Relevant bibliographies by topics / Biochemistry

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Biochemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 January 2025

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Journal articles on the topic "Biochemistry"

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Jovičić, Snežana, and Nada Majkić-Singh. "Medical Biochemistry as Subdiscipline of Laboratory Medicine in Serbia." Journal of Medical Biochemistry 36, no. 2 (April 1, 2017): 177–86. http://dx.doi.org/10.1515/jomb-2017-0010.

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SummaryMedical biochemistry is the usual name for clinical biochemistry or clinical chemistry in Serbia, and medical biochemist is the official name for the clinical chemist (or clinical biochemist). This is the largest sub-discipline of the laboratory medicine in Serbia. It includes all aspects of clinical chemistry, and also laboratory hematology with coagulation, immunology, etc. Medical biochemistry laboratories in Serbia and medical biochemists as a profession are part of Health Care System and their activities are regulated through: the Health Care Law and rules issued by the Chamber of Medical Biochemists of Serbia. The first continuous and organized education for Medical Biochemists (Clinical Chemists) in Serbia dates from 1945, when the Department of Medical Biochemistry was established at the Pharmaceutical Faculty in Belgrade. In 1987 at the same Faculty a five years undergraduate study program was established, educating Medical Biochemists under a special program. Since the academic year 2006/2007 the new five year undergraduate (according to Bologna Declaration) and four-year postgraduate program according to EC4 European Syllabus for Postgraduate Training in Clinical Chemistry and Laboratory Medicine has been established. The Ministry of Education and Ministry of Public Health accredited these programs. There are four requirements for practicing medical biochemistry in the Health Care System: University Diploma of the Faculty of Pharmacy (Study of Medical Biochemistry), successful completion of the professional exam at the Ministry of Health after completion of one additional year of obligatory practical training in the medical biochemistry laboratories, membership in the Serbian Chamber of Medical Biochemists and licence for skilled work issued by the Serbian Chamber of Medical Biochemists. In order to present laboratory medical biochemistry practice in Serbia this paper will be focused on the following: Serbian national legislation, healthcare services organization, sub-disciplines of laboratory medicine and medical biochemistry as the most significant, education in medical biochemistry, conditions for professional practice in medical biochemistry, continuous quality improvement, and accreditation. Serbian healthcare is based on fundamental principles of universal health coverage and solidarity between all citizens.
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Majkić-Singh, Nada. "Education and Recognition of Professional Qualifications in the Field of Medical Biochemistry in Serbia." Journal of Medical Biochemistry 30, no. 4 (October 1, 2011): 279–86. http://dx.doi.org/10.2478/v10011-011-0013-7.

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Education and Recognition of Professional Qualifications in the Field of Medical Biochemistry in Serbia Medical biochemistry is the usual name for clinical biochemistry or clinical chemistry in Serbia, and medical biochemist is the official name for the clinical chemist (or clinical biochemist). This is the largest sub-discipline of the laboratory medicine in Serbia. It includes all aspects of clinical chemistry, and also laboratory hematology with coagulation, immunology, etc. Medical biochemistry laboratories in Serbia and medical biochemists as a profession are part of Health Care System and their activities are regulated through: the Health Care Law and rules issued by the Chamber of Medical Biochemists of Serbia. The first continuous and organized education for Medical Biochemists (Clinical Chemists) in Serbia dates from 1945, when the Department of Medical Biochemistry was established at the Pharmaceutical Faculty in Belgrade. In 1987 at the same Faculty a five years undergraduate branch was established, educating Medical Biochemists under a special program. Since school-year 2006/2007 the new five year undergraduate (according to Bologna Declaration) and postgraduate program of four-year specialization according to EC4 European Syllabus for Post-Gradate Training in Clinical Chemistry and Laboratory Medicine has been established. The Ministry of Education and Ministry of Public Health accredits the programs. There are four requirements for practicing medical biochemistry in the Health Care System: University Diploma of the Faculty of Pharmacy (Study of Medical Biochemistry), successful completion of the profession exam at the Ministry of Health after completion of one additional year of obligatory practical training in the medical biochemistry laboratories, membership in the Serbian Chamber of Medical Biochemists and licence for skilled work issued by the Serbian Chamber of Medical Biochemists. The process of recognition of a foreign higher education document for field of medical biochemistry is initiated on request by Candidate. The process of recognition of foreign higher education documents is performed by the University. In the process of recognition in Serbia national legislations are applied as well as international legal documents of varying legal importance.
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Majkic-Singh, Nada. "Society of medical biochemists of Serbia and Montenegro: 50 years anniversary." Jugoslovenska medicinska biohemija 24, no. 3 (2005): 157–70. http://dx.doi.org/10.2298/jmh0503157m.

