Results 71 to 80 of about 888,200 (233)

Manual for starch gel electrophoresis: A method for the detection of genetic variation [PDF]

open access: yes, 1987
The procedure to conduct horizontal starch gel electrophoresis on enzymes is described in detail. Areas covered are (I) collection and storage of specimens, (2) preparation of tissues, (3) preparation of a starch gel, (4) application of enzyme extracts ...
Aebersold, Paul B.   +4 more
core  

The Development of a Direct Homologous Radioimmunoassay for Serum Cortisol [PDF]

open access: yes, 1981
Peer ...
Giesemann, G.   +4 more
core   +2 more sources

PLPP/CIN Regulates Seizure Activity by the Differential Modulation of Calsenilin Binding to GluN1 and Kv4.2 in Mice

open access: yesFrontiers in Molecular Neuroscience, 2017
Calsenilin (CSEN) binds to Kv4.2 (an A-type K+ channel) as well as N-methyl-D-aspartate receptor (NMDAR), and modulates their activities. However, the regulatory mechanisms for CSEN-binding to Kv4.2 or NMDAR remain elusive. Here, we demonstrate the novel
Ji-Eun Kim   +6 more
doaj   +1 more source

Theoretical activity prediction, structure-based design, molecular docking and pharmacokinetic studies of some maleimides against Leishmania donovani for the treatment of leishmaniasis

open access: yesBulletin of the National Research Centre, 2022
Background Leishmaniasis is a neglected tropical disease caused by a group of protozoan of the genus Leishmania and transmitted to humans majorly through the bite of the female sand fly.
Fabian Audu Ugbe   +3 more
doaj   +1 more source

Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcome [PDF]

open access: yes, 2017
Mutations in PNPO are a known cause of neonatal onset seizures that are resistant to pyridoxine but responsive to pyridoxal phosphate (PLP). Mills etal. show that PNPO mutations can also cause neonatal onset seizures that respond to pyridoxine but worsen
Bala, Pronab   +25 more
core  

Structural and functional studies on Salmonella typhimurium pyridoxal kinase: the first structural evidence for the formation of Schiff base with the substrate

open access: yesThe FEBS Journal, 2019
A large number of enzymes depend on the ubiquitous cofactor pyridoxal 5′ phosphate (PLP) for their activity. Pyridoxal kinase (PLK) is the key enzyme involved in the synthesis of PLP from the three forms of vitamin B6 via the salvage pathway.
G. Deka   +5 more
semanticscholar   +1 more source

Mitochondrial Protein Import [PDF]

open access: yes, 1987
The role of nucleoside triphosphates (NTPs) in mitochondrial protein import was investigated with the precursors of N. crassa ADP/ATP carrier, F1-ATPase subunit β, F0-ATPase subunit 9, and fusion proteins between subunit 9 and mouse dihydrofolate ...
Arends   +72 more
core   +1 more source

Integrating gene and protein expression data with genome-scale metabolic networks to infer functional pathways [PDF]

open access: yes, 2013
This article has been made available through the Brunel Open Access Publishing Fund. Copyright @ 2013 Pey et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://
Beasley, JE   +4 more
core   +1 more source

Brain Pyridoxal Kinase. Mobility of the Substrate Pyridoxal and Binding of Inhibitors to the Nucleotide Site [PDF]

open access: yesEuropean Journal of Biochemistry, 1979
Pyridoxal kinase has been purified 2000‐fold from pig brain. The enzyme preparation migrates as a single protein and activity band on analytical gel electrophoresis. The interactions of the substrate pyridoxal and the inhibitor N‐dansyl‐2‐oxopyrrolidine (dansyl = 5‐dimethylaminonaph‐thalene‐1‐sulfonyl) with the catalytic site were examined by means of ...
F, Kwok, J E, Churchich
openaire   +2 more sources

The Concise Guide to PHARMACOLOGY 2015/16:Enzymes [PDF]

open access: yes, 2015
The Concise Guide to PHARMACOLOGY 2015/16 provides concise overviews of the key properties of over 1750 human drug targets with their pharmacology, plus links to an open access knowledgebase of drug targets and their ligands (www.guidetopharmacology.org),
Aldrich, R   +151 more
core   +4 more sources

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