Academic literature on the topic 'Etabolism'

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Journal articles on the topic "Etabolism"

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Taylor, Sarah A., and Richard M. Green. "Bile A cids, M icrobiota, and M etabolism." Hepatology 68, no. 4 (October 2018): 1229–31. http://dx.doi.org/10.1002/hep.30078.

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Schnitzler, Jörg-Peter, and Hanns Ulrich Seitz. "Rapid Responses of Cultured Carrot Cells and Protoplasts to an Elicitor from the Cell Wall of Pythium aphanidermatum (Edson) Fitzp." Zeitschrift für Naturforschung C 44, no. 11-12 (December 1, 1989): 1020–28. http://dx.doi.org/10.1515/znc-1989-11-1223.

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Abstract , Allgem eine Botanik und Pflanzenphysiologie, Auf der Morgenstelle Suspension cultured cells of an anthocyanin-containing cell line (DCb) from Daucus carota L. ssp. sativus respond very rapidly to treatment with a soluble carbohydrate elicitor from the wall of the oom ycete Pythium aphanidermatum by synthesizing 4-hydroxybenzoic acid which is incorpo­ rated into the plant cell wall. Enzym es of phenol m etabolism , phenylalanine am m onia-lyase (P A L) and chalcone synthase (C H S), respond to elicitor treatment in different ways. Both the catalytic activity of PAL and its subunit concentration, measured by means of immunoblotting, show a transient increase upon elicitation, whereas CHS the initial enzyme of the flavonoid pathway, is inhibited after administration of the elicitor. and consequently anthocyanin accum ula­ tion ceases. In protoplasts derived from the cultured cells a very similar elicitor-induced response has been observed. Lacking a cell wall, the protoplasts secrete the 4-hydroxybenzoic acid into the culture fluid. The carrot protoplasts isolated by wall degrading enzym es retain their responsive­ ness to the fungal carbohydrate elicitor. The value of the protoplast system for studying the im m ediate events following elicitor treatment is discussed.
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Varga, Zoltan V., Katalin Erdelyi, Janos Paloczi, Resat Cinar, Zsuzsanna K. Zsengeller, Tony Jourdan, Csaba Matyas, et al. "Disruption of R enal A rginine M etabolism P romotes K idney I njury in H epatorenal S yndrome in M ice." Hepatology 68, no. 4 (October 2018): 1519–33. http://dx.doi.org/10.1002/hep.29915.

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Palmieri, Vittorio, Giovanni de Simone, Mary J. Roman, Joseph E. Schwartz, Thomas G. Pickering, and Richard B. Devereux. "Ambulatory Blood Pressure and M;etabolic Abnormalities in Hypertensive Subjects With Inappropriately High Left Ventricular Mass." Hypertension 34, no. 5 (November 1999): 1032–40. http://dx.doi.org/10.1161/01.hyp.34.5.1032.

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Gao, Xin, and Jian‐Gao Fan. "Diagnosis and management of non‐alcoholic fatty liver disease and related metabolic disorders: Consensus statement from the S tudy G roup of L iver and M etabolism, C hinese S ociety of E ndocrinology (非酒精性脂肪性肝病与相关代谢紊乱诊疗共识——中华医学会内分泌学分会肝病与代谢学组)." Journal of Diabetes 5, no. 4 (June 4, 2013): 406–15. http://dx.doi.org/10.1111/1753-0407.12056.

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Lopez-Ridaura, Ruy, Karl P. Puchner, Eduardo Ortiz-Panozo, Isabel Vieitez, and Martín Lajous. "Stature is inversely associated with self-reported diabetes in middle-aged Mexican women." Revista Panamericana de Salud Pública 41 (March 6, 2017): 1. http://dx.doi.org/10.26633/rpsp.2017.32.