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Medical biochemistry (synonyms: clinical chemistry or clinical biochemistry) in the terms of professional and scientific discipline, stems from and/or has developed along with the natural sciences and its influences (mathematics, physics, chemistry and biochemistry) and medical sciences as well (physiology, genetics, cell biology). As a scientific discipline, medical biochemistry studies metabolic processes of physiological and pathological changes with humans and animals. Applying analytical chemistry's and biochemistry's techniques enables medical biochemists to gain plenty of information related to diagnosis and prognosis which serve physicians to asses the gravity of illness and prescribe healing therapy. Therefore medical biochemistry is an integral part of modern medicine. This discipline was dubbed various, often confusing names such as pathology, physiology, clinical biology, clinical pathology, chemical pathology, clinical biochemistry, medical biochemistry, clinical chemistry and laboratory medicine, all depending on place of origin. The official, internationally accepted name - clinical chemistry, was mentioned for the first time in 1912 by Johan Scherer, who described his laboratory as Clinical Chemistry Laboratory (Klinisch Chemische Laboratorium) in the hospital Julius in Wurzburg in Germany. After creating national societies of clinical chemists, Professor Earl J. King of Royal Postgraduate Medical School from London incited an initiative to unite national societies into the organization with worldwide character - it was the International Association of Clinical Biochemists, monitored by the International Union for Pure and Applied Chemistry (IUPAC). On 24 July 1952 in Paris, a Second International Congress of Biochemistry was held. A year later, in Stockholm, the name of a newly formed association was altered into International Federation of Clinical Chemistry, which was officially accepted in 1955 in Brussels. Today this federation-s name is International Federation for Clinical Chemistry and Laboratory Medicine (IFCC). Right after the World War II our medical biochemists began to gather within their expert societies. Even before 1950 Pharmaceutical Society of Serbia hosted laboratory experts among whom the most active were Prof. Dr. Aleksandar Damanski for bromatology, Prof. Dr. Momcilo Mokranjac for toxicology and Docent Dr. Pavle Trpinac for biochemistry. When the Managing Board of the Pharmaceutical Society of National Republic of Serbia held its session on 22 December 1950, an issue was raised with reference to creation of a Section that would gather together the laboratory experts. Section for Sanitary Chemistry, combining all three profiles of laboratory staff, i.e. medical biochemists, sanitary chemists and toxicologists, was founded on 1st of January 1951. On 15 May 1955, during the sixth plenum of the Society of Pharmaceutical Societies of Yugoslavia (SFRY) held in Split, the decision was passed to set up a Section for Medical Biochemistry in SFDJ. The Section for Medical Biochemistry in SFDJ was renamed into Society for Medical Biochemistry of SFDJ based on the decision passed during the 16th plenum of SFDJ, held on 15 May 1965 in Banja Luka. Pursuant to the decision passed by SMBY on 6 April 1995 and based on the historic data, 15 May was declared as being the official Day of the Society of Medical Biochemists of Yugoslavia. The purpose of YuSMB (currently SMBSCG) is to gather medical biochemists who would develop and enhance all the branches of medical biochemistry in health industry. Its tasks are as following: to standardize operations in clinical-biochemical laboratories, education of young biochemists on all levels, encouraging scientific research, setting up of working norms and implementation, execution and abiding by the ethics codices with health workers. SMBSCG is to promote the systemized standards in the field of medical biochemistry with the relevant federal and republican institutions. SMBSCG is to enable exchange of experiences of its members with the members of affiliate associations in the country and abroad. .
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Fartushok, Tetiana V., Nadiia V. Fartushok, Yu M. Fedevych, and Vladyslav V. Pyndus. "HISTORY OF BIOCHEMISTRY IN LVIV." Wiadomości Lekarskie 75, no. 4 (2022): 881–90. http://dx.doi.org/10.36740/wlek202204124.

