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1-Alkyl-2-acetylglycerophosphocholine Esterase
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks., Peloso, Gina M., Auer Paul L., Bis Joshua C., Voorman Arend, Morrison Alanna C., Stitziel Nathan O., Brody Jennifer A., Khetarpal Sumeet A., Crosby Jacy R., Fornage Myriam, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.223-32, (2014) Abstract
Genotype-by-diet effects on co-variation in Lp-PLA2 activity and LDL-cholesterol concentration in baboons fed an atherogenic diet., Vinson, Amanda, Mahaney Michael C., Diego Vince P., Cox Laura A., Rogers Jeffrey, VandeBerg John L., and Rainwater David L. , Journal of lipid research, 2008 Jun, Volume 49, Issue 6, p.1295-302, (2008) Abstract
3' Untranslated Regions
Integrated analyses of microRNAs demonstrate their widespread influence on gene expression in high-grade serous ovarian carcinoma., Creighton, Chad J., Hernandez-Herrera Anadulce, Jacobsen Anders, Levine Douglas A., Mankoo Parminder, Schultz Nikolaus, Du Ying, Zhang Yiqun, Larsson Erik, Sheridan Robert, et al. , PloS one, 2012, Volume 7, Issue 3, p.e34546, (2012) Abstract
5' Untranslated Regions
The DNA sequence and analysis of human chromosome 14., Heilig, Roland, Eckenberg Ralph, Petit Jean-Louis, Fonknechten Núria, Da Silva Corinne, Cattolico Laurence, Levy Michaël, Barbe Valérie, de Berardinis Véronique, Ureta-Vidal Abel, et al. , Nature, 2003 Feb 6, Volume 421, Issue 6923, p.601-7, (2003) Abstract
Abdominal Pain
Gastrointestinal microbiome signatures of pediatric patients with irritable bowel syndrome., Saulnier, Delphine M., Riehle Kevin, Mistretta Toni-Ann, Diaz Maria-Alejandra, Mandal Debasmita, Raza Sabeen, Weidler Erica M., Qin Xiang, Coarfa Cristian, Milosavljevic Aleksandar, et al. , Gastroenterology, 2011 Nov, Volume 141, Issue 5, p.1782-91, (2011) Abstract
Abnormalities, Multiple
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms., Campeau, Philippe M., Lu James T., Dawson Brian C., Fokkema Ivo F. A. C., Robertson Stephen P., Gibbs Richard A., and Lee Brendan H. , Human mutation, 2012 Nov, Volume 33, Issue 11, p.1520-5, (2012) 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
ABO Blood-Group System
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels., Barbalic, Maja, Dupuis Josée, Dehghan Abbas, Bis Joshua C., Hoogeveen Ron C., Schnabel Renate B., Nambi Vijay, Bretler Monique, Smith Nicholas L., Peters Annette, et al. , Human molecular genetics, 2010 May 1, Volume 19, Issue 9, p.1863-72, (2010) Abstract
Absorptiometry, Photon
A preliminary report on the feeding of cynomolgus monkeys (Macaca fascicularis) with a high-sugar high-fat diet for 33 weeks., Mubiru, James N., Garcia-Forey Magdalena, Higgins Paul B., Hemmat Peggah, Cavazos Nicole E., Dick Edward J., Owston Michael A., Bauer Cassondra A., Shade Robert E., Comuzzie Anthony G., et al. , Journal of medical primatology, 2011 Oct, Volume 40, Issue 5, p.335-41, (2011) Abstract
Serum prostate specific antigen changes in cynomolgus monkeys (Macaca fascicularis) on a high sugar high fat diet., Mubiru, James N., Garcia-Forey Magdalena, Cavazos Nicole, Hemmat Peggah, Dick Edward J., Owston Michael A., Bauer Cassondra A., Shade Robert E., and Rogers Jeffrey , The Prostate, 2012 Apr, Volume 72, Issue 5, p.469-75, (2012) Abstract
Abstracting and Indexing as Topic
Automated MeSH indexing of the World-Wide Web., Fowler, J., Kouramajian V., Maram S., and Devadhar V. , Proceedings / the ... Annual Symposium on Computer Application [sic] in Medical Care. Symposium on Computer Applications in Medical Care, 1995, p.893-7, (1995) Abstract
Access to Information
Prepublication data sharing., Birney, Ewan, Hudson Thomas J., Green Eric D., Gunter Chris, Eddy Sean, Rogers Jane, Harris Jennifer R., Ehrlich Dusko S., Apweiler Rolf, Austin Christopher P., et al. , Nature, 2009 Sep 10, Volume 461, Issue 7261, p.168-70, (2009) Abstract
Acetyl-CoA Carboxylase
