Academic literature on the topic 'Albumin and Transferrin'

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Journal articles on the topic "Albumin and Transferrin"

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Cooper, J. A., and A. B. Malik. "Pulmonary transvascular flux of transferrin." Journal of Applied Physiology 67, no. 5 (1989): 1850–54. http://dx.doi.org/10.1152/jappl.1989.67.5.1850.

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We compared the pulmonary transvascular fluxes of transferrin and albumin in the intact sheep lung. Anesthetized sheep were prepared with lung lymph fistulas. The vascular blood pool was marked with 99mTc-erythrocytes, autologous transferrin was labeled with 113mIn, and albumin was labeled with 125I. Samples of blood, plasma, lymph, and lung were obtained up to 180 min after tracer infusion. Lymph tissue radioactivities were corrected for the intravascular component and expressed as extravascular-to-plasma concentration ratios. Clearance of transferrin and albumin from the plasma space followe
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Kratz, Felix. "Drug conjugates with albumin and transferrin." Expert Opinion on Therapeutic Patents 12, no. 3 (2002): 433–39. http://dx.doi.org/10.1517/13543776.12.3.433.

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Franks, J. J., J. B. Kruskal, R. E. Kirsch, A. P. G. Beechey, D. F. Morrell, and G. G. Harrison. "Halothane Decreases Albumin and Transferrin Synthesis." Anesthesiology 68, no. 4 (1988): 529–33. http://dx.doi.org/10.1097/00000542-198804000-00009.

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BRAEND, M., G. EFREMOV, M. K. FAGERHOL, and O. HARTMANN. "ALBUMIN AND TRANSFERRIN VARIANTS IN NORWEGIANS." Hereditas 53, no. 1-2 (2009): 137–42. http://dx.doi.org/10.1111/j.1601-5223.1965.tb01986.x.

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Barber, B. J., and V. L. Stanhope. "Bromcresol green assay is nonspecific for rat plasma albumin." American Journal of Physiology-Heart and Circulatory Physiology 262, no. 1 (1992): H299—H302. http://dx.doi.org/10.1152/ajpheart.1992.262.1.h299.

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Bromcresol green (BCG) assay has been used in microvascular studies to determine albumin in rat plasma. The purpose of this study was to demonstrate that BCG overestimates rat plasma albumin partly because BCG binds to transferrin, a beta-globulin. The light absorbance of a transferrin-BCG reagent solution is shown to increase with time; appreciable binding occurs within a few seconds. Pure transferrin produced BCG assay results (P less than 0.001) that could be expressed as pseudoalbumin concentrations. Albumin and transferrin solutions of equal concentrations were mixed in equal parts; a plo
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Williams, Carolyn L., Paul K. Priscott, I. T. Oliver, and George C. T. Yeoh. "Albumin and transferrin synthesis in whole rat embryo cultures." Development 92, no. 1 (1986): 33–41. http://dx.doi.org/10.1242/dev.92.1.33.

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The uptake of [3H]leucine by the rat yolk sac and embryo and the subsequent synthesis of albumin and transferrin have been studied in whole embryo culture. Rat embryos of 12 days gestation were used in all experiments. Isotopically labelled transferrin was detectable in yolksac and embryo tissue extracts. In contrast, [3H]albumin could not be found in either tissue extract. Levels of radioactive transferrin in the yolk sac of cultured whole conceptuses decreased during 12 h in cold media. Embryonic transferrin showed an opposite trend in that it increased over 12 h by nearly 30-fold. In view o
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SCHNEIDER, H., M. P. C. SCHNEIDER, B. T. F. DA SILVA, and F. M. SALZANO. "Transferrin and albumin polymorphisms in buffaloes from Brazil." Animal Genetics 21, no. 3 (1990): 335–37. http://dx.doi.org/10.1111/j.1365-2052.1990.tb03246.x.

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Hsu, S. L., Y. F. Lin, and C. K. Chou. "Transcriptional regulation of transferrin and albumin genes by retinoic acid in human hepatoma cell line Hep3B." Biochemical Journal 283, no. 2 (1992): 611–15. http://dx.doi.org/10.1042/bj2830611.

