Results 111 to 120 of about 40,643 (298)

Structural insights into the orthosteric inhibition of P2X receptors by non-ATP analog antagonists

open access: yeseLife
P2X receptors are extracellular ATP-gated ion channels that form homo- or heterotrimers and consist of seven subtypes. They are expressed in various tissues, including neuronal and nonneuronal cells, and play critical roles in physiological processes ...
Danqi Sheng   +7 more
doaj   +1 more source

Purification and properties of diaminopimelate decarboxylase of Micrococcus glutamicus [PDF]

open access: yes, 1981
Diaminopimelate decarboxylase (EC 4.1.1.20) of Micrococcus glutamicus ATCC 13059 was purified to homogeneity. The enzyme had an apparent molecular weight of 191,000 as determined by gel filtration on Sephadex G-200. At protein concentrations of 20 and 10
Lakshman, Meena   +2 more
core   +1 more source

Impact of polysaccharides on advancing plant‐based meat alternatives

open access: yesFood Biomacromolecules, EarlyView.
An outline of plant‐based meat production by incorporating polysaccharides. Abstract Plant‐based meat products are a valued choice for vegetarians and others. Their production has been perceived as an innovation promoting animal welfare and sustainability.
Prashant Dahal   +2 more
wiley   +1 more source

Structural and biophysical analysis of important biomedical enzymes and nano-architectures [PDF]

open access: yes, 2008
Dopa decarboxylase (DDC) is an important enzyme in the catecholamine biosynthesis pathways. Catecholamines, e.g., dopamine, serotonin, etc. often are the major neuromodulators or neurotransmitters.
Chattopadhyay, Arundhati
core   +1 more source

Molecular and cellular mechanisms underlying gyrate atrophy: Why is the retina primarily affected?

open access: yesActa Ophthalmologica, EarlyView.
Abstract Gyrate atrophy of the choroid and retina (GACR; OMIM #258870) is a rare early‐onset autosomal recessive disorder, caused by bi‐allelic pathogenic variants in the gene coding for ornithine aminotransferase (OAT) resulting in hyperornithinaemia.
Mark J. N. Buijs   +12 more
wiley   +1 more source

Plasma Pyridoxal 5´-Phosphate Level in Children with Intractable and Controlled Epilepsy [PDF]

open access: yes
Objective Intractable epilepsy is a serious neurologic problem with different etiologies. Decreased levels of pyridoxal phosphate in cerebral spinal fluid of patients with intractable epilepsy due to pyridoxine dependency epilepsy are reported.
Ghofrani, Mohammad   +2 more
core  

Inflammation causes tissue-specific depletion of vitamin B(6) [PDF]

open access: yes, 2005
Previously we observed strong and consistent associations between vitamin B(6 )status and several indicators of inflammation in patients with rheumatoid arthritis.
Chiang, En-Pei   +5 more
core   +3 more sources

Bioinformatics Comparison of \u3cem\u3eM. ruber\u3c/em\u3e Mrub_2507 to \u3cem\u3eE. coli\u3c/em\u3e pdxK/b1636 and \u3cem\u3eM. ruber\u3c/em\u3e Mrub_2888 to \u3cem\u3eE. coli\u3c/em\u3e pdxH/b1638 to Determine the Orthologous Nature [PDF]

open access: yes, 2016
This project is part of the Meiothermus ruber genome analysis project, which uses the bioinformatics tools associated with the Guiding Education through Novel Investigation – Annotation Collaboration Toolkit (GENI-ACT) to predict gene function.
Bernardi, Adam, Scott, Dr. Lori
core   +1 more source

Highly efficient generation of pulsed photon pair using a bulk Periodically Poled Potassium Titanyl Phosphate [PDF]

open access: yes, 2003
In this paper, we demonstrate efficient generation of collinearly propagating, degenerate pulsed photon pairs based on a bulk Periodically Poled Potassium Titanyl Phosphate pumped by an ultrashort pulse laser. Using a single-mode fiber as a spatial mode filter, we detect about 3200 coincidence counts per second per milliwatt pump power.
arxiv   +1 more source

Potassium current inactivation as a novel pathomechanism for KCNQ2 developmental and epileptic encephalopathy

open access: yesEpilepsia, EarlyView.
Abstract De novo variants in KCNQ2 cause neonatal onset developmental and epileptic encephalopathy (KCNQ2‐DEE; Online Mendelian Inheritance in Man #613720), most often by loss‐of‐function in vitro effects. In this study, we describe a neonatal onset DEE proband carrying a recurrent de novo KCNQ2 variant (c.794C>T; p.A265V) affecting the pore domain of ...
Ingride Luzio Gaspar   +6 more
wiley   +1 more source

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