검색어 : 통합검색[Human molecular genetics 3]
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51
- Pseudoautosomal genes in man
- Goodfellow, P. J.; Darling, S.; Banting, G.; Pym, B.; Mondello, C.; Goodfellow, P. N.; 1 Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, Lincoln’s Inn Fields. London, WC2A 3PX. UK; 1 Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, Lincoln’s Inn Fields. London, WC2A 3PX. UK; 1 Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, Lincoln’s Inn Fields. London, WC2A 3PX. UK; 1 Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, Lincoln’s Inn Fields. London, WC2A 3PX. UK; 2 lslituto di Gené tica lliochemica ed Evoluzionistica. Via Abbialegrasso. 207-27100 Pavia. Italy; 1 Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, Lincoln’s Inn Fields. London, WC2A 3PX. UK; (Development, v.101, 1987, pp.119-125)
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52
- Insights into social insects from the genome of the honeybee Apis mellifera
- The Honeybee Genome Sequencing Consortium,; Weinstock, George M.; Robinson, Gene E.; Gibbs, Richard A.; Weinstock, George M.; Weinstock, George M.; Robinson, Gene E.; Worley, Kim C.; Evans, Jay D.; Maleszka, Ryszard; Robertson, Hugh M.; Weaver, Daniel B.; Beye, Martin; Bork, Peer; Elsik, Christine G.; Evans, Jay D.; Hartfelder, Klaus; Hunt, Greg J.; Robertson, Hugh M.; Robinson, Gene E.; Maleszka, Ryszard; Weinstock, George M.; Worley, Kim C.; Zdobnov, Evgeny M.; Hartfelder, Klaus; Amdam, Gro V.; Bitondi, Mrcia M. G.; Collins, Anita M.; Cristino, Alexandre S.; Evans, Jay D.; Michael, H.; Lattorff, G.; Lobo, Carlos H.; Moritz, Robin F. A.; Nunes, Francis M. F.; Page Jr, Robert E.; Simes, Zil L. P.; Wheeler, Diana; Carninci, Piero; Fukuda, Shiro; Hayashizaki, Yoshihide; Kai, Chikatoshi; Kawai, Jun; Sakazume, Naoko; Sasaki, Daisuke; Tagami, Michihira; Maleszka, Ryszard; Amdam, Gro V.; Albert, Stefan; Baggerman, Geert; *Lists of participants and affiliations appear at the end of the paper.; [1] Human Genome Sequencing Center, [2] Department of Molecular and Human Genetics, and; [1] Department of Entomology, [2] Department of Cell and Developmental Biology, [3] Neuroscience Program, [4] Program in Ecology and Evolutionary Biology, and; [1] Human Genome Sequencing Center, [2] Department of Molecular and Human Genetics, and; [1] Human Genome Sequencing Center, [2] Department of Molecular and Human Genetics, and; [1] Human Genome Sequencing Center, [2] Department of Molecular and Human Genetics, and; [1] Department of Entomology, [2] Department of Cell and Developmental Biology, [3] Neuroscience Program, [4] Program in Ecology and Evolutionary Biology, and; [1] Human Genome Sequencing Center, [2] Department of Molecular and Human Genetics, and; Bee Research Laboratory, BARCE, and; ARC Special Centre for the Molecular Genetics of Development, Visual Sciences, Research School of Biological Science; (Nature, v.443, 2006, pp.931-949)
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53
- Age as a Risk Factor for Myocardial Infarction in Leiden Mutation Carriers
- Baranovskaya, S.; Kudinov, S.; Fomicheva, E.; Vasina, V.; Solovieva, D.; Khavinson, V.; Schwartz, E.; ; (Molecular genetics and metabolism, v.64, 1998, pp.155-157)
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54
- Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
- Smith, Christopher A.; Driscoll, Deborah A.; Emanuel, Beverly S.; McDonald-McGinn, Donna M.; Zackai, Elaine H.; Sullivan, Kathleen E.; < !--label omitted: 1--> Division of Immunologic and Infectious Diseases1 and; < !--label omitted: 2--> Department of Obstetrics and Gynecology, The University of Pennsylvania School of Medicine,2 Philadelphia, Pennsylvania; < !--label omitted: 3--> Division of Human Genetics and Molecular Biology,3 The Children’s Hospital of Philadelphia, and; < !--label omitted: 3--> Division of Human Genetics and Molecular Biology,3 The Children’s Hospital of Philadelphia, and; < !--label omitted: 3--> Division of Human Genetics and Molecular Biology,3 The Children’s Hospital of Philadelphia, and; < !--label omitted: 1--> Division of Immunologic and Infectious Diseases1 and; (Clinical and diagnostic laboratory immunology, v.5, 1998, pp.415-417)
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56
- Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss