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The aim: The purpose of this literature review is to shed light on the development of biochemical knowledge in the Lviv region and on prominent figures in the development of biochemistry during the Second World War. Materials and methods: Review of literature published before 2020. We searched the literature using the search terms ‘biochemists’, ‘ Lviv National Medical University’, ‘second World War’. Conclusions: The development of biological research in Lviv can be divided into two historical stages: 1) from the beginning of the founding of Lviv University in 1661 to the First World War; 2) between the First and Second World Wars and after the Second World War. Biochemical research was initiated at the Medical Faculty of Lviv University. In 1939, the Lviv State Medical Institute was established on the basis of the Medical Faculty of the University, where a powerful department of biochemistry functioned, which was headed by a worldclass biochemist – Jakub Parnas.
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Jia, Jun. "Teaching Reform and Practice Exploration of Medical Biochemistry Theory Course." Lifelong Education 9, no. 6 (September 28, 2020): 60. http://dx.doi.org/10.18282/le.v9i6.1298.

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Biochemists lack understanding of professional medical knowledge, and clinicians have very little understanding of biochemistry, which makes it difficult to teach medical biochemistry theory. However, with the rapid development of life sciences, the demand for high-quality medical personnel in today’s society has also become higher and higher. Therefore, it is necessary to link biochemistry with medicine, and at the same time learn from the teaching concepts of biochemistry, to explore several ways to improve the teaching quality of medical biochemistry theory courses.
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Milosevic Georgiev, Andrijana, Dušanka Krajnović, Jelena Manojlović, Svetlana Ignatović, and Nada Majkić Singh. "Seventy Years of Biochemical Subjects’ Development in Pharmacy Curricula: Experience from Serbia/ Sedamdeset godina razvoja biohemijskih predmeta u kurikulumu farmacije: iskustvo iz srbije." Journal of Medical Biochemistry 35, no. 1 (January 1, 2016): 69–79. http://dx.doi.org/10.1515/jomb-2015-0018.

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Summary Introduction: The pharmacists played an important role in the development of biochemistry as applied chemistry in Serbia. What is more, the first seven state chemists in Ser bia were pharmacists. State chemists performed the chemicaltoxicological analysis as well as some medical and biochemical ones. When it comes to the education of medical biochemists as health workers, the period after the beginning of the second half of the twentieth century should be taken into account because that is when the training of pharmaceutical staff of the Faculty of Pharmacy, University of Belgrade, begins on the territory of Serbia. This paper presents the development of medical biochemistry through the development of curriculum, personnel and literature since the foundation of the Faculty of Pharmacy in Serbia until today. Objective: The aim of this paper is to present the historical development of biochemistry at the Faculty of Pharmacy, University of Belgrade, through analysis of three indicators: undergraduate and postgraduate education of medical biochemists, teaching literature and professional associations and trade associations. Method: The method of direct data was applied in this paper. Also, desktop analysis was used for analyzing of secondary data, regulations, curricula, documents and bibliographic material. Desktop research was conducted and based on the following sources: Archives of the University of Belgrade- Faculty of Pharmacy, Museum of the History of Pharmacy at the University of Belgrade-Faculty of Pharmacy, the Society of Medical Biochemists of Serbia and the Serbian Chamber of Biochemists. Results and conclusion: The curricula, the Bologna process of improving education, the expansion of the range of subjects, the number of students, professional literature for teaching biochemistry, as well as professional associations and trade associations are presented through the results.
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Gürler, Mukaddes. "Postmortem biochemistry." Dicle Medical Journal 41, no. 4 (December 1, 2014): 773–80. http://dx.doi.org/10.5798/diclemedj.0921.2014.04.0519.

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Flesch, Juliet. "'A Biochemist of the Best Type': The Contribution of Arthur Cecil Hamel Rothera to Biochemistry in Australia." Historical Records of Australian Science 23, no. 2 (2012): 120. http://dx.doi.org/10.1071/hr12015.

