Pesquisas alternativas:
compared cause » compared case (Expandir a Pesquisa), compared cases (Expandir a Pesquisa), complex cause (Expandir a Pesquisa)
null compared » pull compared (Expandir a Pesquisa), cell compared (Expandir a Pesquisa), nacl compared (Expandir a Pesquisa)
dairy company » day company (Expandir a Pesquisa), dairy companies (Expandir a Pesquisa), family company (Expandir a Pesquisa)
ada computer » pada computer (Expandir a Pesquisa), data computer (Expandir a Pesquisa), area computer (Expandir a Pesquisa)
company law » company a (Expandir a Pesquisa)
computer a » computer _ (Expandir a Pesquisa)
cause non » causes non (Expandir a Pesquisa)
law noted » law note (Expandir a Pesquisa), law notes (Expandir a Pesquisa), law united (Expandir a Pesquisa)
2 dairy » 2 daily (Expandir a Pesquisa)
j null » k null (Expandir a Pesquisa), h null (Expandir a Pesquisa), j nuelle (Expandir a Pesquisa)
i ada » i adam (Expandir a Pesquisa), i adha (Expandir a Pesquisa), _ ada (Expandir a Pesquisa)
a non » _ non (Expandir a Pesquisa)
compared cause » compared case (Expandir a Pesquisa), compared cases (Expandir a Pesquisa), complex cause (Expandir a Pesquisa)
null compared » pull compared (Expandir a Pesquisa), cell compared (Expandir a Pesquisa), nacl compared (Expandir a Pesquisa)
dairy company » day company (Expandir a Pesquisa), dairy companies (Expandir a Pesquisa), family company (Expandir a Pesquisa)
ada computer » pada computer (Expandir a Pesquisa), data computer (Expandir a Pesquisa), area computer (Expandir a Pesquisa)
company law » company a (Expandir a Pesquisa)
computer a » computer _ (Expandir a Pesquisa)
cause non » causes non (Expandir a Pesquisa)
law noted » law note (Expandir a Pesquisa), law notes (Expandir a Pesquisa), law united (Expandir a Pesquisa)
2 dairy » 2 daily (Expandir a Pesquisa)
j null » k null (Expandir a Pesquisa), h null (Expandir a Pesquisa), j nuelle (Expandir a Pesquisa)
i ada » i adam (Expandir a Pesquisa), i adha (Expandir a Pesquisa), _ ada (Expandir a Pesquisa)
a non » _ non (Expandir a Pesquisa)
1
Por Jiang, Shiming, Katz, Tiffany A., Garee, Jason P., DeMayo, Francesco J., Lee, Adrian V., Oesterreich, Steffi
Publicado no Dis Model Mech (2015)
“... and expression upon deletion of SAFB2. Thus, despite a high degree of sequence similarity, SAFB1(−/−) and SAFB2...”Publicado no Dis Model Mech (2015)
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2
Por Schmidt, Sigrun A. J., Ording, Anne G., Horváth-Puhó, Erzsébet, Sørensen, Henrik T., Henderson, Victor W.
Publicado no PLoS One (2017)
“...) and all-cause dementia. Using Danish medical databases, we identified adults diagnosed with NMSC between 1...”Publicado no PLoS One (2017)
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3
Por Rajadhyaksha, Anjali M., Ra, Stephen, Kishinevsky, Sarah, Lee, Anni S., Romanienko, Peter, DuBoff, Mariel, Yang, Chingwen, Zupan, Bojana, Byrne, Maureen, Daruwalla, Zeeba R., Mark, Willie, Kosofsky, Barry E., Toth, Miklos, Higgins, Joseph J.
Publicado no Behav Brain Res (2011)
“...A nonsense mutation in the human cereblon gene (CRBN) causes a mild type of autosomal recessive non...”Publicado no Behav Brain Res (2011)
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4
Por del Junco, Deborah J., Bulger, Eileen M., Fox, Erin E., Holcomb, John B., Brasel, Karen J., Hoyt, David B., Grady, James J., Duran, Sarah, Klotz, Patricia, Dubick, Michael A., Wade, Charles E.
Publicado no Injury (2015)
“...BACKGROUND: Collider bias, or stratifying data by a covariate consequence rather than cause...”Publicado no Injury (2015)
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5
Comparative Safety of Sulfonylureas and the Risk of Sudden Cardiac Arrest and Ventricular Arrhythmia
Por Leonard, Charles E., Brensinger, Colleen M., Aquilante, Christina L., Bilker, Warren B., Boudreau, Denise M., Deo, Rajat, Flory, James H., Gagne, Joshua J., Mangaali, Margaret J., Hennessy, Sean
Publicado no Diabetes Care (2018)
“... fatal) for a crude incidence rate of 3.6 per 1,000 person-years. Compared with glipizide, propensity...”Publicado no Diabetes Care (2018)
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6
Por Goodyear, Richard J., Cheatham, Mary Ann, Naskar, Souvik, Zhou, Yingjie, Osgood, Richard T., Zheng, Jing, Richardson, Guy P.
Publicado no Front Mol Neurosci (2019)
“...gal/βgal) null mutant mice on a C57Bl/6J background, the incidence of spontaneous otoacoustic...”Publicado no Front Mol Neurosci (2019)
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7
Por Sathiakumar, N., Delzell, E., Hovinga, M., Macaluso, M., Julian, J. A., Larson, R., Cole, P., Muir, D. C.