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Objective. To investigate whether stature is associated with two highly prevalent cardiom- etabolic disorders—diabetes mellitus (DM) and high blood pressure (HBP) —in middle-aged Mexican women. Methods. We conducted a cross-sectional analysis of a sample of 93 481 middle-aged Mexican female teachers, all participating in the Mexican Teachers Cohort (MTC, or ESMaestras) study. We used a multivariable regression model to investigate the association of stature quintiles with the self-reported outcomes of DM and HBP. Results. After adjusting for birth cohort, ethnicity, family history, birthweight, occupation of household’s head during participant’s childhood, menopausal status, and geographical region of birthplace, stature was inversely associated with DM, with the odds for DM being 9% higher in the lowest stature quintile when compared to the highest stature quintile. Stratification for location of residence resulted in confirmation of the above-mentioned findings only in partici- pants living in urban environments. Conclusions. We found an inverse association of stature with DM but not with HBP. Our data suggest that urban setting might be an important effect modifier of this association, which merits further investigation since it might provide valuable insights into the epidemiological transition occurring in developing countries.
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Jägers, Erhard, Vinayagar Pasupathy, Anke Hovenbitzer, and Wolfgang Steglich. "Suillin, ein charakteristischer Inhaltsstoff von Röhrlingen der Gattung Suillus (Boletales) / Suillin, a Characteristic M etabolite from Boletes of the Genus Suillus (Boletales)." Zeitschrift für Naturforschung B 41, no. 5 (May 1, 1986): 645–48. http://dx.doi.org/10.1515/znb-1986-0517.

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Abstract Fruiting bodies of several Suillus species contain a colourless compound, suillin, which is concentrated in the cuticle of the pileus. Its structure has been established as 4-acetoxy-3-geranyl-geranyl-1,2 -dihydroxybenzene (1) by spectroscopic evidence, conversion into a cyclic carbonate 2 and synthesis of its deacetyl derivative 3.
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Basov, Alexander, Ilya Bykov, Lilia Fedulova, Stepan Dzhimak, and Michael Baryshev. "Correction of oxidative m etabolism in blood and tissues of the internal organs in laboratory animals using isotopic D/H exchange reactions." Medical news of the North Caucasus 11, no. 1 (2016). http://dx.doi.org/10.14300/mnnc.2016.11010.

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Fotelli, Mariangela N., Fani G. Lyrou, Dimitrios N. Avtzis, Daniel Maurer, Heinz Rennenberg, Gavriil Spyroglou, Andrea Polle, and Kalliopi Radoglou. "Effective Defense of Aleppo Pine Against the Giant Scale Marchalina hellenica Through Ecophysiological and Metabolic Changes." Frontiers in Plant Science 11 (December 10, 2020). http://dx.doi.org/10.3389/fpls.2020.581693.

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Aleppo pine (Pinus halepensis) is widely distributed in the Mediterranean region and in other areas of the world, where it has been introduced due to its adaptive capacity to xerothermic conditions. The giant pine scale Marchalina hellenica often infests Aleppo pine, as well as other pines, in several southeastern European countries, causing pine declines. When combined with the expected intensified heat and drought events in eastern Mediterranean, the impact of this biotic parameter on the host pines may be exacerbated. The importance of understanding the defense mechanisms of Aleppo pine is emphasized by the recent invasion of the pine scale in new regions, like Australia, lacking the insect’s natural enemies, where more intense negative effects on pine species may occur. To date, Aleppo pine’s physiological responses to the infestation by M. hellenica are largely unknown. This study aimed at assessing the responses of Aleppo pine to the giant pine scale attack, both on an ecophysiological and a metabolic level. For this purpose, gas exchange, needle water status, and carbon and nitrogen content were measured during 1 year on healthy and infested adult trees. M etabolic profiling of Aleppo pine needles was also performed before, during, and after the high feeding activity of the insect. The maintenance of stable relative water content, δ13C signatures, and chlorophyll fluorescence in the needles of infested pines indicated that infestation did not induce drought stress to the host pines. At the peak of infestation, stomatal closure and a pronounced reduction in assimilation were observed and were associated with the accumulation of sugars in the needles, probably due to impaired phloem loading. At the end of the infestation period, tricarboxylic acids were induced and phenolic compounds were enhanced in the needles of infested pines. These metabolic responses, together with the recovery of photosynthesis after the end of M. hellenica intense feeding, indicate that in the studied region and under the current climate, Aleppo pine is resilient to the infestation by the giant pine scale. Future research should assess whether these promising defense mechanisms are also employed by other host pines, particularly in regions of the world recently invaded by the giant pine scale, as well as under more xerothermic regimes.
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Dissertations / Theses on the topic "Etabolism"

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Huf, Peter A., and mikewood@deakin edu au. "Androgen metabolism in the Australian lizard Tiliqua Rugosa." Deakin University. School of Sciences, 1989. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20051111.134448.