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Biochemistry was an early concern of physiologists and agricultural scientists in the universities of Australia. Much more is known and recorded about such early biochemists as Osborne, Robertson and Young than about Arthur Rothera, whose contribution from 1906 to 1915 is the principal focus of this paper. Rothera was the first lecturer in biochemistry in Australia, the author of a number of significant papers and, through his ketone test, is still influential in diagnosis of diabetes today. At his death, he left biochemistry at Melbourne in new laboratories, and several students able to take his place.
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Quaresma, Abel Botelho, Armando José d'Acampora, Ricardo Tramonte, Débora Cadore de Farias, and Fabrícia Slomsky Joly. "Histological study of the liver and biochemistry of the blood of Wistar rats following ligature of right hepatic duct." Acta Cirurgica Brasileira 22, no. 1 (February 2007): 68–78. http://dx.doi.org/10.1590/s0102-86502007000100013.

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PURPOSE: To observe the histological alterations in the liver and biochemistry in the blood that can happen in Wistar rat, after the ligature of right hepatic duct. METHODS: In this study were used rats (n=46) of Wistar pedigree. The animal groups (n=46) were distributed in 6 experimented sub-groups (n=6). It was held a ligature surgery of the right hepatic duct and euthanasia in 7, 14, 21, 28, 60 and 90 days and the biochemistry control group (n=10), that animals had 2ml of their blood taken by cardiac puncture for biochemistry study with value analyses of bilirubins, transaminasis, lactic desidrogenasis, alkaline phophatase and gamma-glutamil-transferase. Given the expected time of each group, the animals were submitted to anesthesia procedure and cavity re-opening, being held intra-cardiac puncture and with 2ml blood collected for biochemistry analyses. It was proceeded the liver resection, being the liver putted in formol solution to 10% for a period of 24 hours and taken to the histology. RESULTS: It was not possible to identify results that express significant differences as the existence of alterations histological and biochemistrily between the different groups. CONCLUSION: At the end of the study, it was not possible to identify histological and biochemistrily alterations that express significant differences between livers of the animals from the right linked hepatic duct and the animals of the control group.
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Hunter, Tony. "My biochemical journey from a Cambridge undergraduate to the discovery of phosphotyrosine." Biochemist 43, no. 6 (December 23, 2021): 74–77. http://dx.doi.org/10.1042/bio_2021_197.

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The most notable moment in my career as a biochemist was the discovery of phosphotyrosine, a somewhat serendipitous finding that turned out to have some very important consequences, notably, in human cancer. My career as a biochemist which has spanned nearly 60 years, began when I was 16. At the time, I was in the sixth form at Felsted School, a boarding school in Essex England, and my biology master, David Sturdy, elected to teach me some extracurricular biochemistry, giving me one-on-one tutorials on glycolysis and the TCA cycle. These early biochemistry lessons turned out to be invaluable because I was able to regurgitate them to answer a question in the University of Cambridge scholarship exam in the autumn of 1960. As a result, I was lucky enough to be awarded an Exhibition at Gonville and Caius College, the college where my father had studied for a medical degree during World War II. When I arrived in Cambridge in October 1962 to read natural sciences (see Figure 1), it was a natural choice to take biochemistry as one of my three required first-year courses. The Part I biochemistry course was taught by a series of excellent lecturers, including Philip Randle (a prominent diabetes researcher who described the Randle Cycle), Brian Chappell (who discovered mitochondrial transporters) and Asher Korner (a pioneer of cell free systems to study protein synthesis). It quickly became clear that biochemistry was an exciting subject, and Brian Chappell, my biochemistry supervisor at Caius, made supervisions a lot of fun. I also took Part I courses in invertebrate zoology and, importantly, organic chemistry, which gave me insights into how the metabolites we were learning about in biochemistry worked as chemicals.
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Dissertations / Theses on the topic "Biochemistry"

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Suttisansanee, Uthaiwan. "Biochemistry in Bacterioferritin." Thesis, University of Waterloo, 2006. http://hdl.handle.net/10012/2983.

