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Journal articles on the topic 'Long chain'

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Published: 4 June 2021
Last updated: 10 March 2023

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1

de Gennes, P. G. "One long chain among shorter chains." Journal of Polymer Science: Polymer Symposia 61, no. 1 (March 8, 2007): 313–15. http://dx.doi.org/10.1002/polc.5070610130.

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2

Jefferson, A., and S. Wangchareontrakul. "Long-chain phenols." Journal of Chromatography A 367 (January 1986): 145–54. http://dx.doi.org/10.1016/s0021-9673(00)94823-4.

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3

Mcleish, T. C. B. "Long Chain Branching." Chemical Engineering Research and Design 78, no. 1 (January 2000): 12–32. http://dx.doi.org/10.1205/026387600527031.

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4

Bragg, William Henry. "Long Chain Molecules." Journal of the Society of Dyers and Colourists 42, no. 8 (October 22, 2008): 237–42. http://dx.doi.org/10.1111/j.1478-4408.1926.tb01390.x.

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5

Zelnik, Iris D., Giora Volpert, Leena E. Viiri, Dimple Kauhanen, Tamar Arazi, Katriina Aalto-Setälä, Reijo Laaksonen, and Anthony H. Futerman. "Different rates of flux through the biosynthetic pathway for long-chain versus very-long-chain sphingolipids." Journal of Lipid Research 61, no. 10 (July 10, 2020): 1341–46. http://dx.doi.org/10.1194/jlr.ra120000984.

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The backbone of all sphingolipids (SLs) is a sphingoid long-chain base (LCB) to which a fatty acid is N-acylated. Considerable variability exists in the chain length and degree of saturation of both of these hydrophobic chains, and recent work has implicated ceramides with different LCBs and N-acyl chains in distinct biological processes; moreover, they may play different roles in disease states and possibly even act as prognostic markers. We now demonstrate that the half-life, or turnover rate, of ceramides containing diverse N-acyl chains is different. By means of a pulse-labeling protocol using stable-isotope, deuterated free fatty acids, and following their incorporation into ceramide and downstream SLs, we show that very-long-chain (VLC) ceramides containing C24:0 or C24:1 fatty acids turn over much more rapidly than long-chain (LC) ceramides containing C16:0 or C18:0 fatty acids due to the more rapid metabolism of the former into VLC sphingomyelin and VLC hexosylceramide. In contrast, d16:1 and d18:1 ceramides show similar rates of turnover, indicating that the length of the sphingoid LCB does not influence the flux of ceramides through the biosynthetic pathway. Together, these data demonstrate that the N-acyl chain length of SLs may not only affect membrane biophysical properties but also influence the rate of metabolism of SLs so as to regulate their levels and perhaps their biological functions.
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6

Pourabdollahi, Zahra, Behzad Karimi, Abolfazl K. Mohammadian, and Kazuya Kawamura. "Shipping Chain Choices in Long-Distance Supply Chains." Transportation Research Record: Journal of the Transportation Research Board 2410, no. 1 (January 2014): 58–66. http://dx.doi.org/10.3141/2410-07.

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7

Tolentino, Ainhoa, Abdelilah Alla, Antxon Martínez de Ilarduya, Mercè Font-Bardía, Salvador León, and Sebastián Muñoz-Guerra. "Thermal behavior of long-chain alkanoylcholine soaps." RSC Adv. 4, no. 21 (2014): 10738–50. http://dx.doi.org/10.1039/c3ra47049k.

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Long-chain alkanoylcholines prepared from fatty acids adopt a diversity of thermally interconvertible phases made of a bilayered structure with alkanoyl chains crystallized or interdigitated in a more or less extent depending on temperature and alkanoyl chain length.
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8

Moss, Robert A., and Chuan-Sheng Ge. "Long-chain (polyfluoroalkyl)oxacarbenes." Journal of Fluorine Chemistry 73, no. 1 (July 1995): 101–5. http://dx.doi.org/10.1016/0022-1139(94)03213-j.

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9

Minton, Kirsty. "A long-chain reaction." Nature Reviews Immunology 15, no. 12 (October 30, 2015): 726–27. http://dx.doi.org/10.1038/nri3934.

