scholarly article | Q13442814 |
review article | Q7318358 |
P6179 | Dimensions Publication ID | 1033751246 |
P356 | DOI | 10.1186/S12976-016-0042-5 |
P3181 | OpenCitations bibliographic resource ID | 1011826 |
P932 | PMC publication ID | 4896004 |
P698 | PubMed publication ID | 27267202 |
P50 | author | Felix Scholkmann | Q56605899 |
P2093 | author name string | Felix Scholkmann | |
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Testes of Astyanax altiparanae: the Sertoli cell functions in a semicystic spermatogenesis | Q46898562 | ||
Estimation of the number of biophotons involved in the visual perception of a single-object image: biophoton intensity can be considerably higher inside cells than outside | Q48149427 | ||
Hypothesis about brilliant lights by bioluminescent photons in near death experiences | Q48541914 | ||
Endogenous spontaneous ultraweak photon emission in the formation of eye-specific retinogeniculate projections before birth | Q49162454 | ||
Actin filaments as the fast pathways for calcium ions involved in auditory processes | Q50351962 | ||
Wiring through tunneling nanotubes--from electrical signals to organelle transfer | Q37991687 | ||
Electric fields generated by synchronized oscillations of microtubules, centrosomes and chromosomes regulate the dynamics of mitosis and meiosis | Q38022780 | ||
Tunneling nanotubes, an emerging intercellular communication route in development | Q38068038 | ||
Membrane nanotubes: novel communication between distant cells | Q38134575 | ||
Non-chemical and non-contact cell-to-cell communication: a short review | Q38149129 | ||
Biophoton signal transmission and processing in the brain. | Q38181718 | ||
Tunneling nanotubes: Diversity in morphology and structure | Q38207996 | ||
Biological wires, communication systems, and implications for disease. | Q38275476 | ||
Cell cycle regulation of mitochondrial function | Q38281167 | ||
Two emerging topics regarding long-range physical signaling in neurosystems: Membrane nanotubes and electromagnetic fields. | Q38472861 | ||
Emerging physiological and pathological implications of tunneling nanotubes formation between cells | Q38545340 | ||
Mitochondrial synapses: intracellular communication and signal integration. | Q38549716 | ||
Role of nonlinear localized Ca(2+) pulses along microtubules in tuning the mechano-sensitivity of hair cells. | Q38553646 | ||
Centrosome function and assembly in animal cells. | Q38587415 | ||
Mitochondrial Retrograde Signaling: Triggers, Pathways, and Outcomes | Q38638197 | ||
Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects. | Q39326113 | ||
Mitochondria are morphologically and functionally heterogeneous within cells. | Q39646958 | ||
Luminescence research and its relation to ultraweak cell radiation | Q39654293 | ||
The mammalian centrosome and its functional significance | Q36661673 | ||
Dynamin-like protein 1 reduction underlies mitochondrial morphology and distribution abnormalities in fibroblasts from sporadic Alzheimer's disease patients | Q36778260 | ||
Dynamics and environment of mitochondrial water as detected by 1H NMR. | Q36799165 | ||
Intercellular transfer mediated by tunneling nanotubes | Q37154491 | ||
Mitochondrial fusion, fission and autophagy as a quality control axis: the bioenergetic view | Q37179623 | ||
Percolation and criticality in a mitochondrial network. | Q37357761 | ||
Picture representation during REM dreams: a redox molecular hypothesis | Q37687560 | ||
Evidence for conduction of protons along the interface between water and a polar lipid monolayer | Q37687981 | ||
Microtubule ionic conduction and its implications for higher cognitive functions | Q37768755 | ||
Emergence of intrinsic representations of images by feedforward and feedback processes and bioluminescent photons in early retinotopic areas | Q37855761 | ||
Emission of mitochondrial biophotons and their effect on electrical activity of membrane via microtubules. | Q37855763 | ||
