Results 201 to 210 of about 95,409 (213)
Aberrant cellular signaling plays a pivotal role in the pathogenesis of acute myeloid leukemia (AML). Identifying key signaling components and their dependencies is crucial for advancing AML therapy. Here, we conducted a focused CRISPR library screen targeting 427 cell signaling-related genes with 3,416 sgRNAs (8 sgRNAs per gene) in the
Leisi Zhang +9 more
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In this communication we present some preliminary findings on the “cross-over points” which we observed when isolated electron transport complexes III and IV from beef heart mitochondria were studied in 90% glycerol. Three considerations led us to study electron transport in a medium of low water activity: 1) Such studies might allow the resolution of ...
H, Baum, J S, Rieske
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AbstractThe mitochondrial cytochrome oxidase (CO) genes are involved in complex IV of the electron transport system, and dysfunction of CO genes leads to several diseases. However, no work has been reported on the codon usage pattern of these genes. We used bioinformatic methods to analyze the compositional properties and the codon usage pattern of the
Arif Uddin +2 more
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Introduction: We have previously documented in a rat model of VF and closed-chest resuscitation that administration of erythropoietin (EPO) preserves left ventricular distensibility - yielding hemodynamically more effective CPR - and attenuates post-resuscitation myocardial dysfunction ...
Jeejabai Radhakrishnan +2 more
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AbstractMitochondrial encephalomyopathies resulting from electron transport chain (ETC) dysfunction can present with a wide spectrum of clinical manifestations having significant neuropathology and a progressive nature. Despite advances in diagnosis of ETC disorders, treatment still remains inadequate.
Nicola, Ioannou +5 more
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Abstract: l‐3,4‐Dihydroxyphenylalanine (l‐DOPA) is toxic for human neuroblastoma cells NB69 and its toxicity is related to several mechanisms including quinone formation and enhanced production of free radicals related to the metabolism of dopamine via monoamine oxidase type B.
B, Pardo, M A, Mena, J G, de Yébenes
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