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Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 22 lutego 2023

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1

Graba, Yacine. Hox genes: Methods and protocols. New York: Humana Press, 2014.

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How proteins work. New York: Garland Science, 2012.

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1946-, Liepa George U., red. Dietary proteins: How they alleviate disease and promote better health. Champaign, Ill: American Oil Chemistsʼ Society, 1992.

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Allen, John F. How does protein phosphorylation regulate photosynthesis?. Amsterdam: Elsevier, 1992.

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Gelderloos, Peter. How nonviolence protects the state. Cambridge, Mass: South End Press, 2007.

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Gelderloos, Peter. How nonviolence protects the state. Harrisonburg, VA: Signalfire Press, 2005.

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Gelderloos, Peter. How nonviolence protects the state. Cambridge, MA: South End Press, 2006.

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Susanne, Brakmann, i Johnsson Kai, red. Directed molecular evolution of proteins: Or how to improve enzymes for biocatalysis. Weinheim: Wiley-VCH, 2002.

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Ezrin, Calvin. The endocrine control diet: How to beat the metabolic trap and lose weight permanently. New York: Harper & Row, 1990.

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Church discipline: How the church protects the name of Jesus. Wheaton, Ill: Crossway, 2012.

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United States. Animal and Plant Health Inspection Service. Veterinary Services. The Animal Welfare Act: How it protects your dog and cat. --. [Washington, D.C.?]: U.S. Dept. of Agriculture, Animal and Plant Health Inspection Service, Veterinary Services, 1986.

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How to lower your property taxes. New York: Simon & Schuster, 1991.

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Johnson, Rick. That's my girl: How a father's love protects and empowers his daughter. Grand Rapids, MI: Revell, 2012.

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England), Stock Exchange (London. Fair trade: How the Stock Exchange regulates its markets and protects investors. London: StockExchange, 1985.

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Smith-Llera, Danielle. Lunch counter sit-ins: How photographs helped foster peaceful civil rights protests. North Mankato, Minnesota]: Compass Point Books, 2019.

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Fundación Estudios de Derecho Administrativo. Contencioso tributario hoy: Jornadas internacionales. Caracas: Fundación Estudios de Derecho Administrativo, 2004.

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17

Rezsohazy, René, i Yacine Graba. Hox Genes: Methods and Protocols. Springer New York, 2016.

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18

Frederic M. Richards (Series Editor), David S. Eisenberg (Series Editor) i Peter S. Kim (Series Editor), red. Advances in Protein Chemistry: Volume 48: Enzymes and Proteins from Hyperthermophilic Microorganisms (Advances in Protein Chemistry). Academic Press, 1996.

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19

Divan, Aysha, i Janice A. Royds. 4. Proteins. Oxford University Press, 2016. http://dx.doi.org/10.1093/actrade/9780198723882.003.0004.

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Biological functions require protein and the protein makeup of a cell determines its behaviour and identity. Proteins, therefore, are the most abundant molecules in the body except for water. The approximately 20,000 protein coding genes in the human genome can, by alternative splicing, multiple translation starts, and post-translational modifications, produce over 1,000,000 different proteins, collectively called ‘the proteome’. It is the size of the proteome and not the genome that defines the complexity of an organism. ‘Proteins’ describes the composition and structure of proteins and how they are studied. What information is required in order to understand how proteins work and what happens when this function is impaired in disease?
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20

Bagni, Claudia, i Eric Klann. Molecular Functions of the Mammalian Fragile X Mental Retardation Protein: Insights Into Mental Retardation and Synaptic Plasticity. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199744312.003.0008.

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Chapter 8 discusses how Fragile X syndrome (FXS) is caused by the absence of the RNA-binding protein fragile X mental retardation protein (FMRP). FMRP is highly expressed in the brain and gonads, the two organs mainly affected in patients with the syndrome. Functionally, FMRP belongs to the family of RNA-binding proteins, shuttling from the nucleus to the cytoplasm, and, as shown for other RNA-binding proteins, forms large messenger ribonucleoparticles.
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21

Nakamura, Tomohiro, i Stuart A. Lipton. Neurodegenerative Diseases as Protein Misfolding Disorders. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190233563.003.0002.

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Neurodegenerative diseases (NDDs) often represent disorders of protein folding. Rather than large aggregates, recent evidence suggests that soluble oligomers of misfolded proteins are the most neurotoxic species. Emerging evidence points to small, soluble oligomers of misfolded proteins as the cause of synaptic dysfunction and loss, the major pathological correlate to disease progression in many NDDs including Alzheimer’s disease. The protein quality control machinery of the cell, which includes molecular chaperones as found in the endoplasmic reticulum (ER), the ubiquitin-proteasome system (UPS), and various forms of autophagy, can counterbalance the accumulation of misfolded proteins to some extent. Their ability to eliminate the neurotoxic effects of misfolded proteins, however, declines with age. A plausible explanation for the age-dependent deterioration of the quality control machinery involves compromise of these systems by excessive generation of reactive oxygen species (ROS), such as superoxide anion (O2-), and reactive nitrogen species (RNS), such as nitric oxide (NO). The resulting redox stress contributes to the accumulation of misfolded proteins. Here, we focus on aberrantly increased generation of NO-related species since this process appears to accelerate the manifestation of key neuropathological features, including protein misfolding. We review the chemical mechanisms of posttranslational modification by RNS such as protein S-nitrosylation of critical cysteine thiol groups and nitration of tyrosine residues, showing how they contribute to the pathogenesis of NDDs.
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22

Williamson, Michael. How Proteins Work. Garland Science, 2012. http://dx.doi.org/10.1201/9781136665493.

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Williamson, Michael. How Proteins Work. CRC Press LLC, 2012.

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Williamson, Michael. How Proteins Work. CRC Press LLC, 2012.

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Roe, Simon, red. Protein Purification Techniques. Oxford University Press, 2001. http://dx.doi.org/10.1093/oso/9780199636747.001.0001.

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Proteins are an integral part of molecular and cellular structure and function and are probably the most purified type of biological molecule. In order to elucidate the structure and function of any protein it is first necessary to purify it. Protein purification techniques have evolved over the past ten years with improvements in equipment control, automation, and separation materials, and the introduction of new techniques such as affinity membranes and expanded beds. These developments have reduced the workload involved in protein purification, but there is still a need to consider how unit operations linked together to form a purification strategy, which can be scaled up if necessary. The two Practical Approach books on protein purification have therefore been thoroughly updated and rewritten where necessary. The core of both books is the provision of detailed practical guidelines aimed particularly at laboratory scale purification. Information on scale-up considerations is given where appropriate. The books are not comprehensive but do cover the major laboratory techniques and common sources of protein. Protein Purification Techniques focuses on unit operations and analytical techniques. It starts with an overview of purification strategy and then covers initial extraction and clarification techniques. The rest of the book concentrates on different purification methods with the emphasis being on chromatography. The final chapter considers general scale-up considerations. Protein Purification Applications describes purification strategies from common sources: mammalian cell culture, microbial cell culture, milk, animal tissue, and plant tissue. It also includes chapters on purification of inclusion bodies, fusion proteins, and purification for crystallography. A purification strategy that can produce a highly pure single protein from a crude mixture of proteins, carbohydrates, lipids, and cell debris to is a work of art to be admired. These books (available individually or as a set)are designed to give the laboratory worker the information needed to undertake the challenge of designing such a strategy.
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Eisenberg, David S., Frederic M. Richards i Peter S. Kim. Enzymes and Proteins from Hyperthermophilic Microorganisms. Elsevier Science & Technology Books, 1996.

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How Much Carb How Much Protein. Jane Curry Publishing, 2004.

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Nestec Limited. Documentation Centre. Corporate Affaires Department., red. Proteins: What for, where from, how much? Vevey: Nestec Ltd., 1987.

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Chapter Resource 10 How Proteins/Made Biology. Holt, Rinehart & Winston, 2004.

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White, Stephen, Gunnar Von Heijne i Don Engelman. Cell Boundaries: How Membranes and Their Proteins Work. CRC Press LLC, 2022.

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White, Stephen, Gunnar Von Heijne i Don Engelman. Cell Boundaries: How Membranes and Their Proteins Work. CRC Press LLC, 2022.

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Heijne, Gunnar von, Don Engelman i John Stephen White. Cell Boundaries: How Membranes and Their Proteins Work. CRC Press LLC, 2022.

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White, Stephen, Gunnar Von Heijne i Don Engelman. Cell Boundaries: How Membranes and Their Proteins Work. CRC Press LLC, 2022.

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Brakmann, Susanne, i Kai Johnsson. Directed Molecular Evolution of Proteins: Or How to Improve Enzymes for Biocatalysis. Wiley-VCH Verlag GmbH, 2003.

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Gelderloos, Peter. How Nonviolence Protects the State. Detritus Books, 2018.

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Gelderloos, Peter. How Nonviolence Protects the State. South End Press, 2007.

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Henderson, Daniel A., R. J. Boys, Carole J. Proctor i Darren J. Wilkinson. Linking systems biology models to data: A stochastic kinetic model of p53 oscillations. Redaktorzy Anthony O'Hagan i Mike West. Oxford University Press, 2018. http://dx.doi.org/10.1093/oxfordhb/9780198703174.013.7.

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This article discusses the use of a stochastic kinetic model to study protein level oscillations in single living cancer cells, using the p53 and Mdm2 proteins as examples. It describes the refinement of a dynamic stochastic process model of the cellular response to DNA damage and compares this model to time course data on the levels of p53 and Mdm2. The article first provides a biological background on p53 and Mdm2 before explaining how the stochastic kinetic model is constructed. It then introduces the stochastic kinetic model and links it to the data and goes on to apply sophisticated MCMC methods to compute posterior distributions. The results demonstrate that it is possible to develop computationally intensive Markov chain Monte Carlo (MCMC) methods for conducting a Bayesian analysis of an intra-cellular stochastic systems biology model using single-cell time course data.
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LaGarry, Alison, i Timothy Conder. How “Identity Play” Protects White Privilege. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190676087.003.0008.

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This chapter, “How ‘Identity Play’ Protects White Privilege: A Meta-Ethnographic Methodological Test,” presents the findings of a 2013 meta-ethnographic analysis on White identity in preservice teachers (PSTs), as well as a methodological test of those findings in light of recent publications on Second-Wave White Teacher Identity Studies (SWWTIS). In the 2013 meta-ethnography, the authors first found a reciprocal argument in which the authors described similar tools or strategies by which White PSTs defended their own privilege. Through further reflexive interpretation, the authors then found a line of argument that situated the multiple theories used in the studies as contested spaces in a larger figured world of whiteness. In testing findings from 2013 against recently published studies on SWWTIS, the authors found that the earlier study anticipated a shift in thinking and theorizing within the field.
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Mason, Peggy. Receiving the Synaptic Message. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190237493.003.0013.

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Ionotropic and metabotropic receptors differ in their speed of action, the variety of effects produced after ligand-binding, and in the number of types present in the nervous system. The participation of two ionotropic glutamate receptors in synaptic plasticity is thought to be the cellular basis of learning. The actions of acetylcholine on nicotinic acetylcholine receptors present at the neuromuscular junction are described. The pharmacological profile of the GABAA receptor, central to most neural functions, is introduced. The properties of metabotropic receptors that are coupled to G proteins, termed G protein-coupled receptors (GPCRs), are detailed. Three canonical second-messenger systems through which GPCRs act are briefly described. An introduction to clinical pharmacology focused on how drugs acting on muscarinic and adrenergic receptors produce peripheral and central psychotropic effects is provided. Finally, the role of connexins and gap junctions in myelination and hearing is introduced.
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Davis, Garth, i Howard Jacobson. Proteinaholic: How Our Obsession with Meat Is Killing Us and What We Can Do about It. HarperCollins Publishers, 2015.

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author, Jacobson Howard 1930, red. Proteinaholic: How our obsession with meat is killing us and what we can do about it. 2015.

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Munro, Daniel Colin. You Can Live Longer Than You Think: A Doctor Tells You How To Eat Your Way To Added Years Of Happiness And Vigor. Kessinger Publishing, LLC, 2007.

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Pilon, Brad. Eat Stop Eat How Much Protein: How much protein do you need to build muscle, lose fat and be healthy? Brad Pilon, 2019.

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(Editor), Susanne Brakmann, i Kai Johnsson (Editor), red. Directed Molecular Evolution of Proteins: Or How to Improve Enzymes for Biocatalysis. Wiley-VCH, 2002.

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Brakmann, Susanne, i Kai Johnsson. Directed Molecular Evolution of Proteins: Or How to Improve Enzymes for Biocatalysis. Wiley & Sons, Incorporated, John, 2020.

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D, Garth Davis M., i Howard Jacobson. Proteinaholic: How Our Obsession with Meat Is Killing Us and What We Can Do About It. HarperOne, 2016.

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Iversen, Les. 2. How drugs work. Oxford University Press, 2016. http://dx.doi.org/10.1093/actrade/9780198745792.003.0002.

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‘How drugs work’ outlines the basic mechanisms of pharmacology. Drugs are chemicals that can be naturally occurring or man-made, and which can be administered in a variety of ways. They can act on receptors—often highly specific proteins in cells which can up-regulate or down-regulate processes—or on other targets, such as DNA or enzymes. The molecular action of drugs can be investigated in a lab, but the effects on the whole organism are more important. Effective doses need to be determined, taking into account metabolic rates, drug interactions, and side effects. Prolonged drug use can cause tolerance and substance addiction.
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Meurig Thomas, John. Architects of Structural Biology. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780198854500.001.0001.

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Designed for the non-specialist, the explanations and illustrations used here describe the work, personalities, collaborations, and idiosyncrasies of four of the most distinguished Nobel Laureates of the twentieth century. They exploited a discovery made over a century ago about the nature of X-rays, and thereby created a new branch of science. This enabled them to elucidate, in atomic detail, the structure and mode of action of molecules of the living world: enzymes, vitamins, and viruses, as well as antibiotics. Perutz and Kendrew, from their pioneering work using X-ray diffraction on haemoglobin and myoglobin, the proteins that transport and store oxygen in all animals, led them to establish in 1962 one of the most successful research centres ever—the Laboratory of Molecular Biology (LMB) in Cambridge. Medicines discovered there are used worldwide to treat leukaemia, arthritis, and other diseases. Their work also led to the creation in the United States of the Protein Data Bank that guides scientists in understanding the misfolding of proteins, which cause Alzheimer’s disease, Parkinson’s disease, and other neurodegenerative diseases. This book is first a memoir of these scientists and their contemporaries, many of them friends of the author. Second, it is an insight into the great excitement associated with structural molecular biology, which directly informs our understanding of ourselves. Third, it describes how two renowned research centres in the United Kingdom—the LMB and the Davy-Faraday Research Laboratory—achieved iconic status. It also highlights the importance of the popularization of science, of which Bragg, Perutz, and Kendrew, as well as Dorothy Hodgkin (who solved the structures of penicillin and vitamin B12) were experts.
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Press, Yum Treats. My Favorite High Protein Recipes: My Best Collection of Healthy, High Protein Foods and How to Cook Them. Independently Published, 2018.

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Immune: How Your Body Defends and Protects You. Bloomsbury Publishing Plc, 2017.

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