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The following term was not found in PubMed: 19 2231
Page 1
What Have We Learned from Studies of IFN-λ Variants and Hepatitis C Virus Infection?
O'Brien TR, Jackson SS. O'Brien TR, et al. J Interferon Cytokine Res. 2019 Oct;39(10):618-626. doi: 10.1089/jir.2019.0048. Epub 2019 Jun 4. J Interferon Cytokine Res. 2019. PMID: 31161939 Free PMC article. Review.
Chronic infection with the hepatitis C virus (HCV) is a major cause of cirrhosis and hepatocellular carcinoma. In 2009, genome-wide association studies (GWAS) strongly linked genetic variants in the interferon lambda (IFN-lambda) chromosomal region to HCV clearance. …
Chronic infection with the hepatitis C virus (HCV) is a major cause of cirrhosis and hepatocellular carcinoma. In 2009, genome
Mouse models for human otitis media.
Trune DR, Zheng QY. Trune DR, et al. Brain Res. 2009 Jun 24;1277:90-103. doi: 10.1016/j.brainres.2009.02.047. Epub 2009 Mar 6. Brain Res. 2009. PMID: 19272362 Free PMC article. Review.
Genetic predisposition is recognized as an important factor in OM and increasing numbers of mouse models are helping to uncover the potential genetic bases for human OM. Furthermore, the completion of the mouse genome sequence has offered a powerful set of tools for invest …
Genetic predisposition is recognized as an important factor in OM and increasing numbers of mouse models are helping to uncover the potentia …
The Mouse Genome Database genotypes::phenotypes.
Blake JA, Bult CJ, Eppig JT, Kadin JA, Richardson JE; Mouse Genome Database Group. Blake JA, et al. Nucleic Acids Res. 2009 Jan;37(Database issue):D712-9. doi: 10.1093/nar/gkn886. Epub 2008 Nov 3. Nucleic Acids Res. 2009. PMID: 18981050 Free PMC article.
The Mouse Genome Database (MGD, http://www.informatics.jax.org/), integrates genetic, genomic and phenotypic information about the laboratory mouse, a primary animal model for studying human biology and disease. ...MGI can be accessed by a variety of methods including web- …
The Mouse Genome Database (MGD, http://www.informatics.jax.org/), integrates genetic, genomic and phenotypic information about the la …
The Mouse Genome Database: enhancements and updates.
Bult CJ, Kadin JA, Richardson JE, Blake JA, Eppig JT; Mouse Genome Database Group. Bult CJ, et al. Nucleic Acids Res. 2010 Jan;38(Database issue):D586-92. doi: 10.1093/nar/gkp880. Epub 2009 Oct 27. Nucleic Acids Res. 2010. PMID: 19864252 Free PMC article.
The Mouse Genome Database (MGD) is a major component of the Mouse Genome Informatics (MGI, http://www.informatics.jax.org/) database resource and serves as the primary community model organism database for the laboratory mouse. ...MGD contains comprehensive data and …
The Mouse Genome Database (MGD) is a major component of the Mouse Genome Informatics (MGI, http://www.informatics.jax.org/) da …
Comparative genomics of the fungal pathogens Candida dubliniensis and Candida albicans.
Jackson AP, Gamble JA, Yeomans T, Moran GP, Saunders D, Harris D, Aslett M, Barrell JF, Butler G, Citiulo F, Coleman DC, de Groot PW, Goodwin TJ, Quail MA, McQuillan J, Munro CA, Pain A, Poulter RT, Rajandream MA, Renauld H, Spiering MJ, Tivey A, Gow NA, Barrell B, Sullivan DJ, Berriman M. Jackson AP, et al. Genome Res. 2009 Dec;19(12):2231-44. doi: 10.1101/gr.097501.109. Epub 2009 Sep 10. Genome Res. 2009. PMID: 19745113 Free PMC article.
Therefore, to identify C. albicans-specific genes that may be responsible for an increased capacity to cause disease, we have sequenced the C. dubliniensis genome and compared it with the known C. albicans genome sequence. Although the two genome sequences ar …
Therefore, to identify C. albicans-specific genes that may be responsible for an increased capacity to cause disease, we have sequenced the …
Do genetic recombination and gene density shape the pattern of DNA elimination in rice long terminal repeat retrotransposons?
