Differential regulation of mTORC1 by leucine and glutamine

A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity

Jinek, M., Chylinski, K., Fonfara, I., Hauer, M., Doudna, J. A., & Charpentier, E. (2012) · Science · doi:10.1126/science.1225829 · Cited by 17,116

Multiplex Genome Engineering Using CRISPR/Cas Systems

Cong, L., Ran, F. A., Cox, D., Lin, S., Barretto, R., Habib, N., Hsu, P. D., Wu, X., Jiang, W., Marraffini, L. A., et al. (2013) · Science · doi:10.1126/science.1231143 · Cited by 15,339

RNA-Guided Human Genome Engineering via Cas9

Mali, P., Yang, L., Esvelt, K. M., Aach, J., Guell, M., DiCarlo, J. E., Norville, J. E., & Church, G. M. (2013) · Science · doi:10.1126/science.1232033 · Cited by 9,210

mTOR Signaling in Growth Control and Disease

Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509

DNA targeting specificity of RNA-guided Cas9 nucleases

Hsu, P. D., Scott, D. A., Weinstein, J. A., Ran, F. A., Konermann, S., Agarwala, V., Li, Y., Fine, E. J., Wu, X., Shalem, O., et al. (2013) · Nature Biotechnology · doi:10.1038/nbt.2647 · Cited by 4,741

The Rag GTPases Bind Raptor and Mediate Amino Acid Signaling to mTORC1

Sancak, Y., Peterson, T. R., Shaul, Y. D., Lindquist, R. A., Thoreen, C. C., Bar-Peled, L., & Sabatini, D. M. (2008) · Science · doi:10.1126/science.1157535 · Cited by 2,773

Ragulator-Rag Complex Targets mTORC1 to the Lysosomal Surface and Is Necessary for Its Activation by Amino Acids

Sancak, Y., Bar-Peled, L., Zoncu, R., Markhard, A. L., Nada, S., & Sabatini, D. M. (2010) · Cell · doi:10.1016/j.cell.2010.02.024 · Cited by 2,464

RNA-programmed genome editing in human cells

Jinek, M., East, A., Cheng, A., Lin, S., Ma, E., & Doudna, J. (2013) · eLife · doi:10.7554/elife.00471 · Cited by 2,098

Bidirectional Transport of Amino Acids Regulates mTOR and Autophagy

Nicklin, P., Bergman, P., Zhang, B., Triantafellow, E., Wang, H., Nyfeler, B., Yang, H., Hild, M., Kung, C., Wilson, C., et al. (2009) · Cell · doi:10.1016/j.cell.2008.11.044 · Cited by 1,798

mTORC1 Senses Lysosomal Amino Acids Through an Inside-Out Mechanism That Requires the Vacuolar H + -ATPase

Zoncu, R., Bar-Peled, L., Efeyan, A., Wang, S., Sancak, Y., & Sabatini, D. M. (2011) · Science · doi:10.1126/science.1207056 · Cited by 1,673

Amino acids and their roles in tumor immunotherapy of breast cancer

Xia, H., Zhu, J., Zheng, Z., Xiao, P., Yu, X., Wu, M., Xue, L., Xu, X. Y., Wang, X., Guo, Y., et al. (2023) · The Journal of Gene Medicine · doi:10.1002/jgm.3647 · Cited by 3

Glutamine supplementation versus functional overload in extensor digitorum longus muscle hypertrophy

de Souza, D. R., de Vasconcelos, D. A. A., Murata, G. M., Fortes, M. A. S., Marzuca-Nassr, G. N., Levada‐Pires, A. C., Vitzel, K. F., Abreu, P., Scervino, M. V. M., Hirabara, S. M., et al. (2020) · PharmaNutrition · doi:10.1016/j.phanu.2020.100236 · Cited by 4

Stress Relief Downstream of TOR

Stocker, H. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.04.013 · Cited by 3

Molecular Processes and Regulation of Autophagy

Nasb, M., Kirberger, M., & Chen, N. (2021) · Springer eBooks · doi:10.1007/978-981-16-4525-9_1 · Cited by 3

Response by Xu et al to Letter Regarding Article, “Branched-Chain Amino Acid Catabolism Promotes Thrombosis Risk by Enhancing Tropomodulin-3 Propionylation in Platelets”

Xu, Y., Jiang, H., & Liu, J. (2020) · Circulation · doi:10.1161/circulationaha.120.051367 · Cited by 3

Glutamine metabolism enables NKT cell homeostasis and function through the AMPK-mTORC1 signaling axisPreprint

