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Relevant bibliographies by topics / Mammalian genomics / Books

Books on the topic 'Mammalian genomics'

To see the other types of publications on this topic, follow the link: Mammalian genomics.

Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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1

Ruvinsky, A., and J. A. Marshall Graves, eds. Mammalian genomics. Wallingford: CABI, 2005. http://dx.doi.org/10.1079/9780851999104.0000.

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2

Organisation for Economic Co-operation and Development., ed. Mammalian embryo genomics. Paris: Organisation for Economic Co-operation and Development, 2003.

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3

Hu, Wei Shou, and An-Ping Zeng, eds. Genomics and Systems Biology of Mammalian Cell Culture. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-28350-5.

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4

An-Ping, Zeng, and SpringerLink (Online service), eds. Genomics and Systems Biology of Mammalian Cell Culture. 2nd ed. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.

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5

Foreign DNA in mammalian systems. Weinheim: Wiley-VCH, 2000.

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6

Manocha, Marcus M. S. Isolation and characterization of genomic DNA sequences that enhance the stability of plasmid DNA in mammalian cells. St. Catharines, Ont: Brock University, Centre for Biotechnology, 2005.

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7

Mammalian Embryo Genomics. OECD, 2003. http://dx.doi.org/10.1787/9789264104273-en.

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8

(Editor), A. Ruvinsky, and J. A. Marshall Graves (Editor), eds. Mammalian Genomics (Cabi Publishing). CABI, 2005.

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9

Genomics And Systems Biology Of Mammalian Cell Culture. Springer, 2012.

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10

Zeng, An-Ping, and Wei Shou Hu. Genomics and Systems Biology of Mammalian Cell Culture. Springer, 2012.

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11

Zeng, An-Ping, and Wei Shou Hu. Genomics and Systems Biology of Mammalian Cell Culture. Springer, 2014.

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12

Organisation for economic co-operation and development. Mammalian Embryo Genomics (Biological Resource Management in Agriculture). OECD, 2003.

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13

Gamete and Embryo Selection: Genomics, Metabolomics and Morphological Assessment. Springer, 2014.

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14

Katz-Jaffe, Mandy G., Denny Sakkas, and Carlos E. Sueldo. Gamete and Embryo Selection: Genomics, Metabolomics and Morphological Assessment. Springer, 2014.

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15

Tonin, Patricia N. Characterization of genomic sequences coamplified with the M2 gene in hydroxyurea-resistant mammalian cells. 1989.

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16

Becker, Richard C., and Frederick A. Spencer. Fibrinolytic and Antithrombotic Therapy. Oxford University Press, 2006. http://dx.doi.org/10.1093/oso/9780195155648.001.0001.

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Thrombotic disorders of the circulatory system represent the leading cause of morbidity, motality, and health care expenditure in the United States. Fibrinolytic and Antithrombotic Therapy provides a practical, evidence-based approach to the management of thrombotic disorders for all clinicians involved in the care of patients with these disorders. It provides not only vital conceptual information on fibrinolytic and antithrombotic therapy, but also the means to apply it to everyday decision making and patient care. Focusing on managment guidelines and critical pathways, the text stresses practicality and usability. It will be a valuable resource for the wide range of clinicians involved in the care of patients with these disorders, including cardiologists, emergency physicians, primary care physicians, hematologists, neurologists, intensivists, pharmacists, and nurse practitioners. The origins of mammalian blood coagulation can be traced back over 400 million years. Despite its long history, it is only within the past century that this complex and pivotal teleologic system has begun to be understood. Most recently, the intricacies of hemostasis and pahtologic thrombosis have come to light, leading the way toward new, more effective, and safer treatment modalities. The Second Edition of Fibrinolytic and Antithrombotic Therapy, even more concise and clinically relevant than the First, provides vital, evidence-based information on management of patients with arterial and venous thrombotic disorders. Since the First Edition, the text has been expanded to cover the evolving topics of atherothrombosis, thrombocardiology, hematologic/thrombophilic conditions, and vascular medicine. It includes up-to-date guidelines for antithrombotic and fibrinolytic therapy, and offers concise summaries of current "standards of care." Chapters are dedicated to discussions of patient-specific therapeutics and to the importance of genomics, proteomics, and metabolomics in defining genotype-phenotype relationships, while throughout the book coagulation, inflammation, and vascular medicine are newly examined as elements in an intricatley-linked triad of biochemical and cellular based phenomenology.

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17

Patisaul, Heather B., and Scott M. Belcher. Receptor and Enzyme Mechanisms as Targets for Endocrine Disruptors. Oxford University Press, 2017. http://dx.doi.org/10.1093/acprof:oso/9780199935734.003.0005.

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In this chapter, the current understanding of the mechanisms of endocrine disruption on the brain and nervous system are presented. Because the overwhelming majority of mechanistic studies on EDCs have focused on the actions mediated by nuclear hormone receptors, this mechanisms is described in detail. The chapter also discusses the classic transcriptional mechanisms of steroid action and the impact of EDCs on rapid signaling (non-genomic) mechanisms. It presents an overview of the enzymes and pathways involved in the biosynthesis of steroid hormones, which are critical to proper functioning of the HPA and HPG axis, and the neuroactive steroids synthesized and active in the mammalian brain. The potential for EDCs to alter metabolic enzymes, with a focus on possible targets in the metabolic blood-brain barrier, is presented as a potential, though largely unexplored, mode of EDC action in the brain.

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18

Ellis, James Ryall. Gene targetting and retroviral recombination with mammalian genomes: pathways deduced from progeny structures of selected recombination events. 1990.

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