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Transferrin and albumin, which are both secreted from the human hepatoma cell line Hep3B, were regulated transcriptionally by retinoic acid (RA) in a dose-dependent manner. The cell growth rate was little affected under the same conditions. The treatment of Hep3B cells with RA (10 microM for 48 h) resulted in an 8-fold increase in transferrin protein synthesis, a 10-fold increase in the steady-state transferrin mRNA level, and a 5-fold increase in its transcriptional rate. The same treatment led to 4-fold decrease in albumin synthesis, as well as a 7-fold decline in the steady-state albumin mR
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Lim, Su-Lin, and Jamie Lye. "Nutritional Intervention Incorporating Expedited 10 g Protein Counter (EP-10) to Improve the Albumin and Transferrin of Chronic Hemodialysis Patients." ISRN Nutrition 2013 (October 22, 2013): 1–5. http://dx.doi.org/10.5402/2013/396570.

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Objective. The expedited 10 g protein counter (EP-10) is a quick and valid clinical tool for dietary protein quantification. This study aims to assess the clinical effectiveness of the EP-10 in improving serum albumin and transferrin in chronic hemodialysis patients. Methods. Forty-five patients with low serum albumin (<38 g/L) were enrolled in this study. Parameters measured included dry weight, height, dietary intake, and levels of serum albumin, transferrin, potassium, phosphate, and kinetic modeling (Kt/V). The nutritional intervention incorporated the EP-10 in two ways (1) to quantify
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Das, Bhabani S., David I. Thurnham, and Deba B. Das. "Influence of malaria on markers of iron status in children: implications for interpreting iron status in malaria-endemic communities." British Journal of Nutrition 78, no. 5 (1997): 751–60. http://dx.doi.org/10.1079/bjn19970192.

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To investigate Fe nutritional indices in malaria infection in children, haematology (blood haemoglobin, plasma ferritin, transferrin, Fe, and transferrin saturation), acute phase markers (albumin and caeruloplasmin) and liver function tests were studied in fifty consecutive cases of severe and mild falciparum malaria, fifty matched controls and twenty-three cases of asymptomatic malaria. Blood haemoglobin and transferrin were lower, while ferritin and transferrin saturation were higher, in groups with symptomatic malaria in comparison with the control group. The differences were greatest with
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Dissertations / Theses on the topic "Albumin and Transferrin"

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Kim, Jonghan. "Pharmacokinetics and pharmacodynamics of protein turnover and production in vivo." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1100554543.

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Thesis (Ph. D.)--Ohio State University, 2004.<br>Title from first page of PDF file. Document formatted into pages; contains xxi, 203 p.; also includes graphics. Includes bibliographical references (p. 191-203).
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Zablith, Nadine. "The association between amniotic fluid albumin, prealbumin or transferrin and the fetal growth /." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=98526.

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The study objectives were to measure the concentrations of albumin, prealbumin and transferrin in amniotic fluid (AF), and to establish if these concentrations were associated with infant birth weight (BW). At St Mary's Hospital (Montreal, Quebec), 294 AF samples were collected from mothers undergoing routine amniocentesis (12-19 weeks gestation). Exclusion criteria included subjects having gestational diabetes, multiple births or fetal genetic abnormalities. AF samples were analyzed by capillary electrophoresis (CE) at 190 nm. Analysis of variance and multiple linear regressions were performe
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Hunjan, Anoop Singh, and Anoop Singh Hunjan. "Chronic Arsenite Exposure in Lung Epithelium Modulates Endocytosis." Thesis, The University of Arizona, 2017. http://hdl.handle.net/10150/626765.

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Arsenic exposure in humans has been implicated in the development of a myriad of non-cancerous and cancerous diseases. A reductionist approach to understanding this unusual phenomenon would suggest that arsenic-induced perturbation of a small number of fundamental biological processes could manifest as this diverse array of disease endpoints. Endocytosis is a fundamental cellular process involved in the internalization and transport of various extracellular molecules and membranous components. BEAS-2B, a human bronchial epithelial cell line, was used to characterize the effects of chronic arse
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Sanches, Rute Nazaré Fernandes. "Estudo da interação de metalofármacos de dirutênio-anti-inflamatórios com as proteínas séricas transferrina e albumina." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-17082016-084123/.

