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An integrated map of genetic variation from 1,092 human genomes., Abecasis, Goncalo R., Auton Adam, Brooks Lisa D., DePristo Mark A., Durbin Richard M., Handsaker Robert E., Kang Hyun Min, Marth Gabor T., and McVean Gil A. , Nature, 2012 Nov 1, Volume 491, Issue 7422, p.56-65, (2012) Abstract
Further evidence for phenotypic signatures of hybridization in descendent baboon populations., Ackermann, Rebecca R., Schroeder Lauren, Rogers Jeffrey, and Cheverud James M. , Journal of human evolution, 2014 Jun 13, (2014) Abstract
The genome sequence of Drosophila melanogaster., Adams, M. D., Celniker S. E., Holt R. A., Evans C. A., Gocayne J. D., Amanatides P. G., Scherer S. E., Li P. W., Hoskins R. A., Galle R. F., et al. , Science (New York, N.Y.), 2000 Mar 24, Volume 287, Issue 5461, p.2185-95, (2000) Abstract
Porin interaction with hexokinase and glycerol kinase: metabolic microcompartmentation at the outer mitochondrial membrane., Adams, V., Griffin L., Towbin J., Gelb B., Worley K., and McCabe E. R. , Biochemical medicine and metabolic biology, 1991 Jun, Volume 45, Issue 3, p.271-91, (1991) Abstract
Biological characterization and next-generation genome sequencing of the unclassified Cotia virus SPAn232 (Poxviridae)., Afonso, Priscila P., Silva Patrícia M., Schnellrath Laila C., Jesus Desyreé M., Hu Jianhong, Yang Yajie, Renne Rolf, Attias Marcia, Condit Richard C., Moussatché Nissin, et al. , Journal of virology, 2012 May, Volume 86, Issue 9, p.5039-54, (2012) Abstract
Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida., Agopian, A. J., Bhalla Angela D., Boerwinkle Eric, Finnell Richard H., Grove Megan L., Hixson James E., Shimmin Lawrence C., Sewda Anshuman, Stuart Colin, Zhong Yu, et al. , Birth defects research. Part A, Clinical and molecular teratology, 2013 Sep, Volume 97, Issue 9, p.597-601, (2013) Abstract
Exome sequencing of head and neck squamous cell carcinoma reveals inactivating mutations in NOTCH1., Agrawal, Nishant, Frederick Mitchell J., Pickering Curtis R., Bettegowda Chetan, Chang Kyle, Li Ryan J., Fakhry Carole, Xie Tong-Xin, Zhang Jiexin, Wang Jing, et al. , Science (New York, N.Y.), 2011 Aug 26, Volume 333, Issue 6046, p.1154-7, (2011) Abstract
The Glanville fritillary genome retains an ancient karyotype and reveals selective chromosomal fusions in Lepidoptera., Ahola, Virpi, Lehtonen Rainer, Somervuo Panu, Salmela Leena, Koskinen Patrik, Rastas Pasi, Välimäki Niko, Paulin Lars, Kvist Jouni, Wahlberg Niklas, et al. , Nature communications, 2014, Volume 5, p.4737, (2014) Abstract
Progress and prospects in rat genetics: a community view., Aitman, Timothy J., Critser John K., Cuppen Edwin, Dominiczak Anna, Fernandez-Suarez Xose M., Flint Jonathan, Gauguier Dominique, Geurts Aron M., Gould Michael, Harris Peter C., et al. , Nature genetics, 2008 May, Volume 40, Issue 5, p.516-22, (2008) Abstract
DNA polymerase III from Escherichia coli cells expressing mutA mistranslator tRNA is error-prone., Al Mamun, Abu Amar M., Marians Kenneth J., and Humayun Zafri M. , The Journal of biological chemistry, 2002 Nov 29, Volume 277, Issue 48, p.46319-27, (2002) Abstract
Elevated expression of DNA polymerase II increases spontaneous mutagenesis in Escherichia coli., Al Mamun, Abu Amar M. , Mutation research, 2007 Dec 1, Volume 625, Issue 1-2, p.29-39, (2007) Abstract
Detection and characterization of the flagellar master operon in the four Shigella subgroups., Al Mamun, A. A., Tominaga A., and Enomoto M. , Journal of bacteriology, 1996 Jul, Volume 178, Issue 13, p.3722-6, (1996) Abstract
