The basal proton conductance of mitochondria depends on adenine nucleotide translocase content

DETERMINATION OF SERUM PROTEINS BY MEANS OF THE BIURET REACTION

Gornall, A. G., Bardawill, C. J., & David, M. M. (1949) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)57021-6 · Cited by 16,164

Mitochondrial superoxide: production, biological effects, and activation of uncoupling proteins

Brand, M. D., Affourtit, C., Esteves, T. C., Green, K., Lambert, A. J., Miwa, S., Pakay, J. L., & Parker, N. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.05.034 · Cited by 1,032

Uncoupling: new approaches to an old problem of bioenergetics

Skulachev, V. P. (1998) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(97)00091-1 · Cited by 893

Role of uncoupled and non-coupled oxidations in maintenance of safely low levels of oxygen and its one-electron reductants

Skulachev, V. P. (1996) · Quarterly Reviews of Biophysics · doi:10.1017/s0033583500005795 · Cited by 703

A signalling role for 4‐hydroxy‐2‐nonenal in regulation of mitochondrial uncoupling

Echtay, K. S., Esteves, T. C., Pakay, J. L., Jekabsons, M. B., Lambert, A. J., Portero‐Otín, M., Pamplona, R., Vidal‐Puig, A. J., Wang, S., Roebuck, S. J., et al. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg412 · Cited by 597

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

Graham, B. H., Waymire, K. G., Cottrell, B. A., Trounce, I. A., MacGregor, G. R., & Wallace, D. C. (1997) · Nature Genetics · doi:10.1038/ng0797-226 · Cited by 556

Uncoupling Protein 2, in Vivo Distribution, Induction upon Oxidative Stress, and Evidence for Translational Regulation

Pecqueur, C., Alves‐Guerra, M., Gelly, C., Lévi-Meyrueis, C., Couplan, E., Collins, S., Ricquier, D., Bouillaud, F., & Miroux, B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006938200 · Cited by 483

The causes and functions of mitochondrial proton leak

Brand, M. D., Chien, L.-F., Ainscow, E. K., Rolfe, D. F. S., & Porter, R. K. (1994) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(94)90099-x · Cited by 466

Reversible Inhibition of Mitochondrial Adenosine Diphosphate Phosphorylation by Long Chain Acyl Coenzyme A Esters

Pande, S. V., & Blanchaer, M. C. (1971) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)62505-0 · Cited by 355

Mitochondrial carrier proteins

Palmieri, F. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00329-7 · Cited by 341

Differential Ca2+ handling by isolated synaptic and non-synaptic mitochondria: roles of Ca2+ buffering and efflux

Mishra, J., Bevers, K., Li, K., Zare, A., Heisner, J. S., Tong, A., Kwok, W., Stowe, D. F., & Camara, A. K. S. (2025) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2025.1562065 · Cited by 7

Effects of artificial light at night on basal thermogenesis and gut microbiota in two small passerine birds

Xu, R., Gu, C., Wang, X., Zou, D., Wang, T., Chang, H., He, X., Huang, K., Liu, J., & Wang, D. (2025) · Journal of Experimental Biology · doi:10.1242/jeb.250060 · Cited by 7

Mammals to membranes: A reductionist story

Else, P. L. (2020) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2020.110552 · Cited by 7

Exploring the multifaceted role of adenosine nucleotide translocase 2 in cellular and disease processes: A comprehensive review

Pan, T., Yang, B., Yao, S., Wang, R., & Zhu, Y. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122802 · Cited by 5

Adaptogen Technology for Skin Resilience Benefits

Cavagnino, A., Breton, L., Ruaux, C., Grossgold, C., Levoy, S., Abdayem, R., Roumiguiere, R., Cheilian, S., Bouchara, A., Baraibar, M. A., et al. (2023) · Cosmetics · doi:10.3390/cosmetics10060155 · Cited by 6

Functional characterization of an uncoupling protein in goldfish white skeletal muscle

dos Santos, R. S., Peçanha, F. L. M., & da‐Silva, W. S. (2013) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-013-9512-1 · Cited by 6