- Nagamani, Sandesh Chakravarthy Sreenath; Erez, Ayelet; Eng, Christine; Ou, Zhishuo; Chinault, Craig; Workman, Laura; Coldwell, James; Stankiewicz, Pawel; Patel, Ankita; Lupski, James R; Cheung, Sau Wai; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Sutter Medical Center, Sacramento, CA, USA; Children's Medical Center, Tulsa, OK, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; [1] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA [2] Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA [3] Texas Children's Hospital, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor Colle; (European journal of human genetics : EJHG, v.17, 2009, pp.573-581)
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57
- The mini-driver model of polygenic cancer evolution
- Castro-Giner, Francesc; Ratcliffe, Peter; Tomlinson, Ian; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.; Henry Wellcome Building for Molecular Physiology, Nuffield Department of Clinical Medicine, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.; Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.; (Nature reviews. Cancer, v.15, 2015, pp.680-685)
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58
- PCNA directs type 2 RNase H activity on DNA replication and repair substrates
- Bubeck, Doryen; Reijns, Martin A. M.; Graham, Stephen C.; Astell, Katy R.; Jones, E. Yvonne; Jackson, Andrew P.; Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN and Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, Western General Hospital, Edinburgh EH4 2XU, UK; Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN and Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, Western General Hospital, Edinburgh EH4 2XU, UK; Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN and Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, Western General Hospital, Edinburgh EH4 2XU, UK; Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN and Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, Western General Hospit; (Nucleic acids research, v.39, 2011, pp.3652-3666)
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59
- Proteomic identification of host and parasite biomarkers in saliva from patients with uncomplicated <i>Plasmodium falciparum</i> malaria
- Huang, Honglei; Mackeen, Mukram M; Cook, Matthew; Oriero, Eniyou; Locke, Emily; Thé zé nas, Marie L; Kessler, Benedikt M; Nwakanma, Davis; Casals-Pascual, Climent; Wellcome Trust Centre for Human Genetics and Centre for Cellular and Molecular Physiology, Roosevelt Drive, Oxford, OX3 7BN, UK; Wellcome Trust Centre for Human Genetics and Centre for Cellular and Molecular Physiology, Roosevelt Drive, Oxford, OX3 7BN, UK; Wellcome Trust Centre for Human Genetics and Centre for Cellular and Molecular Physiology, Roosevelt Drive, Oxford, OX3 7BN, UK; MRC Laboratories, Banjul, The Gambia; The PATH Malaria Vaccine Initiative, Washington, DC, 20001, USA; Wellcome Trust Centre for Human Genetics and Centre for Cellular and Molecular Physiology, Roosevelt Drive, Oxford, OX3 7BN, UK; Wellcome Trust Centre for Human Genetics and Centre for Cellular and Molecular Physiology, Roosevelt Drive, Oxford, OX3 7BN, UK; MRC Laboratories, Banjul, The Gambia; Wellcome Trust Centre for Human Genetics and Centre for Cellular and Molecular Physiology, Roosevelt Drive, Oxford, OX3 7BN, UK; (Malaria journal, v.11, 2012, pp.178-178)
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- A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at <i>DPYD</i> and a putative role for <i>ENOSF1</i> rather than <i>TYMS</i>
- Rosmarin, Dan; Palles, Claire; Pagnamenta, Alistair; Kaur, Kulvinder; Pita, Guillermo; Martin, Miguel; Domingo, Enric; Jones, Angela; Howarth, Kimberley; Freeman-Mills, Luke; Johnstone, Elaine; Wang, Haitao; Love, Sharon; Scudder, Claire; Julier, Patrick; Ferná ndez-Rozadilla, Ceres; Ruiz-Ponte, Clara; Carracedo, Angel; Castellvi-Bel, Sergi; Castells, Antoni; Gonzalez-Neira, Anna; Taylor, Jenny; Kerr, Rachel; Kerr, David; Tomlinson, Ian; Molecular and Population Genetics Laboratory , Oxford , UK; Molecular and Population Genetics Laboratory , Oxford , UK; Oxford NIHR Comprehensive Biomedical Research Centre, Wellcome Trust Centre for Human Genetics , Oxford , UK; Oxford NIHR Comprehensive Biomedical Research Centre, Wellcome Trust Centre for Human Genetics , Oxford , UK; Human Genotyping Unit-CeGen, Human Cancer Genetics Programme , Spanish National Cancer Research Centre, Melchor Ferná ndez Almagro 3 , Madrid , Spain; Department of Medical Oncology , Instituto de Investigacion Sanitaria Hospital General Universitario Gregorio Marañ ó n, Universidad Complutense , Madrid , Spain; Molecular and Population Genetics Laboratory , Oxford , UK; Molecular and Population Genetics Laboratory , Oxford , UK; Molecular; (Gut: journal of the British Society of Gastroenterology, v.64, 2015, pp.111-120)
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