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  1. 5001
    “…Fruits and vegetables have alkalizing properties and beneficially affect DAL. It has thus been suggested that a plant‐based diet (restricting or excluding animal products) may be a powerful tool in reducing DAL; yet studies in that particular field are scarce. …”
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  2. 5002
    “…In addition, the methylation status of selected genomic regions of CRC biomarkers (ADAMTS16, MGMT, PROM1 (CD133), LGR5 and ALCAM) was investigated by pyrosequencing in a cohort of patients from Martin University Hospital, Martin, Slovakia. …”
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  3. 5003
    “…Endosulfan, a challenging analyte with poor affinity to metal surfaces, was captured near the metal surface by using self-assembled alkane thiol monolayers (hexanethiol and octanethiol), as demonstrated by the thorough vibrational band analysis, and supported by density functional theory (DFT) calculations. …”
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  4. 5004
    “…In modern times, increased freshwater runoff to the lake surface waters resulted in stratification and dilution of the upper water column followed by microbial blooms. …”
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  5. 5005
  6. 5006
  7. 5007
    “…Methods: The study was performed as a prospective cohort in patients referred to Hazrat Rasoul Akram Hospital in Tehran for two years (April 2019-April 2021). …”
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  8. 5008
    “…The GC-MS profiling of n-butanol and chloroform fractions revealed the existence of several (110) important compounds presenting different classes (fatty acids, phenols, alkanes, monoterpenes, diterpenes, sesquiterpenoids, and sterols), while LC-ESI-MS tentatively identified the presence of 44 clinically important secondary metabolites. …”
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  9. 5009
    “…A comparison of the δ(13)C of Pr and Ph with the δ(13)C of the n-C17 and n-C18 alkanes reveals a shift in the mode of carbon cycling/export (autotrophy versus heterotrophy) in the Yanchang Formation and that there was dominant heterotrophic bacterial activity or bacterial biomass in the Chang 7 member. …”
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  10. 5010
    “…Broad and weak bands of aliphatic ether (C–O), alkane (C–H), and other functional groups were also found on these AuNPs. …”
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  11. 5011
    “…In situ Fourier transform infrared results showed that the adsorption of alkane occurred through the interaction with Ce–OH. …”
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  12. 5012
    por Aggarwal, M.M., Agnihotri, A., Ahammed, Z., Angelis, A.L.S., Antonenko, V., Arefiev, V., Astakhov, V., Avdeitchikov, V., Awes, T.C., Baba, P.V.K.S., Badyal, S.K., Baldine, A., Barabach, L., Barlag, C., Bathe, S., Batiounia, B., Bernier, T., Bhalla, K.B., Bhatia, V.S., Blume, C., Bock, R., Bohne, E.-M., Borocz, Z.K., Bucher, D., Buijs, A., Busching, H., Carlen, L., Chalyshev, V., Chattopadhyay, S., Cherbatchev, R., Chujo, T., Claussen, A., Das, A.C., Decowski, M.P., Djordjadze, V., Donni, P., Doubovik, I., Dutta Majumdar, M.R., El Chenawi, K., Eliseev, S., Enosawa, K., Foka, P., Fokin, S., Frolov, V., Ganti, M.S., Garpman, S., Gavrishchuk, O., Geurts, F.J.M., Ghosh, T.K., Glasow, R., Gupta, S.K., Guskov, B., Gustafsson, H.A., Gutbrod, H.H., Higuchi, R., Hrivnacova, I., Ippolitov, M., Kalechofsky, H., Kamermans, R., Kampert, K.-H., Karadjev, K., Karpio, K., Kato, S., Kees, S., Kim, H., Kolb, B.W., Kosarev, I., Koutcheryaev, I., Krumpel, T., Kugler, A., Kulinich, P., Kurata, M., Kurita, K., Kuzmin, N., Langbein, I., Lebedev, A., Lee, Y.Y., Lohner, H., Luquin, L., Mahapatra, D.P., Manko, V., Martin, M., Maximov, A., Mehdiyev, R., Mgebrichvili, G., Miake, Y., Mikhalev, D., Mishra, G.C., Miyamoto, Y., Morrison, D., Mukhopadhyay, D.S., Myalkovski, V., Naef, H., Nandi, B.K., Nayak, S.K., Nayak, T.K., Neumaier, S., Nianine, A., Nikitine, V., Nikolaev, S., Nilsson, P., Nishimura, S., Nomokonov, P., Nystrand, J., Obenshain, F.E., Oskarsson, A., Otterlund, I., Pachr, M., Parfenov, A., Pavliouk, S., Pietzmann, T., Patracek, V., Pinanaud, W., Plasil, F., Purschke, M.L., Raeven, B., Rak, J., Raniwala, R., Raniwala, S., Ramamurthy, V.S., Rao, N.K., Retiere, F., Reygers, K., Roland, G., Rosselet, L., Roufanov, I., Roy, C., Rubio, J.M., Sako, H., Sambyal, S.S., Santo, R., Sato, S., Schlagheck, H., Schmidt, H.-R., Shabratova, G., Sibiriak, I., Siemiarczuk, T., Silvermyr, D., Sinha, B.C., Slavine, N., Soderstrom, K., Solomey, N., Sorensen, S.P., Stankus, P., Stefanek, G., Steinberg, P., Stenlund, E., Stuken, D., Sumbera, M., Svensson, T., Trivedi, M.D., Tsvetkov, A., Twenhofel, C., Tykarski, L., Urbahn, J., Eijndhoven, N.v., Nieuwenhuizen, G.J.v., Vinogradov, A., Viyogi, Y.P., Vodopianov, A., Voros, S., Wyslouch, B., Yagi, K., Yokota, Y., Young, G.R.