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10

Stephanou, E. "Long-chain n-aldehydes." Naturwissenschaften 76, no. 10 (October 1989): 464–67. http://dx.doi.org/10.1007/bf00366223.

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11

Maghrebi, R., M. Buffi, P. Bondioli, and D. Chiaramonti. "Isomerization of long-chain fatty acids and long-chain hydrocarbons: A review." Renewable and Sustainable Energy Reviews 149 (October 2021): 111264. http://dx.doi.org/10.1016/j.rser.2021.111264.

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12

Turon, Xavier. "Algae Oil, a Valuable Source of Long Chain Polyunsaturated Fatty Acids." Journal of Life Medicine 01, no. 01 (April 20, 2013): 11–14. http://dx.doi.org/10.14511/jlm.2013.010102.

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13

Gournellos, Theodore. "A theoretical Markov chain model of the long term landform evolution." Zeitschrift für Geomorphologie 41, no. 4 (December 26, 1997): 519–29. http://dx.doi.org/10.1127/zfg/41/1997/519.

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14

F Maliwad, Jyotsna, Pankajkumar B Parmar, Jaydev K Dave, Kalpita S Shringarpure, and Raman D Damor. "Injection with long chain triglyceride or long chain triglyceride/medium chain triglyceride propofol: Which is less painful?" Indian Journal of Clinical Anaesthesia 7, no. 1 (February 15, 2020): 54–58. http://dx.doi.org/10.18231/j.ijca.2020.010.

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15

Kretzschmar, Tom, Mohamed M. Bekhite, Jasmine M. F. Wu, Daniela Haase, Martin Förster, Tina Müller, Sandor Nietzsche, et al. "Long-Chain and Very Long-Chain Ceramides Mediate Doxorubicin-Induced Toxicity and Fibrosis." International Journal of Molecular Sciences 22, no. 21 (November 1, 2021): 11852. http://dx.doi.org/10.3390/ijms222111852.

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Doxorubicin (Dox) is a chemotherapeutic agent with cardiotoxicity associated with profibrotic effects. Dox increases ceramide levels with pro-inflammatory effects, cell death, and fibrosis. The purpose of our study was to identify the underlying ceramide signaling pathways. We aimed to characterize the downstream effects on cell survival, metabolism, and fibrosis. Human fibroblasts (hFSF) were treated with 0.7 µM of Dox or transgenically overexpressed ceramide synthase 2 (FLAG-CerS2). Furthermore, cells were pre-treated with MitoTempo (MT) (2 h, 20 µM) or Fumonisin B1 (FuB) (4 h, 100 µM). Protein expression was measured by Western blot or immunofluorescence (IF). Ceramide levels were determined with mass spectroscopy (MS). Visualizations were conducted using laser scanning microscopy (LSM) or electron microscopy. Mitochondrial activity was measured using seahorse analysis. Dox and CerS2 overexpression increased CerS2 protein expression. Coherently, ceramides were elevated with the highest peak for C24:0. Ceramide- induced mitochondrial ROS production was reduced with MT or FuB preincubation. Mitochondrial homeostasis was reduced and accompanied by reduced ATP production. Our data show that the increase in pro-inflammatory ceramides is an essential contributor to Dox side-effects. The accumulation of ceramides resulted in a lipotoxic shift and subsequently mitochondrial structural and functional damage, which was partially reversible following inhibition of ceramide synthesis.
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16

Svensson, L. Thomas, Stefan E. H. Alexson, and J. Kalervo Hiltunen. "Very Long Chain and Long Chain Acyl-CoA Thioesterases in Rat Liver Mitochondria." Journal of Biological Chemistry 270, no. 20 (May 19, 1995): 12177–83. http://dx.doi.org/10.1074/jbc.270.20.12177.

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17

Hu, Yanling, Yunqi Shao, Zhen Liu, Xuelian He, and Boping Liu. "Dominant Effects of Short-Chain Branching on the Initial Stage of Nucleation and Formation of Tie Chains for Bimodal Polyethylene as Revealed by Molecular Dynamics Simulation." Polymers 11, no. 11 (November 8, 2019): 1840. http://dx.doi.org/10.3390/polym11111840.

