The Sedoheptulose Kinase CARKL Directs Macrophage Polarization through Control of Glucose Metabolism

Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

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On the origin of cancer cells

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Alternative activation of macrophages: mechanism and functions

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Approaching the asymptote? Evolution and revolution in immunology.Preprint

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The Inflammasomes: Guardians of the Body

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Nonresolving Inflammation

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Inflammation 2010: New Adventures of an Old Flame

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HIF1α–dependent glycolytic pathway orchestrates a metabolic checkpoint for the differentiation of TH17 and Treg cells

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SOCS proteins, cytokine signalling and immune regulation

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Toll-like receptor–induced changes in glycolytic metabolism regulate dendritic cell activation

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Towards high resolution analysis of metabolic flux in cells and tissues

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Kinome siRNA screen identifies novel cell-type specific dengue host target genes

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First two unrelated cases of isolated sedoheptulokinase deficiency: A benign disorder?

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Rhein ameliorates septic lung injury and intervenes in macrophage metabolic reprogramming in the inflammatory state by Sirtuin 1

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The multi-faceted role of NADPH in regulating inflammation in activated myeloid cells

Ting, K. K. Y., Jongstra‐Bilen, J., & Cybulsky, M. I. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1328484 · Cited by 15

Mitochondrial perturbation in immune cells enhances cell-mediated innate immunity in Drosophila

Salminen, T. S., Vesala, L., Basikhina, Y., Kutzer, M. A. M., Tuomela, T., Lucas, R., Monteith, K., Prakash, A., Tietz, T., & Vale, P. F. (2024) · BMC Biology · doi:10.1186/s12915-024-01858-5 · Cited by 15

Studies on the effects of LPS , ß‐glucan and metabolic inhibitors on the respiratory burst and gene expression in Atlantic salmon macrophages

Ulvestad, J. S., Kumari, J., Seternes, T., Chi, H., & Dalmo, R. A. (2018) · Journal of Fish Diseases · doi:10.1111/jfd.12806 · Cited by 15

Glycolytic Activation of CD14+ Intestinal Macrophages Contributes to the Inflammatory Responses via Exosomal Membrane Tumor Necrosis Factor in Crohn’s Disease

Zeng, Z., Cheng, S., Li, X., Liu, H., Lin, J., Liang, Z., Liu, X., Cao, C., Li, S., He, X., et al. (2023) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izad117 · Cited by 14

Metabolic reprogramming of macrophages in chronic obstructive pulmonary disease

Qin, Z., Liu, W., Huang, C., & Zhang, W. Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1684075 · Cited by 15

Induction of MTHFD2 in Macrophages Inhibits Reactive Oxygen Species–mediated NF-κB Activation and Protects against Inflammatory Responses

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Tumor-Associated Macrophages—Implications for Molecular Oncology and Imaging

Kimm, M. A., Klenk, C., Alunni‐Fabbroni, M., Kästle, S., Stechele, M., Ricke, J., Eisenblätter, M., & Wildgruber, M. (2021) · Biomedicines · doi:10.3390/biomedicines9040374 · Cited by 16

Fasting metabolism modulates the interleukin-12/interleukin-10 cytokine axis

Kovarik, J. J., Kernbauer, E., Hölzl, M. A., Hofer, J., Gualdoni, G. A., Schmetterer, K. G., Miftari, F., Sobanov, Y., Meshcheryakova, A., Mechtcheriakova, D., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180900 · Cited by 14

The Role of the Pentose Phosphate Pathway in Cardiovascular Diseases

Chen, Z., Zhang, Y., Qian, C., & Xia, L. (2025) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-025-07788-w · Cited by 14

Novel insights into the regulation of cellular catabolic metabolism in macrophages through nuclear receptors

Stifel, U., Caratti, G., & Tuckermann, J. P. (2022) · FEBS Letters · doi:10.1002/1873-3468.14474 · Cited by 14