    Publicado 1998
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  13. 5013
    por Aggarwal, M.M., Agnihotri, A., Ahammed, Z., Angelis, A.L.S., Antonenko, V., Arefev, V., Astakhov, V., Avdeitchikov, V., Awes, T.C., Baba, P.V.K.S., Badyal, S.K., Barlag, C., Bathe, S., Batiounia, B., Bernier, T., Bhalla, K.B., Bhatia, V.S., Blume, C., Bock, R., Bohne, E.M., Borocz, Z., Bucher, D., Buijs, A., Busching, H., Carlen, L., Chalyshev, V., Chattopadhyay, S., Cherbatchev, R., Chujo, T., Claussen, A., Das, A.C., Decowski, M.P., Delagrange, H., Djordjadze, V., Donni, P., Doubovik, I., Dutt, S., Dutta Majumdar, M.R., El Chenawi, K., Eliseev, S., Enosawa, K., Foka, P., Fokin, S., Ganti, M.S., Garpman, S., Gavrishchuk, O., Geurts, F.J.M., Ghosh, T.K., Glasow, R., Gupta, S.K., Guskov, B., Gustafsson, H.A., Gutbrod, H.H., Higuchi, R., Hrivnacova, I., Ippolitov, M., Kalechofsky, H., Kamermans, R., Kampert, K.H., Karadjev, K., Karpio, K., Kato, S., Kees, S., Klein-Boesing, Christian, Knoche, S., Kolb, B.W., Kosarev, I., Koutcheryaev, I., Krumpel, T., Kugler, A., Kulinich, P., Kurata, M., Kurita, K., Kuzmin, N., Langbein, I., Lebedev, A., Lee, Y.Y., Lohner, H., Luquin, L., Mahapatra, D.P., Manko, V., Martin, M., Martinez, G., Maximov, A., Mgebrichvili, G., Miake, Y., Mir, M.F., Mishra, G.C., Miyamoto, Y., Mohanty, B., Morrison, Douglas R.O., Mukhopadhyay, D.S., Naef, H., Nandi, B.K., Nayak, S.K., Nayak, T.K., Neumaier, S., Nianine, A., Nikitine, V., Nikolaev, S., Nilsson, P., Nishimura, S., Nomokonov, P., Nystrand, J., Obenshain, F.E., Oskarsson, A., Otterlund, I., Pachr, M., Pavliouk, S., Peitzmann, T., Petracek, V., Pinganaud, W., Plasil, F., von Poblotzki, U., Purschke, M.L., Rak, J., Raniwala, R., Raniwala, S., Ramamurthy, V.S., Rao, N.K., Retiere, F., Reygers, K., Roland, G., Rosselet, L., Roufanov, I., Roy, C., Rubio, J.M., Sako, H., Sambyal, S.S., Santo, R., Sato, S., Schlagheck, H., Schmidt, H.R., Schutz, Y., Shabratova, G., Shah, T.H., Sibiriak, I., Siemiarczuk, T., Silvermyr, D., Sinha, B.C., Slavine, N., Soderstrom, K., Solomey, N., Sorensen, S.P., Stankus, P., Stefanek, G., Steinberg, P., Stenlund, E., Stuken, D., Sumbera, M., Svensson, T., Trivedi, M.D., Tsvetkov, A., Tykarski, L., Urbahn, J., van de Pijll, E.C., van Eijndhoven, N., van Nieuwenhuizen, G.J., Vinogradov, A., Viyogi, Y.P., Vodopianov, A.S., Voros, S., Wyslouch, B., Yagi, K., Yokota, Y.
