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Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation., Lalani, Seema R., Safiullah Arsalan M., Fernbach Susan D., Harutyunyan Karine G., Thaller Christina, Peterson Leif E., McPherson John D., Gibbs Richard A., White Lisa D., Hefner Margaret, et al. , American journal of human genetics, 2006 Feb, Volume 78, Issue 2, p.303-14, (2006) Abstract
Initial sequencing and analysis of the human genome., Lander, E. S., Linton L. M., Birren B., Nusbaum C., Zody M. C., Baldwin J., Devon K., Dewar K., Doyle M., FitzHugh W., et al. , Nature, 2001 Feb 15, Volume 409, Issue 6822, p.860-921, (2001) Abstract
The importance of context to the genetic architecture of diabetes-related traits is revealed in a genome-wide scan of a LG/J × SM/J murine model., Lawson, Heather A., Lee Arthur, Fawcett Gloria L., Wang Bing, Pletscher Susan L., Maxwell Taylor J., Ehrich Thomas H., Kenney-Hunt Jane P., Wolf Jason B., Semenkovich Clay F., et al. , Mammalian genome : official journal of the International Mammalian Genome Society, 2011 Apr, Volume 22, Issue 3-4, p.197-208, (2011) Abstract
Genetic, epigenetic, and gene-by-diet interaction effects underlie variation in serum lipids in a LG/JxSM/J murine model., Lawson, Heather A., Zelle Kathleen M., Fawcett Gloria L., Wang Bing, Pletscher Susan L., Maxwell Taylor J., Ehrich Thomas H., Kenney-Hunt Jane P., Wolf Jason B., Semenkovich Clay F., et al. , Journal of lipid research, 2010 Oct, Volume 51, Issue 10, p.2976-84, (2010) Abstract
Comprehensive evaluation of apolipoprotein H gene (APOH) variation identifies novel associations with measures of lipid metabolism in GENOA., Leduc, Magalie S., Shimmin Lawrence C., Klos Kathy L. E., Hanis Craig, Boerwinkle Eric, and Hixson James E. , Journal of lipid research, 2008 Dec, Volume 49, Issue 12, p.2648-56, (2008) Abstract
Landscape of somatic retrotransposition in human cancers., Lee, Eunjung, Iskow Rebecca, Yang Lixing, Gokcumen Omer, Haseley Psalm, Luquette Lovelace J., Lohr Jens G., Harris Christopher C., Ding Li, Wilson Richard K., et al. , Science (New York, N.Y.), 2012 Aug 24, Volume 337, Issue 6097, p.967-71, (2012) Abstract
PLD3 variants in population studies., van der Lee, Sven J., Holstege Henne, Wong Tsz Hang, Jakobsdottir Johanna, Bis Joshua C., Chouraki Vincent, van Rooij Jeroen G. J., Grove Megan L., Smith Albert V., Amin Najaf, et al. , Nature, 2015 Apr 2, Volume 520, Issue 7545, p.E2-3, (2015)
Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase., Lee, C. C., Wu X. W., Gibbs R. A., Cook R. G., Muzny D. M., and Caskey C. T. , Science (New York, N.Y.), 1988 Mar 11, Volume 239, Issue 4845, p.1288-91, (1988) Abstract
Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia., Lee, Sangkyou, Jeong Joon, Majewski Tadeusz, Scherer Steven E., Kim Mi-Sook, Tuziak Tomasz, Tang Kuang S., Baggerly Keith, Grossman Herbert Barton, Zhou Jain-Hua, et al. , Proceedings of the National Academy of Sciences of the United States of America, 2007 Aug 21, Volume 104, Issue 34, p.13732-7, (2007) Abstract
Single nucleotide polymorphism (SNP) analysis of mouse pulmonary adenoma susceptibility loci 1-4 for identification of candidate genes., Lemon, W. J., Swinton C. H., Wang M., Berbari N., Wang Y., and You M. , Journal of medical genetics, 2003 Apr, Volume 40, Issue 4, p.e36, (2003)
A bioinformatics analysis of memory consolidation reveals involvement of the transcription factor c-rel., Levenson, Jonathan M., Choi Sangdun, Lee Sun-Young, Cao Yun Anna, Ahn Hyung Jin, Worley Kim C., Pizzi Marina, Liou Hsiou-Chi, and Sweatt David J. , The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004 Apr 21, Volume 24, Issue 16, p.3933-43, (2004) Abstract
A comparative transcription map of the murine bare patches (Bpa) and striated (Str) critical regions and human Xq28., Levin, M. L., Chatterjee A., Pragliola A., Worley K. C., Wehnert M., Zhuchenko O., Smith R. F., Lee C. C., and Herman G. E. , Genome research, 1996 Jun, Volume 6, Issue 6, p.465-77, (1996) Abstract
