A Cellular Perspective on Brain Energy Metabolism and Functional Imaging

On the origin of cancer cells

Warburg, O. (1956) · Science · doi:10.1126/science.123.3191.309 · Cited by 13,425

Neurophysiological investigation of the basis of the fMRI signal

Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,551

Brain magnetic resonance imaging with contrast dependent on blood oxygenation.

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THE [ 14 C]DEOXYGLUCOSE METHOD FOR THE MEASUREMENT OF LOCAL CEREBRAL GLUCOSE UTILIZATION: THEORY, PROCEDURE, AND NORMAL VALUES IN THE CONSCIOUS AND ANESTHETIZED ALBINO RAT 1

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A Paravascular Pathway Facilitates CSF Flow Through the Brain Parenchyma and the Clearance of Interstitial Solutes, Including Amyloid β

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Astrocytes: Biology and pathology

Sofroniew, M. V., & Vinters, H. V. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0619-8 · Cited by 5,196

An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex

Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875

Glutamate uptake

Danbolt, N. C. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00067-8 · Cited by 4,227

An Energy Budget for Signaling in the Grey Matter of the Brain

Attwell, D., & Laughlin, S. B. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200110000-00001 · Cited by 3,543

Metabolic Reprogramming: A Cancer Hallmark Even Warburg Did Not Anticipate

Ward, P. S., & Thompson, C. B. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.02.014 · Cited by 3,233

Intelligence in Multiple Dimensions: Evolutionary Framework for the Study of Human Cognition

Geary, D. C. (2026) · Intelligence & Cognitive Abilities · doi:10.65550/001c.154815 · Cited by 3

Cholinergic Phenotypes of Acetyl-CoA with ATP-Citrate Lyase Link

Gul‐Hinc, S., Jankowska-Kulawy, A., & Szutowicz, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020782 · Cited by 4

Mechanical Stretch Disrupts Calcium Dynamics and Redistributes Piezo1 in Human Astrocytes

Shiravi, S., Chakka, A., Xiao, X., García, M. F., Yufa, A., Mitevska, A., Seah, C., Gao, H., Huckins, L. M., Brennand, K., et al. (2026) · Annals of Biomedical Engineering · doi:10.1007/s10439-026-03995-0 · Cited by 3

Metabolic alterations after traumatic neural injury: Mechanistic insights and potential translational targets for axon regeneration

Cao, Q., Zhao, W., Yan, J., Belin, S., Yu, B., Nawabi, H., & Mao, S. (2026) · Science Signaling · doi:10.1126/scisignal.adx9003 · Cited by 3

Glial lactate metabolism and transport in Alzheimer’s disease

Wang, Y., Feng, B., Hong, R., Qiu, D., Zhao, J., & Zhao, L. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2026.1731089 · Cited by 3

Metabolism Controls the Timing of Human Brain Development and Maturation

Rava, V., Cannone, E., Francolini, M., & Taverna, E. (2026) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.70180 · Cited by 3

Acetyl-CoA metabolism in skeletal biology and bone disorders: From mechanisms to therapeutic implications

Yang, Q., Shi, R., Zhang, C. H. I., Sun, W., & Chen, G. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108346 · Cited by 3

Protective Effects of a Novel Glycogen Phosphorylase Inhibitor Against Cerebral ischemia–reperfusion Injury in Mice

Yan, Z., Li, S., Wang, Y., Guo, Y., & Zhang, L. (2023) · Future Medicinal Chemistry · doi:10.4155/fmc-2023-0038 · Cited by 3

Thermodynamic Analysis to Evaluate the Effect of Diet on Brain Glucose Metabolism: The Case of Fish Oil

Yıldız, C., & Medina, I. (2024) · Nutrients · doi:10.3390/nu16050631 · Cited by 3

Combination of RNA-seq and proteomics reveals the mechanism of DL0410 treatment in APP/PS1 transgenic mouse model of Alzheimer's disease

Zhang, B., Zhao, J., Yan, C., Bai, Y., Guo, P., Wang, C., Wang, Z., Du, G., & Liu, A. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116940 · Cited by 3