Targeting the Nrf2/HO-1 aixs: A therapeutic strategy against regulated cell death in Alzheimer’s disease

Wang, Z., Feng, W., Li, X., Yun, X., Wu, S., Du, L., & Wang, H. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103035 · Cited by 15

Mitochondrial Regulation of Macrophages in Innate Immunity and Diverse Roles of Macrophages During Cochlear Inflammation

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The potential role of Hippo pathway regulates cellular metabolism via signaling crosstalk in disease-induced macrophage polarization

An, Y., Tan, S., Yang, J., Gao, T., & Dong, Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1344697 · Cited by 14

Metabolic adaptation of macrophages in chronic diseases

Conza, G. D., & Ho, P. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.11.023 · Cited by 12

The Underexplored Landscape of Hypoxia-Inducible Factor 2 Alpha and Potential Roles in Tumor Macrophages: A Review

Steinberger, K. J., & Eubank, T. D. (2023) · Oxygen · doi:10.3390/oxygen3010005 · Cited by 15

Metabolomics in cancer and cancer-associated inflammatory cells

dos Santos, G. C., Saldanha-Gama, R. F. G., de Brito, N. M., Renovato‐Martins, M., & Barja‐Fidalgo, C. (2021) · Journal of Cancer Metastasis and Treatment · doi:10.20517/2394-4722.2020.86 · Cited by 12

Exploring the versatile roles of the endocannabinoid system and phytocannabinoids in modulating bacterial infections

Barker, H., & Ferraro, M. J. (2024) · Infection and Immunity · doi:10.1128/iai.00020-24 · Cited by 11

Natural products that target macrophages in treating non-alcoholic steatohepatitis

Li, C., Zhou, W., Ji, G., & Zhang, L. R. (2020) · World Journal of Gastroenterology · doi:10.3748/wjg.v26.i18.2155 · Cited by 11

An Army Marches on Its Stomach: Metabolic Intermediates as Antimicrobial Mediators in Mycobacterium tuberculosis Infection

Hackett, E. E., & Sheedy, F. J. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00446 · Cited by 11

Growth hormone remodels the 3D-structure of the mitochondria of inflammatory macrophages and promotes metabolic reprogramming

Palacios, B. S., Villares, R., Lucas, P., Rodrı́guez-Frade, J. M., Cayuela, A., Piccirillo, J., Lombardía, M., Gestoso, D. D., Fernández-García, M., Risco, C., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1200259 · Cited by 10

Macrophage immunometabolism in diabetes-associated atherosclerosis

dos Santos, B. G., & Goedeke, L. (2023) · Immunometabolism · doi:10.1097/in9.0000000000000032 · Cited by 11

Metabolic evolutionary roots of the macrophage immune response in amoeba-bacteria interactions: The conserved role of hypoxia-induced Factor and AMP kinase

Dzik, J. (2021) · Acta Biochimica Polonica · doi:10.18388/abp.2020_5683 · Cited by 10

Metabolic Pathways as a Novel Landscape in Pancreatic Ductal Adenocarcinoma

Ali, A. H., Chianese, U., Papulino, C., Toraldo, A., Abakar, M. E. A., Passaro, E., Cennamo, R., Gaudio, N. D., Altucci, L., & Benedetti, R. (2022) · Cancers · doi:10.3390/cancers14153799 · Cited by 10

Sirtuin-3-Mediated Cellular Metabolism Links Cardiovascular Remodeling with Hypertension

Gao, J., & Shen, W. (2023) · Biology · doi:10.3390/biology12050686 · Cited by 9

Decoding macrophage immunometabolism in human viral infection

Malemnganba, T., Rattan, A., & Prajapati, V. K. (2024) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2023.12.003 · Cited by 9

Single-cell multiomics reveals macrophage-derived IL-23 and CXCL9/10 drive pathogenic IFNG + IL17 + T cells in immunotherapy-related colitis

