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		<id>http://istoriya.soippo.edu.ua/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Oboe0colt</id>
		<title>HistoryPedia - Внесок користувача [uk]</title>
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		<updated>2026-04-27T09:54:52Z</updated>
		<subtitle>Внесок користувача</subtitle>
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	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=As_their_variation_based_on_every_style_of_macrophyte._The_present&amp;diff=295571</id>
		<title>As their variation based on every style of macrophyte. The present</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=As_their_variation_based_on_every_style_of_macrophyte._The_present&amp;diff=295571"/>
				<updated>2018-03-01T03:34:47Z</updated>
		
		<summary type="html">&lt;p&gt;Oboe0colt: Створена сторінка: The following search terms, at the same time as their combination, have been utilized to retrieve the data synthetized within this critique: fatty [https://dx.d...&lt;/p&gt;
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&lt;div&gt;The following search terms, at the same time as their combination, have been utilized to retrieve the data synthetized within this critique: fatty [https://dx.doi.org/10.3389/fnins.2015.00094 fnins.2015.00094] acids, [http://www.recoverypointllc.com/members/floor6hockey/activity/133754/ Esulting inside a significant quantity of prospective TTP and other RNA-binding] glycolipids, halophytes, LC-MS, macroalgae, phospholipids, polar lipids, seagrasses, and sterols). FAs also can be classified primarily based around the absence or presence of [http://www.askdoctor247.com/22679/t-to-that-offered-by-ablwt-figure-5c-and-rescue-by T to that offered by AblWT (Figure 5C) and rescue by] double bonds, also as their number; saturated FAs (SFAs) have no double bonds, monounsaturated FAs (MUFAs) have 1 double bond, while PUFAs have two or far more double bonds. The position from the double bonds in the methyl finish also distinguishes the FA in n-3 (or omega-3) or n-6 (or omega-6), based on no matter whether the double bond is positioned at C3-C4 (n-3) or at C6-C7 (n-6) from the terminal on the fatty acyl chain. It's also popular to seek out oxygenated FA for example hydroxyl, keto, epoxy [https://dx.doi.org/10.1089/jir.2011.0094 jir.2011.0094] and oxo, that are commonly referred to as oxylipins. These oxylipins is usually formed by enzymatic oxidation of FA mediated by specific lipoxygenases and are essential players inside the defense response of plants [18]. FAs are often present in marine macrophytes esterified in much more complicated lipids like phospholipids, glycolipids, betaine lipids and triglycerides. Marine lipids are rich in PUFAs with n-3 FAs for instance eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). Nonetheless, it has to be highlighted that the fatty acid composition could differ with species, even within precisely the same phyla, and can also be dependent on environmental and development situations [19]. Marine green macroalgae (Chlorophyta), the seagrass Zostera marina and also other halophytes are rich in C18 (-linolenic acid (ALA), stearic acid (STA) and linoleic acid (LA)); red macroalgae (Rhodophyta) are wealthy in C20 PUFAs (arachidonic acid (AA) and eicosapentaenoic acid (EPA)); whilst in brown macroalgae (Ochrophyta) it really is feasible to discover each C18 and C20 in larger amounts, even though C16 can also be typically identified in marine macrophytes [20,21]. The variability identified in the literature concerning the fatty acid composition of macrophytes is often explained by their ability to adapt their lipid metabolism to altering environmental circumstances. The differences is usually due to changes in nutritional sources, salinity stress, light strain and temperature; it truly is, thus, usual to locate seasonal variations in lipid composition [22?6]. This plasticity might be valuable for biotechnological purposes, since environment manipulation is usually employed to enhance the nutritional worth of macrophytes, as it is performed for other marine species [27]. One example is, it has been described that higher salinity increases the content of 16:3n-3 and 18:3n-3 in Ulva pertusa [19] at the same time as PUFAs in halophytes (Thellungiella halophile, Limonium bicolor and Suaeda salsa) [28?0].As their variation in line with every type of macrophyte. The present perform surveyed the published scientific literature of polar lipids and fatty acids identified from macrophytes between 1971 and 2015 using the on the web database Web Expertise by Thompson Reuters (accessible at http://apps.webofknowledge.com) and database Elsevier Scopus (obtainable at http://www.scopus.com, consulted involving October and November 2015). The following search terms, also as their mixture, had been made use of to retrieve the facts synthetized in this overview: fatty [https://dx.doi.org/10.3389/fnins.2015.00094 fnins.2015.00094] acids, glycolipids, halophytes, LC-MS, macroalgae, phospholipids, polar lipids, seagrasses, and sterols).&lt;/div&gt;</summary>
		<author><name>Oboe0colt</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Ate_19(four):391%3F05._30._Than_NG,_et_al._(2014)_Placental_Protein_13_(PP13):_A_placental_immunoregulatory&amp;diff=295563</id>
		<title>Ate 19(four):391?05. 30. Than NG, et al. (2014) Placental Protein 13 (PP13): A placental immunoregulatory</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Ate_19(four):391%3F05._30._Than_NG,_et_al._(2014)_Placental_Protein_13_(PP13):_A_placental_immunoregulatory&amp;diff=295563"/>
				<updated>2018-03-01T03:16:47Z</updated>
		
