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law non » law note (Expandir a Pesquisa), thaw non (Expandir a Pesquisa)
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1
Por Herman J. Kempen, Dorota B. Schranz, Bela F. Asztalos, James Otvos, Elias Jeyarajah, Denise Drazul-Schrader, Heidi L. Collins, Steven J. Adelman, Peter L. J. Wijngaard
Publicado em 2014-01-01
“... plasma or serum with MDCO-216 on cholesterol efflux capacity from J774 cells, on prebeta-1 high density...”Publicado em 2014-01-01
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2
Por Da Costa, Marc M. J., Allen, Claire E., Higginbottom, Adrian, Ramesh, Tennore, Shaw, Pamela J., McDermott, Christopher J.
Publicado em 2014
“...Mutations in the superoxide dismutase gene (SOD1) are one cause of familial amyotrophic lateral...”Publicado em 2014
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3
“... in Valparaísos city services. Experiments with new ways of organizing business accompanied the new technology...”
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4
Por Andreoletti, Gaia, Seaby, Eleanor G, Dewing, Jennifer M, O'Kelly, Ita, Lachlan, Katherine, Gilbert, Rodney D, Ennis, Sarah
Publicado no J Med Genet (2017)
Assuntos:
“...New Loci...”Publicado no J Med Genet (2017)
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5
Por Ogryzko, Nikolay V., Hoggett, Emily E., Solaymani-Kohal, Sara, Tazzyman, Simon, Chico, Timothy J. A., Renshaw, Stephen A., Wilson, Heather L.
Publicado em 2014
“... comes from in vitro monocytic cell culture models as lines or primary isolates, in which a range...”Publicado em 2014
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6
Por Frosk, Patrick, Arts, Heleen H, Philippe, Julien, Gunn, Carter S, Brown, Emma L, Chodirker, Bernard, Simard, Louise, Majewski, Jacek, Fahiminiya, Somayyeh, Russell, Chad, Liu, Yangfan P, Hegele, Robert, Katsanis, Nicholas, Goerz, Conrad, Del Bigio, Marc R, Davis, Erica E
Publicado no J Med Genet (2017)
Assuntos:
“...New Loci...”Publicado no J Med Genet (2017)
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7
Por Sinha, Sutapa, Mondal, Gourish, Hwang, Eun Ju, Han, Da Woon, Dutta, Shamit K., Iyer, Seethalakshmi, Karumanchi, S. Ananth, Kim, Keun Il, Couch, Fergus J., Mukhopadhyay, Debabrata
Publicado em 2011
“... caused failure to localize the ESCRT-1 interacting protein Alix and the v-SNARE complex component...”Publicado em 2011
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8
“... and leaves. Sub1 lines restored new leaf and tiller production faster. During submergence, FR13A showed...”
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9
“... of Hh function in zebrafish does not affect dorsoventral and mediolateral otic patterning, we now show...”
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10
SARS-CoV replication and pathogenesis in an in vitro model of the human conducting airway epithelium
“... Calu-3 that can be inoculated by viruses either as a non-polarized monolayer of cells or polarized...”Obter o texto integral
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11
Por Rintoul, Robert C, Rassl, Doris M, Gittins, Jacki, Marciniak, Stefan J
Publicado no Thorax (2016)
“... patients with mesothelioma. Twenty-six new cell lines have also been developed. MesobanK meets all...”Publicado no Thorax (2016)
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12
Por Shin, John J., Aftab, Qurratulain, Austin, Pamela, McQueen, Jennifer A., Poon, Tak, Li, Shu Chen, Young, Barry P., Roskelley, Calvin D., Loewen, Christopher J. R.