Regulation of avian uncoupling protein (av-UCP) expression by cytokines and hormonal signals in quail myoblast cells

Ferver, A., & Dridi, S. (2020) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2020.110747 · Cited by 6

Mitochondrial respiration supports cancer growth independent of OXPHOS

Chinopoulos, C. (2026) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2026.189593 · Cited by 5

Mitochondrial Physiology

Bottje, W. G. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-407160-5.00004-x · Cited by 5

Uncoupling effect of palmitate is exacerbated in skeletal muscle mitochondria of sea-acclimatized king penguins (Aptenodytes patagonicus)

Rey, B., Duchamp, C., & Roussel, D. (2017) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2017.06.009 · Cited by 5

Non-Mammalian Vertebrates: Distinct Models to Assess the Role of Ion Gradients in Energy Expenditure

Geisler, C. E., Kentch, K. P., & Renquist, B. J. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00224 · Cited by 5

Reduction of Elevated Proton Leak Rejuvenates Mitochondria in the Aged CardiomyocytePreprint

Zhang, H., Alder, N. N., Wang, W., Szeto, H. H., Marcinek, D. J., & Rabinovitch, P. S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.02.893362 · Cited by 5

Adenine Nucleotide Translocase 1 Promotes Functional Integrity of Mitochondria via Activating DDIT3-CytC Pathway and Intensifying Actin Filament Structures

Liu, J., Ding, W., Chen, Q., Peng, Y., Kong, Y., Ma, L., & Zhang, W. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-04710-1 · Cited by 4

Adjustments of Mitochondrial Energy Transduction in Response to Physiological and Environmental Challenge

Jastroch, M. (2012) · Springer eBooks · doi:10.1007/978-3-642-28678-0_34 · Cited by 4

Interplay Between Hippocampal Glutathione Depletion and pH Increment in Alzheimer’s Disease

Mandal, P. K., Dwivedi, D., Shukla, D., Samkaria, A., Roy, R. G., Arora, Y., & Jindal, K. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-215729 · Cited by 4

Cortisol Regulates Cerebral Mitochondrial Oxidative Phosphorylation and Morphology of the Brain in a Region-Specific Manner in the Ovine Fetus

Davies, K., Smith, D. J., El‐Bacha, T., Wooding, F. B. P., Forhead, A. J., Murray, A. J., Fowden, A. L., & Camm, E. J. (2022) · Biomolecules · doi:10.3390/biom12060768 · Cited by 6

Ecological, functional, and thermodynamic prerequisites and consequences of the origin and development of homoiothermy: A case study of avian energetics

Gavrilov, V. M. (2013) · Biology Bulletin Reviews · doi:10.1134/s2079086413010040 · Cited by 4

Mild Mitochondrial Uncoupling for True Ectopic Lipid Disposal

Lee, H. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26167740 · Cited by 3

Potential health benefits of cold‐water immersion: the central role of PGC‐1α

Hohenauer, E., Douzi, W., & Burtscher, J. (2025) · The Journal of Physiology · doi:10.1113/jp289536 · Cited by 4

Characterization of the Intracellular Distribution of Adenine Nucleotide Translocase (ANT) in Drosophila Indirect Flight Muscles

Vishnudas, V. K., Guillemette, S., Lekkas, P., Maughan, D. W., & Vigoreaux, J. O. (2013) · CellBio · doi:10.4236/cellbio.2013.23017 · Cited by 3

Adaptation of striated muscles to Wolframin deficiency in mice: Alterations in cellular bioenergetics

Tepp, K., Puurand, M., Timohhina, N., Aid, J., Reile, I., Shevchuk, I. N., Chekulayev, V. A., Eimre, M., Peet, N., Kadaja, L., et al. (2020) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2020.129523 · Cited by 3

Can thermogenic adipocytes protect from obesity?