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Nonmammalian vertebrates possess some unusual features in their hormonal systems/ when compared to mammals. As a consequence, they can make an important contribution in investigations concerning the fundamental mechanisms operating in endocrinology. Such studies concerning androgens include inter alia their effects on developmental aspects in the brain of birds and related singing behaviour; the role of neural enzymes in reproductive processes in fish; and the relation between androgens and the stages of spermatogenesis in amphibia, The present thesis examines the biochemistry of androgens in the Australian lizard Tiliqua rugosa. The major compounds studied were testosterone and epitestosterone, which are known to be present in high concentrations in the plasma of the male animal. Previous investigations are expanded, particularly in the areas of steroid identification and testicular biosynthesis. In addition, preliminary studies on the metabolism in the brain (and other tissues) and plasma protein binding are reported. The presence of epitestosterone as a major free androgen in the plasma of the male lizard was confirmed. Other steroids were found in the sulphate fraction. Testosterone sulphate was the most rigorously identified compound, while some evidence was also found for the presence of conjugated 5-androstene-3β,17-diols, etiocholanolone and dehydroepiandrosterone (DHA). Epitestosterone does not appear to be extensively conjugated in this animal. Steroids were not found to be conjugated as glucuronides. The identification studies employed a novel method of electrochemical detection of steroids. This technique was investigated and extended in the current thesis. Biosynthetic studies were carried out on androgen interconversions in the testis, in vitro. The major enzyme activities detected were 17α-arid 17β-oxidoreductases (17α-OR and l7β-OR) and 3β-hydroxysteroid dehydrogenase (3β-HSD)/isonerase. No evidence was found for the presence of a steroid-17-epimerase that would directly interconvert testosterone and epitestosterone. The 17-oxidoreductases were found to be dependent on the cofactor NBDFH. Testosterone appears to be formed mainly via the 4-ene pathway, whereas epitestosterone is formed from both the 4- and 5-ene routes. The compound 5-androstene-3β, 17α-diol was found to be an intermediate in the synthesis of epitestosterone from DHA. Temperature was found to significantly affect 17α-OR activity (maximum at 32°C). In contrast,17β-OR activity was independent of this factor in the testis. Androgen metabolism in the testis was found to be regulated by cofactors, temperature and season. The major enzyme activities found in the male brain were 17α- and 17β-OR. 3βHSD/isomerase was not found; however a low activity of 5α-reductase was identified. Aromatase activity was not positively identified, but preliminary results suggest that it may be present at low levels. The 17-oxidoreductases were widespread throughout the brain. The 17α-OR was significantly lower in the forebrain than other brain sections. The 170-OR activity did not vary significantly throughout the organ, although there was a trend for its activity to be higher in the midbrain region (containing the hypothalamus in these sections). The concentration of endogenous steroids in brain tissue was estimated by radioimmunoassay. Epitestosterone was found throughout the organ structure, whereas testosterone was found mainly in the midbrain (containing hypothalamic regions in these sections). Correlations between enzyme activities and steroid concentrations in brain regions suggested that the main function of 17α-OR is to produce epitestosterone, whereas the 17β-OR may catalyse a more reversible reaction in vivo. Temperature was found to significantly affect both 17α- and 17β-OR activities in the brain. In contrast to the testis, the maximum activity of the brain enzymes occurred at 37°C. The level of 17α-OR activity in the male lizard (100 nmol/g tissue/h) is the highest reported for this enzyme in vertebrates. Both activities were found to be quantitatively similar in the whole brain homogenates of male and female animals, and did not vary seasonally when examined in the male. The 17-oxidoreductases were also found in most other tissues in T.rugosa, including epididymis, adrenal, kidney and liver (but not blood). This suggests that the high activities of both 17α-OR and 17β-OR are dominant features of the steroid system in this animal. The formation of 11-oxygenated compounds was found in the adrenal, in addition to the formation of polar metabolites in the kidney and liver (possibly polyhydroxylated and conjugated steroids). A preliminary investigation into the plasma binding of androgens was carried out. The insults suggest that there are several binding sites for testosterone; one with high affinity and low capacity; the other with low affinity and high capacity. Binding experiments were carried out at 32°C. At this temperature, specific binding was greater than at 25 or 37°C. From the results of competition studies it was suggested that epitestosterone (with a K(i)= 3 X 10 (-6)M for testosterone binding) regulates the binding of testosterone (K(i)=10(-7)M) and hence the concentrations of the latter steroid as a free compound in plasma. In general, the study has shown that the biochemistry of androgens in the reptile T.rugosa is largely similar to that found in other vertebrates. The major difference is a greatly increased activity of 17α-OR, which causes a higher concentration of 17α-compounds to be present in the tissues of this lizard. The physiological roles for epitestosterone are not yet clear. However it appears from this study that this steroid regulates testosterone concentrations in several tissues by either steroidogenic or binding mechanisms. Several major influences on this regulation include temperature, availability of cofactors and seasonal effects.
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Salvato, Flavia. "Fermentação de mosto industrial por linhagens de Saccharomyces cerevisiae com transportador de sacarose e sobreexpressão de invertase interna: estudo comparativo com linhagens com alta e baixa atividade de invertase externa." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/11/11138/tde-17092010-174743/.

