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Книги з теми "Biological Active Molecules"

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Автор: Grafiati
Опубліковано: 10 грудня 2022
Оновлено: 29 січня 2023

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1

Schlunegger, Urs Peter, ed. Biologically Active Molecules. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74582-9.

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2

Mahapatra, Debarshi Kar, and Sanjay Kumar Bharti. Biologically Active Small Molecules. New York: Apple Academic Press, 2022. http://dx.doi.org/10.1201/9781003283119.

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3

Brenna, Elisabetta, ed. Synthetic Methods for Biologically Active Molecules. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527665785.

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4

Hiroyasu, Aizawa, ed. Metabolic maps: Pesticides, environmentally relevant molecules, and biologically active molecules. San Diego, Calif: Academic Press, 2001.

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5

Necib, Y. Biochemical evaluation of lectins and other biologically active molecules. Salford: University of Salford, 1987.

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6

Ion-exchange sorption and preparative chromatography of biologically active molecules. New York: Consultants Bureau, 1986.

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7

Samsonov, G. V. Ion-Exchange Sorption and Preparative Chromatography of Biologically Active Molecules. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-8908-8.

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8

NATO Advanced Research Workshop on Molecular and Cellular Mechanisms of H [plus] transport (1993 York, England). Molecular and cellular mechanisms of H [plus] transport. Berlin: Springer-Verlag, 1994.

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9

P, Schlunegger Urs, and Schweizerischer Chemiker-Verband, eds. Biologically active molecules: Identification, characterization, and synthesis : proceedings of a Seminar on Chemistry on Biologically Active Compounds and Modern Analytical Methods, Interlaken, September 5-7, 1988. Berlin: Springer-Verlag, 1989.

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10

International, Symposium on Molecular Basis of Biomembrane Transport (1988 Bari Italy). Molecular basis of biomembrane transport: Proceedings of the International Symposium on Molecular Basis of Biomembrane Transport, Bari, Italy, 30 May-2 June 1988. Amsterdam: Elsevier, 1988.

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11

Wood, Chris M., and T. J. Shuttleworth. Cellular and molecular approaches to fish ionic regulation. San Diego: Academic Press, 1995.

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12

Andre, Herchuelz, and New York Academy of Sciences, eds. Sodium-calcium exchange and the plasma membrane Ca2+-ATPase in cell function: Fifth international conference. Boston, Mass: Blackwell Pub. on behalf of the New York Academy of Sciences, 2007.

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13

International Symposium on Molecular and Cellular Biology of Insulin and IGFs (3rd 1990 Gainesville, Fla.). Molecular biology and physiology of insulin and insulin-like growth factors. New York: Plenum Press, 1991.

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14

E, Vance Dennis, and Vance Jean E, eds. Biochemistry of lipids, lipoproteins, and membranes. Amsterdam: Elsevier, 1991.

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15

Marino, Ana. Dynamic modification of graphite surfaces with surfactants for electrochemical detection of biological molecules. 1994.

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16

(Editor), J. K. Broome-Smith, S. Baumberg (Editor), C. J. Stirling (Editor), and F. B. Ward (Editor), eds. Transport of Molecules across Microbial Membranes (Society for General Microbiology Symposia). Cambridge University Press, 1999.

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17

Schlunegger, Urs Peter. Biologically Active Molecules. Springer, 2011.

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18

Aizawa, Hiroyasu. Metabolic Maps: Pesticides, Environmentally Relevant Molecules and Biologically Active Molecules. Elsevier Science & Technology Books, 2001.

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19

Kováčik, Anton, and Eva Tvrdá, eds. Research in Animal Physiology: Proceedings of scientific papers. Slovak University of Agriculture in Nitra, Slovakia, 2020. http://dx.doi.org/10.15414/2020.9788055222349.

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Анотація:
Proceedings of scientific papers ranges across a breadth of research in animal physiology. The main chapters of this publication are “Animal Physiology - Health Status Observations; Biologically Active Compounds in Animal Physiology; Animal Toxicology”. Animal physiology is the scientific study of the life-supporting properties, functions and processes of animals or their parts. It focuses on how organisms, organ systems, organs, cells, and bio-molecules carry out the chemical or physical functions that exist in a living system. Therefore, the proper studying of animal physiology is crucial for understanding and evaluating underlying biological processes, behavioral states and animal response to different biological, social and environmental stimuli. As such, the principal aim of this proceedings of scientific papers was to gather original papers on research in the fields of animal physiology, animal nutrition, reproduction and toxicopathology. We hope the publication will serve as a forum for presenting contemporary knowledge on basic and applied research, thus making new findings, methods, and techniques easily accessible and applicable in practice.
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20

Mahapatra, Debarshi Kar, and Sanjay Kumar Bharti. Biologically Active Small Molecules: Modern Applications and Therapeutic Perspectives. Apple Academic Press, Incorporated, 2023.