Kumar, A., Yarosz, E. L., Andren, A. C., Zhang, L., Lyssiotis, C. A., & Chang, C. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.07.463490 · Cited by 3

Biallelic Loss of Molecular Chaperone Molecule AIP Results in a Novel Severe Multisystem Disease Defined by Defective ProteostasisPreprint

Korbonits, M., Wang, X., Barry, S., Lim, C. T., Suleyman, O., Tito, S. D., Uddin, N., Vignola, M. L., Hall, C. L., Perna, L., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.08.604602 · Cited by 3

Synergistic Role of Amino Acids in Enhancing mTOR Activation Through Lysosome PositioningPreprint

Kolaczkowski, O. M., Goodson, B. A., Vazquez, V. F. M., Jia, J., Bhat, A. Q., Kim, T., & Pu, J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.12.618047 · Cited by 3

Arf1 promotes porcine intestinal epithelial cell proliferation via the mTORC1 signaling pathway

Fang, Y.-X., Lu, E.-Q., Xu, H. E., Zhang, Y., & Zhu, M. (2024) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-024-00942-y · Cited by 2

Amino acid sensing in cancer

Lin, Z., He, L., Wang, J., Zhang, H., Yao, S., Guo, J., Zhang, X., Liang, T., & Bai, X. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.108003 · Cited by 3

Glutamine synthetase modulates YAP activation by stabilizing LATS under glutamine homeostasis

Li, S., Ling, T., Wang, Y., Shi, J., Wang, Q., Lv, J., Li, J., Liu, Y., Zhang, Y., Liu, C., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116620 · Cited by 2

LAT1 / SLC7A5 ‐mediated amino acid uptake is regulated by redox signals triggered by formyl‐peptide receptor 2

Cassese, M., Brignola, C., Marrone, S., Esposito, G., Ammendola, R., & Cattaneo, F. (2025) · FEBS Journal · doi:10.1111/febs.70370 · Cited by 2

Peripheral lysosome levels dictate mTORC1 inactivation even when catabolically impaired

Dang, H. Q., Forssén, T., Pantelios, S., Chatzioglou, A. N., Kurzejamska, E., Vincent, C. T., Ibrahim, Y., & Mutvei, A. P. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02659-9 · Cited by 2

Reconstruction and Exploratory Analysis of mTORC1 Signaling Pathway and Its Applications to Various Diseases Using Network-Based Approach

Buddham, R., Chauhan, S., Narad, P., & Mathur, P. (2022) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2108.08007 · Cited by 2

Metabolite profiling in assessing ulcerative colitis activity: A systematic review

Cui, D., Han, X., Jin, J., Wang, Y., Chen, Z., Yang, G., & Jiang, M. (2025) · Human Nutrition & Metabolism · doi:10.1016/j.hnm.2025.200298 · Cited by 2

A Novel Approach for Cisplatin‐Resistant Esophageal Squamous Cell Carcinoma via Amino Acid Transporter LAT1 Inhibition

Mozumi, T., Harada‐Shoji, N., Ozawa, Y., Yamazaki, Y., Niikuni, R., Imai, K., Taniyama, Y., Sato, C., Okamoto, H., Ishida, H., et al. (2025) · Cancer Medicine · doi:10.1002/cam4.71234 · Cited by 2

Systems biology insights into the molecular drivers of childhood stunting and implications for intervention

Dable-Tupas, G., Maraon, A. B. A., Bernolo, L. J. L., Toñacao, N. G. F., Taylaran, A. D. M., Plata, M. A. C., Alcano, J. C., Björvang, R. D., Zain, S. M., Kobayashi, V., et al. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1761376 · Cited by 3

Regulation of Macroautophagy by Nutrients and Metabolites

Lorin, S., Pattingre, S., Meijer, A. J., & Codogno, P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802167-5.00014-1 · Cited by 2

Protein Metabolism in the Elderly

Dillon, E. L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802167-5.00007-4 · Cited by 3

Nutrient sensing

Venugopal, A., & Bishu, S. (2021) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000000709 · Cited by 2

Metabolic dysregulation in cancer progression

Arfin, S., Agrawal, K., Kumar, A., Kumar, A. J., Rathi, B., & Kumar, D. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-99879-6.00008-0 · Cited by 2

Macronutrient Deprivation: Biological Mechanisms and Effects on Early NeurodevelopmentPreprint

Doom, J. R. (2018) · OSF Preprints (OSF Preprints) · Cited by 2

Spatially and Functionally Distinct mTORC1 Entities Orchestrate the Cellular Response to Amino Acid AvailabilityPreprint

