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Human adipose tissue as a reservoir for memory CD4+ T cells and HIV., Couturier, Jacob, Suliburk James W., Brown Jeremy M., Luke David J., Agarwal Neeti, Yu Xiaoying, Nguyen Chi, Iyer Dinakar, Kozinetz Claudia A., Overbeek Paul A., et al. , AIDS (London, England), 2015 Mar 27, Volume 29, Issue 6, p.667-74, (2015) Abstract
Homozygous loss-of-function mutations in SOHLH1 in patients with non-syndromic hypergonadotropic hypogonadism., Bayram, Yavuz, Gulsuner Suleyman, Guran Tulay, Abaci Ayhan, Yesil Gozde, Gulsuner Hilal Unal, Atay Zeynep, Pierce Sarah B., Gambin Tomasz, Lee Ming, et al. , The Journal of clinical endocrinology and metabolism, 2015 Mar 16, p.jc20151150, (2015) Abstract
High-Quality Draft Genome Sequence of Francisella tularensis subsp. holarctica Strain OR96-0246., Atkins, L. M., Holder M. E., Ajami N. J., Metcalf G. A., Weissenberger G. M., Wang M., Vee V., Han Y., Muzny D. M., Gibbs R. A., et al. , Genome announcements, 2015, Volume 3, Issue 4, (2015) Abstract
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome, Wangler, Michael F., Gonzaga-Jauregui Claudia, Gambin Tomasz, Penney Samantha, Moss Timothy, Chopra Atul, Probst Frank J., Xia Fan, Yang Yaping, Werlin Steven, et al. , PLoS Genetics, 3/2014, Volume 10, Issue 3, p.e1004258, (2014)
Human Metabolome Associates With Dietary Intake Habits Among African Americans in the Atherosclerosis Risk in Communities Study., Zheng, Yan, Yu Bing, Alexander Danny, Steffen Lyn M., and Boerwinkle Eric , American journal of epidemiology, 2014 May 6, (2014) Abstract
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome., Wangler, Michael F., Gonzaga-Jauregui Claudia, Gambin Tomasz, Penney Samantha, Moss Timothy, Chopra Atul, Probst Frank J., Xia Fan, Yang Yaping, Werlin Steven, et al. , PLoS genetics, 2014 Mar, Volume 10, Issue 3, p.e1004258, (2014) Abstract
A homozygous missense mutation in NEUROD1 is associated with non-syndromic autosomal recessive retinitis pigmentosa., Wang, Feng, Li Huajin, Xu Mingchu, Li Hui, Zhao Li, Yang Lizhu, Zaneveld Jacques E., Wang Keqing, Li Yumei, Sui Ruifang, et al. , Investigative ophthalmology & visual science, 2014 Dec 4, (2014) Abstract
Human CLP1 Mutations Alter tRNA Biogenesis, Affecting Both Peripheral and Central Nervous System Function., Karaca, Ender, Weitzer Stefan, Pehlivan Davut, Shiraishi Hiroshi, Gogakos Tasos, Hanada Toshikatsu, Jhangiani Shalini N., Wiszniewski Wojciech, Withers Marjorie, Campbell Ian M., et al. , Cell, 2014 Apr 24, Volume 157, Issue 3, p.636-50, (2014) Abstract
High throughput sequencing methods for microbiome profiling: application to food animal systems., Highlander, Sarah K. , Animal health research reviews / Conference of Research Workers in Animal Diseases, 2012 Jun, Volume 13, Issue 1, p.40-53, (2012) Abstract
Human genome sequencing in health and disease., Gonzaga-Jauregui, Claudia, Lupski James R., and Gibbs Richard A. , Annual review of medicine, 2012, Volume 63, p.35-61, (2012) Abstract
A high-resolution map of human evolutionary constraint using 29 mammals., Lindblad-Toh, Kerstin, Garber Manuel, Zuk Or, Lin Michael F., Parker Brian J., Washietl Stefan, Kheradpour Pouya, Ernst Jason, Jordan Gregory, Mauceli Evan, et al. , Nature, 2011 Oct 27, Volume 478, Issue 7370, p.476-82, (2011) Abstract
High-resolution characterization of a hepatocellular carcinoma genome., Totoki, Yasushi, Tatsuno Kenji, Yamamoto Shogo, Arai Yasuhito, Hosoda Fumie, Ishikawa Shumpei, Tsutsumi Shuichi, Sonoda Kohtaro, Totsuka Hirohiko, Shirakihara Takuya, et al. , Nature genetics, 2011 May, Volume 43, Issue 5, p.464-9, (2011) Abstract
