Results 201 to 210 of about 56,803 (290)

Cardiovascular β‐Adrenergic Receptor Distribution and Function: Influence of Species, Sex, Age, and Tissue

open access: yesComprehensive Physiology, Volume 16, Issue 3, June 2026.
Estrogen modulates β‐AR signaling in a context‐dependent manner influenced by species, sex, age, tissue, and vascular health, highlighting challenges in translating findings from experimental models to human cardiovascular physiology. ABSTRACT Cardiovascular diseases remain the leading global cause of morbidity and mortality, with notable sex‐specific ...
Basant Elsaid   +5 more
wiley   +1 more source

The Recycling Endosomal (Na+, K+)/H+ Exchanger NHE6/SLC9A6 Facilitates Signal Transduction by Shuttling Cyclin‐Dependent Kinase 5 to the Plasma Membrane

open access: yesActa Physiologica, Volume 242, Issue 6, June 2026.
ABSTRACT Aim The alkali cation/proton exchanger NHE6/SLC9A6 regulates luminal pH homeostasis and trafficking of recycling endosomes in most tissues, especially neurons. Loss‐of‐function mutations in NHE6 cause Christianson Syndrome, an X‐linked neurodevelopmental and neurodegenerative disorder; however, the underlying molecular and cellular mechanisms ...
Rebecca Flessner   +6 more
wiley   +1 more source

FUNCTIONS OF MICRODOMAINS OF VACUOLAR MEMBRANE [PDF]

open access: yesBook of proceedings of The Second All-Russian Scientific Conference with international participation "Regulation Mechanisms of Eukariotic Cell Organelle Functions", 2018
I.S. Nesterkina   +5 more
openaire   +1 more source

Mitochondrial Transplantation as a New Therapeutic Approach Against Cardiac and Renal Consequences in Male Rats With Myocardial Infarction

open access: yesActa Physiologica, Volume 242, Issue 6, June 2026.
ABSTRACT Aim Myocardial infarction (MI) is one of the leading causes of death worldwide. MI is associated with cardiac structural and functional alterations. Among these, cardiac fibrosis may be significantly influenced by mitochondrial dysfunction. We sought to evaluate whether the injection of functional mitochondria from healthy muscle could improve
María Cuesta‐Corral   +13 more
wiley   +1 more source

Molecular Probes for Tracking Reactive Oxygen Species at the Organelle Interface

open access: yesAnalysis &Sensing, Volume 6, Issue 3, May 2026.
This perspective charts the frontier of visualizing compartmentalized redox signaling across mitochondria, the ER, lysosomes, and the underexplored peroxisome. It discusses evolving molecular probe designs, the integration of multiplexed imaging, and the specific engineering challenges for tracking ROS at organelle interfaces.
Daniela Ceballos‐Ávila   +1 more
wiley   +1 more source

Rational Design and Operando Characterization of Hierarchical α‐FeOOH‐FeP/Ni3S2 Catalysts for High‐Rate Alkaline Water Electrolysis

open access: yesENERGY &ENVIRONMENTAL MATERIALS, Volume 9, Issue 3, May 2026.
A hierarchical FeOOH–FeP@Ni3S2 electrocatalyst is engineered on 3D Ni foam to enable efficient alkaline oxygen evolution. Operando spectroscopic techniques reveal dynamic surface reconstruction and proton‐coupled electron transfer (PCET) kinetics. The catalyst exhibits low overpotential and industrial‐level current operation, driving high‐performance ...
Maria S. Metaxa   +2 more
wiley   +1 more source

Lipidome Analysis of Cancer Cells and Their Extracellular Vesicles Reveals Cancer‐Type‐Specific Lipid Signatures and Enables the Design of EV‐Mimetic Liposomes

open access: yesJournal of Extracellular Vesicles, Volume 15, Issue 5, May 2026.
ABSTRACT Lipid metabolism reprogramming is a hallmark of cancer, yet the global lipidome of cancer cells and their extracellular vesicles (EVs) remains poorly understood. Using mass spectrometry, we analyzed the lipid profiles of a panel of human cancer and non‐cancer cell lines along with their secreted EVs.
Noélie Douanne   +14 more
wiley   +1 more source

Differential Trafficking Phenotypes of NPC1 Mutant Proteins Reveal Distinct Cholesterol Accumulation Profiles

open access: yesJournal of Inherited Metabolic Disease, Volume 49, Issue 3, May 2026.
ABSTRACT Niemann‐Pick disease type C (NPC) is a rare autosomal recessive lysosomal storage disorder that affects approximately 1 in 100 000 live births. It is primarily caused by mutations in the NPC1 gene, which disrupts intracellular cholesterol transport and leads to lipid accumulation in late endosomes and lysosomes.
Sanaa Abdelmalek Mahmoud   +3 more
wiley   +1 more source

Missense mutations on SynGAP C2 domain impair membrane diffusion

open access: yesProtein Science, Volume 35, Issue 5, May 2026.
Abstract SYNGAP1 mutations have been linked to a range of neuropathological disorders and, more recently, to the insurgence of cancer. SynGAP is a postsynaptic Ras GTPase‐activating protein that regulates Ras/ERK signaling and synaptic plasticity. All SynGAP isoforms share a conserved C2–RasGAP core, where the C2 domain may mediate interactions with ...
Mattia Miotto   +4 more
wiley   +1 more source

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