Relevant bibliographies by topics / Pyruvate / Books

Books on the topic 'Pyruvate'

To see the other types of publications on this topic, follow the link: Pyruvate.
Author: Grafiati
Published: 4 June 2021
Last updated: 14 March 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 48 books for your research on the topic 'Pyruvate.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse books on a wide variety of disciplines and organise your bibliography correctly.

1

B, Keech D., and Wallace J. C, eds. Pyruvate carboxylase. Boca Raton, Fla: CRC Press, 1985.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Yazdanpanah, Mehrdad. Pyruvate improves myocardial functional recovery after ischemia and reperfusion. Ottawa: National Library of Canada, 1998.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Dykshoorn, Philip. Identification of an upstream activating sequence of the yeast pyruvate kinase gene (PYK). Ottawa: National Library of Canada, 1990.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Lesicki, Andrzej. Fosfofruktokinaza i kinaza pirogronianowa w tkankach skorupiaków i owadów. 3rd ed. Poznań: Wydawn. Nauk. Uniwersytetu im. Adama Mickiewicza, 1993.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Staples, Elizabeth M. The effects of R(+)-lipoic acid supplementation on regulation of human skeletal muscle pyruvate dehydrogenase. St. Catharines, Ont: Brock University, Faculty of Applied Health Science, 2006.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

MacPherson, Laura Lynn. Adaptations of skeletal muscle pyruvate dehydrogenase kinase in response to food-restriction in mitochondrial subpopulations. St. Catharines, Ont: Brock University, Faculty of Applied Health Sciences, 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

International Meeting on the Function of Thiamin Diphosphate Enzymes (1990 Blaubeuren, Germany). Biochemistry and physiology of thiamin diphosphate enzymes: Proceedings of the International Meeting on the Function of Thiamin Diphosphate Enzymes, held in Blaubeuren, October 1990. Weinheim: VCH, 1991.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Parker, James N., and Philip M. Parker. Pyruvate carboxylase deficiency: A bibliography and dictionary for physicians, patients, and genome researchers [to Internet references]. San Diego, CA: ICON Health Publications, 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Pyruvate: The natural dietary supplement that increases exercise endurance, promotes fat loss, and regulates blood sugar metabolism. New Canaan, Conn: Keats Pub., 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Bornemann, Stephen. Studies on pyruvate decarboxylase-catalysed acyloin formation and the effects of surfactants on lipase-catalysedhydrolysis of esters. [s.l.]: typescript, 1992.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
11

Bigrigg, Jonathan Kent. Carbohydrate refeeding rapidly reverses the adaptive upregulation of human skeletal muscle pyruvate dehydrogenase kinase following a high fat diet. St. Catharines, Ont: Brock University, Dept. of Physical Education and Kinesiology, 2004.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
12

Shahi, B. Chopra. Studies on the uptake and utilization of pyruvate and glucose by isolated segmental ganglia of the leech Haemopis Sanguisuga. Salford: University of Salford, 1987.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
13

Keogh, Adrian Colin. Anti-mitochondrial antigen on human biliary epithelial cells [: A study of membrane expression of dihydrolipoamide acetyltransferase sub unit of pyruvate dehydrogenase on human biliary epithelial cells]. Birmingham: University of Birmingham, 2001.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
14

Bjorkman, Camilla. Methodological and biochemical aspects of acetylcholinesterase and acetate in blood from cattle , and acetyl-CoA synthesizing enzymes in spinal cord from ruminants and monogastric animals. Uppsala: Sveriges Lantbruksuniversitet, 1989.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
15

Burke, Edmund R. Pyruvate. McGraw-Hill, 1998.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
16

Keech. Pyruvate Carboxylase. Edited by D. B. Keech and J. C. Wallace. CRC Press, 2018. http://dx.doi.org/10.1201/9781351076142.