Medvedev, L. N., & Elsukova, E. I. (2015) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-015-0443-7 · Cited by 3

Cytosolic Adaptation to Mitochondrial Precursor Overaccumulation Stress Induces Progressive Muscle WastingPreprint

Wang, X., Middleton, F. A., Tawil, R., & Chen, X. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/733097 · Cited by 3

Exploring Immediate Photon Effects From 635 nm Light on Mitochondrial Bioenergetics

Mezzacappo, N. F., Inada, N. M., Siqueira‐Santos, E. S., Vollet‐Filho, J. D., Castilho, R. F., Denton, M. L., & Bagnato, V. S. (2025) · Journal of Biophotonics · doi:10.1002/jbio.202500162 · Cited by 2

Saccharomyces cerevisiae as a Model for Reprogramming of Eukaryotic Cells: Implications for the Study of the Relationship Between Metabolism and Inflammation in Chronic Disease

Friedman, N. S., Britto, G. J. D., & Lehner, A. N. (2025) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-025-01844-w · Cited by 2

Nitric oxide and hypoxia at adaptation to muscular work (brief review)

Radchenko, A. S. (2016) · Reviews on Clinical Pharmacology and Drug Therapy · doi:10.17816/rcf14178-88 · Cited by 2

Adenine Nucleotide Translocase 1 Expression Modulates the Immune Response in Ischemic Hearts

Yergöz, F., Friebel, J., Kränkel, N., Rauch-Kroehnert, U., Schultheiß, H., Landmesser, U., & Dörner, A. (2021) · Cells · doi:10.3390/cells10082130 · Cited by 3

Dietary fatty acids alter mitochondrial phospholipid fatty acyl composition and proton leak in Drosophila melanogaster

Ocloo, A. (2010) · Biokemistri · doi:10.4314/biokem.v18i2.56411 · Cited by 2

New Insights into the Bioenergetic and Immunomodulatory Properties of Phospholipases A2 from Bothrops diporus Venom

Sasovsky, D. J., Oliveira, A. K., Silva, D. T., Ojeda, G. A., Almarza, C., Lomonte, B., Fox, J. W., Urra, F. A., & Bustillo, S. (2026) · Toxins · doi:10.3390/toxins18020114 · Cited by 1

Conformation and Ion Transport of Neuronal Uncoupling Proteins

Hoang, T. A., Smith, M. D., & Jelokhani‐Niaraki, M. (2011) · Biophysical Journal · doi:10.1016/j.bpj.2010.12.2148 · Cited by 1

Conformation and ion transport of neuronal uncoupling proteins: UCP2, UCP4, and UCP5

Hoang, T. A. (2011) · Scholars Commons (Wilfrid Laurier University) · Cited by 1

Regulatory design in a simple system integrating membrane potential generation and metabolic ATP consumption. Robustness and the role of energy dissipating processes

Acerenza, L., Cristina, E., & Hernández, J. A. (2011) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2011.09.003 · Cited by 1

Obesity: A Multi Perspective of Physiology and Neurobiology Energy Regulation

Meiliana, A., Dewi, N. M., & Wijaya, A. (2024) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v16i1.2840 · Cited by 1

How Fast Do Mitochondria Work? A Kinetic Study of Oxidative Phosphorylation

Pastrana-Pineda, C., Melgoza-Ramírez, L. J., Islas-Flores, E. M., Gómez-Monsivais, W. L., Gonce, J., López, N., Limón-González, J. B., Rodríguez‐Zavala, J. S., Saavedra, E., & Belmont-Díaz, J. (2025) · Journal of Chemical Education · doi:10.1021/acs.jchemed.4c00992 · Cited by 1

Thyroid Hormone and Myocardial Mitochondria

Marín-García, J. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4599-9_22 · Cited by 2

Nuclear Encoded Mitochondrial Proteins in Metabolite Transport and Oxidation Pathway Connecting Metabolism of Nutrients

Vašková, J., Firment, J., & Vaško, L. (2018) · InTech eBooks · doi:10.5772/intechopen.72937 · Cited by 1

Dietary inorganic nitrate : role in exercise physiology, cardiovascular and metabolic regulation