High-resolution identity by descent mapping uncovers the genetic basis for blood pressure differences between spontaneously hypertensive rat lines., Bell, Rebecca, Herring Stacy M., Gokul Nisha, Monita Monique, Grove Megan L., Boerwinkle Eric, and Doris Peter A. , Circulation. Cardiovascular genetics, 2011 Jun, Volume 4, Issue 3, p.223-31, (2011) Abstract
The hypofunctional effect of P335L single nucleotide polymorphism on SSTR5 function., Zhou, Guisheng, Gingras Marie-Claude, Liu Shi-He, Li Donghui, Li Zhijun, Catania Robbi L., Stehling Kelly M., Li Min, Paganelli Giovanni, Gibbs Richard A., et al. , World journal of surgery, 2011 Aug, Volume 35, Issue 8, p.1715-24, (2011) Abstract
Heritability of alveolar bone loss from periodontal disease in a baboon population: a pilot study., Miley, Douglas D., Baumgartner Mark H., Cheverud James M., Roseman Charles C., Rogers Jeffrey, McLeod Dwight E., Reyes Elio, and Hildebolt Charles F. , Journal of periodontology, 2011 Apr, Volume 82, Issue 4, p.575-80, (2011) Abstract
Hsp90 modulates CAG repeat instability in human cells., Mittelman, David, Sykoudis Kristen, Hersh Megan, Lin Yunfu, and Wilson John H. , Cell stress & chaperones, 2010 Sep, Volume 15, Issue 5, p.753-9, (2010) Abstract
Human Lymphatic Architecture and Dynamic Transport Imaged Using Near-infrared Fluorescence., Rasmussen, John C., Tan I-Chih, Marshall Milton V., Adams Kristen E., Kwon Sunkuk, Fife Caroline E., Maus Erik A., Smith Latisha A., Covington Kyle R., and Sevick-Muraca Eva M. , Translational oncology, 2010, Volume 3, Issue 6, p.362-72, (2010) Abstract
High-quality genomic DNA extraction from formalin-fixed and paraffin-embedded samples deparaffinized using mineral oil., Lin, Jianghai, Kennedy Stephen H., Svarovsky Therese, Rogers Jeffrey, Kemnitz Joseph W., Xu Anlong, and Zondervan Krina T. , Analytical biochemistry, 2009 Dec 15, Volume 395, Issue 2, p.265-7, (2009) Abstract
High-throughput multiplex sequencing to discover copy number variants in Drosophila., Daines, Bryce, Wang Hui, Li Yumei, Han Yi, Gibbs Richard, and Chen Rui , Genetics, 2009 Aug, Volume 182, Issue 4, p.935-41, (2009) Abstract
Horizontal gene transfer in cyanobacterial signature genes., Yerrapragada, Shailaja, Siefert Janet L., and Fox George E. , Methods in molecular biology (Clifton, N.J.), 2009, Volume 532, p.339-66, (2009) Abstract
Hepatocyte nuclear factor 1 and hypertensive nephropathy., Dmitrieva, Renata I., Hinojos Cruz A., Boerwinkle Eric, Braun Michael C., Fornage Myriam, and Doris Peter A. , Hypertension, 2008 Jun, Volume 51, Issue 6, p.1583-9, (2008) Abstract
High-precision, whole-genome sequencing of laboratory strains facilitates genetic studies., Srivatsan, Anjana, Han Yi, Peng Jianlan, Tehranchi Ashley K., Gibbs Richard, Wang Jue D., and Chen Rui , PLoS genetics, 2008, Volume 4, Issue 8, p.e1000139, (2008) Abstract
Heritability of brain volume, surface area and shape: an MRI study in an extended pedigree of baboons., Rogers, Jeffrey, Kochunov Peter, Lancaster Jack, Shelledy Wendy, Glahn David, Blangero John, and Fox Peter , Human brain mapping, 2007 Jun, Volume 28, Issue 6, p.576-83, (2007) Abstract
High mobility group (HMG-box) genes in the honeybee fungal pathogen Ascosphaera apis., Aronstein, K. A., Murray K. D., de León J. H., Qin X., and Weinstock G. M. , Mycologia, 2007 Jul-Aug, Volume 99, Issue 4, p.553-61, (2007) Abstract
Human-specific changes of genome structure detected by genomic triangulation., Harris, R. A., Rogers J., and Milosavljevic A. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.235-7, (2007) Abstract

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