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Bacterioferritin, an iron storage protein having a 24-subunit quaternary structure, was used as a model for the study of host-guest interactions and guest encapsulation, making use of its spherical cage-like structure. A hexahistidine-affinity tag fused to the C-terminus of each bacterioferritin subunit was constructed. The C-terminus of each subunit points toward the inside of the cavity, while the N-terminus is exposed on the surface of the protein. The hexaHistag was able to form strong interactions with a nickel-nitrilotriacetic acid linked dye molecule (guest) and this interaction was used in attempts to develop a principle to control guest molecule encapsulation within the spherical cavity of the 24-mer bacterioferritin protein molecule. The procedure involved (1) subunit dissociation under acidic pH, (2) affinity controlled dye-Histag binding with exposed C-terminal hexahistidine residues and (3) reassociation of the subunits at neutral pH. The encapsulation conditions involving step 1 and 3 were studied preliminarily using laser light scattering to measure size (hydrodynamic radius) of the protein particle with apoferritin as a model system as it resembles the size and structure of bacterioferritin. In order to encapsulate guest molecules, the emptied shell of bacterioferritin was generated by site-directed mutagenesis resulting in ferroxidase- as well as heme-free bacterioferritin mutants (E18A/M52L/E94A), and these mutants were used to examine protein stability before conducting encapsulation experiments. However, wild-type bacterioferritin possessed highest stability in maintaining its multisubunit structure; hence, it was used for the encapsulation studies. It was found that 100% bacterioferritin with hexahistidine tag at the C-terminus, and a combination of 60% bacterioferritin with hexahistidine tag at the C-terminus and 40% bacterioferritin without hexahistidine tag at the C-terminus yielded similar amounts of encapsulated guest molecules. This suggested that all hexahistidine at the C-terminus were not equally available for dye molecule binding.
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Hoh, Hon Bing. "Biochemistry of keratoconus." Thesis, University of Bristol, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266879.

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Chen, Xiaoren. "Biochemistry of Prox1 function /." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 160 p, 2007. http://proquest.umi.com/pqdweb?did=1456284231&sid=8&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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Rix, Louise Katharine. "Biochemistry of heart disease." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334889.

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Chapman, A. "Biochemistry of Trichomonas vaginalis." Thesis, Bucks New University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373578.

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Lawrence, Fiona Jane. "The biochemistry of keratoconus." Thesis, University of Bristol, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268784.

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Beacham, Tracey. "Biochemistry of transgenic wheats." Thesis, Cardiff University, 2006. http://orca.cf.ac.uk/55160/.

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This investigation uses transgenic wheat lines carrying the Pisum sativum glycerol 3-phosphate acyl transferase gene and /or the Arabidopsis thaliana acyl ACP thioesterase gene to determine their role of these genes in producing the altered metabolic and physiological traits seen in wild type plants grown under enhanced greenhouse conditions. We identified and analysed lines with insertions of the lipid metabolism genes. Plant lines bombarded with the same transgenes, showed a huge diversity in genotypes and demonstrated the haphazard nature of particle bombardment. Gene stability was observed following crossing of genetically modified lines and in all instances the transgenic material was found to be active in fourth generation plants. None of the transgenic lines showed the phenotype expected (increased growth and yield), but all showed aspects. This could indicate that more than these two genes are affected by the enhanced greenhouse effect, or that neither gene is in fact involved and the phenotypes observed are merely a happy coincidence. It is also possible that the full effect of gene up-regulation was not observed since only one of the lines observed showed ubiquitous expression of the transgenes and all showed some changes in expression of the native thioesterase gene. The lipid metabolism of plants from the four genetic groups (GPAT +, thioesterase+, Dual+ and Null) was analysed and, while alterations in lipid and fatty acid metabolism were observed in all transgenic lines, the differences were highly variable between plant lines of the same group, making an overall analysis of changes difficult. It was also found that the null lines showed as much variation in lipid metabolism as the transgenic lines indicating that chromosomal damage introduced into the plant lines during the original bombardment and tissue culturing process may have had a huge impact on the phenotype of the transgenic plants.
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Huang, Po-Ssu Rees Douglas C. "Biochemistry and molecular biophysics /." Diss., Pasadena, Calif. : California Institute of Technology, 2004. http://resolver.caltech.edu/CaltechETD:etd-06012004-214823.

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Woodhouse, Jennifer Ann. "Plutonium pharmacokinetics and blood biochemistry." Thesis, University of Central Lancashire, 1997. http://clok.uclan.ac.uk/20148/.