Tang, Z., Shi, J., Xu, S., Liu, S., Yin, W., Xiang, Y., Li, J., He, Z., Yao, X., Zhou, L., et al. (2025) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2025-011959 · Cited by 10

Metabolic reprogramming and signalling networks in microglial activation: Implications for neurodegeneration

El-Hamri, M.-A., & Abboussi, O. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103138 · Cited by 9

Attenuating Effect of Chlorella Extract on NLRP3 Inflammasome Activation by Mitochondrial Reactive Oxygen Species

Nakashima, Y., Gotoh, K., Mizuguchi, S., Setoyama, D., Takata, Y., Kanno, T., & Kang, D. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.763492 · Cited by 10

Macrophage origin, phenotypic diversity, and modulatory signaling pathways in the atherosclerotic plaque microenvironment

Liu, N., Zhang, B., Sun, Y., Song, W., & Guo, S.-D. (2021) · Vessel Plus · doi:10.20517/2574-1209.2021.25 · Cited by 10

Macrophage polarization by potential nutraceutical compounds: A strategic approach to counteract inflammation in atherosclerosis

Sottero, B., Testa, G., Gamba, P., Staurenghi, E., Giannelli, S., & Leonarduzzi, G. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.02.010 · Cited by 9

Microbial dysbiosis in the gut–mammary axis as a mechanism for mastitis in dairy cows

Wang, Z., Ma, Z., Tian, Z., Jia, H., Zhang, L., Mao, Y., Yang, Z., Liu, X., & Li, M. (2024) · International Journal of Dairy Technology · doi:10.1111/1471-0307.13150 · Cited by 8

Macrophage metabolism in inflammatory heart disease: new insights and therapeutic implications

Xiang, A., Chang, A., Zhou, J., Jin, J., Zhang, X., & Wang, Q. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1664538 · Cited by 11

The metabolic regulation of tumor-associated macrophage reprogramming

Fan, H., Lu, D., Yin, X., Sun, H., Wang, Z., Sun, H., Li, Y., Li, Y., Zhou, Z., Chen, L., et al. (2025) · Molecular Immunology · doi:10.1016/j.molimm.2025.10.006 · Cited by 9

Glucose Metabolic Reprogramming of Macrophages Against Mycobacterium tuberculosis Infection

Liu, T., Yang, Z., Tong, J., Gao, M., & Pang, Y. (2025) · ImmunoTargets and Therapy · doi:10.2147/itt.s552746 · Cited by 9

Quantitative Proteomics of Polarised Macrophages Derived from Induced Pluripotent Stem Cells

Murugesan, G., Davidson, L., Jannetti, L., Crocker, P. R., & Weigle, B. (2022) · Biomedicines · doi:10.3390/biomedicines10020239 · Cited by 9

Metabolic regulation of intrasynovial flexor tendon repair: The effects of dichloroacetate administration on early tendon healing in a canine model

Gelberman, R. H., Lane, R. A., Sakiyama‐Elbert, S. E., Thomopoulos, S., & Shen, H. (2022) · Journal of Orthopaedic Research® · doi:10.1002/jor.25354 · Cited by 8

Parkinsonian Neurotoxins Impair the Pro-inflammatory Response of Glial Cells

Rabaneda‐Lombarte, N., Xicoy-Espaulella, E., Serratosa, J., Saura, J., & Solà, C. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00479 · Cited by 8

When size matters – coordination of growth and cell cycle in bacteria

Morcinek-Orłowska, J., Galińska, J., & Glinkowska, M. K. (2019) · Acta Biochimica Polonica · doi:10.18388/abp.2018_2798 · Cited by 8

Stromal-induced mitochondrial re-education: Impact on epithelial-to-mesenchymal transition and cancer aggressiveness

Bacci, M., Ippolito, L., Magnelli, L., Giannoni, E., & Chiarugi, P. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.05.009 · Cited by 8