Long-distance electrical coupling via tunneling nanotubes | Q37935203 | ||
The centrosome in cells and organisms | Q37979201 | ||
Mitochondrial fission, fusion, and stress | Q29616536 | ||
During autophagy mitochondria elongate, are spared from degradation and sustain cell viability. | Q29616569 | ||
Topology of superoxide production from different sites in the mitochondrial electron transport chain | Q29619855 | ||
ER tubules mark sites of mitochondrial division | Q29619991 | ||
Mitochondrial transmission during mating in Saccharomyces cerevisiae is determined by mitochondrial fusion and fission and the intramitochondrial segregation of mitochondrial DNA | Q29622864 | ||
Light Effect on Water Viscosity: Implication for ATP Biosynthesis | Q30407009 | ||
When microbial conversations get physical | Q30470148 | ||
Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons | Q30477062 | ||
The fundamental organization of cardiac mitochondria as a network of coupled oscillators | Q30478263 | ||
A hyperfused mitochondrial state achieved at G1-S regulates cyclin E buildup and entry into S phase | Q30488844 | ||
Mesenchymal stem cells rescue cardiomyoblasts from cell death in an in vitro ischemia model via direct cell-to-cell connections | Q30494495 | ||
Preferential transfer of mitochondria from endothelial to cancer cells through tunneling nanotubes modulates chemoresistance | Q30540212 | ||
Dynamic imaging of mammalian neural tube closure | Q30560773 | ||
Transfer of mitochondria via tunneling nanotubes rescues apoptotic PC12 cells | Q30664746 | ||
Fluctuations in mitochondrial membrane potential caused by repetitive gating of the permeability transition pore | Q30785418 | ||
Change of the mitochondrial distribution in mouse ooplasm during in vitro maturation | Q31017782 | ||
Microtubular origin of mitotic spindle form birefringence. Demonstration of the applicability of Wiener's equation | Q31114481 | ||
Mitochondrial filaments and clusters as intracellular power-transmitting cables | Q31879149 | ||
Propagation of electromagnetic radiation in mitochondria? | Q33205655 | ||
Mitochondrial subpopulations and heterogeneity revealed by confocal imaging: possible physiological role? | Q33244123 | ||
Tomographic phase microscopy | Q33293939 | ||
Surface extensions of 3T3 cells towards distant infrared light sources | Q33349940 | ||
Heterogeneity of mitochondria and mitochondrial function within cells as another level of mitochondrial complexity | Q33452558 | ||
A reaction-diffusion model of ROS-induced ROS release in a mitochondrial network | Q33529043 | ||
Saccamoeba lacustris, sp. nov. (Amoebozoa: Lobosea: Hartmannellidae), a new lobose amoeba, parasitized by the novel chlamydia 'Candidatus Metachlamydia lacustris' (Chlamydiae: Parachlamydiaceae). | Q33546859 | ||
Membrane nanotubes drawn by optical tweezers transmit electrical signals between mammalian cells over long distances | Q33641566 | ||
Primary and secondary mechanisms of action of visible to near-IR radiation on cells | Q33655624 | ||
Intercellular communication by exchange of cytoplasmic material via tunneling nano-tube like structures in primary human renal epithelial cells. | Q33954765 | ||
Endoplasmic reticulum: ER stress regulates mitochondrial bioenergetics | Q33986242 | ||
Imaging in five dimensions: time-dependent membrane potentials in individual mitochondria | Q34020166 | ||
Spatio-temporal oscillations of individual mitochondria in cardiac myocytes reveal modulation of synchronized mitochondrial clusters | Q34069487 | ||
Energetic communication between mitochondria and nucleus directed by catalyzed phosphotransfer. | Q34099463 | ||
Cancer physics: diagnostics based on damped cellular elastoelectrical vibrations in microtubules. | Q34169966 | ||
Animal cells connected by nanotubes can be electrically coupled through interposed gap-junction channels | Q34182848 | ||