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Since its discovery in the early 1940s the element plutonium has been seen by mankind as both an opportunity and a threat. As a radioactive nuclide plutonium presents health hazards in its handling and if mankind is to make the most of this element's potential benefits it is essential that these hazards be understood. Both overestimation and underestimation of these hazards are damaging to its proper utilisation. Many studies have been carried out to determine the effects of plutonium exposure and a broad picture of the biological behaviour of plutonium has been built up. Radiological protection standards are based on such broad understanding and a "Central Dogma" has arisen viz, plutonium is bound avidly in liver and bone; clearance half-lives from these organs differ (by a factor of 2.5) but are very long - a minimum of 50 years for bone; this is why plutonium urinary excretion levels are very low. Despite all the research work that has been carried out there are many important areas of plutonium behaviour which are not well understood or in which the central ideas adopted for radiological protection purposes are questionable. One such questionable area is extended half-life in the body. Two rather different areas relate to the molecular binding interactions which plutonium enters into in body tissues and transfer mechanisms from blood into cellular organelles. Very little is known about these processes and the speciation that plutonium demonstrates within the body. This thesis explores understanding of plutonium behaviour by application of pharmacokinetic theory to observed human behaviour, both following occupational exposure and experimental injection. Occupational exposure data demonstrated behaviour consistent with pharmacokinetic expectations over periods of 25 years or more. Long-term half-lives were 10 to 30 years rather than 50 to 100 years or more. There was no evidence of differing half-lives between liver and bone. Very low renal clearance was seen in intravenous injection studies suggesting either very extensive plutonium binding to the protein transferrin in blood or pointing to reabsorption in the kidney tubule after glomerular filtration. This latter possibility might lead to a "Plutonium blood pressure" which effectively forces activity into tissues irrespective of the strength of binding forces. Experimental work indicated species differences in transferrin binding which may have relevance for extrapolation from animals to humans.
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Nasir-ud-Din. "Glycoconjugate biochemistry : structure-function relationship." Thesis, University of Edinburgh, 1996. http://hdl.handle.net/1842/27105.

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In this thesis studies on the following glycoconjugates are presented: bacterial, Micrococcus lysodeikticus, cell wall, simian cervical mucin, human pulmonary mucin, bovine gallbladder mucin, sperm surface glycoproteins and glycoconjugates of malarial parasite, Plasmodium falciparum. The information obtained on the structure of these complex carbohydrates utilising chemical, enzymatic, immunological and physical methods provided insight into the understanding, in particular, of structure-function relationship, degradation and biosynthesis of these macromolecules. Studies on model compounds and analytical methods, all of which are vitally important tools in the study of glycoconjugates, are also described. The carbohydrate prosthetic group of Micrococcus lysodeikticus cell wall was shown to consist of a glycan moiety linked to the protein and an antigenic polysaccharide attached to the glycan moiety of the peptidoglycan through a phosphodiester group. A variety of model compounds were synthesised to establish the structure of the carbohydrate moiety as well as to study the kinetics if the acid hydrolysis of the phosphodiester group linked to muramic acid and to the reducing terminus of glucose. The study was performed on Micrococcus lysodeikticus cell wall polymer resistant to lysozyme, elaborating the structural requirement for stability to the enzyme. Furthermore, a water soluble polymer from the Micrococcus lysodeikticus cell wall was isolated and characterised, a novel observation. The study on this polymer suggested the possible deficiencies in the biosynthesis or possible autolysis of the cell wall polymer. A large number of model compounds were chemically synthesised to identify the structural features of the cell wall peptidoglycans and those of the antigenic polysaccharide. In addition, several compounds were chemically synthesised to obtain the model compounds necessary to conduct kinetic studies to define the type of linkage, i.e. differentiate between the monophosphate or pyrophosphate, between the cell wall polysaccharide and peptidoglycan, more precisely the linkage between muramic acid 6-phosphate of the peptidoglycan and the reducing terminal residue, glucose, of the polysaccharide.
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Books on the topic "Biochemistry"

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Carr, Martin. Biochemistry. Walton-on-Thames: Nelson, 1992.

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Rawn, J. David. Biochemistry. Burlington, N.C: Neil Patterson Publishers, 1989.

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Stenesh, J. Biochemistry. New York: Plenum Press, 1998.

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Briggs, Thomas, and Albert M. Chandler, eds. Biochemistry. New York, NY: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-0294-0.

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Briggs, Thomas, and Albert M. Chandler, eds. Biochemistry. New York, NY: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4684-0437-1.

