Gotowe bibliografie tematyczne / Peas Physiology

Gotowa bibliografia na temat „Peas Physiology”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 1 lutego 2022

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Artykuły w czasopismach na temat "Peas Physiology"

Craven, Kimberley B., i William N. Zagotta. "CNG AND HCN CHANNELS: Two Peas, One Pod". Annual Review of Physiology 68, nr 1 (styczeń 2006): 375–401. http://dx.doi.org/10.1146/annurev.physiol.68.040104.134728.

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Galloway, C. M., i W. M. Dugger. "Boron inhibition of phosphoglucomutase from peas". Journal of Plant Nutrition 13, nr 7 (lipiec 1990): 817–25. http://dx.doi.org/10.1080/01904169009364119.

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Wszelaki, Annette, Karla Deza-Duran i Carol Harper. "(44) Postharvest Physiology and Quality of Pigeon Pea [Cajanus cajan (L.) Millsp.]". HortScience 40, nr 4 (lipiec 2005): 1030B—1030. http://dx.doi.org/10.21273/hortsci.40.4.1030b.

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Pigeon pea is an important food crop for the Puerto Rican diet, as well as the economy. Pigeon pea ranks fourth in production among edible legumes in production worldwide. It can be consumed dried or as a vegetable (fresh, frozen, or canned). Canned, frozen, and dried peas are commonly used when fresh peas are no longer available. Due to the preferred flavor of fresh pigeon pea, it commands a higher market premium, selling for more than twice the price of the dried product. Although there is a great demand for this vegetable in Puerto Rico, virtually no research has been done on fresh pigeon pea postharvest physiology and its overall keeping quality. Baseline data on pigeon pea physiology, including respiration and ethylene production rates, soluble solids, titratable acidity, color reflectance, chlorophyll content, and responses to ethylene are presented here in order to establish the optimum storage temperature. Using this information, fresh pigeon pea consumption could increase locally, and exporting opportunities for shipping pigeon pea to alternative markets could be expanded.

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MELCHER, INGA M. "GLUTAMATE METABOLISM IN INTACT SEEDLINGS AND SEEDLING SEGMENTS OF PEAS". New Phytologist 103, nr 4 (sierpień 1986): 685–88. http://dx.doi.org/10.1111/j.1469-8137.1986.tb00842.x.

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Galloway, Cynthia M., i W. Mack Dugger. "Purification and characterization of phosphoglucomutase from peas". Physiologia Plantarum 92, nr 3 (listopad 1994): 479–86. http://dx.doi.org/10.1111/j.1399-3054.1994.tb08839.x.

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Mollard, Rebecca C., Bohdan L. Luhovyy, Christopher Smith i G. Harvey Anderson. "Acute effects of pea protein and hull fibre alone and combined on blood glucose, appetite, and food intake in healthy young men – a randomized crossover trial". Applied Physiology, Nutrition, and Metabolism 39, nr 12 (grudzień 2014): 1360–65. http://dx.doi.org/10.1139/apnm-2014-0170.

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Whether pulse components can be used as value-added ingredients in foods formulated for blood glucose (BG) and food intake (FI) control requires investigation. The objective of this study was to examine of the effects of pea components on FI at an ad libitum meal, as well as appetite and BG responses before and after the meal. In a repeated-measures crossover trial, men (n = 15) randomly consumed (i) pea hull fibre (7 g), (ii) pea protein (10 g), (iii) pea protein (10 g) plus hull fibre (7 g), (iv) yellow peas (406 g), and (v) control. Pea hull fibre and protein were served with tomato sauce and noodles, while yellow peas were served with tomato sauce. Control was noodles and tomato sauce. FI was measured at a pizza meal (135 min). Appetite and BG were measured pre-pizza (0–135 min) and post-pizza (155–215 min). Protein plus fibre and yellow peas led to lower pre-pizza BG area under the curve compared with fibre and control. At 30 min, BG was lower after protein plus fibre and yellow peas compared with fibre and control, whereas at 45 and 75 min, protein plus fibre and yellow peas led to lower BG compared with fibre (p < 0.05). Following the pizza meal (155 min), yellow peas led to lower BG compared with fibre (p < 0.05). No differences were observed in FI or appetite. This trial supports the use of pea components as value-added ingredients in foods designed to improve glycemic control.

