Latest papers

Heterogeneity amongst 5-HT₃ receptor subunits: is this significant?

[Voltage-dependent calcium channels of different types in the neuro-muscular synapses of vertebrates and their contribution to modulation of the neurosecretion process].

The N-terminal domain of the V-ATPase subunit 'a' is regulated by pH in vitro and in vivo.

Cooperativity of protein binding to vesicles.

Crystallography and electron microscopy of chaperone/usher pilus systems.

[Activation of the phosphatidylinositol-3'-kinase pathway with lectin-induced signal through sialo-containing glycoproteins of leukocyte membranes under type 1 diabetes mellitus].

The Ccr4-Not complex interacts with the mRNA export machinery.

[Molecular mechanisms of glutamic AMPA receptors functioning and regulation in chronic pain].

Head swivel on the ribosome facilitates translocation by means of intra-subunit tRNA hybrid sites.

Association of the subunits of the calcium-independent receptor of α-latrotoxin.

Subunit exchange rates in Hepatitis B virus capsids are geometry- and temperature-dependent.

ATP synthases: cellular nanomotors characterized by LILBID mass spectrometry.

Low (60 cGy) doses of (56)Fe HZE-particle radiation lead to a persistent reduction in the glutamatergic readily releasable pool in rat hippocampal synaptosomes.

Growth factor receptor-bound protein 14: a new modulator of photoreceptor-specific cyclic-nucleotide-gated channel.

Beta-adrenergic-regulated phosphorylation of the skeletal muscle Ca(V)1.1 channel in the fight-or-flight response.

Two abundant proteasome subtypes that uniquely process some antigens presented by HLA class I molecules.

The proteasome antechamber maintains substrates in an unfolded state.

Cytochrome c oxidase loses catalytic activity and structural integrity during the aging process in Drosophila melanogaster.

Dimerization of G protein-coupled purinergic receptors: increasing the diversity of purinergic receptor signal responses and receptor functions.

The vacuolar ATPase in bone cells: a potential therapeutic target in osteoporosis.