Larsen, F. J. (2011) · Figshare · Cited by 1

Limiting factors in ATP synthesis

Kramarova, T. V. (2006) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · Cited by 1

Antidiabetic activity of Vaccinium vitis-idaea, a medicinal plant from the traditional pharmacopeia of the James Bay Cree

Eid, H. M. (2010) · doi:10.71781/30008 · Cited by 1

Die mitochondriale Funktion bei Coxsackievirus-B3-induzierter Myokarditis Wirkung einer kardialen Überexpression des Adeninnukleotid-Translokators

Ebermann, L. (2011) · Cited by 1

Developmental Regulation of Mitochondrial Function in Ovine Fetal Skeletal Muscle

Davies, K. (2018) · Apollo (University of Cambridge) · doi:10.17863/cam.22845 · Cited by 1

The Role of Thyroid Hormone across Avian Development Spectrum: Investigations on Systemic Development, Metabolism and Ontogeny of Endothermy

Sirsat, T. S. (2017) · University of North Texas Digital Library (University of North Texas) · doi:10.12794/metadc1011746 · Cited by 1

Mitochondria, lipotoxicity and skeletal muscle metabolism : implications for type 2 diabetes mellitus

van Bree, B. W. J. (2014) · Research Publications (Maastricht University) · doi:10.26481/dis.20141017bb

Thyroid Hormone and Energy Expenditure

Yehuda‐Shnaidman, E., Kalderon, B., & Bar-T, J. (2012) · InTech eBooks · doi:10.5772/48309

Papel de la proteína desacoplante UCP2 en el estrés oxidativo provocado por la metformina en el adipocito blanco

Anedda, A. (2010) · Tesis Doctorals en Xarxa (Consorci de Serveis Universitaris de Catalunya)

Mitochondrial form and function in pancreatic β-cells and brown adipocytes

Wikström, J. D. (2010) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Mechanistic insights into the function of the mitochondrial uncoupling protein in Caenorhabditis elegans

Pfeiffer, M. E. (2010) · Texas ScholarWorks (Texas Digital Library)

NOVEL MECHANISMS GOVERNING SKELETAL MUSCLE MITOCHONDRIAL BIOENERGETICS : OXPHOS EFFICIENCY AND cAMP/PKA SIGNALING

Lark, D. S. (2014) · The Scholarship East Carolina University's Institutional Repository (East Carolina University)

Mitochondrial uncoupling protein 3 blocks skin carcinogenesis and drives bulge stem cell differentiation and epidermal turnover

Lago, C. U. (2009) · Texas ScholarWorks (Texas Digital Library)

Correction: A Novel High-Throughput Assay for Islet Respiration Reveals Uncoupling of Rodent and Human Islets

Wikström, J. D., Sereda, S. B., Stiles, L., Elorza, Á. A., Allister, E. M., Neilson, A., Ferrick, D. A., Wheeler, M. B., & Shirihai, O. S. (2013) · PLoS ONE · doi:10.1371/annotation/f21efac9-2906-4a2f-ad22-befcb7714dd0

Pharmacological Induction of Molecular Chaperones Restores Mitochondrial Function in Hyperglycemically Stressed Sensory Neurons

Zhang, L. (2012) · KU ScholarWorks (The University of Kansas)

Characterizing the Relationship Between Energy Metabolism and Mesenchymal Stem Cell Therapy in the Infarcted Heart

Hughey, C. C. (2013) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/25306

LeakRegulation and Physiology of Mitochondrial Proton

Dalton, N. D., Peterson, K. L., Gu, Y., Matkovich, S. J., Murphy, A. N., Ling, H., Divakaruni, A. S., Zambon, A. C., King, M. S., Kunji, E. R. S., et al. (2015)

Métabolisme énergétique au cours de la cachexie cancereuse

Johnson, G. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique)

Mitochondria and energetics stress : signaling pathways and cellular adaptations.