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Metalofármacos baseados em rutênio têm se mostrado promissores com relação à atividade anticancerígena frente a diversos tipos de tumores. Nosso grupo de pesquisa dedica-se ao estudo de compostos contendo o centro dimetálico de valência mista Ru2(II,III) coordenado a ligantes derivados de Faines (Fármacos anti-inflamatórios não esteroides), tendo demostrando o potencial desses complexos frente a glioma. O entendimento do modo de ação destes complexos requer o estudo de suas interações com biomoléculas presentes no meio biológico. Neste cenário, o presente trabalho teve por objetivo investigar
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Rocha, Bianca do Prado Lima Petrucci. "Perfil proteico do fluido folicular durante a foliculogênese da égua." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2014. http://hdl.handle.net/10183/114683.

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O fluido folicular (FF) é um líquido extracelular complexo que se acumula no antro dos folículos ovarianos durante o seu desenvolvimento. É o meio essencial para o crescimento e a maturação das células ovarianas somáticas e germinativas e contém substâncias envolvidas na diferenciação celular, maturação do oócito, qualidade do gameta, ruptura da parede folicular e luteinização. O estudo de seus componentes é fundamental para um melhor entendimento dos mecanismos que envolvem a dinâmica folicular na espécie equina. O objetivo deste trabalho foi comparar o perfil proteico do maior folículo, e en
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Kern, Andrea [Verfasser]. "Stellenwert der Akute-Phase-Proteine, CRP, Albumin, Fibrinogen, Ferritin, Transferrin und Coeruloplasmin in der Diagnostik der Steatosis hepatis - eine Untersuchung an 2445 Probanden einer zufälligen Bevölkerungsstichprobe / Andrea Kern." Ulm : Universität Ulm. Medizinische Fakultät, 2014. http://d-nb.info/1056823607/34.

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Sertillanges, Philippe. "Étude de la purification à l'échelle pilote de l'albumine et de la transferrine humaine par chromatographie d'échange d'ions." Nancy 1, 1991. http://www.theses.fr/1991NAN10445.

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Guerra, Léa Teresinha. "Transferrina e pré-albumina séricas como marcadoras da resposta do suporte nutricional em pacientes com câncer de esôfago." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2008. http://hdl.handle.net/10183/17372.

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Objetivos: O objetivo do presente estudo foi avaliar a dosagem da transferrina e pré-albumina séricas como marcadoras da resposta ao suporte nutricional em pacientes com câncer de esôfago. Métodos: Estudo clínico não-controlado com 45 pacientes internados com câncer de esôfago submetidos ao suporte nutricional antes de iniciar a terapia oncológica. De acordo com o estado nutricional, os pacientes receberam dieta por sonda nasoentérica, via oral ou combinada (via oral e sonda nasoentérica). O gasto energético basal foi estimado pela equação de Harris-Benedict. Pré-albumina e transferrina sérica
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Mendonça, Victor Hugo [UNESP]. "Quantificação de proteínas de fase aguda em éguas doadoras de embrião da raça quarto de milha." Universidade Estadual Paulista (UNESP), 2012. http://hdl.handle.net/11449/88172.

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Made available in DSpace on 2014-06-11T19:23:09Z (GMT). No. of bitstreams: 0 Previous issue date: 2012-08-21Bitstream added on 2014-06-13T18:50:25Z : No. of bitstreams: 1 mendonca_vh_me_araca.pdf: 468913 bytes, checksum: 8c8b58b207927414e570fc0da4f9dd42 (MD5)<br>A eficiência reprodutiva em éguas é geralmente baixa, sendo que 43% de éguas puro-sangue falham em conceber um potro vivo. Infecção bacteriana no lúmen uterino é uma das principais causas de infertilidade em éguas. O exame citológico do endométrio é o mais importante método auxiliar no controle da saúde genital da égua devido ao seu
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Borges, Maria Filomena Parreira Jacinto Pereira. "Avaliação nutricional precoce nos doentes gastrostomizados: perímetro braquial, índice de massa corporal, albumina, transferrina, pré-albumina, e proteína C-reativa no primeiro mês após gastrostomia." Master's thesis, Instituto Superior de Ciências da Saúde Egas Moniz, 2013. http://hdl.handle.net/10400.26/6139.