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21

Mahapatra, Debarshi Kar, and Sanjay Kumar Bharti. Biologically Active Small Molecules: Modern Applications and Therapeutic Perspectives. Apple Academic Press, Incorporated, 2023.

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22

Mahapatra, Debarshi Kar, and Sanjay Kumar Bharti. Biologically Active Small Molecules: Modern Applications and Therapeutic Perspectives. Apple Academic Press, Incorporated, 2023.

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23

Mahapatra, Debarshi Kar, and Sanjay Kumar Bharti. Biologically Active Small Molecules: Modern Applications and Therapeutic Perspectives. Apple Academic Press, Incorporated, 2023.

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24

Schlunegger, Urs Peter. Biologically Active Molecules: Identification, Characterization and Synthesis : Proceedings of a Seminar on Chemistry of Biologically Active Compound. Springer, 1989.

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25

Samsonov, G. V. Ion-Exchange Sorption and Preparative Chromatography of Biologically Active Molecules. Springer London, Limited, 2012.

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26

Samsonov, G. V. Ion-Exchange Sorption and Preparative Chromatography of Biologically Active Molecules. Springer, 2012.

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27

Brenna, Elisabetta. Synthetic Methods for Biologically Active Molecules: Exploring the Potential of Bioreductions. Wiley & Sons, Limited, John, 2013.

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28

Brenna, Elisabetta. Synthetic Methods for Biologically Active Molecules: Exploring the Potential of Bioreductions. Wiley & Sons, Incorporated, John, 2013.

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29

Brenna, Elisabetta. Synthetic Methods for Biologically Active Molecules: Exploring the Potential of Bioreductions. Wiley & Sons, Incorporated, John, 2013.

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30

Brenna, Elisabetta. Synthetic Methods for Biologically Active Molecules: Exploring the Potential of Bioreductions. Wiley & Sons, Incorporated, John, 2013.

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31

Synthetic Methods For Biologically Active Molecules Exploring The Potential Of Bioreductions. Wiley-VCH Verlag GmbH, 2013.

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32

Chow, Freeman Tsz-fung. LATCA: A library of biologically active small molecules for plant chemical genomics. 2007.

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33

Hanahan, Donald J. A Guide to Phospholipid Chemistry. Oxford University Press, 1997. http://dx.doi.org/10.1093/oso/9780195079814.001.0001.

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Анотація:
This book provides a concise introduction to phospholipid chemistry and is intended for a broad audience of biologists, biochemists, and graduate students. Developed as part of a graduate course on lipids, this book also serves as a reference for laboratory investigators on signal transduction and biological membranes. The first part of the text is devoted to an orientation to the chemical nature of lipids in general, how they are thought to be associated in the cell, and the methodology by which the cellular lipids (including the phospholipids) can be recovered from cells and subjected to an initial identification. Subsequent chapters characterize the choline-containing phospholipids, including the sphingolipids, the non-choline containing phospholipids, and finally, the so-called minor phospholipids. The latter compounds, which act as agonists or lipid chemical mediators on cells, form a vanguard of a new category of biologically active substances and have set the study of cellular phospholipids on a new and exiting course. Most importantly, this book provides a basis for further inquiry on these complicated molecules, showing that although the compounds are unique, with care and understanding, they can be studied with ease
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34

1941-, Coxon J. M., ed. Mechanisms of biological importance. Greenwich, Conn: JAI Press, 1992.

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35

Biologically Active Molecules: Identification, Characterization and Synthesis Proceedings of a Seminar on Chemistry of Biologically Active Compounds ... Methods, Interlaken, September 5-7, 1988. Springer, 2011.

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36

Molecular and cellular mechanisms of H⁺ transport. Berlin: Springer-Verlag, 1994.

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37

Schlunegger, Urs P. Biologically Active Molecules: Identification, Characterization and Synthesis Proceedings of a Seminar on Chemistry of Biologically Active Compounds and Modern Analytical Methods, Interlaken, September 5-7 1988. Springer London, Limited, 2012.

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38

Kumar Sharma, Mukesh, and Pallavi Kaushik, eds. Therapeutic Implications of Natural Bioactive Compounds. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150800251220301.

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Анотація:
This volume is a comprehensive compilation of contributions on the state of art knowledge about bioactive compounds including their sources, isolation methods, biological effects, health benefits and potential applications. These bioactive compounds could serve as alternatives in the prevention or treatment of multifactorial diseases for vulnerable population groups. Chapters in the book incorporate the knowledge based on traditional medicine with recent findings on bioactive molecules and their pharmaceutical implications in neurodegenerative diseases, cancer, COVID 19, diabetes, immunomodulation and farm animal diseases. The book also highlights the latest breakthroughs in the field of screening, characterization, and novel applications of natural bioactive compounds from diverse group of organisms ranging from bacteria, algae, fungi, higher plants, and marine sources. Authors from renowned institutions of India, Japan and China have shared their expertise in the contributed chapters with the goal of enhancing readers knowledge about the significance of use of bioactives in therapeutics and nutraceuticals. It is an informative reference for researchers, professors, graduate students, science enthusiasts, and all those who wish to gain insights into various aspects of bioactive compounds and development of new pharmacological active constituents and nutritional science.
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39

Henri, Tiedge, Bloom Floyd E, Richter Dietmar M, and National Academy of Sciences Colloquium on Molecular Kinesis in Cellular Function and Plasticity (2000 : Arnold and Mabel Beckman Center), eds. Colloquium on molecular kinesis in cellular function and plasticity. Washington, D.C: National Academy of Sciences, 2002.