Targeting macrophage polarization for therapy of diabesity–the feasibility of early improvement of insulin sensitivity and insulin resistance-a comprehensive systematic review

Kaur, K. K., Allahbadia, G. N., & Singh, M. (2021) · Journal of Diabetes Metabolic Disorders & Control · doi:10.15406/jdmdc.2021.08.00216 · Cited by 8

Novel Pharmacological Targets for Pulmonary Arterial Hypertension

Klinger, J. R. (2021) · Comprehensive physiology · doi:10.1002/cphy.c200015 · Cited by 10

Metabolically Primed Multipotent Hematopoietic Progenitors Fuel Innate ImmunityPreprint

Cosgrove, J., Lyne, A.-M., Rodríguez‐Ramiro, I., Cabeli, V., Conrad, C., Bento, S. T., Tubeuf, E., Russo, E., Tabarin, F., Belloucif, Y., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.24.525166 · Cited by 9

Metabolic Crossroad Between Macrophages and Cancer Cells: Overview of Hepatocellular Carcinoma

Santarsiero, A., Convertini, P., Iacobazzi, D., Infantino, V., & Todisco, S. (2024) · Biomedicines · doi:10.3390/biomedicines12122684 · Cited by 7

Lactylation modification - a bridge between sepsis and macrophage metabolic reprogramming

Fang, Z., Zhu, G. S., Nie, D. Y., & Xu, B. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1738765 · Cited by 7

Soluble Carrier Transporters and Mitochondria in the Immunometabolic Regulation of Macrophages

Silva, L. F. L., Lee, J., & Moraes‐Vieira, P. M. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0181 · Cited by 7

Metabolic Reprogramming of Immune Cells Following Vaccination: From Metabolites to Personalized Vaccinology

Mussap, M., Puddu, M., & Fanos, V. (2023) · Current Medicinal Chemistry · doi:10.2174/0929867330666230509110108 · Cited by 8

Negative Regulation of Innate Immune Signaling by Components of the Button Mushroom Agaricus bisporus

O'Sullivan, M., Dempsey, E., Case, S., Hackett, E. E., Ledwith, A. E., Prendeville, H., O'Brien, T., Lewis, F., Murphy, D. M., Yadav, S., et al. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202200845 · Cited by 7

Crosstalk between synovial macrophages and fibroblasts in rheumatoid arthritis.

Saeki, N., & Imai, Y. (2023) · PubMed · doi:10.14670/hh-18-628 · Cited by 8

Metabolic Adaptations and Functional Activity of Macrophages in Homeostasis and Inflammation

Yurakova, T. R., Gorshkova, E. A., Nosenko, M. A., & Drutskaya, M. S. (2024) · Biochemistry (Moscow) · doi:10.1134/s0006297924050043 · Cited by 7

Methylglyoxal Drives a Distinct, Nonclassical Macrophage Activation Status

Tsokanos, F., Muley, C., Khani, S., Hass, D., Fleming, T. H., Wolff, G., Bartelt, A., Nawroth, P. P., & Herzig, S. (2021) · Thrombosis and Haemostasis · doi:10.1055/s-0041-1726346 · Cited by 8

Phagocyte metabolism: neutrophils have their cake but don’t eat it

Phelan, J. J., & Sheedy, F. J. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.08.011 · Cited by 7

Cystinose

Cherqui, S. (2023) · médecine/sciences · doi:10.1051/medsci/2023025 · Cited by 7

Bayesian 13C-Metabolic Flux Analysis of Parallel Tracer Experiments in Granulocytes: A Directional Shift within the Non-Oxidative Pentose Phosphate Pathway Supports Phagocytosis

Hogg, M., Wolfschmitt, E.-M., Wachter, U. A., Zink, F., Radermacher, P., & Vogt, J. A. (2023) · Metabolites · doi:10.3390/metabo14010024 · Cited by 7

Mitochondrial Mechanisms in Immunity and Inflammatory Conditions: Beyond Energy Management

Álvarez, S., Vanasco, V., Areán, J. S. A., Magnani, N., & Evelson, P. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0367 · Cited by 6

Sinomenine modulates the metabolic reprogramming induced by sepsis via CHRNA7

Zhao, J., Wang, Z., Zou, X., Liao, J., Zhang, Y., Zhang, W., Yu, J., & Huang, F. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.123332 · Cited by 6

Does oncolytic viruses‐mediated metabolic reprogramming benefit or harm the immune microenvironment?