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Dissertação para obtenção do grau de Mestre em Nutrição Clínica<br>Introdução: A avaliação do estado nutricional nos doentes disfágicos gastrostomizados, no 1º mês após gastrostomia percutânea endoscópica (PEG), é uma importante ferramenta para uma abordagem terapêutica nutricional, eficaz. Torna-se assim um desafio, a procura de novas ferramentas exequíveis e fiáveis que possam fornecer precocemente informação credível sobre o estado nutricional e que possam ter um impacto significativo na monitorização do tratamento destes doentes, nos primeiros 30 dias após a gastrostomia.<br>Objectivos: Av
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Book chapters on the topic "Albumin and Transferrin"

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Lescoat, Gérard, Noëlla Hubert, and Pierre Brissot. "Effect of ornithine on albumin and transferrin secretions in rat and human hepatocyte cultures." In Amino Acids. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_109.

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Jeejeebhoy, K. N., A. Bruce-Robertson, J. Ho, and U. Sodtke. "The Comparative Effects of Nutritional and Hormonal Factors on the Synthesis of Albumin, Fibrinogen and Transferrin." In Ciba Foundation Symposium 9 - Protein Turnover. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719923.ch12.

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Sarich, Vincent M. "Mammalian Systematics: Twenty-Five Years Among Their Albumins and Transferrins." In Mammal Phylogeny. Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4613-9246-0_8.

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Sarne, David H., and Michael Weinberg. "Normal Cellular Uptake of Thyroxine (T4) from Serum of Patients with Familial Dysalbuminemic Hyperthyroxinemia (FDH) or Elevated Thyroxine-Binding Globulin (TBG): T4 Bound to Albumin is not Preferentially Transferred to Tissue." In Frontiers in Thyroidology. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5260-0_99.

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Simões, Sérgio, Pedro Pires, M. Teresa Girão da Cruz, Nejat Düzgüneş, and Maria C. Pedroso de Lima. "Gene Delivery by Cationic Liposome–DNA Complexes Containing Transferrin or Serum Albumin." In Liposomes, Part C. Elsevier, 2003. http://dx.doi.org/10.1016/s0076-6879(03)73024-9.

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Farne, Hugo, Edward Norris-Cervetto, and James Warbrick-Smith. "Jaundice." In Oxford Cases in Medicine and Surgery. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780198716228.003.0020.

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The metabolism of bilirubin in humans is summarized in Figure 14.1 and can be divided into three sequential steps: 1 Production of unconjugated bilirubin. Red blood cells are broken down by macrophages (mainly in the spleen), which degrade haemoglobin into iron and unconjugated (water insoluble) bilirubin. The iron is stored inside transferrin proteins. Unconjugated bilirubin travels to the liver bound to albumin. In disease, unconjugated bilirubin can be produced by haemolysis of red cells intravascularly, rather than in the spleen. 2 Conjugation of bilirubin. Liver hepatocytes uptake unconjugated bilirubin and conjugate it to glucuronate, thus making water soluble, conjugated bilirubin. 3 Excretion of bilirubin. Once conjugated, bilirubin is secreted into the bile canaliculi. Conjugated bilirubin flows with bile down the bile ducts and into the duodenum. Inside the bowel, conjugated bilirubin is metabolized by bacteria into colourless products (urobilinogen, stercobilinogen). Some of these can be reabsorbed by the gut and excreted via the kidneys, but the vast majority are oxidized in the gut into coloured pigments (urobilin, stercobilin) which give faeces their brown colour. Consequently, if there is complete obstruction of the bile ducts there will be no flow of conjugated bilirubin into the gut, no conversion into urobilinogen, and therefore not even a trace of urobilinogen in the urine. The terminology is confusing because different people mean different things. If you are going to use this terminology, make sure that you and your colleagues agree on the definitions. Nonetheless, this is what people usually mean: • Prehepatic jaundice: this refers to jaundice caused by an excessive production of bilirubin. Remember that bilirubin is produced by the breakdown of haemoglobin in the blood vessels or the spleen, hence the term prehepatic. • Hepatic jaundice: for some people, this means any jaundice due to pathology in the liver (anatomically), such as points 3, 4, and 5 in Figure 14.1, and can thus include problems with hepatocytes (e.g. hepatitis) or with the bile canaliculi (e.g. primary sclerosing cholangitis, PSC).
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Galateria, Marinella Mascia. "Dalla scrivania tutta per sé al confino della Massaia." In Italianistica. Fondazione Università Ca’ Foscari, 2020. http://dx.doi.org/10.30687/978-88-6969-422-5/002.