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40

Nelson, Nathan. Organellar Proton-ATPases. Springer, 2013.

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41

Nelson, Nathan. Organellar Proton-ATPases. Springer, 2013.

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42

Advances in Detailed Reaction Mechanisms: Mechanisms of Biological Importance : 1992 (Advances in Detailed Reaction Mechanisms). JAI Press, 1993.

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43

Acri, Jane B., and Phil Skolnick. Novel Approaches for Treating Addiction. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0048.

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Анотація:
Despite remarkable progress in our understanding of the neurobiological bases of drug abuse, no novel pharmacotherapies have recently been approved to treat substance use disorders (SUDs). Thus, while reformulations of established treatments have either been approved or are currently in late stage development (e.g., sustained release formulations of naltrexone (Vivitrol®) and buprenorphine), the development of medications to treat SUDs has lagged well behind other areas of psychiatry. In this chapter, we review some of the factors that have contributed to this dearth of innovative pharmacotherapies. We also review evidence that supports clinical testing of late stage molecules (developed for other indications) acting at promising targets, as well as novel biological approaches to the treatment of SUDs.
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44

(Editor), Jonathan Lytton, Paul P. M. Schnetkamp (Editor), Larry V. Hryshko (Editor), and M. P. Blaustein (Editor), eds. Cellular and Molecular Physiology of Sodium-Calcium Exchange: Proceedings of the Fourth International Conference (Annals of the New York Academy of Sciences). New York Academy of Sciences, 2002.

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45

Cellular and Molecular Physiology of Sodium-Calcium Exchange: Proceedings of the Fourth International Conference (Annals of the New York Academy of Sciences, V. 976). New York Academy of Sciences, 2002.

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46

Lee, Gregory. Epitope/Peptide-Based Monoclonal Antibodies for Immunotherapy of Ovarian Cancer. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190248208.003.0007.

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Анотація:
Two monoclonal antibodies, RP215 and GHR106, were selected, respectively, for the research and development of anti-cancer drugs targeting ovarian cancer and other types of human cancer. RP215 was shown to react with a carbohydrate-associated epitope located mainly in the variable regions of immunoglobulin heavy chains expressed on the surface of almost all cancer cells in humans. GHR106 was generated against a synthetic peptide corresponding to N1-29 amino acid residues in the extracellular domains of human GnRH receptor, which is surface-expressed by most cancer cells as well as the anterior pituitary. This monoclonal antibody was shown to serve as a bioequivalent analog to GnRH-derived decapeptides currently used clinically. The molecular mechanisms of action of these two antibody-based anti-cancer drug candidates were well elucidated following numerous biochemical, immunological, and molecular biological studies, mainly by using ovarian cancer as the model. Further preclinical studies with humanized forms of these two antibodies are essential.
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47

Innominato, Pasquale F., and David Spiegel. Circadian rhythms, sleep, and anti-cancer treatments. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198778240.003.0016.

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The circadian timing system temporally regulates biological functions relevant for psycho-physical wellbeing, spanning all the systems related to health. Hence, disruption of circadian rhythms, along with sleep cycles, is associated with the development of several diseases, including cancer. Moreover, altered circadian and sleep functions negatively impact on cancer patients’ quality of life and survival, above and beyond known determinants of outcome. This alteration can occur as a consequence of cancer, but also of anti-cancer treatments. Indeed, circadian rhythms govern also the ability of detoxifying chemotherapy agents across the 24 hours. Hence, adapting chemotherapy delivery to the molecular oscillations in relevant drug pathways can decrease toxicity to healthy cells, while increasing the number of cancer cells killing. This chronomodulated chemotherapy approach, together with the maintenance of proper circadian function throughtout the whole disease challenge, would finally result in safer and more active anticancer treatments, and in patients experiencing better quality and quantity of life.
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48

Hann, Fred E. Proceedings of the Research Symposium on Complexes of Biologically Active Substances With Nucleic Acids and Their Modes of Action: Held at the Walter ... in Molecular and Subcellular Biology ). Springer, 2012.

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49

Nuclear Import and Export in Plants and Animals (Molecular Biology Intelligence Unit). Springer, 2005.

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50

(Editor), David S. Lester, William SlikkerJr (Editor), and Philip Lazarovici (Editor), eds. Site-Selective Neurotoxicity (Cell and Molecular Mechanisms of Toxinaction, 3). CRC, 2002.

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