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The molecular mechanism of short-chain branching (SCB), especially the effects of methylene sequence length (MSL) and short-chain branching distribution (SCBD) on the initial stage of nucleation, the crystallization process, and particularly the tie chain formation process of bimodal polyethylene (BPE), were explored using molecular dynamics simulation. This work constructed two kinds of BPE models in accordance with commercial BPE pipe resins: SCB incorporated in the long chain or in the short chains. The initial stage of nucleation was determined by the MSL of the system, as the critical MSL for a branched chain to nucleate is about 60 CH2. SCB incorporated in the long chain led to a delay of the initial stage of nucleation relative to the case of SCB incorporated in the short chains. The increase of branch length could accelerate the delay to nucleation. The location of short chain relative to the long chain depended on the MSL of the short chain. As the MSL of the system decreased, the crystallinity decreased, while the tie chains concentration increased. The tie chains concentration of the BPE model with branches incorporated in the long chain was higher than that with branches incorporated in the short chain.
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18

Zhang, Wei, Jian Zhou, Xuejie Zhang, Yan Zhang, and Kun Liu. "Quantitative investigation on force chain lengths during high velocity compaction of ferrous powder." Modern Physics Letters B 33, no. 10 (April 10, 2019): 1950113. http://dx.doi.org/10.1142/s0217984919501136.

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Force chains play an important role in linking the macro- and micro-mechanisms of powder in high velocity compaction (HVC). Force chain lengths, as an important quantitative characteristic, can describe the geometry of force chains. In this study, force chain lengths and their relation to other force chain characteristics in HVC were investigated by discrete element method. Results revealed that force chain length decreased and it can be related to the densification process of ferrous powder in HVC. Moreover, long force chains extended from top to bottom and may play a major role in supporting load, although the percentage of long force chains was low. Probability density functions of force chain lengths further showed the exponential decay. The proportion of short force chains increased and the proportion of long force chains decreased. Long force chains had high strength and can be aligned to the direction of the external load, but force chain lengths did not have clear relation to straightness. These relations were confirmed by Pearson correlation coefficients.
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19

TAKAGI, Yoshiaki. "Long-Chain Fatty Acids. (CnHmCOOH)." Journal of Synthetic Organic Chemistry, Japan 43, no. 2 (1985): 180–81. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.180.

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20

Hamosh, Margit, and Norman Salem Jr. "Long-Chain Polyunsaturated Fatty Acids." Neonatology 74, no. 2 (1998): 106–20. http://dx.doi.org/10.1159/000014017.

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21

Weng, Weiqing, Weiguo Hu, Armenag H. Dekmezian, and Charles J. Ruff. "Long Chain Branched Isotactic Polypropylene." Macromolecules 35, no. 10 (May 2002): 3838–43. http://dx.doi.org/10.1021/ma020050j.

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22

Graupe, Michael, Thomas Koini, Vincent Y. Wang, George M. Nassif, Ramon Colorado, Ramon J. Villazana, Henry Dong, Yasuhiro F. Miura, Olga E. Shmakova, and T. Randall Lee. "Terminally perfluorinated long-chain alkanethiols." Journal of Fluorine Chemistry 93, no. 2 (February 1999): 107–15. http://dx.doi.org/10.1016/s0022-1139(98)00284-x.

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23

Underwood, Robin, Jill Tomlinson-Phillips, and Dor Ben-Amotz. "Are Long-Chain Alkanes Hydrophilic?" Journal of Physical Chemistry B 114, no. 26 (July 8, 2010): 8646–51. http://dx.doi.org/10.1021/jp912089q.

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24

Hilf, Stefan, Frederik Wurm, and Andreas F. M. Kilbinger. "Long-chain branched ROMP polymers." Journal of Polymer Science Part A: Polymer Chemistry 47, no. 24 (December 15, 2009): 6932–40. http://dx.doi.org/10.1002/pola.23733.

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25

Record, Kenneth E., Jimmi H. Kolpek, and Robert P. Rapp. "Invited Review: Long Chain Versus Medium Chain Length Triglycerides." Nutrition in Clinical Practice 1, no. 3 (June 1986): 129–35. http://dx.doi.org/10.1177/088453368600100304.

