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1

Maurer, Karin, and Fritz Mitthof. "Adnotationes epigraphicae III ( 26-33)." TYCHE – Contributions to Ancient History, Papyrology and Epigraphy 27, no. 01 (2013): 229–33. http://dx.doi.org/10.15661/tyche.2012.027.12.

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2

Кельман, Е. И. ""Пороки воли" (Стт. 26-33 Проекта обязательственного права)." Труды цивилистического студенческого кружка при Университете Св. Владимира, Вып. 1, 1915 г. (2009): 64–92.

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3

Lobo, Raul F., Ming Pan, Ignatius Chan, Ronald C. Medrud, Stacey I. Zones, Peter A. Crozier, and Mark E. Davis. "Physicochemical Characterization of Zeolites SSZ-26 and SSZ-33." Journal of Physical Chemistry 98, no. 46 (November 1994): 12040–52. http://dx.doi.org/10.1021/j100097a033.

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4

Abiko, T., and S. Nakatsubo. "Syntheses of Cholecystokin in (Cck) Fragment Analogues (26-33) and Comparative Effect on Decreased Feeding in Rats by Cck Fragment (26-33)." Protein & Peptide Letters 8, no. 2 (April 1, 2001): 153–58. http://dx.doi.org/10.2174/0929866013409652.

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5

Lombaard, C. "The strange case of the patriarchs in Jeremiah 33:26." Acta Theologica 35, no. 2 (October 17, 2016): 36. http://dx.doi.org/10.4314/actat.v35i2.3.

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6

Kusche, Anke. "Rogate – 26. Mai 2019 Johannes 16,23b–28(29–32)33." Homiletische Monatshefte 94, no. 7 (March 6, 2019): 393–401. http://dx.doi.org/10.13109/homh.2018.94.7.393.

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7

Tachibana, Tetsuya, Kiyoko Matsuda, Motoko Kawamura, Hiroshi Ueda, Md Sakirul Islam Khan, and Mark A. Cline. "Feeding-suppressive mechanism of sulfated cholecystokinin (26–33) in chicks." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 161, no. 4 (April 2012): 372–78. http://dx.doi.org/10.1016/j.cbpa.2011.12.010.

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8

Müller, H. V. "Auswertung des Falles "Klaustrophobie" - Allg. homöop. Ztg. 229 (1984), 26-33." Allgemeine Homöopathische Zeitung 229, no. 02 (April 10, 2007): 71–74. http://dx.doi.org/10.1055/s-2006-936050.

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9

Müller, H. V. "Stellungnahme zu den Einsendungen betr. "Klaustrophobie" - AHZ 229 (1984), 26-33." Allgemeine Homöopathische Zeitung 229, no. 03 (April 10, 2007): 113–14. http://dx.doi.org/10.1055/s-2006-936056.

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10

Döhling, Jan-Dirk. "Lukas 1, 26-33 (34-37) 38 19.12.2010 4. Sonntag im Advent." Göttinger Predigtmeditationen 65, no. 1 (October 2010): 34–40. http://dx.doi.org/10.13109/gpre.2010.65.1.34.

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11

Mathis, Jan. "1Kor 11,(17–22) 23–26 (27–29. 33–34a) 18.4.2019 Gründonnerstag." Göttinger Predigtmeditationen 73, no. 2 (January 30, 2019): 217–22. http://dx.doi.org/10.13109/gpre.2018.73.2.217.

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12

Mathis, Jan. "1Kor 11,(17–22) 23–26 (27–29. 33–34a) 18.4.2019 Gründonnerstag." Pastoraltheologie 108, no. 2 (January 30, 2019): 217–22. http://dx.doi.org/10.13109/path.2019.108.2.217.

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13

Dine, Mark S., Sonja S. Hutchins, Ann Thomas, Irene Williams, William J. Bellini, and Stephen C. Redd. "Persistence of Vaccine-Induced Antibody to Measles 26–33 Years after Vaccination." Journal of Infectious Diseases 189, Supplement_1 (May 1, 2004): S123—S130. http://dx.doi.org/10.1086/380308.

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14

Saloga, Tagungsleitung: Joachim, and Mainz. "33. Mainzer Allergie-Workshop – Frühjahrstagung der DGAKI, 25./26. März 2021, Online." Allergologie 44, no. 02 (February 1, 2021): 151–70. http://dx.doi.org/10.5414/alx02217.