Desquiret‐Dumas, V., & Malthièry, Y. (2008) · OpenGrey (Institut de l'Information Scientifique et Technique)

Mitochondrial energetic metabolism in hereditary neuropathies associated with OPA1 and MFN2 genes mutations.

Guillet, V., & REYNIER, P. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)

Role of insulin receptor substrate 1 in energy homeostasis in vivo

Stöhr, O. (2012) · Kölner Universitäts PublikationsServer (Universität zu Köln)

Approche multifonctionnelle mitochondriale par puce à ADN dédiée

Arvier, M. (2008) · OpenGrey (Institut de l'Information Scientifique et Technique)

The mitochondrial complex II and ATP-sensitive potassium channel interaction: quantitation of the channel in heart

Wojtovich, A. P., Nehrke, K. W., & Brookes, P. S. (2010)

changes and passive thermal effects dwarf Siberian hamster: role of active regulated Mitochondrial metabolism during daily torpor in the

Brown, J. C. L., Gerson, A. R., Staples, J. F., Exp, J., Thomas, R., Bernards, M. A., James, F. D., Polymeropoulos, E. T., Heldmaier, G., Frappell, P. B., et al. (2011)

Cloning and analysis of adenine nucleotide translocase gene in Helicoverpa armigera

Niu, B. (2008) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2008.00081

Regulation of In Vivo Mitochondrial Energetics by Oxidative Stress throughout Life: A Multi-Modal Spectroscopy Approach

Siegel, M. P. (2012) · ResearchWorks at the University of Washington (University of Washington)

Powering Up Mitichondrial Functions to Treat Mitochondrial Disease

Wallace, D. C., & Pei, L. (2017)

Role of Protein Phosphorylation among Oxidative Phosphorylation Components

Bou, M., Guedouari, H., Bujold, J. P., & Hébert-Chatelain, É. (2017) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0027586

Investigation into the molecular complexity of Alzheimer's disease : an amyloid-β centered approach

Cioffi, F. (2019) · doi:10.3990/1.9789036548410

Comparison of thermoregulation and metabolic characteristics in Phrynocephalus vlangalii (Lacertilia, Agamidae) from different altitudesPreprint

Tang, X., Wang, H., & Chen, Q. (2020) · Research Square · doi:10.21203/rs.3.rs-64008/v1

Contribution of Mitochondrial F0F1-ATP Synthase and Adenine Nucleotide Translocator to Induced Thermogenesis in the Appendix of Sauromatum venosum Inflorescence

Skubatz, H. (2021) · Journal of Botany Research · doi:10.36959/771/569

Small change, big impact: functional characterization of human SIRT5 variants

Yuan, T. (2021) · doi:10.18174/542143

Lietuvos Respublikos valstybės biudžeto išlaidųanalizė ir jų kitimo tendencijų pagrindimas

Vijūnienė, J. (2010) · Laba (Lietuvos akademinių bibliotekų direktorių asociacija)

Quel est le rôle des protéines découplantes mitochondriales chez les mammifères et les oiseaux ?

DAMON, M., & Collin, A. (2006) · INRAE Productions Animales · doi:10.20870/productions-animales.2006.19.4.3497 · Cited by 3

Characterisation of the ghrelinergic system in human models of neurodegenerative diseases

Carisi, M. C. (2021) · Cronfa (Swansea University) · doi:10.23889/suthesis.58915

Depletion of Toxoplasma adenine nucleotide translocator leads to defects in mitochondrial morphologyPreprint

Liu, Q., Wu, Y., Ying, Z., Liu, J., Sun, Z., & Li, S. (2022) · Research Square · doi:10.21203/rs.3.rs-1472669/v1

Faculty Opinions recommendation of Reduced cytosolic protein synthesis suppresses mitochondrial degeneration.