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Smith, Mary A., Peter J. Davies i James B. Reid. "Role of Polyamines in Gibberellin-Induced Internode Growth in Peas". Plant Physiology 78, nr 1 (1.05.1985): 92–99. http://dx.doi.org/10.1104/pp.78.1.92.

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Ray, Peter M. "Auxin and Fusicoccin Enhancement of β-Glucan Synthase in Peas". Plant Physiology 78, nr 3 (1.07.1985): 466–72. http://dx.doi.org/10.1104/pp.78.3.466.

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Thacher, P. V., S. V. Onyper i Y. Lai. "0196 Whirled Peas: Time Awake, Sleep Problems, And Language Errors". Sleep 41, suppl_1 (kwiecień 2018): A77. http://dx.doi.org/10.1093/sleep/zsy061.195.

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Joy, Kenneth W., i Chander Prabha. "The Role of Transamination in the Synthesis of Homoserine in Peas". Plant Physiology 82, nr 1 (1.09.1986): 99–102. http://dx.doi.org/10.1104/pp.82.1.99.

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Rozprawy doktorskie na temat "Peas Physiology"

Ade-Ademilua, Omobolanle Elizabeth. "Plastochron index - an indicator of plant structure and function a case study using Pisum sativum L". Thesis, Rhodes University, 2006. http://hdl.handle.net/10962/d1003751.

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The use of chronological age for example, using days after sowing (DAS), or days after germination (DAG) as a time variable may result in the inherent variability between plants resulting in differences which can be large enough to obscure subtle developmental trends that become evident among plants sown at the same time. An alternative to DAS or DAG is the plastochron index (PI), first used by Erickson and Michelini (1957) as a morphological time scale and numerical index; which to according to the authors suggested and represented a more accurate reflection of the developmental status of a plant. The research presented in this thesis was therefore aimed specifically at utilizing the index in qualitative and quantitative analyses, to confirm its usefulness in analyzing and predicting plant growth and development. Specifically this research focused on investigating various morphological and physiological events that together, hopefully, would serve as a template for the prediction of the growth, development and reactions of Pisum sativum L. to different growth conditions. In Chapter 3, the use of the average length of the first pair of leaflets on each node as a suitable parameter for calculating PI in P. sativum is suggested. The results presented in Chapter 3 suggest that plant age is best expressed using the plastochron index, as this reflects the time interval between the initiations of successive pairs of leaflets. This section of the research has been published as “Ade-Ademilua OE, Botha CEJ (2005) A re-evaluation of plastochron index in peas - a case for using leaflet length. South African Journal of Botany 71: 76-80”. The PI formula developed was subsequently used in this research to conduct qualitative and quantitative investigations of plant growth and development in which all data and observations were related directly to the plastochron index. In Chapter 4, the sink to source transition in Pisum sativum L. leaves at different plastochron ages in nodulating plants was investigated using the phloem-mobile fluorescent marker, 5,6-carboxyfluorescein (5,6-CF). The results demonstrated that young leaves remained strong sinks up until LPI 0, after which sink-source transition occurred up to LPI 1.8 and leaflets transitioned to strong source systems by LPI 2.0. A well-developed cross-connected phloem system between paired leaflets in peas, and the petiole and the stem vascular supply was observed. The data presented in the second part of Chapter 4 suggest that the phloem transport between leaflet pairs is independent of the sink/source state of the leaflets, or of movement along the source to sink gradient. The data support the presence of a modular transport system which may ensure re-allocation and balancing between leaflets of the same physiological age and photosynthetic and transport status, thereby load-balancing the local transport system, before exporting to other younger (sink) regions. The investigation of leaf development using the plastochron index (Chapter 5) revealed that the formation of air spaces in the palisade and spongy mesophyll, one of the preparatory events for transition from sink to source state in developing leaves, occurs between LPI 0 and LPI 1 in pea leaflets. Results of the anatomical and ultrastructural study related to PI are presented in Chapter 5. The density of wall ingrowths in transfer cells of minor veins increased with LPI and appeared to be associated with the probable transition to source state and the related potential increase in the production of assimilates for export. The onset of wall ingrowth development in leaflets at LPI 0 provided evidence that sink-to-source transition commences at LPI 0 in P. sativum. Presumably-functional plasmodesmata as well as a few mature sieve elements were evident in class IV veins in the apical region of young and older leaflets at LPI 0. The number of mature sieve elements per vein however, increased with increasing LPI. Most class V veins were still undergoing division at LPI 0 and their sieve elements did not show signs of maturity until LPI 1. The increase in the number of mature metaphloem sieve elements in young, supposedly importing tissue at LPI 0 to older, supposedly exporting tissues at LPI 2 is evidence of the association between phloem maturation and transition from importing to exporting status. In Chapter 6, I report on the effects of elevated CO[subscript 2] on the growth and leaf development of nodulating and non-nodulating Pisum sativum L var. Greenfeast grown under controlled environment of the same nitrogen (6mM) and nitrogen- free nutrient solution conditions. Shortterm exposure to elevated CO[subscript 2] induced rapid plant growth, irrespective of treatment. However, long-term elevated CO[subscript 2] treatment did not affect rate of leaf appearance (RLA) in nodulated plants, irrespective of mineral N supply but enhanced RLA in non- nodulating plants supplied with mineral N. Supplied N resulted in a significant increase in leaflet elongation rate (LfER) under both ambient and elevated CO[subscript 2], but LfER was not significantly affected by nodulation but was increased by high CO[subscript 2]. This suggested that the growth of nodulating P. sativum L may not be significantly affected under CO[subscript 2] levels as high as 1000 μmol mol[superscript -1]. The data suggest that elevated CO[subscript 2] will enhance canopy size, provided adequate soil N is available and more so in non-nodulating plants. This section of the research has been published as “Ade-Ademilua OE, Botha CEJ (2004) The effects of elevated CO[subscript 2] and nitrogen availability supersedes the need for nodulation in peas grown under controlled environmental conditions. South African Journal of Botany 70: 816 – 823”. This thesis demonstrates that the similarity in the qualitative analyses results obtained from plants from different CO[subscript 2], nitrogen and nodulation treatment conditions, highlights the fact that plants of same PI value are at the same developmental state, irrespective of the growth condition. Furthermore, changes in plant structure and function observed under different growth conditions can be related simply to changes in plastochron index. The work presented in this thesis demonstrate that changes in plant structure and function analyzed are related to changes in PI. An important finding of this thesis is that with the use of PI, results can be compiled as a template for predicting the structure- function state of pea plants at any plastochron age, under any growth conditions, before using small representative sample populations.

