Base de dados : MEDLINE
Pesquisa : E05.196.401.319 [Categoria DeCS]
Referências encontradas : 3144 [refinar]
Mostrando: 1 .. 10   no formato [Detalhado]

página 1 de 315 ir para página                         

  1 / 3144 MEDLINE  
              next record last record
seleciona
para imprimir
Fotocópia
PubMed Central Texto completo
Texto completo
[PMID]:25780145
[Au] Autor:Brow DA
[Ad] Endereço:Department of Biomolecular Chemistry, University of Wisconsin, Madison, Wisconsin 53706, USA dabrow@wisc.edu.
[Ti] Título:An RNA mystery and its denouement.
[So] Source:RNA;21(4):576-7, 2015 Apr.
[Is] ISSN:1469-9001
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: RNA/química
[Mh] Termos MeSH secundário: Eletroforese em Papel
Editoração
RNA/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
63231-63-0 (RNA)
[Em] Mês de entrada:1505
[Cu] Atualização por classe:150401
[Lr] Data última revisão:
150401
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:150318
[St] Status:MEDLINE
[do] DOI:10.1261/rna.049668.115


  2 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:25456275
[Au] Autor:Luo L; Li X; Crooks RM
[Ad] Endereço:Department of Chemistry, The University of Texas at Austin , 105 East 24th Street Stop A5300, Austin, Texas 78712-1224, United States.
[Ti] Título:Low-voltage origami-paper-based electrophoretic device for rapid protein separation.
[So] Source:Anal Chem;86(24):12390-7, 2014 Dec 16.
[Is] ISSN:1520-6882
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:We present an origami paper-based electrophoretic device (oPAD-Ep) that achieves rapid (∼5 min) separation of fluorescent molecules and proteins. Due to the innovative design, the required driving voltage is just ∼10 V, which is more than 10 times lower than that used for conventional electrophoresis. The oPAD-Ep uses multiple, thin (180 µm/layer) folded paper layers as the supporting medium for electrophoresis. This approach significantly shortens the distance between the anode and cathode, and this, in turn, accounts for the high electric field (>1 kV/m) that can be achieved even with a low applied voltage. The multilayer design of the oPAD-Ep enables convenient sample introduction by use of a slip layer as well as easy product analysis and reclamation after electrophoresis by unfolding the origami paper and cutting out desired layers. We demonstrate the use of oPAD-Ep for simple separation of proteins in bovine serum, which illustrates its potential applications for point-of-care diagnostic testing.
[Mh] Termos MeSH primário: Eletroforese em Papel/métodos
Proteínas/química
[Mh] Termos MeSH secundário: Eletricidade
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Nm] Nome de substância:
0 (Proteins)
[Em] Mês de entrada:1508
[Cu] Atualização por classe:141216
[Lr] Data última revisão:
141216
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:141203
[St] Status:MEDLINE
[do] DOI:10.1021/ac503976c


  3 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:22585473
[Au] Autor:Srinivas PR
[Ad] Endereço:National Heart, Lung, and Blood Institute, National Institutes of Health Bethesda, Bethesda, MD, USA. srinivap@nhlbi.nih.gov
[Ti] Título:Introduction to protein electrophoresis.
[So] Source:Methods Mol Biol;869:23-8, 2012.
[Is] ISSN:1940-6029
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:This chapter discusses, briefly, the developments in electrophoresis of proteins from Tiselius' moving boundary electrophoresis to the modern day two-dimensional polyacrylamide gel electrophoresis. It also touches upon the staining methods used to visualize total proteins postelectrophoresis.
[Mh] Termos MeSH primário: Eletroforese em Gel Bidimensional
Proteínas/isolamento & purificação
[Mh] Termos MeSH secundário: Tampões (Química)
Eletroforese em Papel
Eletroforese em Gel de Poliacrilamida
Seres Humanos
Indicadores e Reagentes/química
Proteínas/química
Corantes de Rosanilina/química
Coloração e Rotulagem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Buffers); 0 (Indicators and Reagents); 0 (Proteins); 0 (Rosaniline Dyes); 78642-64-5 (Coomassie blue)
[Em] Mês de entrada:1209
[Cu] Atualização por classe:120515
[Lr] Data última revisão:
120515
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:120516
[St] Status:MEDLINE
[do] DOI:10.1007/978-1-61779-821-4_2