Publicado em 1998
“... rubber industry. Concerns about a possible association of 1,3-butadiene and styrene...”Publicado em 1998
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8
Por Richard J. Goodyear, Mary Ann Cheatham, Mary Ann Cheatham, Souvik Naskar, Yingjie Zhou, Richard T. Osgood, Jing Zheng, Jing Zheng, Guy P. Richardson
Publicado em 2019-06-01
“.../βgal null mutant mice on a C57Bl/6J background, the incidence of spontaneous otoacoustic emissions...”Publicado em 2019-06-01
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9
Por de Pontual, L, Pelet, A, Trochet, D, Jaubert, F, Espinosa‐Parrilla, Y, Munnich, A, Brunet, J‐F, Goridis, C, Feingold, J, Lyonnet, S, Amiel, J
Publicado em 2006
“... congenital central hypoventilation (CCHS) and Mowat‐Wilson syndrome (MWS), caused by PHOX2B and ZFHX1B gene...”Publicado em 2006
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10
Por Bell, Peter A, Piróg, Katarzyna A, Fresquet, Maryline, Thornton, David J, Boot-Handford, Raymond P, Briggs, Michael D
Publicado em 2012
“... retention of the majority of mutant matrilin 3 was previously observed in a murine model of MED caused by a...”Publicado em 2012
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11
Por Zhu, Bokai, Bai, Robert, Kennett, Mary J., Kang, Boo-Hyon, Gonzalez, Frank J., Peters, Jeffrey M.
Publicado em 2010
“... of cyclooxygenase-2 (COX2) activity by non-steroidal anti-inflammatory drugs (NSAID) can both attenuate skin...”Publicado em 2010
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12
Por Sheldon, I. Martin, Rycroft, Andrew N., Dogan, Belgin, Craven, Melanie, Bromfield, John J., Chandler, Alyssa, Roberts, Mark H., Price, Sian B., Gilbert, Robert O., Simpson, Kenneth W.
Publicado em 2010
“...) purified from EnPEC compared with non-pathogenic E. coli. The EnPEC or their LPS also caused PID when...”Publicado em 2010
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13
Por Bai, Yongsheng, Hassler, Justin, Ziyar, Ahdad, Li, Philip, Wright, Zachary, Menon, Rajasree, Omenn, Gilbert S., Cavalcoli, James D., Kaufman, Randal J., Sartor, Maureen A.
Publicado em 2014
“... Ire1α heterozygous and two Ire1α-null samples. The 26 nt non-canonical splice site in Xbp1...”Publicado em 2014
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14
Por Parnell, Stephen C, Magenheimer, Brenda S, Maser, Robin L, Pavlov, Tengis S, Havens, Mallory A, Hastings, Michelle L, Jackson, Stephen F, Ward, Christopher J, Peterson, Kenneth R, Staruschenko, Alexander, Calvet, James P
Publicado no Hum Mol Genet (2018)
“... that ultimately destroy kidney function. Mutations in the PKD1 and PKD2 genes cause ADPKD. Their protein products...”Publicado no Hum Mol Genet (2018)
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15
Por Felix, Ashley S., Lehman, Amy, Foraker, Randi E., Naughton, Michelle J., Bower, Julie K., Kuller, Lewis, Sarto, Gloria E., Stefanick, Marcia L., Van Horn, Linda, Jackson, Rebecca D., Paskett, Electra D.
Publicado no Cancer Epidemiol (2017)
“...: We compared the incidence of fatal and non-fatal CVD events among 1,179 women who developed Type I EC...”Publicado no Cancer Epidemiol (2017)
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16
Por Abe, Koichiro, Cox, Allison, Takamatsu, Nobuhiko, Velez, Gabriel, Laxer, Ronald M., Tse, Shirley M. L., Mahajan, Vinit B., Bassuk, Alexander G., Fuchs, Helmut, Ferguson, Polly J., Hrabe de Angelis, Martin
Publicado no Proc Natl Acad Sci U S A (2019)
“...) is an autoinflammatory bone disorder that presents with bone pain and localized swelling. Ali18 mice, isolated from a...”Publicado no Proc Natl Acad Sci U S A (2019)
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17
18
Por Iben, James R., Epstein, Jonathan A., Bayfield, Mark A., Bruinsma, Monique W., Hasson, Samuel, Bacikova, Dagmar, Ahmad, Daniel, Rockwell, Denise, Kittler, Ellen L. W., Zapp, Maria L., Maraia, Richard J.
Publicado em 2011
“... protein (Sla1p) mutant. Suppressor pre-tRNA(Ser)UCA-C47:6U with a debilitating substitution in its...”Publicado em 2011
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19
Por Brouns, Madeleine R., De Castro, Sandra C.P., Terwindt-Rouwenhorst, Els A., Massa, Valentina, Hekking, Johan W., Hirst, Caroline S., Savery, Dawn, Munts, Chantal, Partridge, Darren, Lamers, Wout, Köhler, Eleonore, van Straaten, Henny W., Copp, Andrew J., Greene, Nicholas D.E.
Publicado em 2011
“... of Grhl2 causes Axd NTDs, we performed a genetic cross to reduce Grhl2 function in Axd heterozygotes. Grhl...”Publicado em 2011
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20
Por Greenhalgh, J, Bagust, A, Boland, A, Martin Saborido, C, Oyee, J, Blundell, M, Dundar, Y, Dickson, R, Proudlove, C, Fisher, M
Publicado no Health Technol Assess (2011)
“... vascular causes, non-fatal stroke, non-fatal MI or major bleeding complication), the risk of event...”Publicado no Health Technol Assess (2011)
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