A mostrar 1 - 20 resultados de 249 para a pesquisa '(( j l campos coy new ) OR ((( a trait complex cause new ) OR ( 0.9 natl lombana santos nunes ))))*', tempo de pesquisa: 0.35seg Refinar resultados
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... be important contributors to complex trait variation. Therefore, to understand the genetic architecture...
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Por Katsanis, Nicholas
Publicado em 2009
..., testable disease models from such studies. These new realities will probably necessitate a paradigm shift...
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Por Galina A. Kuzmitskaya
Publicado em 2019-11-01
... or large losses of tomatoes in the Far East is a complex, unpredictable, not meeting anywhere else...
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Por Naumova, Anna K., Greenwood, Celia M.T.
Publicado em 2013
...Epigenetics and complex traits provides an overview of basic epigenetic phenomena that influence...
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Por Marian, A.J., Belmont, John
Publicado em 2011
... phenotypes, whether single-gene familial disorders or complex traits without a clear familial aggregation...
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Por Jugessur, Astanand, Murray, Jeffrey C
Publicado em 2005
... recently been applied to investigate the causes of clefts. These include examining Mendelian forms...
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Por O'Shaughnessy, Kevin M
Publicado em 2009
...Genome-wide association scans are beginning to identify risk alleles for a number of complex...
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...<p>Abstract</p> <p>Background</p> <p>Infectious disease of livestock continues to be a cause...
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Por Eyre-Walker, Adam
Publicado em 2010
...A model is investigated in which mutations that affect a complex trait (e.g., heart disease) also...
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Por Barone, A, Di Matteo, A, Carputo, D, Frusciante, L
Publicado em 2009
... of new varieties resistant to pathogens that cause damage to this crop. Many molecular markers highly...
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Por Chami, Nathalie, Chen, Ming-Huei, Slater, Andrew J., Eicher, John D., Evangelou, Evangelos, Tajuddin, Salman M., Love-Gregory, Latisha, Kacprowski, Tim, Schick, Ursula M., Nomura, Akihiro, Giri, Ayush, Lessard, Samuel, Brody, Jennifer A., Schurmann, Claudia, Pankratz, Nathan, Yanek, Lisa R., Manichaikul, Ani, Pazoki, Raha, Mihailov, Evelin, Hill, W. David, Raffield, Laura M., Burt, Amber, Bartz, Traci M., Becker, Diane M., Becker, Lewis C., Boerwinkle, Eric, Bork-Jensen, Jette, Bottinger, Erwin P., O’Donoghue, Michelle L., Crosslin, David R., de Denus, Simon, Dubé, Marie-Pierre, Elliott, Paul, Engström, Gunnar, Evans, Michele K., Floyd, James S., Fornage, Myriam, Gao, He, Greinacher, Andreas, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B., Hayward, Caroline, Hernesniemi, Jussi, Highland, Heather M., Hirschhorn, Joel N., Hofman, Albert, Irvin, Marguerite R., Kähönen, Mika, Lange, Ethan, Launer, Lenore J., Lehtimäki, Terho, Li, Jin, Liewald, David C.M., Linneberg, Allan, Liu, Yongmei, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Mägi, Reedik, Mathias, Rasika A., Melander, Olle, Metspalu, Andres, Mononen, Nina, Nalls, Mike A., Nickerson, Deborah A., Nikus, Kjell, O’Donnell, Chris J., Orho-Melander, Marju, Pedersen, Oluf, Petersmann, Astrid, Polfus, Linda, Psaty, Bruce M., Raitakari, Olli T., Raitoharju, Emma, Richard, Melissa, Rice, Kenneth M., Rivadeneira, Fernando, Rotter, Jerome I., Schmidt, Frank, Smith, Albert Vernon, Starr, John M., Taylor, Kent D., Teumer, Alexander, Thuesen, Betina H., Torstenson, Eric S., Tracy, Russell P., Tzoulaki, Ioanna, Zakai, Neil A., Vacchi-Suzzi, Caterina, van Duijn, Cornelia M., van Rooij, Frank J.A., Cushman, Mary, Deary, Ian J., Velez Edwards, Digna R., Vergnaud, Anne-Claire, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Zonderman, Alan B., Kathiresan, Sekar, Grarup, Niels, Esko, Tõnu, Loos, Ruth J.F., Lange, Leslie A., Faraday, Nauder, Abumrad, Nada A., Edwards, Todd L., Ganesh, Santhi K., Auer, Paul L., Johnson, Andrew D., Reiner, Alexander P., Lettre, Guillaume
Publicado no Am J Hum Genet (2016)
... and mean corpuscular hemoglobin (p < 8 × 10(−9)). Mendelian mutations in ALAS2 are a cause of sideroblastic...
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