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Herdina. "Studies of nodulation, nodule function, and nitrogen fixation of Vicia faba L. and Pisum sativum L". Title page, contents and summary only, 1987. http://web4.library.adelaide.edu.au/theses/09PH/09phh541.pdf.

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Doulis, Andreas G. "Antioxidant responses of pea (Pisum sativum L.) protoplasts". Diss., This resource online, 1994. http://scholar.lib.vt.edu/theses/available/etd-09192008-063125/.

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McCune, Letitia M. "Characterization of galactolipid synthesis in pea root plastids". Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=22858.

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The capacity of pea root plastids for galactolipid synthesis was investigated utilizing radiolabelled acetate and UDP-galactose. Galactolipid biosynthesis was completely dependent on an exogenous supply of UDP-galactose. UDP-galactose stimulated both total lipid biosynthesis from acetate and the proportion of radioactivity accumulated in monogalactosyldiacylglycerol (MGDG). The proportion of MGDG synthesized was saturated at 30$ mu$M UDP-galactose and represented approximately 30% of the total lipid radioactivity after a one hour incubation. However, total lipid biosynthesis continued to increase with concentrations of UDP-galactose up to 75$ mu$M while the proportion of radioactivity in MGDG remained at 30%. MGDG biosynthesis was always accompanied by a corresponding decrease in the amount of diacylglycerol (DAG) accumulated. Digalactosyldiacylglycerol (DGDG) synthesis was not routinely observed in these experiments. These results suggest that the in vitro pathway for MGDG synthesis in the root plastids of pea (an 18:3 plant) is similar to 16:3 plants (FFA's$ to$PA$ to$DAG$ to$MGDG). The endogenous lipids, consistent with the thought of pea as an 18:3 plant, contained 80% C$ sb{18}$ in the fatty acids of MGDG, DGDG, TG and PC. However, in labelled acetate experiments palmitate was the predominately labelled fatty acid in all lipids except PC (where 80% was 18:1). The precursors PA and DAG had ratios of 16:0, 18:0, and 18:1 similar to that of MGDG. 70-80% of the label was associated with the sn-2 position of glycerolipids. The cofactors required for fatty acid synthesis were generally not as required for galactolipid synthesis. The results suggest that galactolipid synthesis relies primarily on endogenous DAG and only partly involves de novo fatty acid synthesis. (Abstract shortened by UMI.)

