS One. 2013;8(1):e53372. doi: 10.1371/journal.pone.0053372. Epub 2013 Jan 10. PLoS One. 2013. PMID: 23326421 Free PMC article.
A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.
Tarczy-Hornoch P, Amendola L, Aronson SJ, Garraway L, Gray S, Grundmeier RW, Hindorff LA, Jarvik G, Karavite D, Lebo M, Plon SE, Van Allen E, Weck KE, White PS, Yang Y. Tarczy-Hornoch P, et al. Genet Med. 2013 Oct;15(10):824-32. doi: 10.1038/gim.2013.120. Epub 2013 Sep 26. Genet Med. 2013. PMID: 24071794 Free PMC article.
Poly peak parser: Method and software for identification of unknown indels using sanger sequencing of polymerase chain reaction products.
Hill JT, Demarest BL, Bisgrove BW, Su YC, Smith M, Yost HJ. Hill JT, et al. Dev Dyn. 2014 Dec;243(12):1632-6. doi: 10.1002/dvdy.24183. Epub 2014 Sep 30. Dev Dyn. 2014. PMID: 25160973 Free PMC article.