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O presente trabalho teve como objetivo avaliar o perfil de metabolização de açúcares por linhagens de S. cerevisiae amplamente utilizadas no setor sucroalcoleiro (CAT-1 e BG-1) e uma linhagem geneticamente modificada (HCJ 003) com o propósito de sobreexpressar invertase intracelular e ainda contém transportadores de sacarose de alta afinidade. Para tal estudo foi realizado 1 ensaio de fermentação simulando as condições industriais de produção de etanol com reciclos de células e mosto misto constituído de melaço e caldo de cana (50% de cada fonte) a 19% de ART. O ensaio de fermentação foi constituído por 4 ciclos sendo os 3 primeiros ciclos destinados a avaliação das cepas CAT -1 e HCJ 003 a qual é diplóide e sobre-expressa somente a invertase intracelular quanto aos diversos parâmetros do processo de fermentação. O 4° ciclo fermentativo foi destinado ao estudo do perfil de metabolização dos açúcares, onde analisou-se os teores de sacarose, glicose e frutose, bem como a formação de glicerol e o teor de trealose na biomassa das linhagens CAT -1, HCJ 003 e BG-1 (ambas com atividades de invertase distintas). No estudo comparativo dos parâmetros fermentativos a cepa HCJ 003 produziu de forma consistente, menos biomassa e mais etanol do que a cepa CAT-1. O rendimento fermentativo em etanol foi maior para a cepa HCJ 003. O fato de transportar a sacarose para o interior da célula faz com que seja gerado apenas 3 moles de ATP (em vez de 4 ATP). Portanto, para repor o ATP que deixa de ser gerado, há um maior direcionamento do metabolismo para as vias fermentativas e conseqüentemente mais etanol é produzido aumentando-se o rendimento da fermentação. No estudo do perfil de metabolização dos açúcares para as cepas CAT -1, HCJ 003 e BG-1 mostrou que a cepa BG -1 hidrolisou mais rapidamente a sacarose devido à alta atividade de invertase e também apresentou quantidades superiores de glicerol em resposta ao aumento da pressão osmótica do meio de fermentação. Já a CAT -1 apresentou maiores níveis de trealose o que pode ser um indicativo da sua maior dominância durante o processo industrial brasileiro. Assim este trabalho resultou no perfil de metabolização de cepas com diferente atividade de invertase e mostrou que a cepa HCJ 003 embora seja uma derivada de uma linhagem laboratorial manteve-se adaptada às condições do processo obtendo-se rendimento superior à CAT-1.
The aim of tis work was to evaluate the metabolic profile of sugars using Saccharomyces cerevisiae strains widely used in industry of sugars and ethanol (CAT-1 e BG-1) and a genetically modified strain in purpose to over-express intracellular invertase and also contains sucrose transporters with high afinity. For this study, 1 test were performed simulating industrial fermentation for ethanol production using cell recycle and mixed must with molasses and sugar cane (50% of each compound) for 19% TRS. The fermentation experiment were composed of 4 recycles and in first 3 cycles were intended for the evaluation of the strains CAT-1 and HCJ 003 wich is diploid and overexpres just the intracellular invertase on the various parameters of the fermentation process. The 4th recycle was designed to study the profile of metabolism of sugars, where were analysed the levels of sucrose, glucose and frutose, as well as the formation of glycerol and trehalose content in biomass of the strains CAT -1, HCJ 003 and BG -1 (all of them with different invertase activity). In the evaluation of the strains on the various parameters of the fermentation process, the strain HCJ 003 produced consistently less biomass and more ethanol than CAT-1. The yield of ethanol fermentation was higher for the strain HCJ 003. The fact that this strain transport sucrose into the cells makes it generated only 3 moles of ATP (instead 4 ATP). So to restore the ATP that is no generated, there is an increase targeting of the metabolism to fermentative pathways and therefore more ethanol is produced increasing the efficiency of fermentation. In the profile of metabolism of sugars to the strains CAT -1 HCJ 003 and BG-1 showed that the strain BG -1 hydrolyzed more rapidly the sucrose due to high invertase activity and also showed higher amounts of glycerol in response to increased osmotic pressure of the fermentation medium. Already CAT -1 showed higher levels of trehalose, which may be indicative of its most dominant during the Brazilian industry. So this work resulted in the profile of metabolism of different strains with invertase activity and showed that strain 003 Hcj although a derivative of a laboratory strain remained adapted to the conditions of the process resulting in higher yield to CAT-1.
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Sharrock, Jessica. "Female sterile (1) homeotic controls metabolic and immune function and enhances survival via AKT and FOXO." Thesis, King's College London (University of London), 2017. https://kclpure.kcl.ac.uk/portal/en/theses/female-sterile-1-homeotic-controls-etabolic-and-immune-function-and-nhances-survival-via-akt-and-foxo(13d32527-d51f-42f8-a90a-586bbbf1986d).html.