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Stenesh, J. Biochemistry. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4757-9427-4.

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Briggs, Thomas, and Albert M. Chandler, eds. Biochemistry. New York, NY: Springer New York, 1995. http://dx.doi.org/10.1007/978-1-4612-4200-0.

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Roskoski, Robert. Biochemistry. Philadelphia: Saunders, 1996.

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Stenesh, J. Biochemistry. New York: Plenum, 1998.

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Davidson, Victor L. Biochemistry. 3rd ed. Philadelphia: Harwal Pub., 1994.

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Book chapters on the topic "Biochemistry"

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Kaul, Mohan L. H. "Biochemistry." In Male Sterility in Higher Plants, 221–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-83139-3_5.

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Jones, G. L., and D. M. Woodbury. "Biochemistry." In Antiepileptic Drugs, 245–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-69518-6_10.

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Kobayashi, Tohru, and Ken Takai. "Biochemistry." In Extremophiles Handbook, 1083–97. Tokyo: Springer Japan, 2011. http://dx.doi.org/10.1007/978-4-431-53898-1_51.

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Gooch, Jan W. "Biochemistry." In Encyclopedic Dictionary of Polymers, 878. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13254.

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Abdel, Ahmad Wagih. "Biochemistry." In Passing the USMLE, 1–24. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-68980-7_11.

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Palmiere, Cristian. "Biochemistry." In Asphyxiation, Suffocation,and Neck Pressure Deaths, 140–47. Boca Raton : CRC Press, [2020]: CRC Press, 2020. http://dx.doi.org/10.1201/9780429188947-16.

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McGhee, Michael F., Caroline A. Saxelby, and Niall McKay. "Biochemistry." In A Guide to Laboratory Investigations, 68–105. 7th ed. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003049685-5.

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Bandyopadhyay, P. K., N. R. Das, and Amit Chattopadhyay. "Biochemistry." In Biochemical, Immunological and Epidemiological Analysis of Parasitic Diseases, 245–61. Singapore: Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-4384-2_6.

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Williams, Michael J. "Biochemistry." In Preventing and Countering Violent Extremism, 38–41. Abingdon, Oxon; New York, NY: Routledge, 2021. | Series: Political violence: Routledge, 2020. http://dx.doi.org/10.4324/9780429441738-8.

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Rubin, Alan E. "Biochemistry." In Surface/Volume, 117–23. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-23749-2_6.

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Conference papers on the topic "Biochemistry"

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Stavrou, Anastasios, Karin Garrie, and David Hindley. "DECOLONISING BIOCHEMISTRY." In 15th International Conference on Education and New Learning Technologies. IATED, 2023. http://dx.doi.org/10.21125/edulearn.2023.1259.

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McKendry, R. "Mechano-biochemistry." In IEE Seminar and Exhibition on MEMS Sensor Technologies. IEE, 2005. http://dx.doi.org/10.1049/ic:20050121.

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"Bioinformatics and Biochemistry." In 2022 International Joint Conference on Neural Networks (IJCNN). IEEE, 2022. http://dx.doi.org/10.1109/ijcnn55064.2022.9892922.

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"Standardizing Biochemistry Dataset for Medical Research." In International Conference on Health Informatics. SCITEPRESS - Science and and Technology Publications, 2014. http://dx.doi.org/10.5220/0004745802050210.

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Ge, Shuna, and Yunrong Zhang. "PBL Teaching Method in Biochemistry Teaching." In CIPAE 2021: 2021 2nd International Conference on Computers, Information Processing and Advanced Education. New York, NY, USA: ACM, 2021. http://dx.doi.org/10.1145/3456887.3456928.

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Ismail, Noor Akmal Shareela, Khaizurin Tajul Arifin, Ekram Alias, Jen Kit Tan, Mohd Hanafi Ahmad Damanhuri, Norwahidah Abdul Karim, Jo Aan Goon, Zakiah Jubri Mohd Zubri, Suzana Makpol, and Yasmin Anum Mohd Yusof. "LEARNING MEDICAL BIOCHEMISTRY THROUGH INTERACTIVE LEARNING." In 10th International Conference on Education and New Learning Technologies. IATED, 2018. http://dx.doi.org/10.21125/edulearn.2018.0966.