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26

Balzano, Sergio, Laura Villanueva, Marijke de Bar, Diana X. Sahonero Canavesi, Caglar Yildiz, Julia C. Engelmann, Eric Marechal, Josselin Lupette, Jaap S. Sinninghe Damst�, and Stefan Schouten. "Biosynthesis of Long Chain Alkyl Diols and Long Chain Alkenols in Nannochloropsis spp. (Eustigmatophyceae)." Plant and Cell Physiology 60, no. 8 (May 6, 2019): 1666–82. http://dx.doi.org/10.1093/pcp/pcz078.

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AbstractWe investigated potential biosynthetic pathways of long chain alkenols (LCAs), long chain alkyl diols (LCDs), and long chain hydroxy fatty acids (LCHFAs) in Nannochloropsis oceanica and Nannochloropsis gaditana, by combining culturing experiments with genomic and transcriptomic analyses. Incubation of Nannochloropsis spp. in the dark for 1 week led to significant increases in the cellular concentrations of LCAs and LCDs in both species. Consistently, 13C-labelled substrate experiments confirmed that both LCA and LCD were actively produced in the dark from C14–18 fatty acids by either condensation or elongation/hydroxylation, although no enzymatic evidence was found for the former pathway. Nannochloropsis spp. did, however, contain (i) multiple polyketide synthases (PKSs) including one type (PKS-Clade II) that might catalyze incomplete fatty acid elongations leading to the formation of 3-OH-fatty acids, (ii) 3-hydroxyacyl dehydratases (HADs), which can possibly form Δ2/Δ3 monounsaturated fatty acids, and (iii) fatty acid elongases (FAEs) that could elongate 3-OH-fatty acids and Δ2/Δ3 monounsaturated fatty acids to longer products. The enzymes responsible for reduction of the long chain fatty acids to LCDs and LCAs are, however, unclear. A putative wax ester synthase/acyl coenzyme A (acyl-CoA): diacylglycerol acyltransferase is likely to be involved in the esterification of LCAs and LCDs in the cell wall. Our data thus provide useful insights in predicting the biosynthetic pathways of LCAs and LCDs in phytoplankton suggesting a key role of FAE and PKS enzymes.
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27

Seki, Motohiro, Derek W. Thurman, James P. Oberhauser, and Julia A. Kornfield. "Shear-Mediated Crystallization of Isotactic Polypropylene: The Role of Long Chain−Long Chain Overlap." Macromolecules 35, no. 7 (March 2002): 2583–94. http://dx.doi.org/10.1021/ma011359q.

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28

Raphaël, E., G. H. Fredrickson, and P. Pincus. "One long chain among shorter chains : the Flory approach revisited." Journal de Physique II 2, no. 10 (October 1992): 1811–23. http://dx.doi.org/10.1051/jp2:1992237.

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29

Young, R. M., A. E. Mendoza, T. Collins, and S. H. Orkin. "Alternatively spliced platelet-derived growth factor A-chain transcripts are not tumor specific but encode normal cellular proteins." Molecular and Cellular Biology 10, no. 11 (November 1990): 6051–54. http://dx.doi.org/10.1128/mcb.10.11.6051-6054.1990.

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Two platelet-derived growth factor A-chain proteins, termed short and long A chains, are generated as a result of alternative mRNA splicing of exon 6 of the A-chain gene. S1 nuclease mapping and polymerase chain reaction analyses demonstrate that both short and long A-chain transcripts are expressed in a variety of normal tissues. In addition, immunohistochemical localization of long A-chain protein reveals a cellular distribution identical to that observed with platelet-derived growth factor heteroserum.
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30

Young, R. M., A. E. Mendoza, T. Collins, and S. H. Orkin. "Alternatively spliced platelet-derived growth factor A-chain transcripts are not tumor specific but encode normal cellular proteins." Molecular and Cellular Biology 10, no. 11 (November 1990): 6051–54. http://dx.doi.org/10.1128/mcb.10.11.6051.

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Two platelet-derived growth factor A-chain proteins, termed short and long A chains, are generated as a result of alternative mRNA splicing of exon 6 of the A-chain gene. S1 nuclease mapping and polymerase chain reaction analyses demonstrate that both short and long A-chain transcripts are expressed in a variety of normal tissues. In addition, immunohistochemical localization of long A-chain protein reveals a cellular distribution identical to that observed with platelet-derived growth factor heteroserum.
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31

Hill, Timothy A., Luke R. Odell, Annie Quan, Ruben Abagyan, Gemma Ferguson, Phillip J. Robinson, and Adam McCluskey. "Long chain amines and long chain ammonium salts as novel inhibitors of dynamin GTPase activity." Bioorganic & Medicinal Chemistry Letters 14, no. 12 (June 2004): 3275–78. http://dx.doi.org/10.1016/j.bmcl.2004.03.096.

