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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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5002por Mersakova, Sandra, Janikova, Katarina, Kalman, Michal, Marcinek, Juraj, Grendar, Marian, Vojtko, Martin, Kycina, Roman, Pindura, Miroslav, Janik, Jan, Mikolajcik, Peter, Gabonova, Eva, Laca, Ludovit, Mejstrikova, Ester, Halasova, Erika, Strnadel, Jan, Lasabova, Zora“…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. …”
Publicado 2022
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5003por Brezestean, I. A., Tosa, N., Falamas, A., Cuibus, D., Muntean, C. M., Bende, A., Cozar, B., Berghian-Grosan, C., Farcău, C.“…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. …”
Publicado 2022
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5004por Levy, Elan J., Thomas, Camille, Antler, Gilad, Gavrieli, Ittai, Turchyn, Alexandra V., Grossi, Vincent, Ariztegui, Daniel, Sivan, Orit“…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. …”
Publicado 2022
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5005“…Among the 97 volatile compounds, 37 compounds belong to alkenes, 29 compounds belong to alkanes, and there were 8 esters, 8 alcohols and 6 ketones. …”
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5006por Hwang, Seon Young, Jang, Hye Ji, Kim, Young Jun, Maeng, Ju Young, Park, Go Eun, Yang, Seo Young, Rhee, Choong Kyun, Sohn, Youngku“…Alkenes were observed to be more produced than alkanes unlike in the conventional F-T synthesis. …”
Publicado 2022
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5007por Shahriari, Saeedeh, Seifi, Sharareh, Khodakarim, Nastaran, Ramim, Tayeb, Dashtpeima, Alireza“…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). …”
Publicado 2022
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5008por Aziz, Marya, Ahmad, Saeed, Khurshid, Umair, Pervaiz, Irfan, Lodhi, Arslan Hussain, Jan, Nasrullah, Khurshid, Sameera, Arshad, Muhammad Adeel, Ibrahim, Mohamed M., Mersal, Gaber A. M., Alenazi, Fahaad S., Awadh Saleh Alamri, Ahmed, Butt, Juwairiya, Saleem, Hammad, El-Bahy, Zeinhom M.“…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. …”
Publicado 2022
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5009por Xu, Huiyuan, Liu, Quanyou, Li, Zhiquan, Hou, Dujie, Han, Xu, Li, Peng, Li, Pengpeng, Zhu, Biqing“…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. …”
Publicado 2023
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5010por Malik, Shiza, Niazi, Maha, Khan, Maham, Rauff, Bisma, Anwar, Sidra, Amin, Faheem, Hanif, Rumeza“…Broad and weak bands of aliphatic ether (C–O), alkane (C–H), and other functional groups were also found on these AuNPs. …”
Publicado 2023
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5011“…In situ Fourier transform infrared results showed that the adsorption of alkane occurred through the interaction with Ce–OH. …”
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5012por 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.Enlace del recurso
Publicado 1998
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5013por 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.Enlace del recurso
Publicado 2000
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5014por 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.Enlace del recurso
Publicado 2001
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5015por Naveed, Muhammad, Makhdoom, Syeda Izma, Rehman, Shafiq ur, Aziz, Tariq, Bashir, Farzana, Ali, Urooj, Alharbi, Metab, Alshammari, Abdulrahman, Alasmari, Abdullah F.“…The synthesized NPs were cylindrical in shape, with a size of 2 nm and (-OH) hydroxyl, (C-H) alkanes and alkynes N-C, N=C, C-O, =CH functional groups attached to the surface of ZVI-NPs. …”
Publicado 2023
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5016por Salem, Mostafa E., Mahrous, Esraa M., Ragab, Eman A., Nafie, Mohamed S., Dawood, Kamal M.“…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. …”
Publicado 2023
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5017por Vonnie, Joseph Merillyn, Rovina, Kobun, ‘Aqilah, Nasir Md Nur, Felicia, Xia Wen Ling“…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. …”
Publicado 2023
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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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5019por Mollard, Rebecca, Cachero, Katrina, Luhovyy, Bohdan, Martin, Heather, Moisiuk, Sharon, Mahboobi, Sepideh, Balshaw, Robert, Collister, David, Cahill, Leah, Tennankore, Karthik K., Tangri, Navdeep, MacKay, Dylan“…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. …”
Publicado 2023
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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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