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15

Gardner, J. D., M. Knight, V. E. Sutliff, and R. T. Jensen. "N-terminal fragments of CCK-(26-33) as cholecystokinin receptor antagonists in guinea pig pancreatic acini." American Journal of Physiology-Gastrointestinal and Liver Physiology 248, no. 1 (January 1, 1985): G98—G102. http://dx.doi.org/10.1152/ajpgi.1985.248.1.g98.

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In the present study we synthesized different N-terminal fragments and analogues of the C-terminal octapeptide of cholecystokinin [CCK-(26-33)] and examined their actions on dispersed acini prepared from guinea pig pancreas. None of the N-terminal fragments or analogues altered basal amylase release. Analogues of CCK-(26-32), CCK-(26-31), and CCK-(26-30) inhibited CCK-(26-33)-stimulated amylase, and there was a close correlation between the ability of an analogue to inhibit stimulated amylase and the analogue's ability to inhibit binding of 125I-cholecystokinin. N-acetyl-CCK-(26-29)-amide at concentrations as high as 100 microM did not inhibit CCK-(26-33)-stimulated amylase release or binding of 125I-CCK. For those analogues that antagonized CCK-(26-33)-stimulated amylase release the antagonism was of the competitive type and was specific for those secretagogues that interact with the cholecystokinin receptor. Removing the C-terminal amide from N-acetyl-CCK-(26-31)-amide caused a 10-fold decrease in the inhibitory potency, whereas removing the C-terminal amide from N-acetyl-CCK-(26-30)-amide did not alter the inhibitory potency of the peptide. Removing the sulfate ester from the tyrosine residue in position 27 of N-acetyl-CCK-(26-31) did not alter the inhibitory potency of the peptide, whereas removing the sulfate ester from the tyrosine residue in position 27 of N-acetyl-(26-30) caused a three- to fivefold decrease in the inhibitory potency of the peptide.(ABSTRACT TRUNCATED AT 250 WORDS)
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16

Inui, A., M. Okita, T. Inoue, N. Sakatani, M. Oya, H. Morioka, M. Oimomi, and S. Baba. "Effect of cholecystokinin octapeptide analogues on food intake in the dog." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 257, no. 4 (October 1, 1989): R946—R951. http://dx.doi.org/10.1152/ajpregu.1989.257.4.r946.

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Cholecystokinin octapeptide, administered into the third cerebral ventricle (icv), suppresses feeding in sheep, pigs, chicken, rats, and dogs. Because of the species differences in the feeding response to cholecystokinin (CCK), we studied the pharmacological characterization of this peptide on feeding in 16-h-fasted dogs. We examined the effects of CCK-(26-33)-NH2 (CCK-8) and a variety of its analogues, nonsulfated CCK-(26-33)-NH2 (desulfated CCK-8), CCK-(26-33)-OH (deamidated CCK-8), (Nle28,31)-CCK-(26-33)-NH2 [(Nle28,31)-CCK-8], succinyl-CCK-(27-33)-NH2 (Suc-CCK-7) succinyl-Thr28, Leu29, MePhe33-CCK-(27-33)-NH2 [Suc-Thr28, Leu29, MePhe33)-CCK-7], CCK-(29-33)-NH2 (CCK-5), and CCK-(30-33)-NH2 (CCK-4) on food intake after iv injection. Systemic dose-response studies appeared to reveal the following rank order of potencies: Suc-CCK-7 = Suc-(Thr28, Leu29, MePhe33)-CCK-7 greater than CCK-8 = (Nle28,31)-CCK-8 greater than desulfated CCK-8 greater than deaminated CCK-8 greater than CCK-5 = CCK-4 = 0. Smaller COOH-terminal fragments acted as antagonists to the satiety effects of CCK-8. These data demonstrate in the dog that the structural requirements for the behavioral activity of CCK-8 are the COOH-terminal amide group, the sulfate ester of the tyrosine moiety, and the conformational constraints observed in CCK-7.
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17

최종원. "A Study on the Significant of Number Seven in Lev 26:14-33." Korean Journal of Old Testament Studies 19, no. 1 (March 2013): 12–42. http://dx.doi.org/10.24333/jkots.2013.19.1.12.

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18

Alagia, Michele, Pietro Candori, Stefano Falcinelli, Fernando Pirani, Maria S. Pedrosa Mundim, Robert Richter, Marzio Rosi, Stefano Stranges, and Franco Vecchiocattivi. "Dissociative double photoionization of benzene molecules in the 26–33 eV energy range." Physical Chemistry Chemical Physics 13, no. 18 (2011): 8245. http://dx.doi.org/10.1039/c0cp02678f.