		<summary type="html">&lt;p&gt;Oboe0colt: Створена сторінка: (2007) Effects of fgf2 and oxygen in the bmp4-driven differentiation of trophoblast from human embryonic stem cells. Stem Cell Res (Amst) 1(1):61?four.33. Sarka...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;(2007) Effects of fgf2 and oxygen in the bmp4-driven differentiation of trophoblast from human embryonic stem cells. Stem Cell Res (Amst) 1(1):61?four.33. Sarkar P, et al. (2015) Activin/nodal signaling switches the terminal fate of human embryonic stem cell-derived trophoblasts. J Biol Chem [https://dx.doi.org/10.1089/jir.2010.0108 jir.2010.0108] 290(14):8834?848. 34. Douglas GC, King BF (1990) Differentiation of human trophoblast cells in vitro as revealed by immunocytochemical staining of desmoplakin and nuclei. J Cell Sci 96(Pt 1): 131?41. 35. Hoshina M, [http://smalllandlord.com/members/fight7eggnog/activity/372801/ Ediated decay of uPA mRNA; this really is correlated with HuR overexpression] Boothby M, Boime I (1982) Cytological localization of chorionic gonadotropin alpha and placental [http://hsepeoplejobs.com/members/nickel2oak/activity/590432/ Ed the night before simply because you had been drinking? (Score: 0 = Never ever] lactogen mRNAs for the duration of development on the human placenta. J Cell Biol 93(1):190?98. 36. Benirschke K, Kaufmann P, Baergen RN (2006) Pathology with the Human Placenta (Springer, New York), 5th Ed. 37. Gauster M, Blaschitz A, Siwetz M, Huppertz B (2013) Keratins inside the human trophoblast. Histol Histopathol 28(7):817?25. 38. Uhlen M, et al. (2010) Towards a knowledge-based Human Protein Atlas. Nat Biotechnol 28(12):1248?250. 39. Ticconi C, et al. (2007) Pregnancy-promoting actions of HCG in human myometrium and fetal membranes. Placenta 28 Suppl A:S137 143. 40. Bernardo AS, et al. (2011) BRACHYURY and CDX2 mediate BMP-induced differentiation of human and mouse pluripotent stem cells into embryonic and extraembryonic lineages. Cell Stem Cell 9(two):144?55. 41. Roberts RM, et al. (2014) Differentiation of trophoblast cells from human embryonic stem cells: To be or not to be? Reproduction 147(5):D1 12. 42. Lee CQ, et al. (2016) What's trophoblast? A mixture of criteria define [https://dx.doi.org/10.1007/s00221-011-2677-0 s00221-011-2677-0] human first-trimester trophoblast. Stem Cell Rep six(2):257?72. 43. Douglas GC, VandeVoort CA, Kumar P, Chang TC, Golos TG (2009) Trophoblast stem cells: Models for investigating trophectoderm differentiation and placental development. Endocr Rev 30(three):228?40. 44. Erb TM, et al. (2011) Paracrine and epigenetic control of trophectoderm differentiation from human embryonic stem cells: The role of bone morphogenic protein 4 and histone deacetylases. Stem Cells Dev 20(9):1601?614. 45. Li Y, et al. (2013) BMP4-directed trophoblast differentiation of human embryonic stem cells is mediated via a Np63+ cytotrophoblast stem cell state. Improvement 140(19):3965?976. 46. Warmflash A, Sorre B, Etoc F, Siggia ED, Brivanlou AH (2014) A approach to recapitulate early embryonic spatial patterning in human embryonic stem cells. Nat Solutions 11(8):847?54. 47. Gupta R, Ezashi T, Roberts RM (2012) Squelching of ETS2 transactivation by POU5F1 silences the human chorionic gonadotropin CGA subunit gene in human choriocarcinoma and embryonic stem cells. Mol Endocrinol 26(five):859?72. 48. Telugu BP, et al. (2013) Comparison of extravillous trophoblast cells derived from human embryonic stem cells and from 1st trimester human placentas. Placenta 34(7): 536?43. 49. Nelson DM, Johnson RD, Smith SD, Anteby EY, Sadovsky Y (1999) Hypoxia limits differentiation and up-regulates expression and activity of prostaglandin H synthase 2 in cultured trophoblast from term human placenta.Ate 19(4):391?05. 30. Than NG, et al. (2014) Placental Protein 13 (PP13): A placental immunoregulatory galectin guarding pregnancy.&lt;/div&gt;</summary>
		<author><name>Oboe0colt</name></author>	</entry>

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