Cognitive Disorders in Type 1 Diabetes: Role of Brain Glucose Variation, Insulin Activity, and Glucocorticoid Exposure

Brossaud, J., Barat, P., & Moisan, M. (2024) · Neuroendocrinology · doi:10.1159/000541989 · Cited by 4

Epilepsy and Oxidative Stress

Lee, H. S., Arulsamy, A., & Shaikh, M. F. (2024) · Springer eBooks · doi:10.1007/978-981-99-7557-0_16 · Cited by 3

Effects of Acute Stress on Metabolic Interactions Related to the Tricarboxylic Acid (TCA) Cycle in the Left Hippocampus of Mice

Yun, C., Hwang, Y. H., Yeon, J., Baek, H., Kim, D. Y., & Han, B. S. (2024) · Metabolites · doi:10.3390/metabo14120699 · Cited by 3

Efficacy of Transcranial Direct Current Stimulation (tDCS) on Neuropsychiatric Symptoms in Multiple Sclerosis (MS)—A Review and Insight into Possible Mechanisms of Action

Chmiel, J., & Stępień–Słodkowska, M. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13247793 · Cited by 3

Interpreting the rich dialogue between astrocytes and neurons: An overview in Rett syndrome

Postogna, F. M., Roggero, O. M., Biella, F., & Frasca, A. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111386 · Cited by 4

The Anatomical and Evolutionary Impact of Pain, Pleasure, Motivation, and Cognition: Integrating Energy Metabolism and the Mind–Body BERN (Behavior, Exercise, Relaxation, and Nutrition) Framework

Stefano, G. B., Büttiker, P., Michaelsen, M. M., & Esch, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26125491 · Cited by 6

MGlu5 Dependent Mitochondrial Translocation of PKCδ : A Mechanism Raising Astrocytic Oxidative Metabolism in Response to Extracellular Glutamate

Farid, K. M. N., Lerchundi, R., Rose, C. R., & Derouiche, A. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70163 · Cited by 3

The interaction between resilience framework and neuron-astrocyte-synapse dynamics in AD

Ma, H., Zhao, H., Feng, X., & Gao, F. (2025) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1644532 · Cited by 4

Mitochondrial Calcium Sparkles Light Up Astrocytes

MacVicar, B. A., & Ko, R. W. Y. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.02.013 · Cited by 3

Imaging Guidance for Therapeutic Delivery: The Dawn of Neuroenergetics

Alambyan, V., Pace, J., Sukpornchairak, P., Yu, X., Alnimir, H., Tatton, R., Chitturu, G., Yarlagadda, A., & Ramos-Estébanez, C. (2020) · Neurotherapeutics · doi:10.1007/s13311-020-00843-4 · Cited by 3

Cellular ATP Synthase

Узлова, Е. В., & Zimatkin, S. M. (2021) · Biology Bulletin Reviews · doi:10.1134/s2079086421020109 · Cited by 3

A novel integrated approach to estimate the mitochondrial content of neuronal cells and brain tissues

Spadini, S., Racchetti, G., Adiletta, A., Lamanna, J., Moro, A. S., Ferro, M., Zimarino, V., & Malgaroli, A. (2021) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2021.109351 · Cited by 3

Voluntary Behavior and Training Conditions Modulate in vivo Extracellular Glucose and Lactate in the Mouse Primary Motor Cortex

Béland-Millar, A., & Messier, C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.732242 · Cited by 4

Hypoglycemia and Brain: The Effect of Energy Loss on Neurons

Martínez‐Piña, D. A., Alvarado-Fernández, G. A., González‐Guevara, E., Castillo‐Pérez, C., Romero-Luna, G., & Torres-Ríos, J. A. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.104210 · Cited by 3

Influences of Prolonged Fasting on Behavioral and Brain Patterns

Papalini, S., Berthold‐Losleben, M., & Kohn, N. (2019) · Springer eBooks · doi:10.1007/978-3-319-55387-0_30 · Cited by 3

Metabolic Heterogeneity of Cerebral Cortical and Cerebellar Astrocytes

Sun, Y., Winters, A., Wang, L., Chaudhari, K., Berry, R., Tang, C., Liu, R., & Yang, S. (2023) · Life · doi:10.3390/life13010184 · Cited by 4

