Publications by authors named "David Monedero Alonso"

Pacinian corpuscles are rapidly adapting mechanoreceptor end-organs that detect transient touch and high-frequency vibration. In the prevailing model, these properties are determined by the outer core, which acts as a mechanical filter limiting static and low-frequency stimuli from reaching the afferent terminal-the sole site of touch detection in corpuscles. Here, we determine the detailed 3D architecture of corpuscular components and reveal their contribution to touch detection.

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The piRNA pathway is a conserved germline-specific small RNA pathway that ensures genomic integrity and continued fertility. In C. elegans and other nematodes, Type-I piRNAs are expressed from >10,000 independently transcribed genes clustered within two discrete domains of 1.

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Article Synopsis
  • - Over 95% of patients with Polycythemia Vera (PV) have a JAK2 V617F mutation, which leads to increased red blood cell production and a higher risk of blood clots.
  • - The study used mass spectrometry to reveal elevated levels of calcium-binding proteins and endoplasmic reticulum proteins in RBC membranes of PV patients compared to healthy individuals.
  • - Research indicates that JAK2 affects calcium balance and ion channel activity in RBCs, which may contribute to dehydration and changes in protein expression during red blood cell development, ultimately impacting potential clotting issues.
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Handbooks of physiology state that the strategy adopted by red blood cells (RBCs) to preserve cell volume is to maintain membrane permeability for cations at its minimum. However, enhanced cation permeability can be measured and observed in specific physiological and pathophysiological situations such as senescence, storage at low temperature, sickle cell anemia and many other genetic defects affecting transporters, membrane or cytoskeletal proteins. Among cation pathways, cation channels are able to dissipate rapidly the gradients that are built and maintained by the sodium and calcium pumps.

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We show that the novel variant p.S314P is a gain-of-function mutation but is less severe than the previously reported p.R352H variant.

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