Peng, C., Xiao, P., & Li, N. (2024) · The FASEB Journal · doi:10.1096/fj.202301947rr · Cited by 6

The multifaceted roles of macrophages in the transition from hepatitis to hepatocellular carcinoma: From mechanisms to therapeutic strategies

Zhang, S., Dong, H., Jin, X., Sun, J., & Li, Y. (2025) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2025.167676 · Cited by 7

Microbial production of D-mannose and D-sedoheptulose with tunable ratios

Palur, D. S. K., Luu, B., Taylor, J. E., Singhal, M., Didzbalis, J., Siegel, J. B., & Atsumi, S. (2025) · Trends in biotechnology · doi:10.1016/j.tibtech.2025.07.017 · Cited by 6

Understanding the role of alternative macrophage phenotypes in human atherosclerosis

Kawai, K., Vozenilek, A. E., Kawakami, R., Sato, Y., Ghosh, S., Virmani, R., & Finn, A. V. (2022) · Expert Review of Cardiovascular Therapy · doi:10.1080/14779072.2022.2111301 · Cited by 6

Mycobacterial infection alters host mitochondrial activity

Mohareer, K., & Banerjee, S. (2023) · International review of cytology · doi:10.1016/bs.ircmb.2023.01.007 · Cited by 7

A detailed insight into macrophages' role in shaping lung carcinogenesis

Aktar, T., Modak, S., Majumder, D., & Maiti, D. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122896 · Cited by 6

Relationship between NADPH and Th1/Th2 ratio in patients with non-Hodgkin lymphoma who have been exposed to pesticides

Aribi, M., Zahzeh, M. R., Loukidi, B., Meziane, W., Haddouche, M., Mesli, N., & Zouaoui, Z. (2015) · Journal of Blood Medicine · doi:10.2147/jbm.s78759 · Cited by 6

Assessing the reliability of gene expression measurements in very-low-numbers of human monocyte-derived macrophages

Geiß, C., Alanis‐Lobato, G., Andrade-Navarro, M. A., & Régnier‐Vigouroux, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-54500-8 · Cited by 7

The Non-canonical Role of Metabolic Enzymes in Immune Cells and Its Impact on Diseases

Alves, R. W., Doretto-Silva, L., da Silva, E. M., Fürstenau, C. R., & Andrade‐Oliveira, V. (2020) · Current Tissue Microenvironment Reports · doi:10.1007/s43152-020-00020-x · Cited by 6

IL17A Depletion Affects the Metabolism of Macrophages Treated with Gemcitabine

Roux, C., Mucciolo, G., Kopecka, J., Novelli, F., Riganti, C., & Cappello, P. (2021) · Antioxidants · doi:10.3390/antiox10030422 · Cited by 6

2-Year-Old and 3-Year-Old Italian ALS Patients with Novel ALS2 Mutations: Identification of Key Metabolites in Their Serum and Plasma

Gautam, M., Carratore, R. D., Helmold, B., Tessa, A., Gözütok, Ö., Chandel, N. S., Idrısoğlu, H. A., Bongioanni, P., Battini, R., & Özdi̇nler, P. H. (2022) · Metabolites · doi:10.3390/metabo12020174 · Cited by 6

The Pivotal Role of Macrophages in Metabolic Distress

Roberts, J., Fallon, P. G., & Hams, E. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.86474 · Cited by 8