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Xue, Lingru. "Glycerolipid biosynthesis in pea root plastids". Thesis, McGill University, 1993. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=26186.

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Pea root plastids were isolated by differential centrifugation and resulting crude plastid fraction was purified by centrifugation through 10%(v/v) Percoll. Marker enzymes indicated that greater than 50% of the plastids were recovered essentially free from mitochondrial and endoplasmic reticulum contamination. The optimum in vitro conditions for glycerolipid biosynthesis from (U-$ sp{14}$C) glycerol-3-phosphate have been determined. Total glycerolipid biosynthesis was approximately 15 nmole/hr/mg protein in the presence of 200 $ mu$M glycerol-3-phosphate, 0.5 mM each of NADH and NADPH, 15 mM KH$ sb2$CO$ sb3$, 0.05 mM CoA, and 2 mM each of ATP and MgCl$ sb2$, 100 mM Bis Tris Propane (pH 7.5) and incubated at the standard temperature of 25$ sp circ$C. ATP, Coenzyme A and a divalent cation are absolutely required for glycerolipid biosynthesis, whereas reduced nucleotides and bicarbonate improve the synthesis to varying degrees. Dihydroxyacetone phosphate had little effect, while dithiothreitol, detergent and Mn$ sp{2+}$ inhibited activity. Under the optimum conditions, isolated pea root plastids mainly synthesized approximately 15% phosphatidic acid, 16% phosphatidylcholine, 13% phosphatidylglycerol, 32% triacylglycerol. Galactolipid synthesis occurred only when UDP-galactose was supplied. Different concentrations of some cofactors resulted in alterations of glycerolipid distribution. Phospholipase A$ sb2$ and Rhizopus lipase digestions of phospholipids and neutral lipids revealed that radioactive fatty acids were preferentially esterified to position sn 2 of each glycerolipid with generally 2-4 times as much radioactivity as position sn 1. Pea root plastids are composed of approximately 62% phospholipid, 24% neutral lipid and 14% glycolipid. Within these classes PG, TAG, and the galactolipids are the major components representing 24, 12, and 12% of the total plastid lipids.

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Qi, Qungang. "The role of glycolytic metabolism in fatty acid and glycerolipid biosynthesis in pea root plastids". Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=39980.

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The interaction between the glycolytic metabolism and fatty acid and glycerolipid biosynthesis in pea root (Pisum sativum L.) plastids was assessed in this study. When various glycolytic intermediates were used to substitute for the APT requirement for fatty acid synthesis from acetate, phosphoenolpyruvate, 2-phosphoglycerate, fructose-6-phosphate and glucose-6-phosphate each gave 48, 17, 23 and 17%, respectively, of the ATP-control activity. Similarly, in the absence of exogenously supplied ATP, the optimized triose-phosphate shuttle, which consists of 2 mM dihydroxyacetone phosphate, 2 mM oxaloacetic acid and 4 mM inorganic phosphate, gave up to 44% the ATP-control activity in promoting fatty acid synthesis from acetate. These results suggest that 3-phosphoglycerate kinase and pyruvate kinase in these plastids can function in intraplastidic ATP production through substrate level phosphorylation. However, in all cases, exogenously supplied ATP gave the greatest rates of fatty acid and glycerolipid synthesis. Radiolabeled pyruvate, glucose, glucose-6-phosphate, and malate in comparison to acetate were all variously utilized for fatty acid and glycerolipid biosynthesis by the root plastid. At the highest concentrations tested (3-5 mM), the rates of incorporation of pyruvate, glucose-6-phosphate and acetate into fatty acids were 183, 154, 125 nd 99 nmol $ rm cdot h sp{-1} cdot mg sp{-1}$, respectively. Malate was the least effective precursor, giving less than 55 nmol $ rm cdot h sp{-1} cdot mg sp{-1}$. Acetate incorporation was approximately 55% dependent on exogenously supplied reduced nuclotides (NADPH and NADH), whereas the utilization of the remaining precursors was only approximately 10-20% dependent on NAD(P)H. These results indicate that the entire pathway of carbon flow from glycolysis, including pyruvate dehydrogenase (PDHase), to fatty acids is operating in pea root plastids. Further, the intraplastidic glycolytic pathway plays an important role in provi