The Escherichia coli UVM response is accompanied by an SOS-independent error-prone DNA replication activity demonstrable in vitro., Al Mamun, A. A., Yadava R. S., Ren L., and Humayun M. Z. , Molecular microbiology, 2000 Oct, Volume 38, Issue 2, p.368-80, (2000) Abstract
Hypermutagenesis in mutA cells is mediated by mistranslational corruption of polymerase, and is accompanied by replication fork collapse., Al Mamun, Abu Amar M., Gautam Satyendra, and Humayun Zafri M. , Molecular microbiology, 2006 Dec, Volume 62, Issue 6, p.1752-63, (2006) Abstract
Identity and function of a large gene network underlying mutagenic repair of DNA breaks., Al Mamun, Abu Amar M., Lombardo Mary-Jane, Shee Chandan, Lisewski Andreas M., Gonzalez Caleb, Lin Dongxu, Nehring Ralf B., Saint-Ruf Claude, Gibson Janet L., Frisch Ryan L., et al. , Science (New York, N.Y.), 2012 Dec 7, Volume 338, Issue 6112, p.1344-8, (2012) Abstract
Escherichia coli cells bearing mutA, a mutant glyV tRNA gene, express a recA-dependent error-prone DNA replication activity., Al Mamun, A. A., Rahman M. S., and Humayun M. Z. , Molecular microbiology, 1999 Aug, Volume 33, Issue 4, p.732-40, (1999) Abstract
Escherichia coli DNA polymerase II can efficiently bypass 3,N(4)-ethenocytosine lesions in vitro and in vivo., Al Mamun, Abu Amar M., and Humayun Zafri M. , Mutation research, 2006 Jan 29, Volume 593, Issue 1-2, p.164-76, (2006) Abstract
Spontaneous mutagenesis is elevated in protease-defective cells., Al Mamun, Abu Amar M., and Humayun Zafri M. , Molecular microbiology, 2009 Feb, Volume 71, Issue 3, p.629-39, (2009) Abstract
Identification of prognosis markers in pediatric high-risk acute lymphoblastic leukemia., Al-Lamki, Zakia, Wali Yasser A., Wasifuddin Shah M., Zachariah Mathew, Al-Mjeni Rayhanah, Li Changping, Muralitharan Shanmugakonar, Al-Kharusi Khalsa, Gunaratne Preethi, Peterson Leif, et al. , Pediatric hematology and oncology, 2005 Oct-Nov, Volume 22, Issue 7, p.629-43, (2005) Abstract
Direct selection of human genomic loci by microarray hybridization., Albert, Thomas J., Molla Michael N., Muzny Donna M., Nazareth Lynne, Wheeler David, Song Xingzhi, Richmond Todd A., Middle Chris M., Rodesch Matthew J., Packard Charles J., et al. , Nature methods, 2007 Nov, Volume 4, Issue 11, p.903-5, (2007) Abstract
Factor XIIIA Val34Leu polymorphism does not predict risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) Study., Aleksic, Nena, Ahn Chul, Wang Yao-Wei, Juneja Harinder, Folsom Aaron R., Boerwinkle Eric, and Wu Kenneth K. , Arteriosclerosis, thrombosis, and vascular biology, 2002 Feb 1, Volume 22, Issue 2, p.348-52, (2002) Abstract
Genetic testing, biotechnology, and GMOs: A snapshot of public opinion, 2003 through 2004., Alford, Raye L., Morris Kelley E., Rives Michelle C., Scherer Steven E., Weinstock George, Gibbs Richard A., Ghonima Karim, Belcher Mark, Valdes Hayden, Sumners Carolyn, et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2005 Jul-Aug, Volume 7, Issue 6, p.454-5, (2005)
Personalized copy number and segmental duplication maps using next-generation sequencing., Alkan, Can, Kidd Jeffrey M., Marques-Bonet Tomas, Aksay Gozde, Antonacci Francesca, Hormozdiari Fereydoun, Kitzman Jacob O., Baker Carl, Malig Maika, Mutlu Onur, et al. , Nature genetics, 2009 Oct, Volume 41, Issue 10, p.1061-7, (2009) Abstract
Complete sequence of a 38.4-kb human cosmid insert containing the polymorphic marker DXS455 from Xq28., Andersson, B., Lu F., Muzny D. M., Warren S. T., and Gibbs R. A. , DNA sequence : the journal of DNA sequencing and mapping, 1995, Volume 5, Issue 4, p.219-23, (1995) Abstract

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