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32

Qin, Linlin, Linling Li, Ye Sha, Ziyu Wang, Dongshan Zhou, Wei Chen, and Gi Xue. "Conformational Transitions of Polymer Chains in Solutions Characterized by Fluorescence Resonance Energy Transfer." Polymers 10, no. 9 (September 10, 2018): 1007. http://dx.doi.org/10.3390/polym10091007.

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The critical overlap concentration C* is an important concept in polymer solutions and is defined as the boundary between dilute and semidilute regimes. In this study, the chain conformational changes of polystyrene (PS) with both high (Mn = 200,000 Da) and low (Mn = 13,000 Da) molecular weights in cis-decalin were compared by intrachain fluorescence resonance energy transfer (FRET). The random labeling of donor and acceptor chromophores strategy was employed for long PS chains, whereas chain-end labeling was used for short PS chains. By monitoring the spectroscopic intensity ratio between acceptor and donor, the concentration dependence on chain conformation from dilute to semidilute solutions was determined. Both long and short chains exhibit a conformational transition concentration, above which the polymer chains begin to collapse with concentration significantly. Interestingly, for randomly labeled polymer long chains, such concentration is consistent with C* determined from the viscosity result, below which only slight conformational change of polymer chain takes place. However, for the chain-end labeled short chain, the conformational transition concentration takes place earlier than C*, below which no significant polymer conformation change is observed.
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33

Zhao, Jun Tian, Shun Zeng Wang, and Xiang Yang. "Elastodynamic Analysis on a Long-Distance Transmission Roller Chain." Applied Mechanics and Materials 607 (July 2014): 209–12. http://dx.doi.org/10.4028/www.scientific.net/amm.607.209.

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Based on the elastic model of a long-distance transmission roller chain, the elastodynamic analysis was taken in this paper, which has given unregulated displacement of chains. With RecurDyn software for the analysis and verification of the theoretical results, the displacement curves of X-axis, Y-axis and total displacement was obtained, which proved that the elastodynamic analysis on long-distance transmission roller chains is feasible with a continuous model.
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34

Kelly, Barbara M., Malcolu E. Rose, Darren Wycherley, and Steven W. Preece. "Electrospray mass spectra of medium-chain and long-chain acylcanitines." Organic Mass Spectrometry 27, no. 8 (August 1992): 924–26. http://dx.doi.org/10.1002/oms.1210270815.

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35

Garić, Dušan, Juan B. De Sanctis, Juhi Shah, Daciana Catalina Dumut, and Danuta Radzioch. "Biochemistry of very-long-chain and long-chain ceramides in cystic fibrosis and other diseases: The importance of side chain." Progress in Lipid Research 74 (April 2019): 130–44. http://dx.doi.org/10.1016/j.plipres.2019.03.001.

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36

Nieto, Susana, Julio Sanhueza, and Alfonso Valenzuela. "Synthesis of structured triacylglycerols containing medium-chain and long-chain fatty acids by interesterification with a stereoespecific lipase from Mucor miehei." Grasas y Aceites 50, no. 3 (June 30, 1999): 199–202. http://dx.doi.org/10.3989/gya.1999.v50.i3.656.

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37

Yamaguchi, Masayuki. "Characterization of Long-chain Branched Polymers." Seikei-Kakou 20, no. 2 (February 20, 2008): 90–93. http://dx.doi.org/10.4325/seikeikakou.20.90.

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38

Soupene, Eric, and Frans A. Kuypers. "Mammalian Long-Chain Acyl-CoA Synthetases." Experimental Biology and Medicine 233, no. 5 (May 2008): 507–21. http://dx.doi.org/10.3181/0710-mr-287.

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39

Evans, Danielle. "A Long Chain of Hidden Things." Sewanee Review 129, no. 4 (2021): 785–804. http://dx.doi.org/10.1353/sew.2021.0063.