Systems-based approach to examine the cytokine responses in primary mouse lung macrophages infected with low pathogenic avian Influenza virus circulating in South East Asia

Taye, B., Chen, H., Myaing, M. Z., Tan, B. H., Maurer‐Stroh, S., & Sugrue, R. J. (2017) · BMC Genomics · doi:10.1186/s12864-017-3803-6 · Cited by 6

Absence of hexose‐6‐phosphate dehydrogenase results in reduced overall glucose consumption but does not prevent 11β‐hydroxysteroid dehydrogenase‐1‐dependent glucocorticoid activation

Marbet, P., Klusoňová, P., Birk, J., Kratschmar, D. V., & Odermatt, A. (2018) · FEBS Journal · doi:10.1111/febs.14642 · Cited by 6

Glutamine metabolism tunes myeloid responses to drive resolution of inflammation during skin repair

Xu, Y., Forni, M. F., Benvie, A. M., Castano, N., King, D. E., Sun, Q., Siebel, S., Tran, V. A., Kibbey, R. G., Miller‐Jensen, K., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117001 · Cited by 5

Crosstalk of mitochondrial dysfunction and macrophage polarization in sepsis

Ji, F., Zhang, L., Lili, N., Zhang, M., & Zhang, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1692597 · Cited by 7

Temporal control of macrophage pro-inflammatory phenotype by a biphasic HIF-1α regulatory program

Davanzo, G. G., Ribeiro, G., dos-Santos, D., Berçot, M. R., Zaidan, I., dos Reis, L. M., Virgílio-da-Silva, J. V., Castelucci, B. G., Estevão, P., Souza, W. D., et al. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.07.001 · Cited by 5

Anti-inflammatory effects of pulsed magnetic field on the immune system

Kim, S., & Lee, H. (2024) · AIP Advances · doi:10.1063/9.0000660 · Cited by 5

Classification and functional analysis of disulfidptosis‐associated genes in sepsis

He, S.-M., Zhang, X.-X., Wang, Z., Zhang, Q.-J., Yao, Y., Pang, J., & Chen, Y.-G. (2024) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70020 · Cited by 4

Longitudinal mitochondrial bioenergetic signatures of blood monocytes and lymphocytes improve during treatment of drug-susceptible pulmonary tuberculosis patients

Cumming, B. M., Addicott, K. W., Maruri, F., Pillay, V., Asmal, R., Moodley, S., Barreto-Durate, B., Araújo‐Pereira, M., Mazibuko, M., Mhlane, Z., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1465448 · Cited by 5

The General Principle of the Warburg Effect as a Possible Approach for Cancer Immunotherapy: The Regulatory Effect of Plant Extracts Could Change the Game

Ivanova, D., Semkova, S., Grigorov, B., Tzanova, M. T., Georgieva, A., Danchev, D., Nikolova, B., & Yaneva, Z. L. (2025) · Molecules · doi:10.3390/molecules30020393 · Cited by 5

Macrophage clock of pregnancy: circadian and metabolic control of decidual macrophage

Yang, D., Thiele, K., Yin, T., & Diao, L. (2025) · Seminars in Immunopathology · doi:10.1007/s00281-025-01057-6 · Cited by 6

Bacterial Discrimination: Dictyostelium’s Discerning Taste

Snyder, M. (2013) · Current Biology · doi:10.1016/j.cub.2013.04.021 · Cited by 5

Aqueous extract of Sedum oxypetalum induces mineralization and osteogenic differentiation by human Periodontal Ligament-Derived cells

Lara‐Issasi, G. R., Ocampo, N. E., Hoz, L., Correa-Prado, R., Cedillo–Cruz, A., Arzate, H., & Aguilar, M. I. (2018) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2018.07.005 · Cited by 5

Deficiency of the sedoheptulose kinase (Shpk) does not alter the ability of hematopoietic stem cells to rescue cystinosis in the mouse model

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