Quantitative Analysis of Spontaneous Mitochondrial Depolarizations | Q34183689 | ||
Electrical coupling and plasticity of the mitochondrial network | Q73293901 | ||
Quantitative analysis of the frequency spectrum of the radiation emitted by cytochrome oxidase enzymes | Q77328447 | ||
Red and far-red action on oxidative phosphorylation | Q79317032 | ||
Electric field generated by axial longitudinal vibration modes of microtubule | Q83010016 | ||
Visible light induced ocular delayed bioluminescence as a possible origin of negative afterimage | Q83779208 | ||
Mesenchymal stem cells rescue injured endothelial cells in an in vitro ischemia-reperfusion model via tunneling nanotube like structure-mediated mitochondrial transfer | Q87212399 | ||
Mitochondrial Genome Transfer to Tumor Cells Breaks The Rules and Establishes a New Precedent in Cancer Biology | Q91834896 | ||
Inhibition of lipid peroxidation in mitochondria isolated from the liver of hypothyroid rabbits | Q99082479 | ||
Long-distance intercellular connectivity between cardiomyocytes and cardiofibroblasts mediated by membrane nanotubes. | Q50676511 | ||
Membrane nanotubes in myeloid cells in the adult mouse cornea represent a novel mode of immune cell interaction. | Q50775904 | ||
Cell-to-cell communication in plants, animals, and fungi: a comparative review. | Q50776978 | ||
The steady-state mechanism of cytochrome c oxidase: redox interactions between metal centres. | Q51181440 | ||
Cell-to-cell communication: current views and future perspectives. | Q51493461 | ||
Nonlinear ionic pulses along microtubules. | Q51565861 | ||
Phosphene perception is due to the ultra-weak photon emission produced in various parts of the visual system: glutamate in the focus. | Q52147076 | ||
Ultraweak photon emission in the brain. | Q52149994 | ||
Energization-induced redistribution of charge carriers near membranes. | Q52426693 | ||
The receptor for advanced glycation end-products (RAGE) plays a key role in the formation of nanotubes (NTs) between peritoneal mesothelial cells and in murine kidneys. | Q54349351 | ||
Temperature dependence of bulk viscosity in water using acoustic spectroscopy | Q56836166 | ||
Spontaneous Ca2+ signaling of interstitial cells in the guinea pig prostate | Q57098749 | ||
Cell-to-Cell Connection of Endothelial Progenitor Cells With Cardiac Myocytes by Nanotubes | Q58816268 | ||
Mitochondrial reticulum for cellular energy distribution in muscle | Q59059572 | ||
Lateral proton conduction at lipid–water interfaces and its implications for the chemiosmotic-coupling hypothesis | Q59094893 | ||
Bioenergetic role of mitochondrial fusion and fission | Q63359585 | ||
Ferrous ion-mediated cytochrome P-450 degradation and lipid peroxidation in adrenal cortex mitochondria | Q67442723 | ||
The spectral distribution of the luminescence emitted during growth of the yeast Saccharomyces cerevisiae and its relationship to mitogenetic radiation | Q67480565 | ||
[Chemoluminescence of mitochondria] | Q68727094 | ||
Spontaneous endogenous ultraweak luminescence of rat liver mitochondria in conditions of normal metabolism | Q69721832 | ||
Distant-optical interaction of mitochondria through quartz | Q70222071 | ||
Vitamin A supplementation inhibits chemiluminescence and lipid peroxidation in isolated rat liver microsomes and mitochondria | Q71284391 | ||
An electromagnetic coupling hypothesis to explain the proton translocation mechanism in mitochondria, bacteria and chloroplasts | Q71739018 | ||
Chemiluminescence associated with doxorubicin-induced lipid peroxidation in rat heart mitochondria | Q72088305 | ||
Roles of catalase and cytochrome c in hydroperoxide-dependent lipid peroxidation and chemiluminescence in rat heart and kidney mitochondria | Q72316115 | ||
Mitochondrial chemiluminescence elicited by acetaldehyde | Q72936311 | ||
Spontaneous Changes in Mitochondrial Membrane Potential in Single Isolated Brain Mitochondria | Q34183696 | ||