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Li, Hongping 1967. "Developmental relationships in the function of pea root plastids". Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=30823.

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Germinating pea (Pisum sativum L.) roots were divided into five sequential 0.5 cm segments from the root tip. Pooled segments were analyzed for their protein, starch and lipid content as an indirect indication of plastid function. Fresh weights of root segments were lowest in the tips (4.45mug per segment) and progressively higher up to the fifth segment (11.09mug per segment). Total protein, starch and lipid content, on a per segment basis, were all highest in zone 1 (tip segment) and progressively lower up to zone 5. Plastids were isolated from each of the five root segments and analyzed for their capacity for lipid biosynthesis under several different in vitro conditions. Collectively, the observations presented here suggest that the relative contributions of plastids to the overall physiology of germinating pea roots gradually diminishes as root development proceeds, and that plastids isolated from progressively older root zones have increased capacity for glycolytic and/or pentose phosphate metabolism. (Abstract shortened by UMI.)

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Stahl, Richard J. (Richard John). "Fatty acid and glycerolipid biosynthesis in pea root plastids". Thesis, McGill University, 1990. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=22389.

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Fatty acid biosynthesis from (1-$ sp{14}$C) acetate was optimized in plastids isolated from primary root tips of 7-day-old germinating pea seeds. Fatty acid synthesis was maximum at 82.3 nmol/hr/mg protein in the presence of 200$ mu$M acetate, 0.5mM each of NADH, NADPH and CoA, 6mM each of ATP and MgCl$ sb2$, 1mM each of MnCl$ sb2$ and glycerol-3-phosphate (G3P), 15mM KHCO$ sb3$, and 0.1M Bis tris propane, pH 8.0 incubated at 35C. At the standard incubation temperature of 25C, fatty acid synthesis was linear for up to 6 hours with 80 to 120 $ mu$g/ml plastid protein. ATP and CoA were absolute requirements, whereas divalent cations, potassium bicarbonate and reduced nucelotides all improved activity by 2 to 10 fold. Mg$ sp{2+}$ and NADH were the preferred cation and nucleotide, respectively. G3P and dihydroxyacetone phosphate had little effect, and dithiothreitol and detergents generally inhibited incorporation of $ sp{14}$C-acetate into fatty acid.
Glycerolipid synthesis was obtained from $ sp{14}$C-acetate, (U-$ sp{14}$C) G3P and (U-$ sp{14}$C) glycerol at relative rates of 3.7:1.0:0.1, respectively. (Abstract shortened by UMI.)

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Saquet, Adriano Arriel. "Physiology and biochemistry of Rocha pear during ripening and long-term controlled atmosphere storage". Doctoral thesis, ISA, 2017. http://hdl.handle.net/10400.5/14943.

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Doutoramento em Engenharia Agronómica - Instituto Superior de Agronomia
Long-term storage of pears is a challenge in the absence of treatment with diphenylamine, due to the development of physiological disorders. Aspects of the ripening physiology and biochemistry of pears, particularly those treated with the ethylene action inhibitor 1-methylcyclopropene, also remain unknown. The aims of this thesis were to map the gradients of adenylate nucleotides and energy charge in the fruit and their changes during fruit ripening and storage period, to compare instrumental and sensory assessments of ripening, to relate the fruit mineral composition to the development of internal storage disorders and determine the optimal storage conditions for long-term storage of ‘Rocha’ pear under controlled atmosphere. Significant radial gradient in energy charge from the skin tissues to the fruit center may be related to internal storage disorders. Significant radial gradients in Ca and B decreasing from the skin tissues toward the fruit center were also consistent with the location of internal storage disorders. However, ‘Rocha’ pear were able to adjust the energy charge during ripening and long-term storage even under low respiration rates induced by 1- methylcyclopropene treatment or low oxygen partial pressure. ‘Rocha’ pear was able to ripen immediately after harvest without chilling or exogenous ethylene application. ‘Rocha’ pear tolerated extremely low 0.5 kPa O2 during 257 d storage without developing storage disorders and kept acceptable firmness and skin color after 7 d shelf life. The 46 d delay in the pull down of O2 partial pressure was detrimental to quality maintenance of ‘Rocha’ pear during long-term controlled atmosphere storage
N/A

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Lomas, Caroline Anne. "The effect of supplementary light on the behaviour, physiology and productivity of cattle". Thesis, Bangor University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239841.

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Książki na temat "Peas Physiology"

Munier-Jolain, Nathalie, i Benoît Carrouée. Agrophysiologie du pois protéagineux. Paris: INRA, 2005.

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Mélissopoulos, Alexandre. La peau: Structure et physiologie. Paris: Tec & Doc Lavoisier, 1998.

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Draguhn, Claudio. Peat: Formation, uses, and biological effects. Hauppauge, N.Y: Nova Science Publisher's, 2011.

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The athlete's guide to recovery: Rest, relax, and restore for peak performance. Boulder, Colo: VeloPress, 2011.

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Michell, A. R. An introduction to veterinary anatomy and physiology. Gloucestershire: British Small Animal Veterinary Association, 1989.

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Michell, A. R. An introduction to veterinary anatomy and physiology. Gloucestershire: British Small Animal Veterinary Association, 1993.

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Bailey, Elisabeth Tova. The sound of a wild snail eating. Chapel Hill, N.C: Algonquin Books of Chapel Hill, 2010.

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Way, Robert F. The anatomy of the horse: A pictorial approach. New York: Breakthrough Publications, 1993.

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Richard, Patton. Ruined by excess, perfected by lack: The paradox of pet nutrition. Nottingham, U.K: Nottingham University Press, 2011.

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Bailey, Elisabeth Tova. The sound of a wild snail eating. Thorndike, Me: Center Point Pub., 2011.

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Części książek na temat "Peas Physiology"

Davies, P. J., i F. J. Muehlbauer. "Peas." W The physiology of vegetable crops, 287–316. Wallingford: CABI, 2020. http://dx.doi.org/10.1079/9781786393777.0287.

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Ferreira, M. E. Saraiva, i M. A. C. Fragoso. "Criteria for fertilization of vining peas in Portugal". W Plant Nutrition — Physiology and Applications, 723–27. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0585-6_121.

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Reid, J. B., i P. J. Davies. "The genetics and physiology of gibberellin sensitivity mutants in peas". W Progress in Plant Growth Regulation, 214–25. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2458-4_24.

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Girling, Simon J. "Basic Avian Anatomy and Physiology". W Veterinary Nursing of Exotic Pets, 131–19. West Sussex, UK: Blackwell Publishing, Ltd,., 2013. http://dx.doi.org/10.1002/9781118782941.ch9.

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Girling, Simon J. "Basic Small Mammal Anatomy and Physiology". W Veterinary Nursing of Exotic Pets, 1–25. West Sussex, UK: Blackwell Publishing, Ltd,., 2013. http://dx.doi.org/10.1002/9781118782941.ch1.

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Girling, Simon J. "Basic Reptile and Amphibian Anatomy and Physiology". W Veterinary Nursing of Exotic Pets, 245–65. West Sussex, UK: Blackwell Publishing, Ltd,., 2013. http://dx.doi.org/10.1002/9781118782941.ch17.

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Rhodes, Jonathan. "Peak Exercise Parameters". W Exercise Physiology for the Pediatric and Congenital Cardiologist, 53–64. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-16818-6_11.

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Lopate, Cheryl, i Kersti Seksel. "Canine Neonatal Physiology, Behavior, and Socialization". W Management of Pregnant and Neonatal Dogs, Cats, and Exotic Pets, 93–127. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118997215.ch7.

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Zambelli, Daniele. "Feline Neonatal Physiology, Behavior, and Socialization". W Management of Pregnant and Neonatal Dogs, Cats, and Exotic Pets, 145–58. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118997215.ch9.