    Publicado 2000
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  14. 5014
    por Aggarwal, M.M., Agnihotri, A., Ahammed, Z., Angelis, A.L.S., Antonenko, V., Arefiev, V., Astakhov, V., Avdeitchikov, V., Awes, T.C., Baba, P.V.K.S., Badyal, S.K., Baldine, A., Barabach, L., Barlag, C., Bathe, S., Batiounia, B., Bernier, T., Bhalla, K.B., Bhatia, V.S., Blume, C., Bohne, E.M., Borocz, Z.K., Bucher, D., Buijs, A., Busching, H., Carlen, L., Chalyshev, V., Chattopadhyay, S., Cherbatchev, R., Chujo, T., Claussen, A., Das, A.C., Decowski, M.P., Delagrange, H., Djordjadze, V., Donni, P., Doubovik, I., Dutt, S., Dutta Majumdar, M.R., El Chenawi, K., Eliseev, S., Enosawa, K., Foka, P., Fokin, S., Frolov, V., Ganti, M.S., Garpman, S., Gavrishchuk, O., Geurts, F.J.M., Ghosh, T.K., Glasow, R., Gupta, S.K., Guskov, B., Gustafsson, H.A., Gutbrod, H.H., Higuchi, R., Hrivnacova, I., Ippolitov, M., Kalechofsky, H., Kamermans, R., Kampert, K.H., Karadjev, K., Karpio, K., Kato, S., Kees, S., Kim, H., Kolb, B.W., Kosarev, I., Koutcheryaev, I., Krumpel, T., Kugler, A., Kulinich, P., Kurata, M., Kurita, K., Kuzmin, N., Langbein, I., Lebedev, A., Lee, Y.Y., Lohner, H., Luquin, L., Mahapatra, D.P., Manko, V., Martin, M., Martinez, G., Maximov, A., Mehdiyev, Rashid R., Mgebrichvili, G., Miake, Y., Mikhalev, D., Mir, Md.F., Mishra, G.C., Miyamoto, Y., Mohanty, B., Mora, M.J., Morrison, Douglas R.O., Mukhopadhyay, D.S., Myalkovski, V., Naef, H., Nandi, B.K., Nayak, S.K., Nayak, T.K., Neumaier, S., Nianine, A., Nikitine, V., Nikolaev, S., Nilsson, P., Nishimura, S., Nomokonov, P., Nystrand, J., Obenshain, F.E., Oskarsson, A., Otterlund, I., Pachr, M., Parfenov, A., Pavliouk, S., Peitzmann, T., Petracek, V., Plasil, F., Pinganaud, W., Purschke, M.L., Raeven, B., Rak, J., Raniwala, R., Raniwala, S., Ramamurthy, V.S., Rao, N.K., Retiere, F., Reygers, K., Roland, G., Rosselet, L., Roufanov, I., Roy, C., Rubio, J.M., Sako, H., Sambyal, S.S., Santo, R., Sato, S., Schlagheck, H., Schmidt, H.R., Schutz, Y., Shabratova, G., Shah, T.H., Sibiriak, I., Siemiarczuk, T., Silvermyr, D., Sinha, B.C., Slavine, N., Soderstrom, K., Solomey, N., Sorensen, S.P., Stankus, P., Stefanek, G., Steinberg, P., Stenlund, E., Stuken, D., Sumbera, M., Svensson, T., Trivedi, M.D., Tsvetkov, A., Tykarski, L., Urbahn, J., van de Pijll, E.C., van Eijndhoven, N., van Nieuwenhuizen, G.J., Vinogradov, A., Viyogi, Y.P., Vodopianov, A.S., Voros, S., Wyslouch, B., Yagi, K., Yokota, Y., Young, G.R.
    Publicado 2001
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  15. 5015
  16. 5016
    “…The symmetric bis-(2-naphthoyl-pyrazol-3-yl)thiazol-2-yl)hydrazono)methyl)phenoxy)alkanes 18a-c and 21a-c were similarly synthesized from reaction of 6 with the appropriate bis-thiosemicarbazones 17a-c and 19a-c, respectively. …”
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  17. 5017
    “…The FTIR indicated that the films contain various functional groups, such as alkane (C-H), hydroxyl (-OH), carbonyl (C=O), carbonate (CO(3)(2−)), and carboxylic acid (-COOH) that can act as biosorption materials. …”
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  18. 5018
    “…These were grouped into 18 classes, including alcohols, aldehydes, alkaloids, alkanes, etc. The number of volatile compounds in A. ilicifolius (176) and B. gymnorrhiza (172) was lower than in the other three species. …”
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  19. 5019
    “…Oral sodium bicarbonate (the current standard of care therapy for metabolic acidosis) is poorly tolerated leading to low adherence. Base-producing or alkalizing Fruit and vegetables have potential as an alternative treatment for metabolic acidosis as they have been shown to reduce acid load arising from the diet. …”
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  20. 5020
    “…The parent tetrahydroxy para-t-butyl-calix[4]arene was dialkylated at the phenolic hydrogen atoms using α,ω-dibromo-alkanes to yield bis(mono-brominated) alkoxy-chains of variable length. …”
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