Long-range forces extending from polymer-gel surfaces | Q34267240 | ||
Nanotubular highways for intercellular organelle transport | Q34298770 | ||
Wavelet analysis reveals heterogeneous time-dependent oscillations of individual mitochondria | Q34357806 | ||
Mitochondrial fusion and fission in mammals | Q34526830 | ||
Analysis of mitochondrial function and localisation during human embryonic stem cell differentiation in vitro. | Q34533356 | ||
Scaling behavior in mitochondrial redox fluctuations | Q34547028 | ||
Structurally distinct membrane nanotubes between human macrophages support long-distance vesicular traffic or surfing of bacteria. | Q34586727 | ||
A biopolymer transistor: electrical amplification by microtubules | Q34646711 | ||
Mitochondrial network morphology: building an integrative, geometrical view | Q34783207 | ||
Active generation and propagation of Ca2+ signals within tunneling membrane nanotubes | Q34800870 | ||
Cellular target of weak magnetic fields: ionic conduction along actin filaments of microvilli | Q34953462 | ||
Fluctuating vs. continuous exposure to H₂O₂: the effects on mitochondrial membrane potential, intracellular calcium, and NF-κB in astroglia | Q35016954 | ||
Mitochondrial membrane potential probes and the proton gradient: a practical usage guide | Q35047150 | ||
Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation | Q35064216 | ||
Tunneling-nanotube development in astrocytes depends on p53 activation | Q35092637 | ||
Protons migrate along interfacial water without significant contributions from jumps between ionizable groups on the membrane surface | Q35197930 | ||
A clinical overview of centrosome amplification in human cancers | Q35479894 | ||
Mitochondrial networks in cardiac myocytes reveal dynamic coupling behavior | Q35529929 | ||
Fission yeast mitochondria are distributed by dynamic microtubules in a motor-independent manner | Q35687446 | ||
Mitochondrial signaling: the retrograde response | Q35739853 | ||
"Nanosized voltmeter" enables cellular-wide electric field mapping | Q35906108 | ||
Connecting Mitochondria, Metabolism, and Stem Cell Fate | Q35977660 | ||
Cutting edge: Membrane nanotubes in vivo: a feature of MHC class II+ cells in the mouse cornea. | Q36083315 | ||
Mitochondrial criticality: a new concept at the turning point of life or death. | Q36293854 | ||
Emerging functions of mammalian mitochondrial fusion and fission | Q36294710 | ||
A microfluidic platform for measuring electrical activity across cells | Q36315075 | ||
Reactive oxygen species (ROS)-induced ROS release: a new phenomenon accompanying induction of the mitochondrial permeability transition in cardiac myocytes | Q36368961 | ||
Mitochondria. II. The nuclear-mitochondrial relationship in Pelomyxa carolinensis Wilson (Chaos chaos L.). | Q36437200 | ||
Interactions of mitochondria with the actin cytoskeleton | Q36453554 | ||
Coupling membranes as energy-transmitting cables. I. Filamentous mitochondria in fibroblasts and mitochondrial clusters in cardiomyocytes | Q36455650 | ||
Exosomes and nanotubes: Control of immune cell communication | Q36483965 | ||
Mitochondrial retrograde signaling | Q36505532 | ||
A wave of reactive oxygen species (ROS)-induced ROS release in a sea of excitable mitochondria | Q36598819 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell | Q7868 |
mitochondrion | Q39572 | ||
cell communication | Q14860133 | ||
signal transduction | Q828130 | ||
manufactured product | Q3406743 | ||
biomedical investigative technique | Q66648976 | ||
P304 | page(s) | 16 | |
P577 | publication date | 2016-06-06 | |
P1433 | published in | Theoretical Biology and Medical Modelling | Q15750144 |
P1476 | title | Long range physical cell-to-cell signalling via mitochondria inside membrane nanotubes: a hypothesis | |
P478 | volume | 13 |
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