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Alvarez Cubero, Maria Jesus, Maria Angel Garcia Chaves, Maria Isabel Rodríguez, Pilar Sánchez, Victoria Sánchez-Martín, Marta Cuadros, and Luis Javier Martinez Gonzalez. "MOTIVATING LEARNING BIOCHEMISTRY IN BIOMEDICAL DEGREES." In 15th International Technology, Education and Development Conference. IATED, 2021. http://dx.doi.org/10.21125/inted.2021.0446.

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Pereira, Jose A. "A biochemistry-inspired artificial chemistry: LAC." In 2005 Purtuguese Conference on Artificial Intelligence. IEEE, 2005. http://dx.doi.org/10.1109/epia.2005.341269.

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Navarro Llorens, Juana Maria, Ana Saborido Modia, Miguel Arroyo Sánchez, Mar Lorente Pérez, Regina Ranz Valdecasa, Teresa López Conejo, Jose Luis Nieto Bueno, et al. "NEW CHALLENGES IN THE BIOCHEMISTRY LABORATORY: CONNECTING SECOND-YEAR STUDENTS OF BIOCHEMISTRY DEGREE TO LABORATORY PRACTICE." In 12th International Technology, Education and Development Conference. IATED, 2018. http://dx.doi.org/10.21125/inted.2018.2192.

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Gorlov, D., Nikolai Jujukin, I. Kuznetsov, and E. Litvinov. "PROSPECTS FOR USING THE ANALYTICAL CAPABILITIES OF CLINICAL CHEMISTRY IN SPORTS BIOCHEMISTRY." In SCIENCE AND INNOVATION IN THE MODERN WORLD. FSBE Institution of Higher Education Voronezh State University of Forestry and Technologies named after G.F. Morozov, 2024. http://dx.doi.org/10.58168/simw2024_59-66.

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Abstract:
The topic related to the use of the analytical capabilities of clinical chemistry in sports biochemistry is quite relevant, in that thanks to it, training has been optimized, and research has also helped improve monitoring of the health of athletes, which is very important in our time. This scientific article is devoted to the study of the physical and chemical principles of the analysis of human biological fluids, which can significantly expand the methodological arsenal of sports biochemistry and sports pharmacology. The work contains a review of the literature of sports biochemistry and clinical biochemistry, examples, as well as new opportunities in the study of organ proteins and muscle tissue proteins. Study results show optimization of training, diagnosis of athletes' condition and prevention of health problems.
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Reports on the topic "Biochemistry"

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Blake, II, R. Biochemistry of Dissimilatory Sulfur Oxidation. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/836587.

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Blake, R. II. Biochemistry of dissimilatory sulfur oxidation. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6599983.

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Alan Hooper. Biochemistry of Ammonia Monoxygenase from Nitrosomonas. Office of Scientific and Technical Information (OSTI), July 2009. http://dx.doi.org/10.2172/958735.

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Nolan, Linda L. Biochemistry and Chemotherapy of Malaria and Leishmaniasis. Fort Belvoir, VA: Defense Technical Information Center, December 1993. http://dx.doi.org/10.21236/ada284195.

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Sharkey, Thomas D. Maltose Biochemistry and Transport in Plant Leaves. Office of Scientific and Technical Information (OSTI), January 2010. http://dx.doi.org/10.2172/971070.

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Whitman, William B. Biochemistry and genetics of autotrophy in Methanococcus. Office of Scientific and Technical Information (OSTI), March 2009. http://dx.doi.org/10.2172/950490.

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Cumberledge, Susan. Biochemistry and Molecular Mechanisms of Wingless Action. Fort Belvoir, VA: Defense Technical Information Center, September 1995. http://dx.doi.org/10.21236/ada305797.

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Weber, Andreas P. M. Maltose Biochemistry and Transport in Plant Leaves. Office of Scientific and Technical Information (OSTI), April 2008. http://dx.doi.org/10.2172/928757.

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Sharkey, Thomas D. Maltose Biochemistry and Transport in Plant Leaves. Office of Scientific and Technical Information (OSTI), May 2012. http://dx.doi.org/10.2172/1039496.

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Whitman, W. B. Biochemistry and genetics of autotrophy in Methanococcus. Progress report. Office of Scientific and Technical Information (OSTI), September 1998. http://dx.doi.org/10.2172/663534.

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