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19

Saloga, J. "Tagungsankündigung: 33. Mainzer Allergie-Workshop – Frühjahrstagung der DGAKI; 25./26. März 2021, Online." Allergologie 44, no. 03 (March 1, 2021): 248. http://dx.doi.org/10.5414/alp44248.

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20

Saloga, J. "Tagungsbericht: 33. Mainzer Allergie Workshop – Frühjahrstagung der DGAKI 25./26. März 2021, Online." Allergologie 44, no. 04 (April 1, 2021): 325–26. http://dx.doi.org/10.5414/alp44325.

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21

Pang, Hui, Yi Jiang, and Kanglin Wan. "Drug Susceptibility of 33 Reference Strains of Slowly Growing Mycobacteria to 19 Antimicrobial Agents." BioMed Research International 2017 (2017): 1–13. http://dx.doi.org/10.1155/2017/1584658.

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Objectives. Slowly growing mycobacteria (SGM) are prevalent worldwide and cause an extensive spectrum of diseases. Methods. In this study, the antimicrobial susceptibility of 33 reference strains of SGM to 19 antimicrobial agents was tested using a modified microdilution method. Results. Cefmetazole (32/33) and azithromycin (32/33) exhibited the highest antimicrobial activity, and dapsone (9/33) exhibited the lowest activity against the tested strains. Cefoxitin (30/33), cefoperazone (28/33), and cefepime (28/33) were effective against a high proportion of strains, and macrolides were also highly effective as well as offering the benefit of convenient oral administration to patients. Linezolid (27/33), meropenem (26/33), sulfamethoxazole (26/33), and tigecycline (25/33) showed the highest activity; clofazimine (20/33) and doxycycline (18/33) showed intermediate activity; and rifapentine (13/33), rifabutin (13/33), and minocycline (11/33) showed low antimicrobial activity, closely followed by thioacetazone (10/33) and pasiniazid (10/33), against the tested organisms. According to their susceptibility profiles, the slowly growing species Mycobacterium avium and Mycobacterium simiae were the least susceptible to the tested drugs, whereas Mycobacterium intracellulare, Mycobacterium asiaticum, Mycobacterium scrofulaceum, Mycobacterium szulgai, Mycobacterium branderi, and Mycobacterium holsaticum were the most susceptible. Conclusions. In summary, cephalosporins and macrolides, particularly cefmetazole, azithromycin, clarithromycin, and roxithromycin, showed good antimicrobial activity against the reference strains of SGM.
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22

Hagen, Stephen J., Ramil F. Latypov, Dimitry A. Dolgikh, and Heinrich Roder. "Rapid Intrachain Binding of Histidine-26 and Histidine-33 to Heme in Unfolded Ferrocytochromec†." Biochemistry 41, no. 4 (January 2002): 1372–80. http://dx.doi.org/10.1021/bi011371a.

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23

Hantous-Zannad, S., M. Lahmandi, I. Ridène, A. Zidi, E. Chaaben, A. Ayadi, I. Baccouche, and K. Ben Miled-M’Rad. "THO-WS-26 Cancer bronchopulmonaire et fibrose pulmonaire idiopathique : a propos de 33 cas." Journal de Radiologie 89, no. 10 (October 2008): 1641. http://dx.doi.org/10.1016/s0221-0363(08)77165-8.

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24

Ron, D., C. Gilon, M. Hanani, A. Vromen, Z. Selinger, and M. Chorev. "N-Methylated analogs of Ac[Nle28,31]CCK(26-33): synthesis, activity, and receptor selectivity." Journal of Medicinal Chemistry 35, no. 15 (July 1992): 2806–11. http://dx.doi.org/10.1021/jm00093a013.

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25

Qin, Wenying, Ruslan Sanishvili, Batya Plotkin, Abel Schejter, and E. Margoliash. "The role of histidines 26 and 33 in the structural stabilization of cytochrome c." Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 1252, no. 1 (September 1995): 87–94. http://dx.doi.org/10.1016/0167-4838(95)00124-d.

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26

Kupatadze, Ketevan. "Study of Alazani River and Surface Water Composition in Some Villages of Kakheti Region of Georgia." Southern Brazilian Journal of Chemistry, Volume 26, No. 26, 2018 26, no. 26 (June 30, 2018): 26–33. http://dx.doi.org/10.37633/sbjc.26(26)2018.26-33.

