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Books on the topic 'Guanosine triphosphatase'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 July 2024

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1

Joan, Marsh, and Goode Jamie, eds. The GTPase superfamily. Chichester: Wiley, 1993.

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2

K, Aktories, Dickey Burton F. 1953-, and Birnbaumer Lutz, eds. GTPases in biology. Berlin: Springer, 1993.

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3

1949-, Balch William Edward, Der Channing J, and Hall A, eds. Regulators and effectors of small GTPases: Rho family. Amsterdam: Elsevier, 2006.

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4

Ed, Manser, and Leung Thomas, eds. GTPase protocols: The Ras superfamily. Totowa, N.J: Humana Press, 2002.

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5

Carlos, Lacal Juan, and McCormick Frank 1950-, eds. The Ras superfamily of GTPases. Boca Raton: CRC Press, 1993.

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6

1949-, Balch William Edward, Der Channing J. 1953-, and Hall A, eds. Small GTPases and their regulators. San Diego: Academic Press, 1995.

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7

Media, Springer Science+Business, ed. Ras signaling: Methods and protocols. New York: Humana Press, 2014.

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8

A, Kahn Richard, ed. ARF family GTPases. Dordrecht: Kluwer Academic Publishers, 2003.

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9

1949-, Balch William Edward, Der Channing J, and Hall A, eds. Small GTPases in disease. London: Academic, 2008.

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10

Corda, D., H. Hamm, and A. Luini. GTPase-controlled molecular machines. Rome: Ares-Serono Symposia Publications, 1994.

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11

1949-, Balch William Edward, Der Channing J, and Hall A, eds. GTPases regulating membrane dynamics. Amsterdam: Elsevier Academic Press, 2005.

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12

1949-, Balch William Edward, Der Channing J, and Hall A, eds. Regulators and effectors of small GTPases. San Diego: Academic Press, 2000.

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13

1949-, Balch William Edward, Der Channing J, and Hall A, eds. Regulators and effectors of small GTPases: Ras family. Amsterdam: Elsevier/Academic Press, 2006.

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14

Nederkoorn, Paul H. J. Signal transduction by G protein-coupled receptors: Bioenergetics and G protein activation : proton transfer and GTP synthesis to explain the experimental findings. New York: Springer, 1997.

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15

Anderson, M. W., K. Aktories, and D. L. Altschuler. Gtpases in Biology I (Handbook of Experimental Pharmacology). Springer-Verlag Telos, 1993.

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16

GTPase Protocols: The Ras Superfamily. Humana Press, 2004.

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17

(Editor), John N. Abelson, Melvin I. Simon (Editor), W. E. Balch (Editor), Channing J. Der (Editor), and Alan Hall (Editor), eds. Regulators and Effectors of Small GTPases, Part D: Rho Family (Methods in Enzymology, Volume 325) (Methods in Enzymology). Academic Press, 2000.

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18

(Editor), Ed Manser, and Thomas Leung (Editor), eds. GTPase Protocols: The Ras Superfamily (Methods in Molecular Biology). Humana Press, 2002.

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19

(Editor), John N. Abelson, Melvin I. Simon (Editor), W. E. Balch (Editor), Channing J. Der (Editor), and Alan Hall (Editor), eds. Regulators and Effectors of Small GTPases, Part D: Rho Family (Methods in Enzymology, Volume 325) (Methods in Enzymology). Academic Press, 2000.

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20

Kahn, Richard A. ARF Family GTPases (Proteins and Cell Regulation). Springer, 2004.

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21

(Editor), John N. Abelson, Melvin I. Simon (Editor), W. E. Balch (Editor), Channing J. Der (Editor), and Alan Hall (Editor), eds. Small Gtpases & Their Regulators: Part A: Ras Family (Methods in Enzymology). Academic Press, 1995.

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22

(Editor), John N. Abelson, Melvin I. Simon (Editor), W. E. Balch (Editor), Channing J. Der (Editor), and Alan Hall (Editor), eds. Small Gtpases & Their Regulators: Part A: Ras Family (Methods in Enzymology). Academic Press, 1995.

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23

Trabalzini, Lorenza, and Saverio Francesco Retta. Ras Signaling: Methods and Protocols. Humana Press, 2016.

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24

Kahn, Richard A. ARF Family GTPases. Springer, 2010.

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25

Kahn, Richard A. ARF Family GTPases. Springer London, Limited, 2006.

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26

(Editor), Mark Rush, and Peter D'Eustachio (Editor), eds. The Small GTPase Ran. Springer, 2001.

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27

(Editor), W. E. Balch, Channing J. Der (Editor), and Alan Hall (Editor), eds. GTPases Regulating Membrane Dynamics, Volume 404 (Methods in Enzymology). Academic Press, 2005.

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28

GTPases Regulating Membrane Dynamics, Volume 404 (Methods in Enzymology). Academic Press, 2005.

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29

Hall, Alan, Channing J. Der, and W. E. Balch. Regulators and Effectors of Small GTPases: Rho Family. Elsevier Science & Technology Books, 2006.

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30

Hall, Alan, Channing J. Der, and W. E. Balch. Regulators and Effectors of Small GTPases: Ras Family. Elsevier Science & Technology Books, 2006.

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31

Ras Superfamily of GTPases (1993). Taylor & Francis Group, 2017.

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32

Lacal, Juan Carlos, and Frank Patrick McCormick. Ras Superfamily of GTPases (1993). Taylor & Francis Group, 2017.

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33

Lacal, Juan Carlos, and Frank Patrick McCormick. Ras Superfamily of GTPases (1993). Taylor & Francis Group, 2017.

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34

Lacal, Juan Carlos, and Frank Patrick McCormick. Ras Superfamily of GTPases (1993). Taylor & Francis Group, 2017.

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35

(Editor), W. E. Balch, Channing J. Der (Editor), Alan Hall (Editor), John N. Abelson (Series Editor), and Melvin I. Simon (Series Editor), eds. Regulators and Effectors of Small GTPases, Part E: GTPases (Methods in Enzymology). Academic Press, 2001.

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36

Regulators and Effectors of Small GTPases: Ras Family, Volume 407 (Methods in Enzymology). Academic Press, 2006.

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37

(Editor), W. E. Balch, Channing J. Der (Editor), and Alan Hall (Editor), eds. Regulators and Effectors of Small GTPases: Ras Family, Volume 407 (Methods in Enzymology). Academic Press, 2006.

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38

Pearl, Phillip L., and William P. Welch. Pediatric Neurotransmitter Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0059.

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Abstract:
The pediatric neurotransmitter disorders represent an enlarging group of neurological syndromes characterized by inherited abnormalities of neurotransmitter synthesis, metabolism, and transport. Disorders involving monoamine synthesis include guanosine triphosphate cyclohydrolase deficiency (Segawa disease or classical Dopa-responsive dystonia as the heterozygous form), aromatic amino acid decarboxylase deficiency, tyrosine hydrolase deficiency, sepiapterin reductase deficiency, and disorders of tetrahydrobiopterin synthesis. These disorders can be classified according to whether they feature elevated serum levels of phenylalanine. Disorders of γ-amino butyric acid (GABA) metabolism include succinic semialdehyde dehydrogenase deficiency and GABA-transaminase deficiency. Glycine encephalopathy is typically manifested by refractory neonatal seizures due to a defect in the glycine degradative pathway. Pyridoxine-responsive seizures have now been associated with deficiency of α-aminoadipic semialdehyde dehydrogenase as well as a variants requiring therapy with pyridoxal-5-phosphate and folinic acid.
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