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phosphoenolpyruvate and Glioblastoma

phosphoenolpyruvate has been researched along with Glioblastoma in 2 studies

Phosphoenolpyruvate: A monocarboxylic acid anion derived from selective deprotonation of the carboxy group of phosphoenolpyruvic acid. It is a metabolic intermediate in GLYCOLYSIS; GLUCONEOGENESIS; and other pathways.
phosphoenolpyruvate : A monocarboxylic acid anion resuting from selective deprotonation of the carboxy group of phosphoenolpyruvic acid.
phosphoenolpyruvic acid : A monocarboxylic acid that is acrylic acid substituted by a phosphonooxy group at position 2. It is a metabolic intermediate in pathways like glycolysis and gluconeogenesis.

Glioblastoma: A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
de Weille, J1
Fabre, C1
Gaven, C1
Bakalara, N1
Chinnaiyan, P1
Kensicki, E1
Bloom, G1
Prabhu, A1
Sarcar, B1
Kahali, S1
Eschrich, S1
Qu, X1
Forsyth, P1
Gillies, R1

Other Studies

2 other studies available for phosphoenolpyruvate and Glioblastoma

ArticleYear
Similar pyruvate kinase modifications in glioblastoma cells by 7β-hydroxycholesterol and glutamine withdrawal.
    Biochemical pharmacology, 2013, Jul-01, Volume: 86, Issue:1

    Topics: AMP-Activated Protein Kinases; Animals; Brain Neoplasms; Cell Cycle; Cell Line, Tumor; Cell Prolifer

2013
The metabolomic signature of malignant glioma reflects accelerated anabolic metabolism.
    Cancer research, 2012, Nov-15, Volume: 72, Issue:22

    Topics: Gas Chromatography-Mass Spectrometry; Glioblastoma; Glioma; Humans; Mesoderm; Metabolomics; Neoplasm

2012