  4 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:21846329
[Au] Autor:Parsons HT; Yasmin T; Fry SC
[Ad] Endereço:The Edinburgh Cell Wall Group, Institute of Molecular Plant Sciences, School of Biological Sciences, The University of Edinburgh, The King's Buildings, Edinburgh EH9 3JH, UK.
[Ti] Título:Alternative pathways of dehydroascorbic acid degradation in vitro and in plant cell cultures: novel insights into vitamin C catabolism.
[So] Source:Biochem J;440(3):375-83, 2011 Dec 15.
[Is] ISSN:1470-8728
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:L-Ascorbate catabolism involves reversible oxidation to DHA (dehydroascorbic acid), then irreversible oxidation or hydrolysis. The precursor-product relationships and the identity of several major DHA breakdown products remained unclear. In the presence of added H2O2, DHA underwent little hydrolysis to DKG (2,3-dioxo-L-gulonate). Instead, it yielded OxT (oxalyl L-threonate), cOxT (cyclic oxalyl L-threonate) and free oxalate (~6:1:1), essentially simultaneously, suggesting that all three product classes independently arose from one reactive intermediate, proposed to be cyclic-2,3-O-oxalyl-L-threonolactone. Only with plant apoplastic esterases present were the esters significant precursors of free oxalate. Without added H2O2, DHA was slowly hydrolysed to DKG. Downstream of DKG was a singly ionized dicarboxy compound (suggested to be 2-carboxy-L-xylonolactone plus 2-carboxy-L-lyxonolactone), which reversibly de-lactonized to a dianionic carboxypentonate. Formation of these lactones and acid was minimized by the presence of residual unreacted ascorbate. In vivo, the putative 2-carboxy-L-pentonolactones were relatively stable. We propose that DHA is a branch-point in ascorbate catabolism, being either oxidized to oxalate and its esters or hydrolysed to DKG and downstream carboxypentonates. The oxidation/hydrolysis ratio is governed by reactive oxygen species status. In vivo, oxalyl esters are enzymatically hydrolysed, but the carboxypentonates are stable. The biological roles of these ascorbate metabolites invite future exploration.
[Mh] Termos MeSH primário: Ácido Ascórbico/metabolismo
Ácido Desidroascórbico/metabolismo
Rosa/citologia
[Mh] Termos MeSH secundário: Ácido 2,3-Dicetogulônico/química
Ácido Ascórbico/química
Células Cultivadas
Ácido Desidroascórbico/química
Eletroforese em Papel
Peróxido de Hidrogênio/química
Hidrólise
Cinética
Modelos Químicos
Oxalatos/química
Oxirredução
Rosa/metabolismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Oxalates); 3409-57-2 (2,3-Diketogulonic Acid); BBX060AN9V (Hydrogen Peroxide); PQ6CK8PD0R (Ascorbic Acid); Y2Z3ZTP9UM (Dehydroascorbic Acid)
[Em] Mês de entrada:1201
[Cu] Atualização por classe:170322
[Lr] Data última revisão:
170322
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:110818
[St] Status:MEDLINE
[do] DOI:10.1042/BJ20110939


  5 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:21319731
[Au] Autor:Zhang S; Zhang W; Wang Y; Jin Z; Wang X; Zhang J; Zhang Y
[Ad] Endereço:Key Laboratory of Radiopharmaceuticals, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing, 100875, China.
[Ti] Título:Synthesis and biodistribution of a novel (99m)TcN complex of norfloxacin dithiocarbamate as a potential agent for bacterial infection imaging.
[So] Source:Bioconjug Chem;22(3):369-75, 2011 Mar 16.
[Is] ISSN:1520-4812
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Achieving a (99m)Tc-labeled fluoroquinolone derivative as a single photon emission computed tomography (SPECT) tracer is considered to be of great interest. The norfloxacin dithiocarbamate (NFXDTC) was synthesized and radiolabeled with a [(99m)TcN]²(+) intermediate to form the (99m)TcN-NFXDTC complex in high yield. The radiochemical purity of (99m)TcN-NFXDTC was over 90%, as measured by thin layer chromatography (TLC) and high performance liquid chromatography (HPLC), without any notable decomposition at room temperature over a period of 6 h. The partition coefficient and electrophoresis results indicated that (99m)TcN-NFXDTC was lipophilic and neutral. The bacterial binding assay studies showed tht (99m)TcN-NFXDTC had a good binding affinity. Biodistribution results in bacterial infected mice showed that (99m)TcN-NFXDTC had a higher uptake at the sites of infection and better abscess/blood and abscess/muscle ratios than those of (99m)Tc-ciprofloxacin and (99m)TcN-CPFXDTC (CPFXDTC = ciprofloxacin dithiocarbamate). The biodistribution results of (99m)TcN-NFXDTC in bacterially infected mice and in mice with turpentine-induced abscesses indicated that (99m)TcN-NFXDTC was suited to be a bacteria-specific infection imaging agent. Single photon emission computed tomography (SPECT) image studies showed there was a visible accumulation in infection sites, suggesting that it would be a promising candidate for bacterial infection imaging.
[Mh] Termos MeSH primário: Infecções Bacterianas/diagnóstico por imagem
Norfloxacino/análogos & derivados
Norfloxacino/síntese química
Norfloxacino/farmacocinética
Compostos de Organotecnécio/química
Tomografia Computadorizada de Emissão de Fóton Único/métodos
[Mh] Termos MeSH secundário: Animais
Estabilidade de Medicamentos
Eletroforese em Papel
Inflamação/diagnóstico por imagem
Marcação por Isótopo
Ligantes
Masculino
Camundongos
Norfloxacino/química
Coelhos
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Ligands); 0 (Organotechnetium Compounds); 0 (norfloxacin dithiocarbamate); N0F8P22L1P (Norfloxacin)
[Em] Mês de entrada:1106
[Cu] Atualização por classe:161125
[Lr] Data última revisão:
161125
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:110216
[St] Status:MEDLINE
[do] DOI:10.1021/bc100357w


  6 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:21222076
[Au] Autor:Fry SC
[Ad] Endereço:The Edinburgh Cell Wall Group, Institute of Molecular Plant Sciences, School of Biological Sciences, University of Edinburgh, Edinburgh, UK.
[Ti] Título:High-voltage paper electrophoresis (HVPE) of cell-wall building blocks and their metabolic precursors.
[So] Source:Methods Mol Biol;715:55-80, 2011.
[Is] ISSN:1940-6029
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:HVPE is an excellent and often overlooked method for obtaining objective and meaningful information about cell-wall "building blocks" and their metabolic precursors. It provides not only a means of analysis of known compounds but also an insight into the charge and/or mass of any unfamiliar compounds that may be encountered. It can be used preparatively or analytically. It can achieve either "class separations" (e.g. delivering all hexose monophosphates into a single pool) or the resolution of different compounds within a given class (e.g. ADP-Glc from UDP-Glc; or GlcA from GalA). All information from HVPE about charge and mass can be obtained on minute traces of analytes, especially those that have been radiolabelled, e.g. by in-vivo feeding of a (3)H- or (14)C-labelled precursor. HVPE does not usually damage the substance under investigation (unless staining is used), so samples of interest can be eluted intact from the paper ready for further analysis. Although HVPE is a technique that has been available for several decades, recently it has tended to be sidelined, possibly because the apparatus is not widely available. Interested scientists are invited to contact the author about the possibility of accessing the Edinburgh apparatus.
[Mh] Termos MeSH primário: Parede Celular/química
Plantas/química
[Mh] Termos MeSH secundário: Aminoácidos/análise
Tampões (Química)
Calibragem
Carboidratos/análise
Eletroforese em Papel/instrumentação
Hidroxibenzoatos/análise
Peso Molecular
Nucleotídeos/análise
Oligossacarídeos/análise
Fosfatos/análise
Plantas/metabolismo
Poliaminas/análise
Coloração pela Prata
Sulfatos/análise
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Amino Acids); 0 (Buffers); 0 (Carbohydrates); 0 (Hydroxybenzoates); 0 (Nucleotides); 0 (Oligosaccharides); 0 (Phosphates); 0 (Polyamines); 0 (Sulfates); 29656-58-4 (phenolic acid)
[Em] Mês de entrada:1106
[Cu] Atualização por classe:171110
[Lr] Data última revisão:
171110
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:110112
[St] Status:MEDLINE
[do] DOI:10.1007/978-1-61779-008-9_4