Rapid-onset dystonia-parkinsonism is associated with reduced cerebral blood flow without gray matter changes

Whitlow, C. T., Atcheson, K. M., Snively, B. M., Cook, J., Kim, J., Haq, I. U., Sweadner, K. J., Ozelius, L. J., & Brashear, A. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1116723 · Cited by 3

Metabolic Covariance Connectivity of Posterior Cingulate Cortex Associated with Depression Symptomatology Level in Healthy Young Adults

Wang, Z., Baeken, C., & Wu, G. (2023) · Metabolites · doi:10.3390/metabo13080920 · Cited by 3

Real-time monitoring of cortical brain activity in response to acute pain using wide-area Ca2+ imaging

Inami, C., Haruta, M., Ohta, Y., Tanaka, M., So, M., Sobue, K., Akay, Y. M., Kume, K., Ohta, J., Akay, M., et al. (2024) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2024.149800 · Cited by 3

A single dose of glycogen phosphorylase inhibitor improves cognitive functions of aged mice and affects the concentrations of metabolites in the brain

Pudełko‐Malik, N., Drulis‐Fajdasz, D., Pruss, Ł., Mielko, K. A., Rakus, D., Gizak, A., & Młynarz, P. (2024) · Scientific Reports · doi:10.1038/s41598-024-74861-z · Cited by 3

Early sensorimotor restriction in rats induces age‐dependent mitochondrial alterations in skeletal muscles and brain structures

Gaever, M. V., Dupuy, O., Dupont, E., Canu, M., & Daussin, F. (2025) · The Journal of Physiology · doi:10.1113/jp287765 · Cited by 3

The Importance of Iron To Support Optimum Cognitive Development

Sekartini, R. (2021) · World Nutrition Journal · doi:10.25220/wnj.v05.s1.0004 · Cited by 3

A Method for Measuring Metabolism in Sorted Subpopulations of Complex Cell Communities Using Stable Isotope Tracing

Roçi, I., Gallart‐Ayala, H., Watrous, J. D., Jain, M., Wheelock, C. E., & Nilsson, R. (2017) · Journal of Visualized Experiments · doi:10.3791/55011 · Cited by 3

Influence of cerebral blood vessel movements on the position of perivascular synapses

Urrecha, M., Romero, I., DeFelipe, J., & Merchán-Pérez, Á. (2017) · PLoS ONE · doi:10.1371/journal.pone.0172368 · Cited by 3

[Progress on loss-of-function hypothesis of presenilin-1 mutations in Alzheimer diseases].

Yan, M., Wang, X., & Guo, X. (2020) · PubMed Central · doi:10.3785/j.issn.1008-9292.2020.08.03 · Cited by 3

Quantitation of cerebral oxygen tension using phasor analysis and phosphorescence lifetime imaging microscopy (PLIM)

Liu, C., Chisholm, A., Fu, B., Su, C. T.-Y., Şencan, İ., Sakadžić, S., & Yaseen, M. A. (2021) · Biomedical Optics Express · doi:10.1364/boe.428873 · Cited by 3

Antioxidant Nutraceuticals as Novel Neuroprotective Agents

Katiyar, P., Ghosh, S., Saini, S., Ghosh, C., Agrawal, H., Sircar, D., & Roy, P. (2022) · Wiley eBooks · doi:10.1002/9781119746843.ch8 · Cited by 4

Additional Proposed Tests of the Soliton/Wave-Action Potential Model, and How the Thermodynamic/Theory-Based Philosophical Approach Abandons the Scientific MethodPreprint

Meissner, S. T. (2022) · Preprints.org · doi:10.20944/preprints202208.0248.v1 · Cited by 4

Lactate potentiates NMDA receptor currents via an intracellular redox mechanism targeting cysteines in the C-terminal domain of GluN2B subunits: implications for synaptic plasticityPreprint

Fiumelli, H., Herrera‐López, G., Lemtiri‐Chlieh, F., Mottier, L., Girgis, J., Benadiba, C., Jourdain, P., Carrano, N., Mahmood, H., Ooi, A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.21.624499 · Cited by 3

Inferring the Metabolic Objectives of Mammalian Cells via Inverse Modeling of Fluxomics and MetabolomicsPreprint

Morrissey, J., Monteiro, M., Betenbaugh, M. J., & Kontoravdi, C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.23.677837 · Cited by 3

Sugar Alcohols as Crosslinking Delay Additives for Fracturing Fluids

Almubarak, T., Alabdrabalnabi, M., Albaiz, A., & Yami, M. (2025) · Gels · doi:10.3390/gels11060457 · Cited by 2

ROS-dependent localization of glycolytic enzymes to mitochondria

Esparza‐Moltó, P. B., Goswami, A. V., Bozkurt, S., Münch, C., Newman, L. E., Moyzis, A. G., Rojas, G. R., Guan, D., Jones, J. R., Gage, F. H., et al. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103812 · Cited by 3

The synthetic cannabinoid THJ-2201 modulates mitochondrial activity and enhances mitochondrial recruitment to newly-forming neurites during neurodifferentiation of NG108-15 cells

Malheiro, R. F., Costa, A. C., Carmo, H., Carvalho, F. D., & Silva, J. P. (2025) · Archives of Toxicology · doi:10.1007/s00204-025-04217-7 · Cited by 2

The neurovascular unit response to cerebral ischemia as a promising area for translational studies – comments on some opened questions

Kowiański, P., Czuba, E., & Lietzau, G. (2025) · Experimental Neurology · doi:10.1016/j.expneurol.2025.115533 · Cited by 4

Does Amyotrophic Lateral Sclerosis (ALS) Have Metabolic Causes from Human Evolution?

Spedding, M. (2025) · Cells · doi:10.3390/cells14211734 · Cited by 2

Spinal cord metabolism in multiple sclerosis: a decade of missed opportunities and future directions

Rudroff, T. (2025) · Spinal Cord · doi:10.1038/s41393-025-01143-4 · Cited by 2

A deep autoencoder for fast spectral–temporal fitting of dynamic deuterium metabolic imaging data at 7T

Osburg, A. P., Shamaei, A., Strasser, B., Niess, F., Duguid, A., Bader, V., Frese, S., Hingerl, L., Fischer, H., Clarke, W. T., et al. (2025) · NeuroImage · doi:10.1016/j.neuroimage.2025.121632 · Cited by 2

Strychni Semen Improves Spatial Memory and Promotes Axon Regeneration Following Vascular Dementia in Mice

Zhang, Y., Liu, M., Zhao, X., Deng, S., Zhou, Z., Wan, B., Yan, Y., Jiang, X., Chen, Z., & Zheng, Y. (2026) · Current Neuropharmacology · doi:10.2174/011570159x388589251030173848 · Cited by 2

Mitochondrial Outer Membrane Voltage-Dependent Anion Channels: Unique Structures, Distinct Functions, and Novel Therapeutic Targets

Srivastava, S., Rawat, A., & Mahalakshmi, R. (2026) · Annual Review of Biophysics · doi:10.1146/annurev-biophys-061124-102155 · Cited by 3

Implantable microelectrode biosensors for monitoring neurometabolic markers

Fernandes, E., Ledo, A., & Barbosa, R. M. (2026) · Bioelectrochemistry · doi:10.1016/j.bioelechem.2026.109286 · Cited by 3

The Glymphatic system: A dynamic regulator of brain health and therapeutic target

Wang, X., Gao, M., Sui, S., Liu, F., Tian, W., Wu, S., Ding, J., Chao, X., Xie, X., Gu, M., et al. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115825 · Cited by 3

Physical Exercise Counteracts Impaired Cognition by Improving Mitochondrial Function

Maciel, P., Lamas, C. B., Araújo, A. C., Chagas, E. F. B., Guiguer, É. L., Curi, R., Pithon‐Curi, T. C., Almeida, M. C. D. S., Sloam, K. C. P., Sloan, L. A., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27104337 · Cited by 3

Neuroglia in traumatic brain injury: Pathophysiology and therapeutic targeting

Suk, K. (2026) · Brain Network Disorders · doi:10.1016/j.bnd.2026.03.002 · Cited by 2

Advancing Brain and Body Vascular Imaging in Bipolar Disorder: A Report From the International Society for Bipolar Disorders Vascular Task Force

Mio, M., Chen, P., Kennedy, K. G., Blumberg, H. P., Bond, D. J., Goldwaser, E. L., Gomes, F. A., Greaney, J. L., Hájek, T., McElroy, S. L., et al. (2026) · Bipolar Disorders · doi:10.1111/bdi.70120 · Cited by 2

Distinct Mitochondrial Central Dogma Gene Expression in the Buffalo Brain: A Comparative Transcriptomic Study with Metabolically Active Organs

Sadeesh, E. M., Lahamge, M. S., Ampadi, A. N., Kumari, S., & Mohiddin, R. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06134-x · Cited by 2

Gene environment interaction in periphery and brain converge to modulate behavioral outcomes: Insights from the SP1 transient early in life interference rat model

Asor, E., & Ben‐Shachar, D. (2016) · World Journal of Psychiatry · doi:10.5498/wjp.v6.i3.294 · Cited by 2

Our hungry brain: Which role do glial cells play for the energy supply?

Deitmer, J. W., Theparambil, S. M., Ruminot, I., & Becker, H. M. (2017) · e-Neuroforum · doi:10.1515/nf-2016-a102 · Cited by 2

Metabolic Plasticity of Astrocytes

Gorina, Y. V., Salmina, A. B., Erofeev, A. I., Can, Z., Bolshakova, A. V., Balaban, P. M., Борисович, Б. И., & Власова, О. Л. (2021) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093021060016 · Cited by 2

Pathophysiology of Cerebellar Degeneration in Mitochondrial Disorders: Insights from the Harlequin Mouse

la Torre, M. F.-D., Fiuza‐Luces, C., Laine-Menéndez, S., Delmiro, A., Arenas, J., Martín, M. A., Lucía, A., & Morán, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310973 · Cited by 2

Involvement of Autophagic Machinery in Neuropathogenesis: Targeting and Relevant Methods of Detection

Sayed, N., Ali, A. E., Elsherbiny, D. A., & Azab, S. S. (2024) · Methods in molecular biology · doi:10.1007/7651_2024_516 · Cited by 2

Electron Microscopic Mapping of Mitochondrial Morphology in the Cochlear Nerve Fibers

Lu, Y., Jiang, Y., Wang, F., Wu, H., & Hua, Y. (2024) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-024-00957-y · Cited by 2

Exploring Mitochondrial Quality in Aging and Neurodegenerative Diseases

Jiao, X., Li, M., Na, D., Meng, M., Zhang, G., & Guo, Y. (2024) · Neurochemical Journal · doi:10.1134/s1819712424700016 · Cited by 2

Interplay of Metastasis, Cancer Stem Cells, and Energy Metabolism in Cancer Progression

Mal, A. (2025) · Current Tissue Microenvironment Reports · doi:10.1007/s43152-025-00059-8 · Cited by 2

Medial prefrontal glutamate response to acute stress is associated with social subordination in female rhesus macaques

Treadway, M. T., Betters, S. A., Cooper, J. A., Li, C.-X., Zhang, X., & Michopoulos, V. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03334-2 · Cited by 3

Starvation Induces Upregulation of Monocarboxylate Transport in Glial Cells at the Drosophila Blood–Brain Barrier

González‐Gutiérrez, A., Gaete, J., Esparza, A., Ibacache, A., Contreras, E. G., & Sierralta, J. A. (2025) · Glia · doi:10.1002/glia.70021 · Cited by 3

DNA glycosylases Ogg1 and Mutyh influence gene expression of PRC2 targets associated with cognition

Abentung, A., Sakshaug, T., Dumaru, R., Liabakk, N., Yang, M., Wang, J., Bjørås, M., & Scheffler, K. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05730-9 · Cited by 4

Reflexiones multidisciplinares para el tratamiento de la competencia artística y la formación cultural

Salido López, P. V., & Irisarri Juste, M. R. (2021) · Ediciones de la Universidad de Castilla-La Mancha eBooks · doi:10.18239/jornadas_2021.29.00 · Cited by 3