Full text
APA, Harvard, Vancouver, ISO, and other styles
17

Pyruvate Carboxylase. Taylor & Francis Group, 2017.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
18

Keech. Pyruvate Carboxylase. Taylor & Francis Group, 2018.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
19

Keech. Pyruvate Carboxylase. Taylor & Francis Group, 2018.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
20

Keech. Pyruvate Carboxylase. Taylor & Francis Group, 2018.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
21

Keech. Pyruvate Carboxylase. Taylor & Francis Group, 2018.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
22

The Power of Pyruvate. Keats Publishing, 1999.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
23

Janssen, Mirian C. H., and Shamima Rahman. Pyruvate Dehydrogenase Complex Deficiency. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0006.

Full text
Abstract:
Pyruvate dehydrogenase complex (PDHc) deficiency usually first manifests at a young age and is rarely diagnosed in adulthood. The clinical picture varies from neonatal death with overwhelming lactic acidosis to a relatively benign course early in life. The three main presentations are congenital lactic acidosis, Leigh syndrome, and episodic ataxia. Treatment consists of a ketogenic diet and cofactor supplementation with thiamine. Successful therapy is rare.
APA, Harvard, Vancouver, ISO, and other styles
24

Grace, Rachael. Fast Facts: Pyruvate Kinase Deficiency. Health Press Limited, 2018.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
25

Glader, B., W. Barcellini, and R. Grace. Fast Facts: Pyruvate Kinase Deficiency. Karger AG, S., 2018.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
26

Molly Theresa L.V Smith. Studies in the purification of phosphoenol-pyruvate. 1985.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
27

Seyda, Agnieszka. Pyruvate dehydrogenase complex-correlation between structure and function. 2001.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
28

The Pyruvate Phenomenon: The Facts, the Benefits, the Unanswered Questions. Woodland Publishing, 1999.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
29

Roy, Shukla. Regulation of hepatic pyruvate carboxylase in 2,3,7,8-Tetrachlorodibenzo-p-dioxin treated C57BL/6J mice and their pair-fed controls. 1998.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
30

Gish, Gerald Daniel. A mechanistic investigation of the thiamin diphosphate-dependent enzyme pyruvate decarboxylase. 1986.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
31

Sparrow, Barney R. Characterization of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induced modification of hepatic pyruvate carboxylase gene expression in C57BL/6J male mice. 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
32

Sparrow, Barney R. Characterization of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induced modification of hepatic pyruvate carboxylase gene expression in C57BL/6J male mice. 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
33

Prokop, David. Pyruvate: The Super Strength, Stamina and Weight-Loss Supplement (Woodland Health Series). Woodland Publishing, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
34

Glader, B., W. Barcellini, and R. Grace. Fast Facts : déficit en Pyruvate Kinase: Sensibilisation à Cette Maladie Génétique Rare. Karger AG, S., 2019.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
35

Carbone, Mary Anna. Human pyruvate carboxylase deficiency: Correlation of genotypes with the clinical and biochemical phenotypes. 2002.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
36

Chun, Kathy M. Characterization of mutations in the E1[alpha] subunit of the pyruvate dehydrogenase complex. 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
37

Schellenberger, Alfred. Thiamin Pyrophosphate Biochemistry, Vol. II: The Pyruvate Dehydrogenase Complex and Prospects for the Future. Crc Pr I Llc, 1988.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
38

Bevacqua, Robert Francis. Mineral nutrition, pyruvate kinase activity, and protein concentration in 'd'Anjou' pear fruit affected by cork spot. 1989.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
39

Veech, Richard L., and M. Todd King. Alzheimer’s Disease. Edited by Detlev Boison. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190497996.003.0026.