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The essay retraces Masino’s life and work from 1938 until 1950 – the period of time she lived in Venice – through her private letters and memoirs (Album di vestiti). Masino transferred to Venice not of her own will, but to follow her companion, writer Massimo Bontempelli, who was compelled by the Fascist Regime to leave Rome. ìTherefore Masino’s relationship with Venice was conditioned from the political situation she lived in and deeply influenced the book she wrote in Venice from 1938 and 1941: Nascita e morte della massaia. Through the publisher’s letters and institutional documents the essay illustrates the censorship’s interventions on the text of her novel before she was allowed to publish it.
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Jones, Alisha Lola. "“Wired”." In Flaming? Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780190065416.003.0006.

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Chapter 5 investigates a case study of Tonéx, a queer preacher-musician who embodies a combination of the most popular archetypes of African-American men’s worship—the preacher and the vocalist head musician—while wielding multifarious rhetorics during his musical performance. Tonéx’s case contests the portrayal of same-gender-loving men as down low, secretive, deceptive, and always withholding information about who they are from their loved ones. Chapter 5 investigates the queer Pentecostal performative strategies behind the creative process of worshipping in Spirit and in truth, as Tonéx grounds his performances in bodily experiences recorded on the Unspoken album. By vocalizing unspoken bodily experiences for gospel music audiences, Tonéx guides his fans through an exploration of what it means to be wired: that is, the occurrence of the embedded, transferred, bestowed, gifted, ridiculed, and surveilled aspects of being a queer masculine survivor of sexual assault in Pentecostal Christian communities.
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Conference papers on the topic "Albumin and Transferrin"

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Konduru, N., K. Zagorovsky, D. Diaz-Diiestra, et al. "Pulmonary Fate and Consequences of Albumin- and Transferrin-Coated Gold Nanoparticles." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a2247.

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Augustine, Shancy, Pan Gu, Xiangjun Zheng, Toshikazu Nishida, and Z. Hugh Fan. "Development of All-Plastic Microvalve Array for Multiplexed Immunoassay." In ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-38154.

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There is a need for low-cost immunoassays that measure the presence and concentration of multiple harmful agents in one device. Currently, comparable immunoassays employ a one-analyte-per-test format that is time consuming and not cost effective for the requirement of detecting multiple analytes in a single sample. For instance, if a spectrum of harmful agents, including E. coli O157, cholera toxin, and Salmonella typhimurium, should be simultaneously monitored in foods and drinking water, then a one-analyte-per-test would be inefficient. This work demonstrates a platform capable of simultaneo
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Miekka, Shirley I. "USE OF ALBUMIN AND TWEEN AS STABILIZERS TO PREVENT ACTIVITY LOSS DURING CLOTTING ASSAYS OF COAGULATION FACTOR IX AND X CONCENTRATES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644065.

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Assays for clotting activities of Vitamin K-dependent coagulation factors in Factor IX complex concentrates are IcnovTn to give variable results depending on the composition of the sample diluent. Higher potency values are obtained when deficient plasma is used for sample pre-dilution compared with dilution in buffer. This discrepancy is more pronounced in assays of higher purity Factor IX (FIX) or Factor X (FX) concentrates. We have found that addition of a mixture of bovine albumin (0.1% w/v) and Tween 20 (0.01% v/v) (BAT) to the dilution buffer can eliminate the discrepancy, giving clotting
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