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40

Steinberg, Steven J., Janine Morgenthaler, Ann K. Heinzer, Kirby D. Smith, and Paul A. Watkins. "Very Long-chain Acyl-CoA Synthetases." Journal of Biological Chemistry 275, no. 45 (August 22, 2000): 35162–69. http://dx.doi.org/10.1074/jbc.m006403200.

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41

Forth, M. A., and S. Smith. "Synthesis of Long Chain ω-Aralkylbromides." Synthetic Communications 24, no. 7 (April 1994): 951–59. http://dx.doi.org/10.1080/00397919408020770.

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42

Kisiel, Wanda, and Jasmin Jakupowic. "Long-Chain Alkyl Hydroxycinnamates fromCrepis taraxacifolia." Planta Medica 61, no. 01 (February 1995): 87–88. http://dx.doi.org/10.1055/s-2006-958012.

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43

Egorov, V. M., and V. A. Marikhin. "Habit of long-chain molecular crystals." Physics of the Solid State 58, no. 11 (November 2016): 2353–57. http://dx.doi.org/10.1134/s1063783416110081.

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44

Maneta-Peyret, Lilly, Bénédicte Sturbois-Balcerzak, Claude Cassagne, and Patrick Moreau. "Antibodies to long-chain acyl-CoAs." Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism 1389, no. 1 (January 1998): 50–56. http://dx.doi.org/10.1016/s0005-2760(97)00146-x.

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45

Winter, R., P. G. Nixon, G. L. Gard, D. H. Radford, N. R. Holcomb, and D. W. Grainger. "New SF5-long chain carbon systems." Journal of Fluorine Chemistry 107, no. 1 (January 2001): 23–30. http://dx.doi.org/10.1016/s0022-1139(00)00340-7.

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46

Leonard, Amanda E., Suzette L. Pereira, Howard Sprecher, and Yung-Sheng Huang. "Elongation of long-chain fatty acids." Progress in Lipid Research 43, no. 1 (January 2004): 36–54. http://dx.doi.org/10.1016/s0163-7827(03)00040-7.

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47

Kawanishi, Kazuko, and Yohei Hashimoto. "Long chain esters of Virola species." Phytochemistry 26, no. 3 (January 1987): 749–52. http://dx.doi.org/10.1016/s0031-9422(00)84778-0.

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48

Calder, Philip C. "Long-chain fatty acids and inflammation." Proceedings of the Nutrition Society 71, no. 2 (February 28, 2012): 284–89. http://dx.doi.org/10.1017/s0029665112000067.

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Inflammation plays a key role in many common conditions and diseases. Fatty acids can influence inflammation through a variety of mechanisms acting from the membrane to the nucleus. They act through cell surface and intracellular receptors that control inflammatory cell signalling and gene expression patterns. Modifications of inflammatory cell membrane fatty acid composition can modify membrane fluidity, lipid raft formation and cell signalling leading to altered gene expression and can alter the pattern of lipid and peptide mediator production. Cells involved in the inflammatory response usually contain a relatively high proportion of the n-6 fatty acid arachidonic acid in their membrane phospholipids. Eicosanoids produced from arachidonic acid have well-recognised roles in inflammation. Oral administration of the marine n-3 fatty acids EPA and DHA increases the contents of EPA and DHA in the membranes of cells involved in inflammation. This is accompanied by a decrease in the amount of arachidonic acid present. EPA is a substrate for eicosanoid synthesis and these are often less potent than those produced from arachidonic acid. EPA gives rise to E-series resolvins and DHA gives rise to D-series resolvins and protectins. Resolvins and protectins are anti-inflammatory and inflammation resolving. Thus, the exposure of inflammatory cells to different types of fatty acids can influence their function and so has the potential to modify inflammatory processes.
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49

Fedenok, L. G., E. V. Plashchenyuk, R. N. Myasnikova, and M. S. Shvartsberg. "Synthesis of long-chain 2-alkadiynylpyridines." Russian Chemical Bulletin 45, no. 3 (March 1996): 667–70. http://dx.doi.org/10.1007/bf01435802.

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50

Rossetti, Ilenia, Chiara Gambaro, and Vincenzo Calemma. "Hydrocracking of long chain linear paraffins." Chemical Engineering Journal 154, no. 1-3 (November 2009): 295–301. http://dx.doi.org/10.1016/j.cej.2009.03.018.

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