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The article reviews the chemical composition of borehole and surface waters in three villages of one of the regions of Georgia - Kakheti, Gurjaani Municipality. The study was specifically focused on iodine content in waters. It turned out that certain amount of iodine really existed in borehole waters, which means that by everyday drinking of water, the human body gets maybe not the complete required amount of iodine, but at least some part of it. It was also discovered, that according to certain parameters, waters are clean, do not contain heavy metals and can be freely used for drinking and cooking. The chemical composition of the Alazani River was also examined according to all four seasons. This river is interesting because of being used for irrigation of vineyards and fruit gardens.
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27

Tian, Na, Guoxian Wei, Detlef Schuppan, and Eva J. Helmerhorst. "Effect of Rothia mucilaginosa enzymes on gliadin (gluten) structure, deamidation, and immunogenic epitopes relevant to celiac disease." American Journal of Physiology-Gastrointestinal and Liver Physiology 307, no. 8 (October 15, 2014): G769—G776. http://dx.doi.org/10.1152/ajpgi.00144.2014.

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Rothia mucilaginosa, a natural microbial inhabitant of the oral cavity, cleaves gluten (gliadin) proteins at regions that are resistant to degradation by mammalian enzymes. The aim of this study was to investigate to what extent the R. mucilaginosa cell-associated enzymes abolish gliadin immunogenic properties. Degradation of total gliadins and highly immunogenic gliadin 33-mer or 26-mer peptides was monitored by SDS-PAGE and RP-HPLC, and fragments were sequenced by liquid chromatography and electrospray ionization tandem mass spectrometer (LC-ESI-MS/MS). Peptide deamidation by tissue transglutaminase (TG2), a critical step in rendering the fragments more immunogenic, was assessed by TG2-mediated cross-linking to monodansyl cadaverine (MDC), and by a +1-Da mass difference by LC-ESI-MS. Survival of potential immunogenic gliadin epitopes was determined by use of the R5 antibody-based ELISA. R. mucilaginosa-associated enzymes cleaved gliadins, 33-mer and 26-mer peptides into smaller fragments. TG2-mediated cross-linking showed a perfect inverse relationship with intact 33-mer and 26-mer peptide levels, and major degradation fragments showed a slow rate of MDC cross-linking of 6.18 ± 2.20 AU/min compared with 97.75 ± 10.72 and 84.17 ± 3.25 AU/min for the intact 33-mer and 26-mer, respectively, which was confirmed by reduced TG2-mediated deamidation of the fragments in mass spectrometry. Incubation of gliadins with Rothia cells reduced R5 antibody binding by 20, 82, and 97% after 30 min, 2 h, and 5 h, respectively, which was paralleled by reduced reactivity of enzyme-treated 33-mer and 26-mer peptides in the R5 competitive ELISA. Our broad complementary approach to validate gluten degrading activities qualifies R. mucilaginosa-associated enzymes as promising tools to neutralize T cell immunogenic properties for treatment of celiac disease.
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28

Kozlova, Svetlana M., Aleksandr I. Kuliapin, and Tatiana G. Cherniaeva. "Russian and Foreign Literature Department of Altai State University: lines of investigation, conferences, publications." Sibirskiy filologicheskiy zhurnal, no. 1 (March 1, 2009): 233–37. http://dx.doi.org/10.17223/18137083/26/33.

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29

Katyshev, Pavel A., and Stanistav V. Olenev. "The influence of language syntactics on a linguistic personality as a problem of rhetorical criticism." Sibirskiy filologicheskiy zhurnal, no. 4 (December 1, 2010): 191–99. http://dx.doi.org/10.17223/18137083/33/26.

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30

Moshnnik, Julia I., and Aimo Rusunen. "REVIEWS OF THE MONOGRAPH BY A. MARTYNOVA “VYBORG, MON REPOS PARK AND ITS ENVIRONS IN THE WORKS OF ARTISTS OF THE XVI–XIX CENTURIES” (A. RUSUNEN, YU.I. MOSHNIK)." Vestnik Tomskogo gosudarstvennogo universiteta. Kul'turologiya i iskusstvovedenie, no. 33 (March 2019): 301–5. http://dx.doi.org/10.17223/22220836/33/26.

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31

Zhunussova, Zh Kh. "The surface to singular solitonic solution of the nonlinear Schrodinger equation." BULLETIN OF THE KARAGANDA UNIVERSITY-MATHEMATICS 88, no. 4 (December 30, 2017): 26–33. http://dx.doi.org/10.31489/2017m4/26-33.

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32

BATE’E, Maria Magdalena, Syah Abadi MENDROFA, Yamolala ZEGA, Syukur Kasieli HULU, LELYSO LELYSO, and Emmanuel ZEBUA. "The Determinant Factors of Foreign Tourists’ Visit to Tourism Destination in North Sumatra." Journal of Environmental Management and Tourism 10, no. 1 (May 19, 2019): 266. http://dx.doi.org/10.14505//jemt.v10.1(33).26.