  7 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:19144525
[Au] Autor:Chu T; Xu H; Yang Z; Wang X
[Ad] Endereço:Beijing National Laboratory for Molecular Sciences, Department of Applied Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China. twchu@pku.edu.cn
[Ti] Título:Synthesis and in vitro evaluation of three 99mTc-labeled hydroxamamide-based ligands as markers for hypoxic cells.
[So] Source:Appl Radiat Isot;67(4):590-3, 2009 Apr.
[Is] ISSN:1872-9800
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Three new hydroxamamide derivatives with different lipophilicity, N'-hydroxy-N-methyl-3-(4-nitro-1H-imidazol-1-yl)propanamidine, N-butyl-N'-hydroxy-3-(4-nitro-1H-imidazol-1-yl)propanamidine, and N'-hydroxy-3-(4-nitro-1H-imidazol-1-yl)-N-octadecylpropanamidine were easily synthesized and labeled with technetium-99m as markers for hypoxic cells. The results of in vitro experiment indicate that the accumulation of three (99m)Tc-complexes steadily increases with time in hypoxic cells, but fluctuates with time and has no fixed trend in aerobic cells; the complex with higher lipophilicity shows more uptake in cells; and the effect of lipophilicity of the (99m)Tc-complexes on the hypoxic/aerobic difference can be neglected.
[Mh] Termos MeSH primário: Amidas/síntese química
Amidas/farmacologia
Hipóxia Celular
Compostos de Organotecnécio/síntese química
Compostos de Organotecnécio/farmacologia
[Mh] Termos MeSH secundário: Avaliação Pré-Clínica de Medicamentos
Eletroforese em Papel
Ligantes
Espectroscopia de Ressonância Magnética
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Amides); 0 (Ligands); 0 (Organotechnetium Compounds)
[Em] Mês de entrada:0904
[Cu] Atualização por classe:090223
[Lr] Data última revisão:
090223
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:090116
[St] Status:MEDLINE
[do] DOI:10.1016/j.apradiso.2008.12.003


  8 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:19128978
[Au] Autor:Zhang J; Song Z; Wang X
[Ad] Endereço:Key Laboratory of Radiopharmaceuticals (Beijing Normal University), Ministry of Education, College of Chemistry, Beijing Normal University, Beijing 100875, PR China. zhjunbo@bnu.edu.cn
[Ti] Título:Synthesis of a bis(2,3-dimethylcyclohexyl-dithiocarbamato)-nitrido 99mTc complex: a potential tracer for myocardial imaging.
[So] Source:Appl Radiat Isot;67(4):577-80, 2009 Apr.
[Is] ISSN:1872-9800
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:The (99m)TcN(DMCHDTC)(2) complex, where DMCHDTC is 2,3-dimethylcyclohexyl dithiocarbamato, has been synthesized through a ligand-exchange reaction. The two-step procedure involved the initial reaction of (99m)TcO(4)(-) with succinic dihydrazide in the presence of stannous chloride as reducing agent and propylenediamine tetraacetic acid as complexant, followed by the addition of 2,3-dimethylcyclohexyl dithiocarbamate. The radiochemical purity of the complex was over 90%, as measured by thin layer chromatography, without any notable decomposition at room temperature over a period of 6h. The partition coefficient and electrophoresis results indicated that this complex was lipophilic and neutral. Biodistribution in mice showed that the complex accumulated in the heart with high uptake and good retention, the heart uptakes being 12.82, 11.37 and 10.64%ID/g at 5, 30 and 60 min post-injection, respectively. The heart/lung, heart/liver and heart/blood ratios of the complex were 1.06, 0.25 and 8.06 at 60 min post-injection, suggesting it has potential for use as a myocardial imaging agent.
[Mh] Termos MeSH primário: Coração/diagnóstico por imagem
Compostos de Organotecnécio/síntese química
Compostos Radiofarmacêuticos/síntese química
[Mh] Termos MeSH secundário: Animais
Eletroforese em Papel
Camundongos
Compostos de Organotecnécio/farmacocinética
Cintilografia
Compostos Radiofarmacêuticos/farmacocinética
Distribuição Tecidual
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Organotechnetium Compounds); 0 (Radiopharmaceuticals); 0 (bis(2,3-dimethylcyclohexyl-dithiocarbamato)-nitrido 99m technetium)
[Em] Mês de entrada:0904
[Cu] Atualização por classe:161125
[Lr] Data última revisão:
161125
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:090109
[St] Status:MEDLINE
[do] DOI:10.1016/j.apradiso.2008.11.006