Full text
Abstract:
Deficits in cerebral glucose utilization in Alzheimer’s disease (AD) arise decades before cognitive impairment and accumulation of amyloid plaques and neurofibrillary tangles in brain. Addressing this metabolic deficit has greater potential in treating AD than targeting later disease processes – an approach that has failed consistently in the clinic. Cerebral glucose utilization requires numerous enzymes, many of which have been shown to decline in AD. Perhaps the most important is pyruvate dehydrogenase (PDH), which links glycolysis with the Krebs cycle and aerobic metabolism, and whose activity is greatly suppressed in AD. The unique metabolism of ketone bodies allows them to bypass the block at pyruvate dehydrogenase and restore brain metabolism. Recent studies in mouse genetic models of AD and in a human Alzheimer’s patient showed the potential of ketones in maintaining brain energetics and function. Oral ketone bodies might be a promising avenue for treatment of Alzheimer’s disease.
APA, Harvard, Vancouver, ISO, and other styles
40

Grace, Rachael. Fast Facts : Pyruvate Kinase Deficiency for Patients and Supporters: A Rare Genetic Disease That Affects Red Blood Cells. Karger AG, S., 2019.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
41

Christofk, Heather Renee. The M2 splice isoform of pyruvate kinase is a phosphotyrosine binding protein critical for tumor cell metabolism and proliferation. 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
42

S, Patel Mulchand, Roche Thomas E, and Harris Robert A. 1939-, eds. Alpha-keto acid dehydrogenase complexes. Boston: Birkhäuser Verlag, 1996.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
43

Sherwood, Dennis, and Paul Dalby. The bioenergetics of living cells. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198782957.003.0024.

Full text
Abstract:
Living systems create order, and appear to break the Second Law. This chapter explains, and resolves, this apparent paradox, drawing on the concept of coupled reactions (as introduced in Chapters 13 and 16), as mediated by ‘energy currencies’ such as ATP and NADH. The chapter then examines the key energy-capturing systems in biological systems – glycolysis and the citric acid cycle, and also photosynthesis. Topics covered include how energy is captured in the conversion of glucose to pyruvate, the mitochondrial membrane, respiration, electron transport, ATP synthase, chloroplasts and thylakoids, photosystems I and II, and the light-independent reactions of photosynthesis.
APA, Harvard, Vancouver, ISO, and other styles
44

Grace, Rachael. Fast Facts : le déficit en Pyruvate Kinase Pour les Patients et les Accompagnants: Une Maladie Génétique Rare Qui Affecte les Globules Rouges. Karger AG, S., 2019.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
45

Hsieh, David T., and Elizabeth A. Thiele. Ketogenic Diet for Other Epilepsies. Edited by Eric H. Kossoff. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190497996.003.0007.

Full text
Abstract:
The ketogenic diet is the treatment of choice for epilepsy in certain disorders of brain metabolism, in particular glucose transporter protein 1 deficiency and pyruvate dehydrogenase deficiency. The International Ketogenic Diet Study Group has listed several other conditions for which the ketogenic diet has been reported as being particularly beneficial and could be offered earlier. Whether efficacy in these conditions is due in part to the broad-spectrum efficacy of the ketogenic diet or to specific mechanisms specific to these conditions is still under investigation. This chapter discusses the use of dietary therapies for the treatment of epilepsy in certain genetic disorders, including Rett syndrome and tuberous sclerosis complex, as listed by the International Ketogenic Diet Study Group, and additionally discusses the use of epilepsy dietary therapies in patients with Angelman syndrome and Sturge-Weber syndrome.
APA, Harvard, Vancouver, ISO, and other styles
46

Provan, Drew, Trevor Baglin, Inderjeet Dokal, and Johannes de Vos. Red cell disorders. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199683307.003.0002.