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Bishop, Cynthia R., i Mark E. Burgess. "Reproductive Physiology, Normal Neonatology, and Neonatal Disorders of Rabbits". W Management of Pregnant and Neonatal Dogs, Cats, and Exotic Pets, 217–38. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118997215.ch13.

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Streszczenia konferencji na temat "Peas Physiology"

Komarova, N. R., A. A. Beloglazova, M. I. Falaleeva i A. T. Eprintsev. "The functioning of the lactate dehydrogenase enzymatic system in the leaves and roots of peas (Pisum sativum L.) for hypoxia". W IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-222.

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Arum Cahyaning Putri, Eka, Raden Argarini, Bambang Purwanto i Lilik Herawati. "Intermittent Physical Training Decreases Peak of Blood Glucose Level after Meals in Rats". W Surabaya International Physiology Seminar. SCITEPRESS - Science and Technology Publications, 2017. http://dx.doi.org/10.5220/0007333100760079.

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Le Goff, Guillaume. "Nutrition physiology of the pear psylla,Cacopsylla pyri". W 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.111371.

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Johnson, Joshua E., Sang-Pil Lee, Terence E. McIff, E. Bruce Toby i Kenneth J. Fischer. "Effects of Surgical Repair or Reconstruction on Radiocarpal Mechanics From Wrists With Scapholunate Injury". W ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53687.

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Scapholunate dissociation (SL ligament disruption) due to trauma can cause changes in joint kinematics and contact patterns, which can lead to scapholunate advanced collapse (SLAC wrist) with secondary radiocarpal osteoarthritis (OA) [1]. The relationship between consequent abnormal mechanics and the onset of OA is not clearly understood, however elevated joint contact pressure is believed to be an associated factor. Knowing how injuries affect joint physiology and mechanics and how well surgical repairs restore the mechanics may improve surgical efficacy and help predict OA risk. Recently a method was proposed to measure joint contact mechanics from in vivo imaging data during functional loading [2]. The objective of this study was to compare radiocarpal joint mechanics (contact forces, contact areas, peak and average contact pressures) of injured and post-operative wrists to contralateral controls using MRI-based contact modeling. We hypothesized that average contact pressures and peak contact pressures would be higher in the injured wrists, and that these measures would decrease post-operatively.

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Moissenet, Florent, Laurence Cheze i Raphaël Dumas. "Simultaneous Prediction of Musculo-Tendon, Joint Contact, Ligament and Bone Forces in the Lower Limb During Gait Using a One-Step Static Optimisation Procedure". W ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14455.

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Instrumented prostheses, by measuring joint contact forces during a movement, give nowadays a unique opportunity to validate the ability of musculo-skeletal models in predicting internal forces. In this study, a rigid multi-body musculo-skeletal model, allowing computing the musculo-tendon, joint contact, ligament and bone forces all together by static optimisation, using a weighted criterion, is presented. The results show that the musculo-tendon forces are generally in accordance with the envelopes of the main peaks of the subject’s EMG signals and that the amplitudes and patterns of the predicted joint contact, ligament and bone forces are in a good agreement with the measurements and with the literature. By allowing the introduction of other forces than the musculo-tendon forces in the static optimisation, this study opens new horizons in order to better model the human physiology (e.g., joint pain).

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Bhushan, Shanti, Manish Borse, Bryan Robinson i Keith Walters. "Turbulent Simulations of Particle Deposition in Feline Aorta Flow for Hypertrophic Cardiomyopathy Heart Conditions". W ASME/JSME/KSME 2015 Joint Fluids Engineering Conference. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/ajkfluids2015-4688.

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Turbulent CFD simulations are performed for feline aorta flow to study the physiology of thrombus localization for hypertrophic cardiomyopathy (HCM) heart condition. Simulations are performed using pulsatile normal and HCM heart cardiac output velocity profiles consisting of a single peak and dual peak pattern, respectively. The predictions for the normal heart conditions are validated using experimental data. The mass outflow through the arteries compares within 1.15% of the expected values. The flow rate through the iliac artery during a cardiac cycle, and shear stress profile at infrarenal aorta cross-section also compares well with the experimental data. Most vortical structures are predicted during decreasing cardiac flow, and are located close to the renal and iliac arteries, consistent with CFD studies in the literature. The model is therefore judged to be reasonably accurate for HCM predictions. For the HCM heart conditions, outflow from all the abdominal arteries shows a trimodal pattern, with reverse flow during the secondary flow. Several vortices are predicted in the increasing secondary cardiac flow. The vortices are mostly located in the lower abdominal aorta between the renal artery and iliac trifurcation. Turbulence plays a significant role in this case, and affects flow in most of the abdominal aorta after the primary peak. Particle deposition occurs in the thoracic aorta, below the renal artery and above the trifurcation. Deposition in the lower abdominal aorta is identified due to presence of flow recirculation and low streamwise velocity.