Effect of Diet as a Factor of Exposome on Brain Function

Fedotova, A., Tiaglik, A. B., & Semyanov, A. V. (2021) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093021030108 · Cited by 2

Autophagy and bioenergetics in aging

Zhang, J., Wang, H., & Fang, E. F. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91617-2.00002-x · Cited by 2

Lipid peroxidation and sphingolipid alterations in the cerebral cortex and hypothalamus of rats fed a high-protein diet

Supruniuk, E., Żebrowska, E., Maciejczyk, M., Zalewska, A., & Chabowski, A. (2022) · Nutrition · doi:10.1016/j.nut.2022.111942 · Cited by 2

Epilepsy and Oxidative Stress

Lee, H. S., Arulsamy, A., & Shaikh, M. F. (2024) · Springer eBooks · doi:10.1007/978-981-19-3949-5_16-1 · Cited by 2

Neurodegenerative Diseases

Ross, I. A. (2024) · Springer eBooks · doi:10.1007/978-3-031-63681-3_6 · Cited by 2

Cerebral Glucose Metabolism

Heiss, W., & Zaro‐Weber, O. (2020) · Springer eBooks · doi:10.1007/978-3-030-53176-8_4 · Cited by 2

Spinal astrocyte-neuron lactate shuttle contributes to the PACAP/PAC1 receptor-induced nociceptive behaviorsPreprint

Kambe, Y., Yokai, M., Takasaki, I., Kurihara, T., & Miyata, A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/317156 · Cited by 2

Chronic pain alters microvascular architectural organization of somatosensory cortexPreprint

Zippo, A. G., del Grosso, V., Patera, A., Riccardi, M. P., Tredici, I. G., Bertoli, G. R., Mittone, A., Valente, M., Stampanoni, M., Coan, P., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/755132 · Cited by 2

Functional Magnetic Resonance Spectroscopy in the mousePreprint

Ligneul, C., Fernandes, F. F., & Shemesh, N. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2001.08505 · Cited by 2

The complexity of the relationship between spontaneous brain activity and glucose metabolismPreprint

Volpi, T., Silvestri, E., Aiello, M., Corbetta, M., & Bertoldo, A. (2021) · Research Square · doi:10.21203/rs.3.rs-728300/v1 · Cited by 2

Adropin expression correlates with age-related neuropathologies in the human brain and improves neuroinflammation and cognitive function in aging micePreprint

Banerjee, S., Ghoshal, S., Clemence, G., DeMars, K. M., Yang, C., Niehoff, M. L., Nguyen, A. D., Jayanth, P., Mersman, B. A., Xu, F., et al. (2021) · doi:10.21203/rs.3.rs-99159/v1 · Cited by 2

Neurovascular development

Adhicary, S., Nakisli, S., Fanelli, K., & Nielsen, C. M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-818872-9.00106-0 · Cited by 2

Altered metabolic function induced by amyloid-beta oligomers and PSEN1-mutations in iPSC-derived astrocytesPreprint

Elsworthy, R. J., Finelli, M. J., Aqattan, S., Dunleavy, C., King, M. C., Ludlam, A., Allen, S. L., Prosser, S., Chen, R. E., Martínez‐Jarquín, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.23.554346 · Cited by 2

Nervous System Disorders

Olsen, E., Witonsky, S. G., Wong, D., van Galen, G., Feary, D., Agne, G. F., Gold, J. R., Kopper, J. J., Madrigal, R., Ruby, R. E., et al. (2024) · Wiley eBooks · doi:10.1002/9781119617228.ch32 · Cited by 2

Human brain anatomy and atlases

Amunts, K., & Zachlod, D. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00187-x · Cited by 2

Glucose-dependent metabolism of hippocampal primary neurons in response to chemically induced long-term potentiationPreprint

Pudełko‐Malik, N., Drulis‐Fajdasz, D., FYDRYSZEWSKI, M. M., Burgess, S. C., Młynarz, P., Rakus, D., & Deja, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.24.639988 · Cited by 2

Role of Astrocytic Serine in Learning and Memory and its Implications in Alzheimer's Disease.

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