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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
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
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
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)
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
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
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
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
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
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
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
Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome., Lalani, Seema R., Zhang Jing, Schaaf Christian P., Brown Chester W., Magoulas Pilar, Tsai Anne Chun-Hui, El-Gharbawy Areeg, Wierenga Klaas J., Bartholomew Dennis, Fong Chin-To, et al. , American journal of human genetics, 2014 Nov 6, Volume 95, Issue 5, p.579-83, (2014) Abstract
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia due to Bi-allelic TANGO2 Mutations., Lalani, Seema R., Liu Pengfei, Rosenfeld Jill A., Watkin Levi B., Chiang Theodore, Leduc Magalie S., Zhu Wenmiao, Ding Yan, Pan Shujuan, Vetrini Francesco, et al. , American journal of human genetics, 2016 Jan 19, (2016) Abstract


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