Pesquisas alternativas:
evan » even (Expandir a Pesquisa), eva (Expandir a Pesquisa)
causes » caused (Expandir a Pesquisa)
oit » oito (Expandir a Pesquisa), doit (Expandir a Pesquisa), orit (Expandir a Pesquisa)
cara » care (Expandir a Pesquisa), cada (Expandir a Pesquisa), casa (Expandir a Pesquisa)
evan » even (Expandir a Pesquisa), eva (Expandir a Pesquisa)
causes » caused (Expandir a Pesquisa)
oit » oito (Expandir a Pesquisa), doit (Expandir a Pesquisa), orit (Expandir a Pesquisa)
cara » care (Expandir a Pesquisa), cada (Expandir a Pesquisa), casa (Expandir a Pesquisa)
1
“... been lacking. To learn more about Spt3–TBP interactions in vivo, we have isolated a new class of spt3...”
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Artigo
2
Por Nagayasu, Eiji, Hwang, Yu-Chen, Liu, Jun, Murray, John M., Hu, Ke
Publicado no Mol Biol Cell (2017)
“.... Their defining characteristic is the apical complex—membranous and cytoskeletal elements at the apical end...”Publicado no Mol Biol Cell (2017)
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Artigo
3
Por Qiu, Zhicheng R., Chico, Lidia, Chang, Jonathan, Shuman, Stewart, Schwer, Beate
Publicado em 2012
“...42 strain, signifying that MER3 splicing is a limiting transaction. These studies reveal a new level...”Publicado em 2012
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4
“...: Developmental Phenotypes -- Transthyretin Null Mice as a Model to Study the Involvement of Transthyretin...”
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Livro
5
Por Vasco M N C S Vieira, Luz Valeria Oppliger, Aschwin H Engelen, Juan A Correa
Publicado em 2015-01-01
“... by permutation tests under the null hypothesis that all demographies come from the same pool. POINT 3:An example...”Publicado em 2015-01-01
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Artigo
6
Por Lalucque, Hervé, Malagnac, Fabienne, Brun, Sylvain, Kicka, Sébastien, Silar, Philippe
Publicado em 2012
“.... Analysis of double and triple mutants inactivated for two or all three MAPK genes undercover new growth...”Publicado em 2012
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Artigo
7
Por Chen, Bohao, Yates, Elena, Huang, Yong, Kogut, Paul, Ma, Lan, Turner, Jerrold R., Tao, Yun, Camoretti-Mercado, Blanca, Lang, Deborah, Svensson, Eric C., Garcia, Joe G. N., Gruber, Peter J., Morrisey, Edward E., Solway, Julian
Publicado em 2009
“...GATA5 is a member of the GATA zinc finger transcription factor family involved in tissue-specific...”Publicado em 2009
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8
Por Vieira, Vasco M. N. C. S., Oppliger, Luz Valeria, Engelen, Aschwin H., Correa, Juan A.
Publicado no PLoS One (2015)
“... by permutation tests under the null hypothesis that all demographies come from the same pool. POINT 3: An example...”Publicado no PLoS One (2015)
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Artigo
9
“...Hypertensive nephropathy (HN) is a medical condition in which chronic high blood pressure causes...”
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Artigo
10
“... of the adult αβ-globin locus and retain only a small 3′ fragment of the α-globin gene. The only exception...”
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11
Por Colares, Renato, Machado, Thuany, Patel, Filipe Machado, Brunelli, Natália da Silva, Viana, Letícia Costa, Martins, Rafael, Longo, Pedro Augusto dos Santos, Cascaes, Mainara Figueiredo
Publicado em 2021
“... rochosos, avaliou-se a relação entre as macroalgas e os gastrópodes associados na Praia da Ribanceira...”Publicado em 2021
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Online
12
Por Li, Hongwu, Jin, Fuquan, Jiang, Keguo, Ji, Shuang, Wang, Li, Ni, Zhaofei, Chen, Xianguo, Hu, Zhongdong, Zhang, Hongbing, Liu, Yehai, Qin, Yide, Zha, Xiaojun
Publicado no Oncotarget (2016)
“...Tuberous sclerosis complex (TSC), caused by loss-of-function mutations in the TSC1 or TSC2 gene...”Publicado no Oncotarget (2016)
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Artigo
13
Por Callegaro, Andrea, Uh, Hae-Won, Helmer, Quinta, Houwing-Duistermaat, Jeanine J
Publicado em 2009
“... of three events: hard coronary heart disease, diabetes, or death from any cause. We use a two-step...”Publicado em 2009
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14
“... and are caused by mutations in the type I collagen genes. During the past several years, a number...”
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15
“...Classical osteogenesis imperfecta (OI) is a dominant genetic disorder of connective tissue caused...”
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16
“... null hypothesis for highly complex and organized systems such as those encountered in the environmental...”
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Artigo
17
“... defects of the class 1 unc-52 mutations have been isolated, and they define a new locus, sup-38. Only...”
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18
“... kinases. Here we describe a new gene, LF5, in which null mutations cause cells to assemble flagella...”
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19
Por Wang, Li, Ni, Zhaofei, Liu, Yujie, Ji, Shuang, Jin, Fuquan, Jiang, Keguo, Ma, Junfang, Ren, Cuiping, Zhang, Hongbing, Hu, Zhongdong, Zha, Xiaojun
Publicado no Oncotarget (2017)
“... inhibited growth of TSC1/TSC2 complex-deficient cells in vitro and in vivo. Therefore, downregulated FOXO3a...”Publicado no Oncotarget (2017)
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Artigo
20
Por Pereiro, Ines, Valverde, Diana, Piñeiro-Gallego, Teresa, Baiget, Montserrat, Borrego, Salud, Ayuso, Carmen, Searby, Charles, Nishimura, Darryl
Publicado em 2010
“.... Therefore, the molecular diagnosis of this complex disorder is a challenging task. METHODS: In this study we...”Publicado em 2010
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Artigo