Publicado no Dis Model Mech (2016)
“..., in resistance to acid stress using a myeloid leukaemia-derived human cell line that we determined to be acid...”Publicado no Dis Model Mech (2016)
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13
Por Westbroek, Wendy, Nguyen, Matthew, Siebert, Marina, Lindstrom, Taylor, Burnett, Robert A., Aflaki, Elma, Jung, Olive, Tamargo, Rafael, Rodriguez-Gil, Jorge L., Acosta, Walter, Hendrix, An, Behre, Bahafta, Tayebi, Nahid, Fujiwara, Hideji, Sidhu, Rohini, Renvoise, Benoit, Ginns, Edward I., Dutra, Amalia, Pak, Evgenia, Cramer, Carole, Ory, Daniel S., Pavan, William J., Sidransky, Ellen
Publicado no Dis Model Mech (2016)
“... disease, a recessive lysosomal storage disorder, is caused by mutations in the gene GBA1. Dysfunctional...”Publicado no Dis Model Mech (2016)
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14
Por Wendy Westbroek, Matthew Nguyen, Marina Siebert, Taylor Lindstrom, Robert A. Burnett, Elma Aflaki, Olive Jung, Rafael Tamargo, Jorge L. Rodriguez-Gil, Walter Acosta, An Hendrix, Bahafta Behre, Nahid Tayebi, Hideji Fujiwara, Rohini Sidhu, Benoit Renvoise, Edward I. Ginns, Amalia Dutra, Evgenia Pak, Carole Cramer, Daniel S. Ory, William J. Pavan, Ellen Sidransky
Publicado em 2016-07-01
“... disease, a recessive lysosomal storage disorder, is caused by mutations in the gene GBA1. Dysfunctional...”Publicado em 2016-07-01
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15
Por Robertson, Anne L., Ogryzko, Nikolay V., Henry, Katherine M., Loynes, Catherine A., Foulkes, Matthew J., Meloni, Marco M., Wang, Xingang, Ford, Christopher, Jackson, Malcolm, Ingham, Philip W., Wilson, Heather L., Farrow, Stuart N., Solari, Roberto, Flower, Roderick J., Jones, Simon, Whyte, Moira K. B., Renshaw, Stephen A.
Publicado no Dis Model Mech (2016)
“...-regulated, persistent neutrophils can cause damage to host tissues and contribute to the pathogenesis...”Publicado no Dis Model Mech (2016)
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16
Por Tessadori, Federico, Roessler, Helen I., Savelberg, Sanne M. C., Chocron, Sonja, Kamel, Sarah M., Duran, Karen J., van Haelst, Mieke M., van Haaften, Gijs, Bakkers, Jeroen
Publicado no Dis Model Mech (2018)
“... zebrafish has also allowed identification of new putative therapeutic drugs. So far, most studies have...”Publicado no Dis Model Mech (2018)
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17
Por Federico Tessadori, Helen I. Roessler, Sanne M. C. Savelberg, Sonja Chocron, Sarah M. Kamel, Karen J. Duran, Mieke M. van Haelst, Gijs van Haaften, Jeroen Bakkers
Publicado em 2018-10-01
“... zebrafish has also allowed identification of new putative therapeutic drugs. So far, most studies have...”Publicado em 2018-10-01
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18
“...Non-small cell lung cancer (NSCLC) accounts for approximately 80-85% of all cases of lung cancer...”
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19
Por Herranz-Martin, Saul, Chandran, Jayanth, Lewis, Katherine, Mulcahy, Padraig, Higginbottom, Adrian, Walker, Callum, Valenzuela, Isabel Martinez-Pena y, Jones, Ross A., Coldicott, Ian, Iannitti, Tommaso, Akaaboune, Mohammed, El-Khamisy, Sherif F., Gillingwater, Thomas H., Shaw, Pamela J., Azzouz, Mimoun
Publicado no Dis Model Mech (2017)
“...Intronic GGGGCC repeat expansions in C9orf72 are the most common genetic cause of amyotrophic...”Publicado no Dis Model Mech (2017)
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20
Por Saul Herranz-Martin, Jayanth Chandran, Katherine Lewis, Padraig Mulcahy, Adrian Higginbottom, Callum Walker, Isabel Martinez-Pena y Valenzuela, Ross A. Jones, Ian Coldicott, Tommaso Iannitti, Mohammed Akaaboune, Sherif F. El-Khamisy, Thomas H. Gillingwater, Pamela J. Shaw, Mimoun Azzouz
Publicado em 2017-07-01
“...Intronic GGGGCC repeat expansions in C9orf72 are the most common genetic cause of amyotrophic...”Publicado em 2017-07-01
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