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Publicado: 11 de marzo de 2023

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1

Rapley, Ralph y David L. Manning, eds. RNA Isolation and Characterization Protocols. Totowa, NJ: Humana Press, 1998. http://dx.doi.org/10.1385/0896034941.

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2

Fields, Gregg B., ed. Peptide Characterization and Application Protocols. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-430-8.

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3

Fields, Gregg B., ed. Peptide Characterization and Application Protocols. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/1-59745-430-3.

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4

Ralph, Rapley y Manning David L, eds. RNA isolation and characterization protocols. Totowa, N.J: Humana Press, 1998.

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5

Selinsky, Barry S. Membrane protein protocols: Expression, purification, and characterization. Totowa, NJ: Humana Press, 2010.

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6

name, No. Membrane protein protocols: Expression, purification, and characterization. Totowa, NJ: Humana Press, Inc., 2003.

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7

Steven, Selinsky Barry, ed. Membrane protein protocols: Expression, purification, and characterization. Totowa, N.J: Humana Press, 2003.

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8

The ciliated protozoa: Characterization, classification, and guide to the literature. New York: Springer, 2008.

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9

Chan, Andrew. Towards the development and characterization of a selective DNA purification protocol by capillary affinity gel electrophoresis. 2006.

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10

B, Fields Gregg, ed. Peptide characterization and application protocols. Totowa, N.J: Humana, 2007.

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11

Fields, Gregg B. Peptide Characterization and Application Protocols. Humana Press, 2007.

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12

Peptide characterization and application protocols. Totowa, NJ: Humana, 2006.

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13

Fields, Gregg B. Peptide Characterization and Application Protocols. Humana Press, 2010.

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14

Manning, David L. y Ralph Rapley. RNA Isolation and Characterization Protocols. Humana Press, 2013.

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15

Bhat, Alangar Ishwara y Govind Pratap Rao. Characterization of Plant Viruses: Methods and Protocols. Springer, 2021.

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16

Bhat, Alangar Ishwara y Govind Pratap Rao. Characterization of Plant Viruses: Methods and Protocols. Springer, 2020.

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17

Lacapere, Jean-Jacques. Membrane Protein Structure and Function Characterization: Methods and Protocols. Springer New York, 2018.

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18

D, Jones Huw y Shewry P. R, eds. Transgenic wheat, barley and oats: Production and characterization protocols. New York, NY: Humana Press, 2009.

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19

Transgenic wheat, barley and oats: Production and characterization protocols. New York, NY: Humana Press, 2009.

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20

Turksen, Kursad. Embryonic Stem Cell Protocols : Volume I: Isolation and Characterization. Humana Press, 2010.

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21

Shewry, Peter R. y Huw D. Jones. Transgenic Wheat, Barley and Oats: Production and Characterization Protocols. Humana Press, 2016.

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22

Embryonic stem cell protocols: Volume 1: isolation and characterization. 2a ed. Totowa, NJ: Humana Press, 2006.

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23

Lacapere, Jean-Jacques. Membrane Protein Structure and Function Characterization: Methods and Protocols. Springer New York, 2017.

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24

Corliss, John O. Ciliated Protozoa: Characterization, Classification and Guide to the Literature. Elsevier Science & Technology Books, 2016.

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25

Selinsky, Barry S. Membrane Protein Protocols: Expression, Purification, and Characterization (Methods in Molecular Biology). Humana Press, 2003.

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26

Lynn, Denis H. The Ciliated Protozoa: Characterization, Classification, and Guide to the Literature. Springer, 2016.

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27

Smolke, Christina D. Metabolic Engineering Protocols: Volume 2: Analysis and Characterization (Methods in Molecular Biology). Humana Press, 2007.

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28

Gene Therapy Protocols : Volume 2: Design and Characterization of Gene Transfer Vectors. Humana Press, 2014.

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29

Turksen, Kursad. Embryonic Stem Cell Protocols: Volume I: Isolation and Characterization (Methods in Molecular Biology). 2a ed. Humana Press, 2006.

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30

Hepatitis B and D Protocols: Volume 1: Detection, Genotypes, and Characterization (Methods in Molecular Medicine). Humana Press, 2004.

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31

Jankowicz-Cieslak, Joanna, Owen A. Huynh, Mayada M. Beshir, Robert G. Laport, Bernhard J. Hofinger y Bradley J. J. Till. Low-Cost Methods for Molecular Characterization of Mutant Plants : Tissue Desiccation, DNA Extraction and Mutation Discovery: Protocols. Springer, 2016.

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32

Jankowicz-Cieslak, Joanna, Bradley J. Till, Owen A. Huynh, Mayada M. Beshir, Robert G. Laport y Bernhard J. Hofinger. Low-Cost Methods for Molecular Characterization of Mutant Plants : Tissue Desiccation, DNA Extraction and Mutation Discovery: Protocols. Springer, 2015.

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33

Lam, Diana L. y Habib Rahbar. Non-Mass Enhancement on MRI. Editado por Christoph I. Lee, Constance D. Lehman y Lawrence W. Bassett. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190270261.003.0031.

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Breast cancer presents on MRI as an enhancing finding on post-contrast T1-weighted images that is distinct from normal background parenchymal enhancement (BPE), and these enhancing lesions can be further described as a focus, mass, or non-mass enhancement (NME). Each enhancing lesion, with the exception of a focus, can be described further with specific morphological features that are defined by the ACR BI-RADS Atlas. This chapter reviews the key imaging and clinical features, imaging protocols and pitfalls, differential diagnoses, and management recommendations of a focus of enhancement and non-mass enhancement on MRI. Topics discussed include distinguishing a focus from normal BPE, benign versus suspicious features of a focus, NME characterization, and kinetic enhancement curves.
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34

Wang, Lilian. Amorphous/Indistinct Calcifications (Group). Editado por Christoph I. Lee, Constance D. Lehman y Lawrence W. Bassett. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190270261.003.0039.

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Amorphous calcifications are calcifications that are sufficiently small and/or hazy that a more specific morphological classification cannot be made. Historically, such calcifications were referred to as “indistinct” calcifications. The likelihood of malignancy and the management of amorphous calcifications largely depend on their distribution. This chapter, appearing in the section on calcifications, reviews the key imaging and clinical features, imaging protocols and pitfalls, differential diagnosis with radiology–pathology correlation, and management recommendations for amorphous/indistinct calcifications in a group. Topics discussed include spot magnification views for characterization, role of distribution in BI-RADS assessment, and pathological entities, including fibrocystic change, milk of calcium, atypical ductal hyperplasia (ADH), and ductal carcinoma in situ (DCIS).
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35

Rosen, Meyer R. A novel synergy of auriculotherapy, kinesiology and temporomandibular dysfunction (TMD) treatment protocols for the quantitative characterization and treatment ... ultra-sensitivity to normal sounds. Interactive Consulting, Inc, 1994.

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36

Ducruix, Arnaud y Richard Giegé, eds. Crystallization of Nucleic Acids and Proteins. Oxford University Press, 1999. http://dx.doi.org/10.1093/oso/9780199636792.001.0001.

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Crystallography is the major method of determining structures of biological macromolecules yet crystallization techniques are still regarded as difficult to perform. This new edition of Crystallization of Nucleic Acids and Proteins: A Practical Approach continues in the vein of the first edition by providing a detailed and rational guide to producing crystals of proteins and nucleic acids of sufficient quantity and quality for diffraction studies. It has been thoroughly updated to include all the major new techniques such as the uses of molecular biology in structural biology (maximizing expression systems, sequence modifications to enable crystallization, and the introduction of anomalous scatterers); diagnostic analysis of prenucleation and nucleation by spectroscopic methods; and the two- dimensional electron crystallography of soluble proteins on planar lipid films. As well as an introduction to crystallogenesis, the other topics covered are: Handling macromolecular solutions, experimental design, seeding, proceeding from solutions to crystals Crystallization in gels Crystallization of nucleic acid complexes and membrane proteins Soaking techniques Preliminary characterization of crystals in order to tell whether they are suitable for diffraction studies. As with all Practical Approach books the protocols have been written by experienced researchers and are tried an tested methods. The underlying theory is brought together with the laboratory protocols to provide researchers with the conceptual and methodological tools necessary to exploit these powerful techniques. Crystallization of Nucleic Acids and Proteins: A Practical Approach 2e will be an invaluable manual of practical crystallization methods to researchers in molecular biology, crystallography, protein engineering, and biological chemistry.
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37

C. M. Souza, Júlio. Métodos de Pesquisa Laboratorial em Biomateriais Dentários. Brazil Publishing, 2021. http://dx.doi.org/10.31012/978-65-5861-448-7.

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This book was designed concerning the struggle of students on finding an updated bibliographic source with scientific terms and clearly focused on the study of biomaterials in dentistry and engineering. The present work is a state of art of fundamentals and scientific data reported in literature regarding the study and application of dental biomaterials and techniques used in experimental in vitro research. The book brings critical questions on the subject and research protocols for study of materials taking into consideration education, research, and clinical applications. The present book involves the following issues divided into chapters: i) properties of materiais; ii) thermal analysis methods for the characterization and processing of materials; iii) mechanical assays; iv) chemical analysis; v) surface analysis; vi) analysis by microscopy; vii) biocompatibility of materials. The participation of professors of dentistry, physics, biology, materials engineering, and biomedical engineering in this work promotes the desired interface between the fields of medicine and engineering. Students, professionals, and professors in Brazil, Portugal and Africa (Portuguese-speaking countries) can gather benefits from this book after the stablishment of the orthographic agreement and the matching of scientific terms.
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38

Teoh, Eugene y Michael J. Weston. Computed tomography. Editado por Christopher G. Winearls. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0014.

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Computed tomography (CT) has increased in use exponentially for the assessment of patients with renal tract pathology. This has been promoted by the availability of multidetector thin-slice CT so that intravenous urography has been superseded by CT urography. The latter may be considered as a ‘one-stop’ imaging investigation for haematuria, with increased detection of both urinary tract cancers and urolithiasis. Multiplanar reformats are made possible with the use of thin slices, allowing clear delineation of other pathologies such as urinary tract injury. In the transplant recipient, protocols have been developed for the assessment of more immediate complications such as thrombotic and stenotic disease. During follow-up, CT continues to inform the management of post-transplant lymphoproliferative disorder and other immunosuppressant-related complications. Unenhanced CT of the urinary tract has established its role in assessment of patients with renal colic, with the ability to detect pathology outside of the urinary tract. Renal CT has been developed for the characterization of renal masses, accompanied by the now well-established Bosniak renal cyst classification system. As the usefulness of CT increases, clear awareness of safety issues has to be maintained. These include the administration of intravenous iodinated contrast medium in higher-risk patient groups, particularly those with renal impairment. The radiation burden that comes with CT poses an added risk to the patient that should not be ignored. This necessitates clear referral guidelines for its use, which should be applied in careful balance with the global assessment of the patient.
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