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Accessibility and physico chemical features
2021-09-06

Accessibility and physico-chemical features of cysteine residues define their redox-reactivity and the 3-dimensional structure of GSNOR allows to identifying such surface-exposed, redox-sensitive cysteine residues. GSNOR crystal structures are available from human (Protein Data Bank code: 1MP0), tom
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Some biguanides can cross the mitochondrial membrane and inc
2021-09-06

Some biguanides can cross the mitochondrial membrane and increase L-lactate formation by inhibiting oxidative fasudil [34]. On the other hand, it has also been reported that levels of fasting plasma lactate in T2DM patients are similar regardless of whether or not metformin is administered [35] and
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br Material and methods br Results
2021-09-06

Material and methods Results The search for proteins selectively expressed in pancreatic islet lgk974 synthesis in the Human Protein Atlas (HPA) yielded 27 hits, including well-known islet cell markers such as insulin, glucagon and pancreatic polypeptide (Table 1). The search algorithm exclud
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The ability of FFA to
2021-09-06

The ability of FFA4 to elevate intracellular levels of Ca2+5, 38, 39, 40 provided early predictions of a key role of the phosphoinositidase C-linked G proteins Gq and/or G11 in transduction of signals from this receptor, while later studies that examined production of inositol phosphates [41] provid
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FSH and LH are glycoprotein dimers that are comprised
2021-09-06

FSH and LH, are glycoprotein dimers that are comprised of two subunits, a common α-subunit (αGSU) and a distinct β-subunit (FSHβ or LHβ, respectively), which determines the biological specificity of the gonadotropins (Ciccone and Kaiser, 2009, Gharib et al., 1990). The Sulfo-NHS-SS-Biotin of the go
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Whereas accurate measurement of glucagon in humans
2021-09-03

Whereas accurate measurement of glucagon in humans has been possible since the early 1950s proper measurements in rodents, have not. That said, plasma concentrations of glucagon have been reported in rodent studies [21] using C-terminal specific methods but what has been lacking is the secretory dyn
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The eradication of agonist activity in compound
2021-09-03

The eradication of agonist activity in compound was also confirmed in the ex vivo growth hormone (GH) release experiment conducted in isolated primary rat pituitary TAME as shown in . Compound did not produce any noticeable GH secretion at up to 10μM concentration. It could also antagonize the stimu
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The membrane metalloendopeptidase MME gene is
2021-09-03

The membrane metalloendopeptidase (MME) gene is located at human chromosome 3q21-27. It encodes a 100-kD type II transmembrane glycoprotein, a widely expressed membrane metalloendopeptidase that degrades a number of substrates. The active site of the enzyme faces the extracellular space. MME is wide
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The effects of C on the NF B pathway
2021-09-03

The effects of C646 on the NF-κB pathway could be explained by the role for p300 that has been described in the regulation of the NF-κB pathway [5]. For instance, acetylations of the p65 NF-κB subunit on lysines 218, 221 and 310 are mediated by the HATs p300 and PCAF [11] and increase transcriptiona
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This crosstalk may be responsible for
2021-09-03

This crosstalk may be responsible for the beneficial effects of histamine H2 receptor inverse agonists on Teneligliptin hydrobromide mg pathologies and may also explain unwanted effects of these drugs on other tissues. In this way, Allen et al. reported an anaphylactoid reaction following cessation
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Accompanied with apoptosis other ways of neuronal death also
2021-09-03

Accompanied with apoptosis, other ways of neuronal death also occur in ischemic salvinorin a due to the impairment of mitochondrial homeostasis [16]. Oxidative DNA damage activates poly (ADP-ribose) polymerase 1 (PARP-1) to induce regulated necrosis, referred to as parthanatos, in the brain [17]. O
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br Biochemical properties and post translational modificatio
2021-09-03

Biochemical properties and post-translational modification of GCAPs GCAPs are hydrophobic proteins that are likely permanently bound to their GC target under physiological conditions [5]. They interact with the photoreceptor GCs through the intracellular domains (reviewed in [17]). GCAP1 has been
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br Conclusions and future perspectives br Declarations of in
2021-09-03

Conclusions and future perspectives Declarations of interest Acknowledgements The authors thank Mrs. Kamala Pandey for the help in the preparation of this manuscript. This work was supported by NIH grants R01HL057531 and R01HL062147. Introduction Separation of short exons by long non-co
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Given that we planned to isolate
2021-09-02

Given that we planned to isolate the GluN1/GluN3A receptor by immunoaffinity chromatography using a Myc epitope tag on GluN3A, we first checked that the tag does not affect the functional properties of the receptor. To do this we co-transfected HEK-293 cells with DNA encoding WT GluN1 and either WT
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In conclusion we demonstrated that the atypical high basal
2021-09-02

In conclusion, we demonstrated that the atypical high-basal activity of the mGlu3 Ranitidine results mostly from its activation by low ambient glutamate concentrations. This is due to a unique interaction network located in the extracellular domain of the mGlu3 receptor. This network acts as “Cl− l
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