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This research aims to investigate the factors influencing the rate of foreign tourists’ visit to tourism destination in North Sumatra, Indonesia. The data were collected using observation, interview, documentation study and questionnaires. The data were analysed using multiple linear regression analysis. The findings of the study indicated that the ancillary facilities are the dominant factor influencing tourists’ visit to tourism destination in North Sumatera. The factors of service quality and facilities and infrastructures provide negative influence on tourists’ visit to tourism destination.
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33

Соф'їн, М. І. "ДО ХАРАКТЕРИСТИКИ ФОРМ І МЕТОДІВ ЗДІЙСНЕННЯ ФІСКАЛЬНОЇ ПОЛІТИКИ В УКРАЇНІ." Прикарпатський юридичний вісник, no. 1(26) (November 28, 2019): 172–76. http://dx.doi.org/10.32837/pyuv.v0i1(26).33.

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У статті на основі аналізу наукових поглядів вчених і норм чинного законодавства України визначено та надано характеристику формам і методам здійснення фіскальної політики в Україні. Обґрунтовано, що форми і методи виконують особливу роль у механізмі здійснення фіскальної політики в Україні. Зокрема, якщо форми виражають способи зовнішнього вираження, існування цієї політики в об’єктивній дійсності, то методи характеризують те, у який спосіб заходи такої політики реалізуються у суспільному житті, застосовуються щодо відповідних суб’єктів. Наголошено, що основною формою контролю у межах фіскальної політики є податковий контроль – система заходів, що вживаються контролюючими органами та координуються центральним органом виконавчої влади, що забезпечує формування та реалізує державну фінансову політику, з метою контролю правильності нарахування, повноти і своєчасності сплати податків і зборів, а також дотримання законодавства з питань регулювання обігу готівки, проведення розрахункових і касових операцій, патентування, ліцензування та іншого законодавства, контроль за дотриманням якого покладено на контролюючі органи. З’ясовано, що, на відміну від переконання, примус метод проведення політики, який передбачає застосування до суб’єктів фіскальних відносин відповідних заходів і мір незалежно від їх волі, бажання. Цей метод використовується у тих випадках, коли переконання на призвело до настання бажаних наслідків і суб’єкти, щодо яких реалізується фіскальна політика, не бажають добровільно належними чином виконувати покладені на них законом обов’язки. У такому разі компетентні контролюючі органи, посадові особи, у цілях захисту суспільних та державних інтересів, застосовують до таких суб’єктів, на підставі, порядку та межах визначених законом, відповідні заходи тиску. Примус виступає важливим засобом відновлення порушеного правопорядку, усунення умов і факторів, що сприяли чи можуть посприяти такому порушенню. Зроблено висновок, що форми і методи є обов’язковими та дуже важливими елементами організаційно-правового механізму здійснення фіскальної політики в Україні. Кожен із них виконує свою роль у цьому механізмі, так, якщо форми виражають способи зовнішнього вираження, існування цієї політики у об’єктивній дійсності, то методи характеризують те, яким чим, у який спосіб заходи цієї політики реалізуються у суспільному житті, застосовуються щодо відповідних суб’єктів. Вивчення проблемних аспектів форм і методів фіскальної політики дозволяє з’ясувати наявні прогалини, недоліки, прорахунки у структурі цієї політики та способах її проведення у практичне життя.
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34

Otsuki, M., Y. Okabayashi, A. Ohki, T. Oka, M. Fujii, T. Nakamura, N. Sugiura, N. Yanaihara, and S. Baba. "Action of cholecystokinin analogues on exocrine and endocrine rat pancreas." American Journal of Physiology-Gastrointestinal and Liver Physiology 250, no. 4 (April 1, 1986): G405—G411. http://dx.doi.org/10.1152/ajpgi.1986.250.4.g405.

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In the present study we have examined the abilities of cholecystokinin-(26-33)-amide [CCK-(26-33)-NH2, CCK-8], nonsulfated CCK-(26-33)-NH2 (desulfated CCK-8), CCK-(30-33)-NH2 (CCK-4), CCK-(26-33)-OH (deamidated CCK-8), and succinyl CCK-(27-31)-NH2 (Suc-Des-Asp6,Phe7-CCK-7) to stimulate exocrine pancreatic secretion from both isolated pancreatic acini and isolated perfused pancreas. We have also compared this action with their ability to cause insulin release. The modification of either the N- or C-terminal amino acid residues of CCK-8 decreased in potency, but the magnitude of the stimulation of enzyme secretion caused by a maximally effective peptide concentration was the same. The minimal effective concentration of CCK-8, desulfated CCK-8, and CCK-4 for insulin release from the isolated rat pancreas in the presence of 8.3 mM glucose was the same as that for pancreatic exocrine secretion. In contrast, the concentrations of deamidated CCK-8 and Suc-Des-Asp6,Phe7-CCK-7 required to produce insulin release were 5-10 times higher than those required to cause stimulation of pancreatic enzyme and juice secretion. It is concluded therefore that the N-terminal 4-amino acid residues or the C-terminal 2-amino acid residues of CCK-8 are not essential for biological activity but do contribute to its potency. In addition, the C-terminal 2-amino acid residues and an amide group in the C-terminal phenylalanine residue of CCK-8 appear to be important determinants of the insulin-releasing activity of the CCK peptides.
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35

Salahuddin, Md Sultan. "Prospect and Challenges of Basic Chemicals Industries in Bangladesh." Journal of Chemical Engineering 26 (March 24, 2012): 27–33. http://dx.doi.org/10.3329/jce.v26i1.10178.

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36

Lobo, R. F., M. Pan, I. Chan, H. X. Li, R. C. Medrud, S. I. Zones, P. A. Crozier, and M. E. Davis. "SSZ-26 and SSZ-33: Two Molecular Sieves with Intersecting 10- and 12-Ring Pores." Science 262, no. 5139 (December 3, 1993): 1543–46. http://dx.doi.org/10.1126/science.262.5139.1543.

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37

Portugal, Crisanta, Luís Sá, and Maria Areias. "Cardiorespiratory effects of maternal sounds in infants born between 26 and 33 weeks of gestation." Revista de Enfermagem Referência IV Série, no. 12 (March 24, 2017): 55–64. http://dx.doi.org/10.12707/riv16075.

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38

Alagia, M., P. Candori, S. Falcinelli, M. S. P. Mundim, F. Pirani, R. Richter, M. Rosi, S. Stranges, and F. Vecchiocattivi. "Dissociative double photoionization of singly deuterated benzene molecules in the 26–33 eV energy range." Journal of Chemical Physics 135, no. 14 (October 14, 2011): 144304. http://dx.doi.org/10.1063/1.3646516.

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39

Knapp, Richard J., Ewa Malatynska, Pam Peterson, Teresa Zalewska, Sunan Fang, Victor J. Hruby, Thomas L. Smith, and Henry I. Yamamura. "[N-methylnorleucine-(28,31)]cholecystokinin-(26–33) (SNF 8702) activity at a cloned rat CCKB receptor." European Journal of Pharmacology: Molecular Pharmacology 269, no. 2 (October 1994): 133–38. http://dx.doi.org/10.1016/0922-4106(94)90079-5.

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40

Čekić, Jovan, and Dušica Dimitrovska-Gajdoska. "Пресекување на хаосот." Identities: Journal for Politics, Gender and Culture 7, no. 3 (June 1, 2008): 26–33. http://dx.doi.org/10.51151/identities.v7i3.240.

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Author(s): Jovan Čekić | Јован Чекиќ Title (Macedonian): Пресекување на хаосот Translated by (Serbian to Macedonian): Dušica Dimitrovska-Gajdoska | Душица Димитровска-Гајдоска Journal Reference: Identities: Journal for Politics, Gender and Culture, Vol. 7, No. 3 (Winter 2008) Publisher: Research Center in Gender Studies - Skopje and Euro-Balkan Institute Page Range: 1-8 (26-33) Page Count: 8 Citation (Macedonian): Јован Чекиќ, „Пресекување на хаосот“, превод од српски Душица Димитровска-Гајдоска, Идентитети: списание за политика, род и култура, т. 7, бр. 3 (зима 2008): 1-8 (26-33).
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41

Jeong, Ka Yeon, Paul V. Nelson, Carl E. Niedziela, William F. Brinton, and William C. Fonteno. "Physical Properties of Peat-based Substrates Amended with a Mature Dairy Cow Manure Compost Before and After Plant Cultivation." Journal of Environmental Horticulture 34, no. 2 (June 1, 2016): 56–62. http://dx.doi.org/10.24266/0738-2898-34.2.56.

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Initial and final physical properties of four substrates based on a sphagnum peat moss:perlite (3:1 v/v) substrate where mature dairy manure compost (DMC) was partially substituted for peat moss at 0, 16, 26, or 33% DMC of total substrate volume (equivalent to DMC to peat moss ratios of 0, 1, 2, or 3 on a dry weight basis, respectively) were evaluated during a 12-week crop of ‘Macumba’ pot chrysanthemum [Dendranthema × grandiflora (Ramat.) Kitam]. The impact of time on physical properties was similar in all substrates, indicating that DMC was as stable as peat moss. Addition of DMC to substrates increased bulk density (Db) and lowered total porosity (TP) and air space (AS). Compared to peat moss plus perlite without DMC, container capacity (CC) increased with 16 and 26% DMC and was similar at 33% DMC. Addition of DMC at 33% resulted in a decrease in available water (AW). Plant shoot dry weight was higher in all substrates containing DMC, with the maximum at 26% DMC, compared to peat moss plus perlite without DMC.
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42

Pei, Albertina, and Kevin Volk. "Dust Features in Carbon-rich Planetary Nebulae." Symposium - International Astronomical Union 209 (2003): 305–6. http://dx.doi.org/10.1017/s0074180900208838.

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Carbon-rich AGB stars, protoplanetary nebulae (PPNe), and PNe show a variety of dust features attributed to carbon-based compounds. Of particular interest are the three dust features peaking near 21, 26 and 33 μm. The 26 and 33 μm features (collectively the “30 μm feature”; see Volk et al. 2002) are always observed together. The 21 μm feature is weak in the AGB phase and becomes more prominent in the PPN phase, which implies carrier evolution. We wish to see how this evolution continues into the PN phase from detailed modelling of the infrared spectra of PNe.
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43

Ortlund, Dane. "Is Jeremiah 33:14-26 a ‘centre’ to the Bible? A test case in inter-canonical hermeneutics." Evangelical Quarterly 84, no. 2 (April 30, 2012): 119–38. http://dx.doi.org/10.1163/27725472-08402003.

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The article draws attention to a neglected passage in the current recovery of biblical-theological sensitivity to the Bible: Jeremiah 33:14-26. Drawing out six intercanonical themes that cluster here as God promises at the conclusion to the Book of Consolation to restore his people, the article suggests that this text forms a unique whole-Bible intersection. The article begins with an introduction clarifying what is (and what is not) being argued before moving on to point out the neglect of Jeremiah 33 in biblical theology. The heart of the article reflects on the six intercanonical themes that emerge. Two objections are handled before the article draws to a close.
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44

Kim, Kyeong-Mi, Grevo S. Gerung, and Sung-Min Boo. "Two-gene sequences and morphology of Gelidium zollingeri (Kutzing) comb. nov. (Gelidiales, Rhodophyta) (26: 33-40)." ALGAE 26, no. 2 (June 15, 2011): 209. http://dx.doi.org/10.4490/algae.2011.26.1.209.

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45

Munro, Gordon. "Comment on Biogenic amine depletion as a putative animal model of fibromyalgia [Pain 2009;146:26–33]." Pain 148, no. 1 (January 2010): 172–73. http://dx.doi.org/10.1016/j.pain.2009.10.018.

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46

Jensen, Niels C., and Frank Linde. "Long-term follow-up on 33 TPR ankle joint replacements in 26 patients with rheumatoid arthritis." Foot and Ankle Surgery 15, no. 3 (September 2009): 123–26. http://dx.doi.org/10.1016/j.fas.2008.08.009.

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47

Patterson, David T. "Temperature and Canopy Development of Velvetleaf (Abutilon theophrasti) and Soybean (Glycine max)." Weed Technology 6, no. 1 (March 1992): 68–76. http://dx.doi.org/10.1017/s0890037x0003431x.

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Velvetleaf from Mississippi and Wisconsin and soybean (var. Williams) were grown in five temperature regimes (12/4, 19/11, 26/18, 33/25, and 40/32 C day/night) in controlled-environment chambers. Leaf appearance rates increased with temperature in both species, ranging from 0.06 to 0.69 leaves per day in velvetleaf and 0.07 to 0.38 leaves per day in soybean. The threshold temperature for leaf appearance in both species was 5 to 6 C. The largest leaves of both species were produced at 26/18 C. By 55 d after emergence, the greatest total leaf area per plant occurred at 26/18 C or above in both species. Reproductive development occurred earliest at 33/25 C in velvetleaf and at 26/18 C in soybean. This limited vegetative growth in velvetleaf more than in soybean. The weed/crop ratio for total leaf area increased with increasing temperature, indicating that velvetleaf probably would be more competitive with soybean under higher temperatures. The two populations of velvetleaf generally responded similarly to temperatures.
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48

Viola, Teresa Herr, Alexandre de Mello Kessler, Andréa Machado Leal Ribeiro, Eduardo Spillari Viola, Luciano Trevizan, and Thomas Aguiar Gonçalves. "Desempenho e peso de frações corporais, na suplementação crescente de lisina, dos 19 aos 40 dias de idade em frangos de corte." Ciência Rural 39, no. 2 (April 2009): 515–21. http://dx.doi.org/10.1590/s0103-84782009000200031.