Full text
Abstract:
The peripheral blood film in anaemias - Anaemia in renal disease - Anaemia in endocrine disease - Anaemia in joint disease - Anaemia in gastrointestinal disease - Anaemia in liver disease - Iron (Fe) deficiency anaemia - Vitamin B12 deficiency - Folate deficiency - Other causes of megaloblastic anaemia - Anaemia in other deficiency states - Haemolytic syndromes - Genetic control of haemoglobin production - Sickling disorders - HbS—sickle-modifying therapies - Sickle cell trait (HbAS) - Other sickling disorders - Other haemoglobinopathies - Unstable haemoglobins - Thalassaemias - α thalassaemia - β thalassaemia - Other thalassaemias - Hereditary persistence of fetal haemoglobin - Hb patterns in haemoglobin disorders - Non-immune haemolysis - Hereditary spherocytosis - Hereditary elliptocytosis - Glucose-6-phosphate dehydrogenase (G6PD) deficiency - Pyruvate kinase deficiency - Other red cell enzymopathies - Drug-induced haemolytic anaemia - Methaemoglobinaemia - Microangiopathic haemolytic anaemia - Acanthocytosis - Autoimmune haemolytic anaemia - Cold haemagglutinin disease - Leucoerythroblastic anaemia - Aplastic anaemia - Paroxysmal nocturnal haemoglobinuria - Pure red cell aplasia - Iron (Fe) overload - Transfusion haemosiderosis
APA, Harvard, Vancouver, ISO, and other styles
47

Provan, Drew, Trevor Baglin, Inderjeet Dokal, Johannes de Vos, Banu Kaya, and Angela Theodoulou. Red cell disorders. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199683307.003.0002_update_001.

Full text
Abstract:
The peripheral blood film in anaemias - Anaemia in renal disease - Anaemia in endocrine disease - Anaemia in joint disease - Anaemia in gastrointestinal disease - Anaemia in liver disease - Iron (Fe) deficiency anaemia - Vitamin B12 deficiency - Folate deficiency - Other causes of megaloblastic anaemia - Anaemia in other deficiency states - Haemolytic syndromes - Genetic control of haemoglobin production - Sickling disorders - HbS—sickle-modifying therapies - Sickle cell trait (HbAS) - Other sickling disorders - Other haemoglobinopathies - Unstable haemoglobins - Thalassaemias - α‎ thalassaemia - β‎ thalassaemia - Other thalassaemias - Hereditary persistence of fetal haemoglobin - Hb patterns in haemoglobin disorders - Non-immune haemolysis - Hereditary spherocytosis - Hereditary elliptocytosis - Glucose-6-phosphate dehydrogenase (G6PD) deficiency - Pyruvate kinase deficiency - Other red cell enzymopathies - Drug-induced haemolytic anaemia - Methaemoglobinaemia - Microangiopathic haemolytic anaemia - Acanthocytosis - Autoimmune haemolytic anaemia - Cold haemagglutinin disease - Leucoerythroblastic anaemia - Aplastic anaemia - Paroxysmal nocturnal haemoglobinuria - Pure red cell aplasia - Iron (Fe) overload - Transfusion haemosiderosis
APA, Harvard, Vancouver, ISO, and other styles
48

Buchaklian, Adam H., and David P. Dimmock. Citrin Deficiency. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0018.

Full text
Abstract:
Citrin deficiency is an inborn error of metabolism that appears to affect both the urea cycle and energy generation. Worldwide, citrin deficiency is likely one of the commonest inborn errors of metabolism, 60,000–80,000 individuals are estimated to have citrin deficiency in China alone. Children typically present with an abnormal newborn screen or neonatal intrahepatic cholestasis with citrin deficiency (NICCD). Adults typically present clinically with neuropsychiatric symptoms, hepatic dysfunction and hyperammonemia. As plasma amino acids typically show an elevated citrulline at the time of crisis, this presentation is known as citrullinemia type II (CTLN2). Without therapy, cases may progress to liver failure. Individuals may also suffer recurrent pancreatitis. In contrast to other urea cycle defects, the treatment for citrin deficiency requires a high protein, low carbohydrate diet. Acute hyperammonemia responds to arginine therapy. Sodium pyruvate has been reported to provide benefit. In addition many cases will require restriction of galactose. Liver transplant fully corrects the CTLN2 phenotype.
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the bibliographies on the topic 'Pyruvate' for other source types:
Journal articles Dissertations / Theses
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography