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Relevant bibliographies by topics / DNA; Chromosomes / Books

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Books on the topic 'DNA; Chromosomes'

Author: Grafiati

Published: 4 June 2021

Last updated: 4 February 2022

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1

Cold, Spring Harbor Symposium on Quantitative Biology (58th 1993 Cold Spring Harbor N. Y. ). DNA and chromosomes. Plainview, N.Y: Cold Spring Harbor Laboratory Press, 1993.

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2

Senshokutai to saibōkaku no dainamikusu: DNA o ayatsuru saibō no shikumi. Kyōto-shi: Kagaku Dōjin, 2013.

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3

The nuclear matrix and spatial organization of chromosomal DNA domains. New York: Chapman & Hall, 1997.

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4

IUBMB Symposium, DNA Enzymes: Structures & Mechanisms (2000 Indian Institute Science, Bangalore). IUBMB Symposium, DNA Enzymes: Structures & Mechanisms, Dec. 1-3, 2000: Abstracts. [Bangalore: Indian Institute of Science], 2000.

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5

Microbial megaplasmids. Berlin: Springer, 2009.

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6

DNA recombination: Methods and protocols. New York: Humana, 2011.

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7

Wyandt, Herman E. Human Chromosome Variation: Heteromorphism and Polymorphism. Dordrecht: Springer Science+Business Media B.V., 2012.

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8

Razin, Sergey V. The nuclear matrix and spatial organization of chomosomal DNA domains. Austin, TX: R.G. Landes, 1997.

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9

Bacterial chromatin. Dordrecht: Springer, 2010.

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10

Khattak, Mohammad Naeem. Chromosomal DNA variations in infections. Manchester: University of Manchester, 1993.

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11

Wang, Ming Li. Development of chromosome-specific DNA libraries in wheat. Norwich: University of East Anglia, 1993.

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12

Dąbrowska, Janina. Chromosome number and DNA content in taxa of Achillea L. in relation to the distribution of the genus. Wrocław: Wydawn. Uniwersytetu Wrocławskiego, 1992.

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13

Hollis, R. J. Chromosome and DNA studies on disorders predisposing to cancer in man. Birmingham: University ofBirmingham, 1986.

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14

Razin, Sergey V. The nuclear matrix and spatial organization of chromosomal DNA domains. New York: Springer, 1997.

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15

Fedorova, S. A. Geneticheskie portrety narodov Respubliki Sakha, I︠A︡kutii︠a︡: Analiz liniĭ mitokhondrialʹnoĭ DNK i Y-khromosomy. I︠A︡kutsk: I︠A︡NT︠S︡ SO RAN, 2008.

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16

Beiler, Allen R. DNA search for the small y bey: America, Switzerland, and beyond : Beiler-Beyeler-Boiler-Byler. New Holland, PA: Bey Research, 2006.

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17

E, Lindsten Jan, Pettersson Ulf, Nobelstiftelsen, and Alfred Nobel's Björkborn Foundation, eds. Etiology of human disease at the DNA level. New York: Raven Press, 1991.

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18

Stifling or stimulating: The role of gene patents in research and genetic testing : hearing before the Subcommittee on Courts, the Internet, and Intellectual Property of the Committee on the Judiciary, House of Representatives, One Hundred Tenth Congress, first session, October 30, 2007. Washington: U.S. G.P.O., 2008.

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19

Primrose, S. B. Principles of gene manipulation and genomics. 7th ed. Malden, MA: Blackwell Pub., 2006.

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20

Primrose, S. B. Principles of genome analysis: A guideto mapping and sequencing DNA from different organisms. Oxford: Blackwell Scientific, 1995.

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21

Principles of genome analysis: A guide to mapping and sequencing DNA from different organisms. 2nd ed. Oxford: Blackwell Science, 1998.

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22

Principles of genome analysis: A guide to mapping and sequencing DNA from different organisms. Oxford [England]: Blackwell Science, 1995.

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23

Kahl, Günter, and Matthias Harbers. Tag-based next generation sequencing. Weinheim: Wiley-Blackwell, 2012.

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24

D, Protopapas Alex, ed. Genomics. Upper Saddle River, NJ: Prentice-Hall, 2005.

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25

European Environmental Mutagen Society. Meeting. Workshop on chromosome instability and cell cycle control: Istituto Superiore di Sanità, Rome, September 3-7, 1996 : abstract book. Roma: L'Istituto, 1996.

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26

NATO Advanced Study Institute on Radiation Carcinogenesis and DNA Alterations (1984 Kerkyra, Greece). Radiation carcinogenesis and DNA alterations. New York: Plenum Press, 1986.

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27

Kotval, Jeroo S. DNA-based tests: Policy implications for New York State : a chairman's report. Albany, NY (Assembly P.O. Box 167, Albany 12248): Legislative Commission on Science and Technology, 1994.

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28

Janitz, Michal. Next-generation genome sequencing: Towards personalized medicine. Weinheim: Wiley-VCH, 2008.

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29

The $1,000 genome: The scientific breakthrough that will change our lives. New York: Free Press, 2010.

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30

At home DNA tests: Marketing scam or medical breakthrough : hearing before the Special Committee on Aging, United States Senate, One Hundred Ninth Congress, second session, Washington, DC, July 27, 2006. Washington: U.S. G.P.O., 2006.

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31

M, Twyman Richard, ed. Principles of gene manipulation and genomics. 8th ed. Malden, MA: Blackwell Pub., 2007.

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32

DNA ploidy and cell cycle analysis in pathology. New York: Igaku-Shoin, 1996.

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33

Rice, Anne. Lasher. Buenos Aires: Libro Express, 1997.

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34

DNA and chromosomes. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory, 1993.

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35

R, Appels, ed. Chromosome biology. Boston: Kluwer Academic Publishers, 1998.

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36

Appels, Rudi. Chromosome Biology. Springer, 2012.

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37

Chromosome Biology. Springer, 2012.

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38

Schwartz, Edward. Microbial Megaplasmids. Springer, 2010.

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39

Divan, Aysha, and Janice A. Royds. 2. DNA. Oxford University Press, 2016. http://dx.doi.org/10.1093/actrade/9780198723882.003.0002.

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Another significant milestone was the publication in 2003 of the complete sequence of the human genome—the entire DNA contained within the forty-six chromosomes located in the nucleus of each human somatic (body) cell. Once this was published, further worldwide projects were launched to work out what the functions of these genes and other regions of the genome actually were. ‘DNA’ outlines the components of the human genome and their organization; DNA replication; mutations and correction mechanisms; polymorphisms; and new DNA technologies, including gene cloning, the polymerase chain reaction, and sequencing methods. Finally, bioinformatics and the subsequent issues of privacy and how this information could be used are discussed.

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40

The Eukaryotic Replisome A Guide To Protein Structure And Function. Springer, 2012.

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41

Wevrick, Rachel. Organization and behaviour of Alpha satellite DNA at the centromeres of human chromosomes. 1992.

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42

McKinlay Gardner, R. J., and David J. Amor. Chromosome Instability Syndromes. Edited by R. J. McKinlay Gardner and David J. Amor. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199329007.003.0016.

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A defect of DNA repair is the factor underlying the chromosome instability syndromes, also known as chromosome breakage syndromes. The “instability” refers to the predisposition of the chromosomes to undergo rearrangement or to display other abnormal cytogenetic behavior. The classic chromosome instability syndromes are individually rare: Fanconi syndrome, ataxia-telangiectasia, and Bloom syndrome. Smaller-print conditions are yet more rare, including Roberts syndrome; the immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome; and Nijmegen breakage syndrome. The role of cytogenetics in diagnosis is less central than formerly, but the interest in these conditions remains, and this chapter provides a full listing. Autosomal recessive inheritance is typical, albeit not universal.

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43

Dame, Remus T., and Charles J. Dorman. Bacterial Chromatin. Springer, 2014.

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44

Dame, Remus T., and Charles J. Dorman. Bacterial Chromatin. Springer, 2010.

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45

Cold Spring Harbor Symposia on Quantitative Biology: DNA and Chromosomes (Cold Spring Harbor Symposia on Quantitative Biology). Cold Spring Harbor Laboratory Press, 1994.

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46

Money, Nicholas P. 1. Microbial diversity. Oxford University Press, 2014. http://dx.doi.org/10.1093/actrade/9780199681686.003.0001.

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‘Microbial diversity’ considers the vast array of microorganisms—the smallest forms of life—which exist everywhere. The three primary groups of microorganisms are bacteria, archaea, and eukaryotes. Bacteria and archaea are prokaryotes with their genetic material held in a single chromosome. In eukaryotes, most of the genome is held in multiple chromosomes. Over 11,000 species of bacteria have been identified using microscopic identification of cell shape and metabolic activity, Gram-staining techniques, and genetic identification of RNA and DNA sequences. There are 500 named species of archaea, divided into two phyla: the euryarchaeota and the crenarchaeota. There are eight supergroupings of eukaryotes, all of them include single-celled organisms, and five are entirely microbial.

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47

Genetics 101: From Chromosomes and the Double Helix to Cloning and DNA Tests, Everything You Need to Know about Genes. New York: Adams Media, 2018.

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48

Roth, Wendy D., and Katherine A. Lyon. Genetic Ancestry Tests and Race. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190465285.003.0008.

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This chapter probes genetic ancestry tests, which are being used increasingly by individuals for a number of reasons. Many are seeking ways to fill in gaps in their family tree; some are hoping to assert membership in certain groups or tribes; and others are simply curious. Nearly 500 test-takers filled out an online survey with questions attempting to form a basis of understanding about the types of people who take these tests, why they take them, and the impact the results have on their identity. There are multiple types of tests offered through various companies, including Y-chromosome tests to infer paternal haplogroup; mitochondrial DNA tests to infer maternal haplogroup; and autosomal or admixture tests, which examine nonsex chromosomes inherited from both parents. The majority of respondents claimed that the tests had an impact on some aspect of their life.

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49

News, PM Medical Health. 21st Century Complete Guide to Human Genome Research: Genetic Mapping, DNA Sequencing, Chromosomes, Bioethics, Tools and Techniques, Gene Variations and Disease. Progressive Management, 2002.

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50

Skwarecki, Beth. Genetics 101: From Chromosomes and the Double Helix to Cloning and DNA Tests, Everything You Need to Know about Genes. Adams Media Corporation, 2018.

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