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Este estudo foi conduzido para avaliar o desempenho e o peso das frações corporais de frangos de corte, recebendo dietas com níveis crescentes de lisina digestível (Lis dig) (0,70; 0,80; 0,90; 1,00; 1,055; 1,11; 1,165 e 1,22%). Foram utilizados 320 frangos machos da linhagem CobbXCobb500, dos 19 aos 40 dias de idade. Foram utilizadas duas dietas basais, com 19,0 e 20,5% de proteína bruta; a primeira para os quatro níveis mais baixos de Lis dig e a segunda, para os quatro restantes. As dietas foram formuladas de forma a manter constante a relação de aminoácidos digestíveis Met, Arg e Tre com a Lis dig. Foram avaliados o peso médio, o ganho de peso, o consumo de ração, o consumo de lisina e a conversão alimentar aos 26, 33 e 40 dias de idade. Também nessas idades, o peso das frações corporais, carcaça, peito, coxa, perna, dorso+asa+pescoço+cabeça+patas +gordura abdominal (D+A), vísceras+sangue (V+S) e penas foi determinado. O ganho de peso e a conversão alimentar apresentaram respostas lineares positivas em função dos níveis de Lis dig. Já o consumo de ração não foi influenciado pelos tratamentos. As respostas das frações corporais foram lineares crescentes para peso do peito e da carcaça, em todos os períodos avaliados (26, 33 e 40 dias), com níveis ótimos de Lis dig ≥1,22%. A mesma resposta se deu para peso da coxa aos 26 e 40 dias, para D+A, aos 33 e 40 dias e para peso de perna, aos 26 e 33 dias, enquanto, para peso de perna, aos 40 dias, a resposta foi quadrática, ainda que com nível ótimo de Lis dig. ≥1,22%. Sugere-se que níveis mais elevados de lisina digestível, nas dietas de frangos machos da linhagem Cobb500, sejam estudados.
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49

Koscinczuk, P., M. N. Alabarcez, and R. P. Cainzos. "Social play traits and environmental exploration in beagle and fox terriers’ puppies." Revista Veterinaria 26, no. 1 (April 18, 2016): 33. http://dx.doi.org/10.30972/vet.261245.

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50

Schjoldager, B., S. P. Powers, and L. J. Miller. "Affinity labeling the bovine gallbladder cholecystokinin receptor using a battery of probes." American Journal of Physiology-Gastrointestinal and Liver Physiology 255, no. 5 (November 1, 1988): G579—G586. http://dx.doi.org/10.1152/ajpgi.1988.255.5.g579.

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Although the gallbladder was the first recognized target of the peptide hormone cholecystokinin (CCK) and is a physiologically important target, only one preliminary report of the biochemical characterization of this receptor exists. Recently, a series of molecular probes for the affinity labeling of different domains of the pancreatic CCK receptor have been developed. In this work we report the application of several of those probes toward the biochemical characterization of the bovine gallbladder muscularis receptor. These include "long" (125I-Bolton-Hunter-CCK-33) and "short" (125I-D-Tyr-Gly-[Nle28,31)CCK-(26-33)]) probes chemically cross-linkable through their amino-terminal amino groups and monofunctional probes with their photolabile moieties at their amino terminus (2-diazo-3,3,3-trifluoropropionyl-125I-D-Tyr-Gly-[(Nle28,31) CCK-(26-33)]) and carboxyl terminus (125I-D-Tyr-Gly-[(Nle28,31,pNO2-Phe33)CCK-(26-33)]), that span the receptor-binding region. Each of these bound specifically and saturably to a preparation enriched in plasma membranes from bovine gallbladder muscularis (mean inhibitor constants: 5.2, 1.1, 0.8, and 1.8 nM, respectively). A major relative molecular weight (Mr) 70,000-85,000 band was specifically and reproducibly labeled with the appropriate apparent affinity by each of the probes, whereas labeling of minor bands of Mr 40,000-50,000, Mr 92,000, Mr 120,000, and Mr 200,000 was dependent on cross-linker type or concentration. These observations support the identification of the Mr 70,000-85,000 protein as the bovine gallbladder CCK-binding subunit and, since this is a different size from the pancreatic CCK-binding subunit, provide biochemical evidence for molecular heterogeneity of peripheral CCK receptors.
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