Tian Z, Rizzon C, Du J, Zhu L, Bennetzen JL, Jackson SA, Gaut BS, Ma J. Tian Z, et al. Genome Res. 2009 Dec;19(12):2221-30. doi: 10.1101/gr.083899.108. Epub 2009 Sep 29. Genome Res. 2009. PMID: 19789376 Free PMC article.
However, the full suite of evolutionary forces that govern the gain or loss of transposable elements (TEs) and their distribution within a genome remains unclear. Here, we investigated the distribution and structural variation of LTR-RTs in relation to the rates of local g …
However, the full suite of evolutionary forces that govern the gain or loss of transposable elements (TEs) and their distribution within a …
Strand selective generation of endo-siRNAs from the Na/phosphate transporter gene Slc34a1 in murine tissues.
Carlile M, Swan D, Jackson K, Preston-Fayers K, Ballester B, Flicek P, Werner A. Carlile M, et al. Nucleic Acids Res. 2009 Apr;37(7):2274-82. doi: 10.1093/nar/gkp088. Epub 2009 Feb 23. Nucleic Acids Res. 2009. PMID: 19237395 Free PMC article.
Considering the wide spread expression of NATs and the gene silencing potential of endo-siRNAs we hypothesized a genome-wide link between antisense transcription and monoallelic expression. ...
Considering the wide spread expression of NATs and the gene silencing potential of endo-siRNAs we hypothesized a genome-wide link bet …
Genetic basis of HDL variation in 129/SvImJ and C57BL/6J mice: importance of testing candidate genes in targeted mutant mice.
Su Z, Wang X, Tsaih SW, Zhang A, Cox A, Sheehan S, Paigen B. Su Z, et al. J Lipid Res. 2009 Jan;50(1):116-25. doi: 10.1194/jlr.M800411-JLR200. Epub 2008 Sep 4. J Lipid Res. 2009. PMID: 18772481 Free PMC article.
To provide such data, we generated 528 F(2) progeny from an intercross of 129S1/SvImJ and C57BL/6 and measured HDL concentrations in F(2) animals first fed chow and then atherogenic diet. A genome wide scan using 508 single-nucleotide polymorphisms (SNPs) identified 19 QTL …
To provide such data, we generated 528 F(2) progeny from an intercross of 129S1/SvImJ and C57BL/6 and measured HDL concentrations in F(2) an …
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors.
Jackson EM, Sievert AJ, Gai X, Hakonarson H, Judkins AR, Tooke L, Perin JC, Xie H, Shaikh TH, Biegel JA. Jackson EM, et al. Clin Cancer Res. 2009 Mar 15;15(6):1923-30. doi: 10.1158/1078-0432.CCR-08-2091. Epub 2009 Mar 10. Clin Cancer Res. 2009. PMID: 19276269 Free PMC article.
EXPERIMENTAL DESIGN: A multiplatform approach using Illumina single nucleotide polymorphism-based oligonucleotide arrays, multiplex ligation-dependent probe amplification, fluorescence in situ hybridization, and coding sequence analysis was used to characterize genome-wide …
EXPERIMENTAL DESIGN: A multiplatform approach using Illumina single nucleotide polymorphism-based oligonucleotide arrays, multiplex ligation …
Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy.
Attiyeh EF, Diskin SJ, Attiyeh MA, Mossé YP, Hou C, Jackson EM, Kim C, Glessner J, Hakonarson H, Biegel JA, Maris JM. Attiyeh EF, et al. Genome Res. 2009 Feb;19(2):276-83. doi: 10.1101/gr.075671.107. Epub 2009 Jan 13. Genome Res. 2009. PMID: 19141597 Free PMC article.
Microarrays are frequently used to profile genome-wide copy number (CN) aberrations. While generally robust for detecting CN variants in germline DNA, the methods used to derive CN from signal intensity values have been suboptimal when applied to cancer genomes. ...This al …
Microarrays are frequently used to profile genome-wide copy number (CN) aberrations. While generally robust for detecting CN variants …
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