Color-blind fluorescence detection for four-color DNA sequencing., Lewis, Ernest K., Haaland Wade C., Nguyen Freddy, Heller Daniel A., Allen Matthew J., MacGregor Robert R., Berger Scott C., Willingham Britain, Burns Lori A., Scott Graham B. I., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2005 Apr 12, Volume 102, Issue 15, p.5346-51, (2005) Abstract
Detection and significance of HIV sequences in HIV infection., Lewis, D. E., and Gibbs R. A. , Progress in medical virology. Fortschritte der medizinischen Virusforschung. Progrès en virologie médicale, 1993, Volume 40, p.19-47, (1993)
A systematic approach to identify functional motifs within vertebrate developmental enhancers., Li, Qiang, Ritter Deborah, Yang Nan, Dong Zhiqiang, Li Hao, Chuang Jeffrey H., and Guo Su , Developmental biology, 2010 Jan 15, Volume 337, Issue 2, p.484-95, (2010) Abstract
Genomic segmental polymorphisms in inbred mouse strains., Li, Jiangzhen, Jiang Tao, Mao Jian-Hua, Balmain Allan, Peterson Leif, Harris Charles, Rao Pulivarthi H., Havlak Paul, Gibbs Richard, and Cai Wei-Wen , Nature genetics, 2004 Sep, Volume 36, Issue 9, p.952-4, (2004) Abstract
Mutation survey of known LCA genes and loci in the Saudi Arabian population., Li, Yumei, Wang Hui, Peng Jianlan, Gibbs Richard A., Lewis Richard Alan, Lupski James R., Mardon Graeme, and Chen Rui , Investigative ophthalmology & visual science, 2009 Mar, Volume 50, Issue 3, p.1336-43, (2009) Abstract
Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease., Li, Alexander H., Morrison Alanna C., Kovar Christie, Cupples Adrienne L., Brody Jennifer A., Polfus Linda M., Yu Bing, Metcalf Ginger, Muzny Donna, Veeraraghavan Narayanan, et al. , Nature genetics, 2015 Apr 27, (2015) Abstract
Gene-Specific Function Prediction for Non-Synonymous Mutations in Monogenic Diabetes Genes, Li, Quan, Liu Xiaoming, Gibbs Richard A., Boerwinkle Eric, Polychronakos Constantin, and Qu Hui-Qi , PLoS ONE, 8/2014, Volume 9, Issue 8, p.e104452, (2014)
PNPLA3 polymorphisms and liver aminotransferase levels in a Mexican American population., Li, Quan, Qu Hui-Qi, Rentfro Anne R., Grove Megan L., Mirza Shaper, Lu Yang, Hanis Craig L., Fallon Michael B., Boerwinkle Eric, Fisher-Hoch Susan P., et al. , Clinical and investigative medicine. Médecine clinique et experimentale, 2012, Volume 35, Issue 4, p.E237-45, (2012) Abstract
Phylogeny of the macaques (Cercopithecidae: Macaca) based on Alu elements., Li, Jing, Han Kyudong, Xing Jinchuan, Kim Heui-Soo, Rogers Jeffrey, Ryder Oliver A., Disotell Todd, Yue Bisong, and Batzer Mark A. , Gene, 2009 Dec 15, Volume 448, Issue 2, p.242-9, (2009) Abstract
Association between somatostatin receptor 5 gene polymorphisms and pancreatic cancer risk and survival., Li, Donghui, Tanaka Motofumi, Brunicardi Charles F., Fisher William E., Gibbs Richard A., and Gingras Marie-Claude , Cancer, 2011 Jul 1, Volume 117, Issue 13, p.2863-72, (2011) Abstract
RNA interference knockdown of DNA methyl-transferase 3 affects gene alternative splicing in the honey bee., Li-Byarlay, Hongmei, Li Yang, Stroud Hume, Feng Suhua, Newman Thomas C., Kaneda Megan, Hou Kirk K., Worley Kim C., Elsik Christine G., Wickline Samuel A., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2013 Jul 30, Volume 110, Issue 31, p.12750-5, (2013) Abstract
In silico genetics: identification of a functional element regulating H2-Ealpha gene expression., Liao, Guochun, Wang Jianmei, Guo Jingshu, Allard John, Cheng Janet, Ng Anh, Shafer Steve, Puech Anne, McPherson John D., Foernzler Dorothee, et al. , Science (New York, N.Y.), 2004 Oct 22, Volume 306, Issue 5696, p.690-5, (2004) Abstract
Evolutionary traces of functional surfaces along G protein signaling pathway., Lichtarge, Olivier, Sowa Mathew E., and Philippi Anne , Methods in enzymology, 2002, Volume 344, p.536-56, (2002)

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