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Showing results for acetyl coenzyme a. Your search for Acetonyl-coenzyme a retrieved no results.

Select item 44036681.

StatPearls [Internet].

Treasure Island (FL): StatPearls Publishing; 2024 Jan-.

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GeneReviews® [Internet].

Adam MP, Feldman J, Mirzaa GM, et al., editors.

Seattle (WA): University of Washington, Seattle; 1993-2024.

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Select item 34012943.

Endotext [Internet].

Feingold KR, Anawalt B, Blackman MR, et al., editors.

South Dartmouth (MA): MDText.com, Inc.; 2000-.

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The Heterogeneity of Cancer Metabolism [Internet]. 2nd edition.

Le A, editor.

Cham (CH): Springer; 2021.

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Basic Neurochemistry: Molecular, Cellular and Medical Aspects. 6th edition.

Siegel GJ, Agranoff BW, Albers RW, et al., editors.

Philadelphia: Lippincott-Raven; 1999.

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Select item 29026906.

Assay Guidance Manual [Internet].

Markossian S, Grossman A, Arkin M, et al., editors.

Bethesda (MD): Eli Lilly & Company and the National Center for Advancing Translational Sciences; 2004-.

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Molecular Biology of the Cell. 4th edition.

Alberts B, Johnson A, Lewis J, et al.

New York: Garland Science; 2002.

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WormBook: The Online Review of C. elegans Biology [Internet].

Pasadena (CA): WormBook; 2005-2018.

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Madame Curie Bioscience Database [Internet].

Austin (TX): Landes Bioscience; 2000-2013.

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Diesel and Gasoline Engine Exhausts and Some Nitroarenes.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 1989. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 46.)

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Molecular Imaging and Contrast Agent Database (MICAD) [Internet].

Bethesda (MD): National Center for Biotechnology Information (US); 2004-2013.

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NTP Technical Report on the Toxicology Studies of Bromodichloroacetic Acid (CASRN 71133-14-7) in F344/N Rats and B6C3F1/N Mice and Toxicology and Carcinogenesis Studies of Bromodichloroacetic Acid in F344/NTac Rats and B6C3F1/N Mice (Drinking Water Studies): Technical Report 583 [Internet].

National Toxicology Program.

Research Triangle Park (NC): National Toxicology Program; 2015 Oct.

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Select item 407287213.

Trichloroethylene, Tetrachloroethylene, and Some Other Chlorinated Agents.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 2014. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 106.)

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Select item 420372014.

Streptococcus pyogenes : Basic Biology to Clinical Manifestations [Internet].

Ferretti JJ, Stevens DL, Fischetti VA, editors.

Oklahoma City (OK): University of Oklahoma Health Sciences Center; 2016-.

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Annual Reviews Collection [Internet].

Bethesda (MD): National Center for Biotechnology Information (US); 2002 Nov.

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NIEHS Report on the In Vivo Repeat Dose Biological Potency Study of 6:1 Fluorotelomer Alcohol (CASRN 375-82-6) in Sprague Dawley (Hsd:Sprague Dawley® SD®) Rats (Gavage Studies): NIEHS Report 07 [Internet].

Auerbach SS, Aillon KL, Ballin JD, et al.

Research Triangle Park (NC): National Institute of Environmental Health Sciences; 2023 Mar.

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Select item 310904217.

Food Components to Enhance Performance: An Evaluation of Potential Performance-Enhancing Food Components for Operational Rations.

Institute of Medicine (US) Committee on Military Nutrition Research; Marriott BM, editor.

Washington (DC): National Academies Press (US); 1994.

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Select item 144161818.

Helicobacter pylori: Physiology and Genetics.

Mobley HLT, Mendz GL, Hazell SL, editors.

Washington (DC): ASM Press; 2001.

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Select item 538535019.

Introduction to Epigenetics [Internet].

Paro R, Grossniklaus U, Santoro R, et al.

Cham (CH): Springer; 2021.

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Select item 441081220.

Some Chemicals Used as Solvents and in Polymer Manufacture.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 2017. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 110.)

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Supplemental Content

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Fig. 1.1

Synthesis and metabolism of acetylcholine (ACh). Choline acetyltransferase (ChAT) and acetylcholinesterase (AChE) are involved in synthesis and metabolism of ACh. ACh is synthesized from Acetyl coenzyme A (Acetyl-CoA) and Choline, releasing Coenzyme A (HS-CoA)

Overview.

Akaike A, Shimohama S, Misu Y, editors. Nicotinic Acetylcholine Receptor Signaling in Neuroprotection [Internet]. Singapore: Springer; 2018.
Figure 2-20Acetyl coenzyme A (acetyl CoA)

This crucial metabolic intermediate is generated when acetyl groups, produced in stage 2 of catabolism, are covalently linked to coenzyme A (CoA).

Food and the Derivation of Cellular Energy .

Alberts B, Bray D, Lewis J, et al. Molecular Biology of the Cell. 3rd edition. New York: Garland Science; 1994.
Figure 14-8Acetyl coenzyme A (acetyl CoA)

This central intermediate is produced during the breakdown of foodstuffs in the mitochondrion. A space-filling model is shown above a common abbreviation (see also Figure2-20). The sulfur atom (S) forms a thioester linkage to acetate. Because this is a "high-energy" linkage, which releases a large amount of free energy when it is hydrolyzed, the acetate group can be readily transferred to other molecules, such as oxaloacetate (see Figure 14-14).

The Mitochondrion .

Alberts B, Bray D, Lewis J, et al. Molecular Biology of the Cell. 3rd edition. New York: Garland Science; 1994.
Figure 6

(a) The chemical structure of acetyl coenzyme A. The characteristic sharp bend observed in the bound forms of AcCoA and CoA in GNAT superfamily members is around the bond highlighted by the starred carbon atoms. (b) The general reaction catalyzed by GCN5-related N-acetyltransferases, showing the presumed tetrahedral intermediate that results from nucleophilic attack of a primary amine on the acyl carbon of the acetyl group.

GCN5-Related N-Acetyltransferases: A Structural Overview.

Annual Reviews Collection [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2002 Nov.