Comprehensive molecular characterization of clear cell renal cell carcinoma., Davis, Caleb F. , Nature, 2013 Jul 4, Volume 499, Issue 7456, p.43-9, (2013) Abstract
Actins
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease., Guo, Dong-Chuan, Papke Christina L., Tran-Fadulu Van, Regalado Ellen S., Avidan Nili, Johnson Ralph Jay, Kim Dong H., Pannu Hariyadarshi, Willing Marcia C., Sparks Elizabeth, et al. , American journal of human genetics, 2009 May, Volume 84, Issue 5, p.617-27, (2009) Abstract
Acute Disease
From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: Part I., Naghavi, Morteza, Libby Peter, Falk Erling, Casscells Ward S., Litovsky Silvio, Rumberger John, Badimon Juan Jose, Stefanadis Christodoulos, Moreno Pedro, Pasterkamp Gerard, et al. , Circulation, 2003 Oct 7, Volume 108, Issue 14, p.1664-72, (2003) Abstract
Acylation
Structure-activity analysis of human ghrelin O-acyltransferase reveals chemical determinants of ghrelin selectivity and acyl group recognition., Darling, Joseph E., Zhao Feifei, Loftus Rosemary J., Patton Leslie M., Gibbs Richard A., and Hougland James L. , Biochemistry, 2015 Feb 3, Volume 54, Issue 4, p.1100-10, (2015) Abstract
Acyltransferases
Structure-activity analysis of human ghrelin O-acyltransferase reveals chemical determinants of ghrelin selectivity and acyl group recognition., Darling, Joseph E., Zhao Feifei, Loftus Rosemary J., Patton Leslie M., Gibbs Richard A., and Hougland James L. , Biochemistry, 2015 Feb 3, Volume 54, Issue 4, p.1100-10, (2015) Abstract
ADAM Proteins
Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura., Lotta, Luca A., Wu Haifeng M., Mackie Ian J., Noris Marina, Veyradier Agnes, Scully Marie A., Remuzzi Giuseppe, Coppo Paul, Liesner Ri, Donadelli Roberta, et al. , Blood, 2012 Jul 12, Volume 120, Issue 2, p.440-8, (2012) Abstract
Adaptation, Physiological
Differential regulation and xenobiotic induction of tandem P450 monooxygenase genes pc-1 (CYP63A1) and pc-2 (CYP63A2) in the white-rot fungus Phanerochaete chrysosporium., Doddapaneni, Harshavardhan, and Yadav Jagjit S. , Applied microbiology and biotechnology, 2004 Oct, Volume 65, Issue 5, p.559-65, (2004) Abstract
Genome sequence of the button mushroom Agaricus bisporus reveals mechanisms governing adaptation to a humic-rich ecological niche., Morin, Emmanuelle, Kohler Annegret, Baker Adam R., Foulongne-Oriol Marie, Lombard Vincent, Nagy Laszlo G., Ohm Robin A., Patyshakuliyeva Aleksandrina, Brun Annick, Aerts Andrea L., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2012 Oct 23, Volume 109, Issue 43, p.17501-6, (2012) Abstract
Adaptor Proteins, Signal Transducing
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum., Davis, Erica E., Zhang Qi, Liu Qin, Diplas Bill H., Davey Lisa M., Hartley Jane, Stoetzel Corinne, Szymanska Katarzyna, Ramaswami Gokul, Logan Clare V., et al. , Nature genetics, 2011 Mar, Volume 43, Issue 3, p.189-96, (2011) Abstract
Stargazin and other transmembrane AMPA receptor regulating proteins interact with synaptic scaffolding protein MAGI-2 in brain., Deng, Fang, Price Maureen G., Davis Caleb F., Mori Mayra, and Burgess Daniel L. , The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006 Jul 26, Volume 26, Issue 30, p.7875-84, (2006) Abstract
MLH1-silenced and non-silenced subgroups of hypermutated colorectal carcinomas have distinct mutational landscapes., Donehower, Lawrence A., Creighton Chad J., Schultz Nikolaus, Shinbrot Eve, Chang Kyle, Gunaratne Preethi H., Muzny Donna, Sander Chris, Hamilton Stanley R., Gibbs Richard A., et al. , The Journal of pathology, 2013 Jan, Volume 229, Issue 1, p.99-110, (2013) Abstract
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies., Khanna, Hemant, Davis Erica E., Murga-Zamalloa Carlos A., Estrada-Cuzcano Alejandro, Lopez Irma, den Hollander Anneke I., Zonneveld Marijke N., Othman Mohammad I., Waseem Naushin, Chakarova Christina F., et al. , Nature genetics, 2009 Jun, Volume 41, Issue 6, p.739-45, (2009) Abstract


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