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The Drosophila melanogaster fat body, analogous to mammalian adipose tissue and the liver, is the primary organ of fat and glycogen storage as well as being responsible for the humoral immune response following infection. Normal functioning of the fat body is of critical importance to the survival of the organism, but many molecular regulators of its function remain ill-defined. Here, for the first time, we demonstrate that the Drosophila bromodomain-containing protein fs(1)h is essential in the fat body for normal lifespan as well as metabolic and immune homeostasis. Under physiological conditions, flies lacking fs(1)h in the fat body exhibit a severely reduced lifespan, abnormally high expression of immune target genes including antimicrobial peptides (AMPs) and cytokines, an inability to utilise triglycerides following periods of starvation, and low basal AKT activity, mostly resulting from systemic defects in insulin signalling. Loss of fs(1)h in the fat body also results in hypoglycemia and a dysregulation of several fat body-derived signals, indicating a role for fat body fs(1)h in the regulation of various systemic endocrine signals. Removing a single copy of the AKT-responsive transcription factor foxo ameliorates almost all the observed phenotypes, restoring lifespan, metabolic function, uninduced immune gene expression, and AKT activity suggesting many of the in vivo effects of fs(1)h in the fat body are foxo-dependent. However, survival is not rescued and AMP expression is still elevated following bacterial infection in fs(1)h knockdown foxo heterozygous flies, indicating some of the phenotypes observed are independent of the FOXO hyperactivation. We propose that the promotion of systemic insulin signalling activity is a key in vivo function of fat body fs(1)h.
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Chapados, Natalie A. "Mécanismes contributifs au développement de la stéatose hépatique non alcoolique (SHNA) : effets de l'entraînement." Thèse, 2009. http://hdl.handle.net/1866/6477.

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Book chapters on the topic "Etabolism"

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"Energy M etabolism." In Advanced Human Nutrition, 301–38. CRC Press, 2014. http://dx.doi.org/10.1201/b16554-15.

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"M etabolism of Acids, Lactones, and Esters." In Handbook of Mammalian Metabolism of Plant Compounds (1991), 147–204. CRC Press, 2017. http://dx.doi.org/10.1201/9780203712504-10.

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"Fundam entals of Cancer Cell M etabolism." In Cancer Cell Metabolism and Cancer Treatment, 11–39. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-7.

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"Controlling Factors of Cancer C ell M etabolism." In Cancer Cell Metabolism and Cancer Treatment, 40–78. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-8.

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"Cancer C ell M etabolism and Cancer M etastasis." In Cancer Cell Metabolism and Cancer Treatment, 155–82. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-12.

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"Cancer C ell M etabolism and M ultidrug Resistance (MDR)." In Cancer Cell Metabolism and Cancer Treatment, 95–118. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-10.

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"Cancer C ell M etabolism , N utrition, and D iet." In Cancer Cell Metabolism and Cancer Treatment, 183–218. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-13.

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"Role of Cancer C ell M etabolism in Cancer Therapy and Cancer Prevention." In Cancer Cell Metabolism and Cancer Treatment, 219–58. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-14.

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"Cancer Cell M etabolism , Cell C ycle, and Cell D eath (Apoptosis, Necrosis)." In Cancer Cell Metabolism and Cancer Treatment, 119–54. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-11.

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"Cancer Cell M etabolism and D evelopm ent of N ovel A nticancer Drugs." In Cancer Cell Metabolism and Cancer Treatment, 259–94. CRC Press, 2001. http://dx.doi.org/10.1201/9780203091906-15.

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