Nairn, A. C., & Wiseman, S. L. (2008) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.720227198.580533

Identification and Design of a Novel Family of Mitochondrial Protonophores for Bioenergetics Analysis and the Treatment of Ischemia-Reperfusion Injury

Kenwood, B. M. (2014) · doi:10.18130/v31n9k

Exercise: Thermodynamic and Bioenergetic Principles

Halling, J. F., Gudiksen, A., Pilegaard, H., & Neufer, P. D. (2022) · Physiology in health and disease · doi:10.1007/978-3-030-94305-9_3 · Cited by 2

ISSIQQONLI VA SOVUQQONLI HAYVONLARNING AEROB METABOLIZMIDAGI FARQ: TERMOGENEZDAGI AHAMIYATI

Rn, A., Karimov, V., Niyazmetov, B. A., & Zaripov, B. Z. (2023) · Scientific journal of the Fergana State University · doi:10.56292/sjfsu/vol29_iss2/a138

Mitochondrial and cellular function in fibroblasts, induced neurons, and astrocytes derived from case study patients: insights into major depression as a mitochondria-associated diseasePreprint

Wetzel, C. H., Cardon, I., Grobecker, S., Kücükoktay, S., Bader, S. M., Jahner, T., Nothdurfter, C., Koschitzki, K., Berneburg, M., Stöhr, H., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3125187/v2 · Cited by 1

Adolescent stress induces behavioral changes and hippocampal excitatory/inhibitory imbalance: involvement of redox dysregulation and mitochondrial dysfunction

Santos‐Silva, T. (2023) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2023.tde-10112023-160657

Targeting Cancer Metabolism with Isoselenazolium Salts. Doctoral Thesis

Dimitrijevs, P. (2024) · doi:10.25143/prom-rsu_2024-01_dt

Additional file 1 of Depletion of Toxoplasma adenine nucleotide translocator leads to defects in mitochondrial morphology

Wu, Y., Ying, Z., Liu, J., Sun, Z., Li, S., & Liu, Q. (2022) · Figshare · doi:10.6084/m9.figshare.19946280

Liver mitochondrial coupling efficiency and its relationship to oxidative capacity and adenine nucleotide translocase content: A comparative study among crocodiles, birds and mammals

Roussel, D., Roussel, N., Voituron, Y., & Rey, B. (2024) · Mitochondrion · doi:10.1016/j.mito.2024.101909

Determination of ADP / ATP translocase isoform ratios in malignancy and cellular senescence

Liblova, Z., Maurencova, D., Šalovská, B., Kratky, M., Mráček, T., Korandová, Z., Pecinová, A., Vašicová, P., Rysanek, D., Anděra, L., et al. (2025) · Molecular Oncology · doi:10.1002/1878-0261.70039 · Cited by 1

Aging Skeletal Muscle: Influence of Obesity and Role of the Exercise Responsive Nuclear Receptor NOR-1

Paez, H. G. (2024) · doi:10.21007/aetd.cghs.2024.0010

How the Mitochondrial Patch-Clamp Technique Establishes the ADP/ATP Carrier as a Major Uncoupling Protein in Non-adipose Tissues

Milner, M. G., & Bertholet, A. M. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190932183.013.25

Nucleoside diphosphate kinase strongly promotes GDP and ADP metabolism in the cell and affects endogenous proton leak in mitochondria – the kinase is hampered by oxidative phosphorylation inhibitors

Woyda-Ploszczyca, A. M. (2025) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756366.2025.2520611

Evolutionary diversity of muscle OXPHOS efficiency in vitro across ectothermic vertebrates

Mueller, R. L., Puma, L. C. L., Itgen, M. W., & Chicco, A. J. (2025) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2025.0374

Parasympathetic and Sympathetic Nervous System Dysfunction and Monitoring

DePace, N. L., Soloway, S., Yayac, M. F., & Colombo, J. (2025) · Springer eBooks · doi:10.1007/978-3-031-88769-7_13

Interconnected roles of mitochondrial carrier proteins ANT, PiT, and UCPs in proton transport

Tabefam, M., Swanson, H. K., Smith, M. D., & Jelokhani‐Niaraki, M. (2025) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2025.1650261

The Role of Mitochondrial Uncoupling in the Development of Diabetic Nephropathy

Persson, M. F. (2012)

