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Items: 1 to 20 of 163


The coding and noncoding transcriptome of Neurospora crassa.

Cemel IA, Ha N, Schermann G, Yonekawa S, Brunner M.

BMC Genomics. 2017 Dec 19;18(1):978. doi: 10.1186/s12864-017-4360-8.


Mechanisms of Long Non-Coding RNAs in the Assembly and Plasticity of Neural Circuitry.

Wang A, Wang J, Liu Y, Zhou Y.

Front Neural Circuits. 2017 Oct 23;11:76. doi: 10.3389/fncir.2017.00076. eCollection 2017. Review.


Human Long Noncoding RNA Regulation of Stem Cell Potency and Differentiation.

Lee S, Seo HH, Lee CY, Lee J, Shin S, Kim SW, Lim S, Hwang KC.

Stem Cells Int. 2017;2017:6374504. doi: 10.1155/2017/6374504. Epub 2017 Aug 30. Review.


Male Mutation Bias Is the Main Force Shaping Chromosomal Substitution Rates in Monotreme Mammals.

Link V, Aguilar-Gómez D, Ramírez-Suástegui C, Hurst LD, Cortez D.

Genome Biol Evol. 2017 Sep 1;9(9):2198-2210. doi: 10.1093/gbe/evx155.


The porcine translational research database: a manually curated, genomics and proteomics-based research resource.

Dawson HD, Chen C, Gaynor B, Shao J, Urban JF Jr.

BMC Genomics. 2017 Aug 22;18(1):643. doi: 10.1186/s12864-017-4009-7.


Whole exome sequencing of wild-derived inbred strains of mice improves power to link phenotype and genotype.

Chang PL, Kopania E, Keeble S, Sarver BAJ, Larson E, Orth A, Belkhir K, Boursot P, Bonhomme F, Good JM, Dean MD.

Mamm Genome. 2017 Oct;28(9-10):416-425. doi: 10.1007/s00335-017-9704-9. Epub 2017 Aug 17.


Biological function in the twilight zone of sequence conservation.

Ponting CP.

BMC Biol. 2017 Aug 16;15(1):71. doi: 10.1186/s12915-017-0411-5. Review.


Complete overview of protein-inactivating sequence variations in 36 sequenced mouse inbred strains.

Timmermans S, Van Montagu M, Libert C.

Proc Natl Acad Sci U S A. 2017 Aug 22;114(34):9158-9163. doi: 10.1073/pnas.1706168114. Epub 2017 Aug 7.


Mechanistic Insight into Long Noncoding RNAs and the Placenta.

McAninch D, Roberts CT, Bianco-Miotto T.

Int J Mol Sci. 2017 Jun 27;18(7). pii: E1371. doi: 10.3390/ijms18071371. Review.


Genome annotation for clinical genomic diagnostics: strengths and weaknesses.

Steward CA, Parker APJ, Minassian BA, Sisodiya SM, Frankish A, Harrow J.

Genome Med. 2017 May 30;9(1):49. doi: 10.1186/s13073-017-0441-1. Review.


Combination of short-read, long-read, and optical mapping assemblies reveals large-scale tandem repeat arrays with population genetic implications.

Weissensteiner MH, Pang AWC, Bunikis I, Höijer I, Vinnere-Petterson O, Suh A, Wolf JBW.

Genome Res. 2017 May;27(5):697-708. doi: 10.1101/gr.215095.116. Epub 2017 Mar 30.


Expressed Structurally-stable Inverted Duplicates in Mammalian Genomes as Functional Noncoding Elements.

Chen ZX, Oliver B, Zhang YE, Gao G, Long M.

Genome Biol Evol. 2017 Mar 13. doi: 10.1093/gbe/evx054. [Epub ahead of print]


Estimating the total number of phosphoproteins and phosphorylation sites in eukaryotic proteomes.

Vlastaridis P, Kyriakidou P, Chaliotis A, Van de Peer Y, Oliver SG, Amoutzias GD.

Gigascience. 2017 Feb 1;6(2):1-11. doi: 10.1093/gigascience/giw015.


Evolution and Diversity of Transposable Elements in Vertebrate Genomes.

Sotero-Caio CG, Platt RN 2nd, Suh A, Ray DA.

Genome Biol Evol. 2017 Jan 1;9(1):161-177. doi: 10.1093/gbe/evw264. Review.


Deficiency of Mkrn2 causes abnormal spermiogenesis and spermiation, and impairs male fertility.

Qian X, Wang L, Zheng B, Shi ZM, Ge X, Jiang CF, Qian YC, Li DM, Li W, Liu X, Yin Y, Zheng JT, Shen H, Wang M, Guo XJ, He J, Lin M, Liu LZ, Sha JH, Jiang BH.

Sci Rep. 2016 Dec 23;6:39318. doi: 10.1038/srep39318.


Expression and epigenomic landscape of the sex chromosomes in mouse post-meiotic male germ cells.

Moretti C, Vaiman D, Tores F, Cocquet J.

Epigenetics Chromatin. 2016 Oct 27;9:47. eCollection 2016.


Epigenetic Aspects of Systemic Lupus Erythematosus.

Relle M, Foehr B, Schwarting A.

Rheumatol Ther. 2015 Jun;2(1):33-46. Epub 2015 Jun 16. Review.


LINC00520 is induced by Src, STAT3, and PI3K and plays a functional role in breast cancer.

Henry WS, Hendrickson DG, Beca F, Glass B, Lindahl-Allen M, He L, Ji Z, Struhl K, Beck AH, Rinn JL, Toker A.

Oncotarget. 2016 Dec 13;7(50):81981-81994. doi: 10.18632/oncotarget.11962.


Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation and homozygous truncating mutations.

Doran AG, Wong K, Flint J, Adams DJ, Hunter KW, Keane TM.

Genome Biol. 2016 Aug 1;17(1):167. doi: 10.1186/s13059-016-1024-y.

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