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Davidson, Lisa Ann, Maegan Carlisle, Richard Utarnachitt, Lori Avaiusini i Elizabeth Bridges. "Utilizing the Transport Risk Index of Physiologic Stability Version Ii (trips Ii): Establishing a Baseline of the Neonates Transported by Airlift Northwest". W Selection of Abstracts From NCE 2016. American Academy of Pediatrics, 2018. http://dx.doi.org/10.1542/peds.141.1_meetingabstract.738.

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Tse, Leonard W., Tina L. T. Shek, Aydin Nabovati i Cristina H. Amon. "Computational Fluid Dynamics Modeling of Redundant Stent-Graft Configurations in Endovascular Aneurysm Repair". W ASME 2010 International Mechanical Engineering Congress and Exposition. ASMEDC, 2010. http://dx.doi.org/10.1115/imece2010-39941.

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An aneurysm is a bulge or localized dilation of an artery that can result in rupture, rapid blood loss, and death. Endovascular aneurysm repair (EVAR) is a minimally-invasive surgical technique that involves delivery of a stent-graft from within the blood vessels. The metallic stents anchor and support the graft (fabric tube), through which blood flow is contained and directed. This relieves the pressure on the weakened aneurysm wall. When the stent-graft is too long for a given patient, the redundant (extra) length adopts a convex configuration in the aneurysm. Based on clinical experience, we hypothesize that redundant stent-graft configurations increase the downward force acting on the device thereby increasing the risk of device dislodgement and failure. This work numerically studies both steady-state and physiologic pulsatile blood flow in redundant stent-graft configurations. Computational fluid dynamics simulations predicted peak downward displacement force for the zero-, moderate- and severe-redundancy configurations of 7.49, 7.65 and 8.04 N, respectively for steady-state flow; and 7.55, 7.70 and 8.31 N, respectively for physiologic pulsatile flow. These results suggest that redundant stent-graft configurations in EVAR do increase the downward force acting on the device, but the clinical consequence depends significantly on device-specific resistance to dislodgement.

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Shahi, Niti, Gabrielle P. Shirek, Kaci Pickett, Alexandra Schwartz, Jamie Shoop, Ryan Phillips, Rachel Workman, Clio Pitula, David W. Kaplan i Steven L. Moulton. "Re-examining Physiologic Diagnostic Criteria: A Pilot Study using the Compensatory Reserve Index to Evaluate Individuals with Postural Orthostatic Tachycardia Syndrome". W AAP National Conference & Exhibition Meeting Abstracts. American Academy of Pediatrics, 2021. http://dx.doi.org/10.1542/peds.147.3_meetingabstract.362-a.

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Chandra, Santanu, Vimalatharmaiyah Gnanaruban, Jaehoon Seong, Barry B. Lieber, Jose F. Rodriguez i Ender A. Finol. "Experimental Validation of a Computational Algorithm for the Zero Pressure Geometry Derivation of Blood Vessels". W ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14716.

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Patient-specific computational assessment of biomechanical parameters such as peak wall stress is a promising tool for rupture risk assessment of blood vessels. However, this assessment is dependent on image based modeling of the vasculature [1] and on either structural or fluid-structure interaction analyses performed with numerical models to compute the stress and strain in the vascular wall. Protocols have been successfully derived to develop 3D models of normal and pathological vessels from individual Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) [2]. While the image based models used for these simulations are essentially in a pressurized state (gated to diastolic pressure), the application of physiologic systolic and diastolic pressures to compute stresses and strains is debatable. Therefore, the derivation of a “simulation ready” computational geometry is of great importance to the research community as the accuracy of the computational results is dependent on it.

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