Additional file 2 of Depletion of Toxoplasma adenine nucleotide translocator leads to defects in mitochondrial morphology

Wu, Y., Ying, Z., Liu, J., Sun, Z., Li, S., & Liu, Q. (2022) · Figshare · doi:10.6084/m9.figshare.19946283

Additional file 1 of AMPK activator-treated human cardiac spheres enhance maturation and enable pathological modeling

Li, D., Armand, L. C., Sun, F., Hwang, H., Wolfson, D., Rampoldi, A., Liu, R., Forghani, P., Hu, X., Yu, W.-M., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24531915

Additional file 3 of AMPK activator-treated human cardiac spheres enhance maturation and enable pathological modeling

Li, D., Armand, L. C., Sun, F., Hwang, H., Wolfson, D., Rampoldi, A., Liu, R., Forghani, P., Hu, X., Yu, W.-M., et al. (2024) · Figshare · doi:10.6084/m9.figshare.24532284

Additional file 3 of Depletion of Toxoplasma adenine nucleotide translocator leads to defects in mitochondrial morphology

Wu, Y., Ying, Z., Liu, J., Sun, Z., Li, S., & Liu, Q. (2022) · Figshare · doi:10.6084/m9.figshare.19946286

Metadichol Orchestrates Cellular Reprogramming and Regenerative Pathways via FOX Transcription Factor Networks: Implications for Immune–Metabolic Rejuvenation

Raghavan, P. R. (2025) · Medical Research Archives · doi:10.18103/mra.v14i1.7160 · Cited by 1

Métabolisme mitochondrial cérébral chez les mâles et les femelles : rôle des stéroïdes endogènes et effet de la progestérone après ischémie transitoire focale

Gaignard, P. (2015) · theses.fr (ABES) · doi:10.70675/4cf11d47z9ce5z496az9f25zf57d697f57e9

Flexibilité mitochondriale au cours du jeûne : étude chez le caneton de barbarie et le poussin de manchot royal

Monternier, P. (2015) · doi:10.70675/bd802cafzb937z4664zbbeaz6e7f4c287966

Rôle protecteur de l'estradiol contre les conséquences systémiques et cellulaires dans un modèle d'apnées obstructives du sommeil : implication des récepteurs nucléaires ERalpha et ERß

Laouafa, S. (2018) · theses.fr (ABES) · doi:10.70675/1b2f3b3az3642z4fbdz8d40za5a67737e2e4

Recherche et études de marqueurs précoces permettant de déterminer l'état de fraicheur de filets de poissons

Cléach, J. (2018) · theses.fr (ABES) · doi:10.70675/498c30b7z90a8z42f0za685zba48bfefb8d7

Rôle de la signalisation calcique dans les troubles métaboliques associés à la dysfonction myocardique

Lacôte, M. (2018) · theses.fr (ABES) · doi:10.70675/bc9b8426z5718z40e1zadc2zaa52fb20a6fd

Uncoupling protein-1 (UCP1) contributes to the basal proton conductance of brown adipose tissue mitochondria

Parker, N., Crichton, P. G., Vidal‐Puig, A., & Brand, M. D. (2009) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-009-9232-8 · Cited by 70

Interaction of adenine nucleotides with the adenine nucleotide translocase regulates the developmental changes in proton conductance of the inner mitochondrial membrane

Valcarce, C., & Vuezva, J. (1991) · FEBS Letters · doi:10.1016/0014-5793(91)81435-b · Cited by 30

S3.25 Complementation of Bacillus subtilis motility with flagellin gene from thermophilic Bacillus sp. PS3

Hayakawa, J., & Ishizuka, M. (2008) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2008.05.124

Energization-dependent endogenous activation of proton conductance in skeletal muscle mitochondria

Parker, N., Affourtit, C., Vidal‐Puig, A., & Brand, M. D. (2008) · Biochemical Journal · doi:10.1042/bj20080006 · Cited by 73

Contribution of mitochondrial carrier proteins to basal proton conductance

Parker, N., & Brand, M. (2008) · UCL Discovery (University College London)