  9 / 3144 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo SciELO Brasil
[PMID]:17581679
[Au] Autor:Yilmaz O; Yurt Lambrecht F; Soylu A; Durkan K; Kavukcu S
[Ad] Endereço:Department of Animal Research Center, Medical Faculty, Dokuz Eylul University, Izmir, Turkey.
[Ti] Título:Biodistribution of 99m technetium- labeled creatinine in healthy rats.
[So] Source:Braz J Med Biol Res;40(6):807-12, 2007 Jun.
[Is] ISSN:0100-879X
[Cp] País de publicação:Brazil
[La] Idioma:eng
[Ab] Resumo:The distribution of creatinine, one of the toxic guanidine compounds, in various tissues has not been studied in detail by using radiolabeled creatinine. Our objective was to investigate the biodistribution of creatinine labeled with 99m technetium (99mTc) by the stannous (II) chloride method in healthy male Wistar rats. Quality controls were carried out by radio thin layer chromatography, high-performance liquid chromatography, and paper electrophoresis. The labeling yield was 85 +/- 2% under optimum conditions (pH 7 and 100 microg stannous chloride). Rats (N = 12) were injected intravenously with 99mTc-creatinine and their blood and visceral organs were evaluated for 99mTc-creatinine uptake as percent of the injected dose per gram wet weight of each tissue (%ID/g). The lowest amount of uptake was detected in the brain and testis. When the rate of uptake was evaluated, only the kidney showed increasing rates of uptake of 99mTc-creatinine throughout the study. Kidneys showed the highest amount of uptake throughout the study (P < 0.001 compared to all other organs), followed by liver, spleen and lung tissue.
[Mh] Termos MeSH primário: Creatinina/farmacocinética
Compostos Radiofarmacêuticos/farmacocinética
Tecnécio/farmacocinética
[Mh] Termos MeSH secundário: Animais
Cromatografia Líquida de Alta Pressão
Creatinina/sangue
Eletroforese em Papel
Masculino
Ratos
Ratos Wistar
Distribuição Tecidual
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Radiopharmaceuticals); 7440-26-8 (Technetium); AYI8EX34EU (Creatinine)
[Em] Mês de entrada:0802
[Cu] Atualização por classe:161018
[Lr] Data última revisão:
161018
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:070622
[St] Status:MEDLINE


  10 / 3144 MEDLINE  
              first record previous record
seleciona
para imprimir
Fotocópia
[PMID]:17438939
[Au] Autor:Song JK; Choi HJ; Chin I
[Ad] Endereço:Department of Polymer Science and Engineering, Inha University, Incheon, Korea.
[Ti] Título:Preparation and properties of electrophoretic microcapsules for electronic paper.
[So] Source:J Microencapsul;24(1):11-9, 2007 Feb.
[Is] ISSN:0265-2048
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:This paper shows two types of microcapsules used for electrophoretic display. One is prepared by in-situ polymerization which is based on urea, melamine and formaldehyde and another by complex coacervation, which is composed of gelatin and gum Arabic. Microcapsules attract interests of many research groups for longer lifetime of electrophoretic display by reducing agglomerization or lateral movements of nanoparticles. The gelatin microcapsules were more attractive in providing more uniform microcapsule coverage on electrodes due to their flexibility as compared to the melamine-urea microcapsules. The properties of microcapsules were characterized by FTIR, OM, SEM and TGA. Migration of nanoparticles in the two types of microcapsules was also observed when an electric field was applied.
[Mh] Termos MeSH primário: Cápsulas/isolamento & purificação
Eletroforese em Papel/métodos
[Mh] Termos MeSH secundário: Cápsulas/química
Composição de Medicamentos
Formaldeído
Gelatina
Goma Arábica
Maleatos/química
Maleatos/isolamento & purificação
Microscopia Eletrônica de Varredura
Polietilenos/química
Polietilenos/isolamento & purificação
Poliestirenos/química
Poliestirenos/isolamento & purificação
Espectroscopia de Infravermelho com Transformada de Fourier
Termogravimetria
Triazinas
Ureia
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Capsules); 0 (Maleates); 0 (Polyethylenes); 0 (Polystyrenes); 0 (Triazines); 1HG84L3525 (Formaldehyde); 70KO0R01RY (polystyrene sulfonic acid); 8W8T17847W (Urea); 9000-01-5 (Gum Arabic); 9000-70-8 (Gelatin); 9006-26-2 (ethylene-maleic anhydride copolymer); N3GP2YSD88 (melamine)
[Em] Mês de entrada:0712
[Cu] Atualização por classe:151119
[Lr] Data última revisão:
151119
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:070419
[St] Status:MEDLINE



página 1 de 315 ir para página                         
   


Refinar a pesquisa
  Base de dados : MEDLINE Formulário avançado   

    Pesquisar no campo  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde