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Libros sobre el tema "Peroxisome"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 25 de mayo de 2024

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1

Lizard, Gérard, ed. Peroxisome Biology: Experimental Models, Peroxisomal Disorders and Neurological Diseases. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-60204-8.

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2

Lizard, Gérard, ed. Peroxisome Biology: Experimental Models, Peroxisomal Disorders and Neurological Diseases. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-60204-8.

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3

Youssef, Jihan A. y Mostafa Z. Badr. Peroxisome Proliferator-Activated Receptors. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-420-3.

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4

Denis, Crane, ed. The peroxisome: A vital organelle. Cambridge: Cambridge University Press, 1995.

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5

Badr, Mostafa Z. y Jihan A. Youssef, eds. Peroxisome Proliferator-Activated Receptors (PPARs). Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-155-4.

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6

Youssef, Jihan A. Peroxisome proliferator-activated receptors: Discovery and recent advances. New York: Humana Press, 2013.

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7

Nwosu, Victor Ugo. Peroxisome enzymes in animal models of obesity. Wolverhampton: The Polytechnic, Wolverhampton, School of Applied Sciences, 1988.

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8

Brocard, Cecile y Andreas Hartig, eds. Molecular Machines Involved in Peroxisome Biogenesis and Maintenance. Vienna: Springer Vienna, 2014. http://dx.doi.org/10.1007/978-3-7091-1788-0.

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9

E, Moody David, ed. Peroxisome proliferators: Unique inducers of drug-metabolizing enzymes. Boca Raton, Fla: CRC Press, 1994.

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10

Fruchart, J. C., A. M. Gotto, R. Paoletti, B. Staels y A. L. Catapano, eds. Peroxisome Proliferator Activated Receptors: From Basic Science to Clinical Applications. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-1171-7.

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11

1945-, Fruchart J. C., ed. Peroxisome proliferator activated receptors: From basic science to clinical applications. Dordrecht: Kluwer Academic Pub., 2002.

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12

The Function of Peroxisome Proliferator-Activated Receptor-Gamma in the Urothelium. [New York, N.Y.?]: [publisher not identified], 2018.

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13

Phipps, Alexander Nicholas. The role of the peroxisome in ether phospholipid metabolism in the small intestine. Manchester: University of Manchester, 1995.

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14

Conlon, Donna Marie. Role of Autophagy and Peroxisome Proliferator-Activated Receptor Gamma2 in Hepatic Lipid Homeostasis. [New York, N.Y.?]: [publisher not identified], 2014.

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15

IARC Working Group on Peroxisome Proliferation. Meeting, ed. Peroxisome proliferation and its role in carcinogenesis: Views and expert opinions of an IARC working group, Lyon, 7-11 December 1994. Geneva: International Agency for Research on Cancer, World Health Organization, 1995.

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16

Holloway, Brian R. Species differences in the effects of clofibrate on peroxisome proliferation and the role of thyroxine. Uxbridge: Brunel University, 1989.

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17

K, Reddy Janardan, ed. Peroxisomes: Biology and role in toxicology and disease. New York, N.Y: New York Academy of Sciences, 1996.

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18

Schrader, Michael, ed. Peroxisomes. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6937-1.

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19

Latruffe, Norbert y Maurice Bugaut, eds. Peroxisomes. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-87807-7.

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20

Norbert, Latruffe y Bugaut M. 1945-, eds. Peroxisomes. Berlin: Springer-Verlag, 1994.

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21

Schrader, Michael, ed. Peroxisomes. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3048-8.

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22

Frank, Roels, Baes Myriam y De Bie Sylvia, eds. Peroxisomal disorders and regulation of genes. New York: Kluwer Academic/Plenum Publishers, 2003.

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23

Frank, Roels, Baes Myriam y De Bie Sylvia, eds. Peroxisomal disorders and regulation of genes. New York: Kluwer Academic / Plenum Publishers, 2003.

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24

Baker, Alison y Ian A. Graham, eds. Plant Peroxisomes. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-015-9858-3.

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25

del Río, Luis A. y Michael Schrader, eds. Proteomics of Peroxisomes. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-2233-4.

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26

Delille, Hannah Katharina. Biogenesis of peroxisomes in mammalian cells: Characterization of the Pex11 proteins and their role in peroxisomal growth and division. Marburg: Philipps-Universität Marburg, 2011.

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27

Roels, Frank. Peroxisomes: A personal account. Brussel: VUB Press, 1991.

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28

M, Coates Paul y Tanaka Kay, eds. New developments in fatty acid oxidation: Proceedings of the Second International Symposium on Clinical, Biochemical, and Molecular Aspects of Fatty Acid Oxidation, held in Philadelphia, Pennsylvania, November 1991. New York, N.Y: Wiley-Liss, 1992.

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29

Fahimi, H. Dariush y Helmut Sies, eds. Peroxisomes in Biology and Medicine. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71325-5.

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30

1933-, Fahimi H. Dariush, Sies H. 1942-, European Cell Biology Organization y International Symposium on Peroxisomes in Biology and Medicine (1986 : Heidelberg, Germany), eds. Peroxisomes in biology and medicine. Berlin: Springer-Verlag, 1987.

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31

Roels, Frank, Sylvia De Bie, Ruud B. H. Schutgens y Guy T. N. Besley, eds. Diagnosis of human peroxisomal disorders. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-9635-2.

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32

Reubsaet, Frans A. Peroxisomal fatty acid [beta]-oxidation. Nijmegen: Univ., 1991.

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33

Imanaka, Tsuneo y Nobuyuki Shimozawa, eds. Peroxisomes: Biogenesis, Function, and Role in Human Disease. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-15-1169-1.

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34

Alison, Baker y Graham Ian A, eds. Plant peroxisomes: Biochemistry, cell biology, and biotechnological applications. Dordrecht: Kluwer Academic Publishers, 2002.

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35

Gordon, Gibson G. y Lake Brian 1948-, eds. Peroxisomes: Biology and importance in toxicology and medicine. London: Taylor & Francis, 1993.

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36

Tappia, Paramjit Singh. Analysis of peroxisomes from mammalian intestine and liver. Wolverhampton: Wolverhampton Polytechnic, 1992.

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37

Roels, Frank, Myriam Baes y Sylvia De Bie, eds. Peroxisomal Disorders and Regulation of Genes. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-9072-3.

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38

Poll-The, Bwee Tien, Ronald J. A. Wanders y Hans R. Waterham. Peroxisomal Disorders. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0062.

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Peroxisomal disorders represent a group of disorders in which there is an impairment in one or more peroxisomal functions. Clinically, a dysfunction of peroxisomes results in most cases in neurologic symptoms of varying extent ranging from severe neurologic symptoms in children to late-onset disease in adults. In most peroxisomal disorders there is ocular and hearing involvement in combination with a multitude of other clinical manifestations. The peroxisomal disorders are subdivided into two major groups: (1) the peroxisome biogenesis disorders (PBDs), and (2) the single peroxisome enzyme deficiencies. The PBD group comprises the Zellweger spectrum disorders (ZSDs) and rhizomelic chondrodysplasia punctate type 1 (RCDP1) whereas the single peroxisomal enzyme deficiency group contains several different disorders including X-linked adrenoleukodystrophy as the most frequent disorder. Laboratory diagnosis of a peroxisomal disorder involves a variety of different biochemical assays in blood and urine, and should be followed up by detailed biochemical and celbiological studies in cultured fibroblasts including complementation analysis. Prenatal diagnosis is possible either by biochemical testing or by molecular analysis.
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39

Lizard, Gérard. Peroxisome Biology: Experimental Models, Peroxisomal Disorders and Neurological Diseases. Springer International Publishing AG, 2021.

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40

Lizard, Gérard. Peroxisome Biology: Experimental Models, Peroxisomal Disorders and Neurological Diseases. Springer International Publishing AG, 2022.

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41

Raymond, Gerald V., Mohamed Y. Jefri, Kristin W. Baranano y Ali Fatemi. Peroxisomal Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0069.

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Disorders of the peroxisome are divided into two major categories. In the first, the organelle fails to develop normally, leading to disruption of multiple peroxisomal enzymes. The second category consists of those disorders in which the peroxisome structure is normal but functioning of a single peroxisomal enzyme or protein is defective. While there is an expanding list of disorders in both categories, this chapter focuses on X-linked adrenoleukodystrophy, the most common peroxisomal disorder, and on peroxisomal assembly/biogenesis disorders.
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42

Peroxisome Proliferatoractivated Receptors Ppars Methods And Protocols. Humana Press, 2012.

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43

Masters, Colin y Denis Crane. The Peroxisome: A Vital Organelle. Cambridge University Press, 2007.

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44

Schuldiner, Maya, Einat Zalckvar, Peter Kijun Kim, Sigrun Reumann y Michael Sattler, eds. Peroxisome Biology: Breakthroughs, Challenges and Future Directions. Frontiers Media SA, 2021. http://dx.doi.org/10.3389/978-2-88971-247-2.

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45

Youssef, Jihan y Mostafa Z. Badr. Peroxisome Proliferator-Activated Receptors: Methods and Protocols. Humana Press, 2016.

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46

Brocard, Cecile y Andreas Hartig. Molecular Machines Involved in Peroxisome Biogenesis and Maintenance. Brocard Cecile, 2014.

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47

Brocard, Cecile y Andreas Hartig. Molecular Machines Involved in Peroxisome Biogenesis and Maintenance. Springer Wien, 2014.

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48

Brocard, Cecile y Andreas Hartig. Molecular Machines Involved in Peroxisome Biogenesis and Maintenance. Brocard Cecile, 2016.

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49

Wylin, Tine. Peroxisome Biogenesis: Characterization of the Import Process of Peroxisomal Integral Membrane Proteins (Acta Biomedica Lovaniensia, 247). Leuven Univ Pr, 2001.

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50

Badr, Mostafa Z. y Jihan A. Youssef. Peroxisome Proliferator-Activated Receptors: Discovery and Recent Advances. Humana Press, 2015.

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