Pesquisas alternativas:
nacl complex » nac56 complex (Expandir a Pesquisa), al complex (Expandir a Pesquisa), all complex (Expandir a Pesquisa)
complex arc » complex area (Expandir a Pesquisa), complex a (Expandir a Pesquisa), complex array (Expandir a Pesquisa)
child from » children from (Expandir a Pesquisa)
can child » can china (Expandir a Pesquisa), own child (Expandir a Pesquisa), can children (Expandir a Pesquisa)
3.5 nacl » 0.9 nacl (Expandir a Pesquisa)
arc non » nrc non (Expandir a Pesquisa), src non (Expandir a Pesquisa)
j neila » j neil (Expandir a Pesquisa), _ neila (Expandir a Pesquisa), j neild (Expandir a Pesquisa)
neila a » neila da (Expandir a Pesquisa), neil a (Expandir a Pesquisa), leila a (Expandir a Pesquisa)
l can » _ can (Expandir a Pesquisa), i can (Expandir a Pesquisa), l con (Expandir a Pesquisa)
nacl complex » nac56 complex (Expandir a Pesquisa), al complex (Expandir a Pesquisa), all complex (Expandir a Pesquisa)
complex arc » complex area (Expandir a Pesquisa), complex a (Expandir a Pesquisa), complex array (Expandir a Pesquisa)
child from » children from (Expandir a Pesquisa)
can child » can china (Expandir a Pesquisa), own child (Expandir a Pesquisa), can children (Expandir a Pesquisa)
3.5 nacl » 0.9 nacl (Expandir a Pesquisa)
arc non » nrc non (Expandir a Pesquisa), src non (Expandir a Pesquisa)
j neila » j neil (Expandir a Pesquisa), _ neila (Expandir a Pesquisa), j neild (Expandir a Pesquisa)
neila a » neila da (Expandir a Pesquisa), neil a (Expandir a Pesquisa), leila a (Expandir a Pesquisa)
l can » _ can (Expandir a Pesquisa), i can (Expandir a Pesquisa), l con (Expandir a Pesquisa)
1
“...Distinguishing self from non-self is a fundamental biological challenge. Many pathogens exploit...”
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2
“.... Both TRS1 proteins bind to double-stranded RNA and, in the cell types in which they can rescue VVΔE3L...”
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3
Por Smith, Alyson J., Graves, Bridget, Child, Robert, Rice, Peter J., Ma, Zuchao, Lowman, Douglas W., Ensley, Harry E., Ryter, Kendal T., Evans, Jay T., Williams, David L.
Publicado no J Immunol (2017)
“... fungal pathogens. Laminarin is a (1→3, 1→6)-β glucan that is widely reported to be a Dectin-1 antagonist...”Publicado no J Immunol (2017)
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4
Por Starr, Tregei, Child, Robert, Wehrly, Tara D., Hansen, Bryan, Hwang, Seungmin, López-Otin, Carlos, Virgin, Herbert W., Celli, Jean
Publicado em 2012
“... elongation proteins ATG5, ATG16L1, ATG4B, ATG7 and LC3B. Furthermore, aBCVs were required to complete...”Publicado em 2012
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5
Por Hein M. Tun, Theodore Konya, Tim K. Takaro, Jeffrey R. Brook, Radha Chari, Catherine J. Field, David S. Guttman, Allan B. Becker, Piush J. Mandhane, Stuart E. Turvey, Padmaja Subbarao, Malcolm R. Sears, James A. Scott, Anita L. Kozyrskyj, the CHILD Study Investigators
Publicado em 2017-04-01
“... large subsample of 746 infants from the Canadian Healthy Infant Longitudinal Development Study (CHILD...”Publicado em 2017-04-01
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6
“...The Maternal and Child Health Information Network--MATCH--was begun in 1984 as a demonstration...”
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7
Por Menon, J. A., Kusanthan, T., Mwaba, S. O. C., Juanola, L., Kok, M. C.
Publicado no PLoS One (2018)
“...; representatives from youth associations, community-based and non-governmental organizations; and district level...”Publicado no PLoS One (2018)
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8
“... changes in infant health and development. Cumulative knowledge from this body of research suggests that a...”
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9
“...A dilemma exists when a doctor is faced with a child or young person who refuses medically...”
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10
Por Simpson, N. E., Dallaire, L., Miller, J. R., Siminovitch, L., Miller, J., Hamerton, J. L.
Publicado em 1979
“... in amniotic fluid is reported from a prospective study of five laboratories testing for 13 Canadian genetic...”Publicado em 1979
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11
“... using wheelchairs, and assistance from caregivers. CONCLUSION. Women with physical disability can...”
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12
Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary...
Por Blum, Werner F., Klammt, Jürgen, Amselem, Serge, Pfäffle, Heike M., Legendre, Marie, Sobrier, Marie-Laure, Luton, Marie-Pierre, Child, Christopher J., Jones, Christine, Zimmermann, Alan G., Quigley, Charmian A., Cutler, Gordon B., Deal, Cheri L., Lebl, Jan, Rosenfeld, Ron G., Parks, John S., Pfäffle, Roland W.
Publicado no EBioMedicine (2018)
“... they were only moderately diminished (3-6 μg/L). Two patients with a GH1 mutation developed TSH deficiency...”Publicado no EBioMedicine (2018)
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13
“...% of those eligible) with a child admitted to hospital for severe trauma with an Abbreviated Injury Scale...”
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14
Por Collins, Chelsea L., Scott, J. Paul, Panepinto, Julie A., Punzalan, Rowena C.
Publicado no J Pediatr Hematol Oncol (2013)
“... from a plasma transfusion. A post-liver transplant patient with a normal platelet count received fresh...”Publicado no J Pediatr Hematol Oncol (2013)
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15
Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary...
Por Werner F. Blum, Jürgen Klammt, Serge Amselem, Heike M. Pfäffle, Marie Legendre, Marie-Laure Sobrier, Marie-Pierre Luton, Christopher J. Child, Christine Jones, Alan G. Zimmermann, Charmian A. Quigley, Gordon B. Cutler, Jr, Cheri L. Deal, Jan Lebl, Ron G. Rosenfeld, John S. Parks, Roland W. Pfäffle
Publicado em 2018-10-01
“... they were only moderately diminished (3-6 μg/L). Two patients with a GH1 mutation developed TSH deficiency...”Publicado em 2018-10-01
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16
“... birth revealed a high level of V3 sequence variability. In contrast, V3 sequences obtained from...”
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17
Por Coatsworth, J. Douglas, Duncan, Larissa G., Greenberg, Mark T., Nix, Robert L.
Publicado em 2009
“...We evaluated the efficacy of a mindful parenting program for changing parents’ mindfulness, child...”Publicado em 2009
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18
“... disease in humans. A closely related bovine RSV is responsible for a remarkably similar disease syndrome...”
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19
Por Komro, Kelli A, Tobler, Amy L, Delisle, Alexis L, O’Mara, Ryan J, Wagenaar, Alexander C
Publicado em 2013
“.... Pediatricians play a vital role in promoting the health of children in the communities they serve and can...”Publicado em 2013
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20
Por Simpson, N. E., Dallaire, L., Miller, J. R., Siminovich, L., Hamerton, J. L., Miller, J., McKeen, C.
Publicado em 1976
“... pregnancy. For 39 fetuses (3.8%) a diagnosis of a genetic abnormality was made and 23 male fetuses were...”Publicado em 1976
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