Fernandes, S. A., Angelidaki, D.-D., Nüchel, J., Pan, J., Gollwitzer, P., Elkis, Y., Artoni, F., Wilhelm, S., Kovacevic-Sarmiento, M., & Demetriades, C. (2023) · bioRxiv · doi:10.1101/2023.10.03.559930 · Cited by 1

LAT4 drives temozolomide induced radiotherapy resistance in glioblastoma by enhancing mTOR pathway activation

Zang, W., Liu, Y., Zheng, J., Huang, Y., Chen, L., Li, C., Zhao, J., Zhou, Q., Xu, Y., Wang, Z., et al. (2024) · Cancer Cell International · doi:10.1186/s12935-024-03590-0 · Cited by 1

The Fanconi Anemia Pathway Inhibits mTOR Signaling and Prevents Accelerated Translation in Head and Neck Cancer Cells

Ruffolo, B., Vicente-Muñoz, S., Mehta, K. Y., Rivera‐Cruz, C. M., Zhao, X., Romick‐Rosendale, L. E., Setchell, K. D. R., Lane, A., & Wells, S. I. (2025) · Cancers · doi:10.3390/cancers17152583 · Cited by 1

Integrated Genomic–Metabolomic Analysis for Tri-Categorical Classification of Type 2 Diabetes Status in the Korean Ansan–Ansung Cohort

Cha, J.-H., & Choi, S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311688 · Cited by 1

F127-CHO/Gelatin-NH₂ hydrogel delivering liposomal eriodictyol suppresses ferroptosis and attenuates retinal ganglion cell loss

Lin, Q., Liu, X., Li, X., Yu, J., Luo, W., Rao, Y., & Xie, L. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.149606 · Cited by 1

Targeting autophagy and metabolism for ewing sarcoma

Antoshina, K., Aniskin, D., Stempen, M., Schroeder, B., Timashev, P. S., Ulasov, I. V., Chaudhary, A., & Kharwar, R. K. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-11304-6 · Cited by 1

Glutamine synthetase sustains cortical circuit development via mTOR-mediated astrocyte maturation

Gong, P., Chen, X. Y., Cong, W., Hong, W., Liu, Y., Qi, G., Song, X., Wang, Z., Leng, Z., Duan, S., et al. (2025) · Protein & Cell · doi:10.1093/procel/pwaf112 · Cited by 1

Development of a severe rat refeeding syndrome model and mathematical modeling of the associated hypophosphatemia

Kato, H., Yamaoka, I., & Kubota, H. (2026) · npj Systems Biology and Applications · doi:10.1038/s41540-026-00658-7 · Cited by 2

IPMK-1 governs C. elegans physiology through ceTOR but lifespan via a distinct IP3-dependent pathway

He, X.-X., Huang, Q., Yu, X., Shi, L., Ou, L., Wu, G.-S., & Luo, H. (2026) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2026.112179 · Cited by 1

Reprogramming regulatory T cell plasticity for cancer immunotherapy

Issa, M. E., Schcolnik‐Cabrera, A., & Monetta, R. (2026) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2026.189605 · Cited by 2

Leucine regulates the mTOR pathway to improve growth and enhance immune responses in Scylla paramamosain challenged with Vibrio parahaemolyticus

Cui, X., Jin, M., Peng, H., Xu, T., Li, X., Xie, S., Zhan, W., Deng, Y., Tian, Y., Tang, Z., et al. (2026) · Animal nutrition · doi:10.1016/j.aninu.2026.03.005 · Cited by 1

LKB1 directly senses glycolytic metabolites to control AMPK activity

Wang, K.-H., Ding, C.-Y., Zou, Y., Sun, C.-C., Li, Q., Cai, Y.-P., Liu, Q., Song, Z.-L., Chen, T., Yang, X., et al. (2026) · Et vita · doi:10.15302/vita.2026.07.0056 · Cited by 1

Methods for Measuring Autophagosome Flux—Impact and Relevance

du Toit, A., Hofmeyr, J. S., & Loos, B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805420-8.00002-0 · Cited by 1

Amino Acid Intricacy

(2015) · Cell · doi:10.1016/j.cell.2015.01.055 · Cited by 1

Exploring phospholipase D signaling in the Warburg effect and cancer

Gideon, D. A., Nadiya, S., Annadurai, P., Murthy, R. G., Srinivasan, V., Nagaraj, K., Vatsan, A. B. K. V. S., Jebastin, T., Sivaramakrishnan, R., & Parashar, A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-95696-3.00014-4 · Cited by 1

Glutamine stimulates the S6K/4E-BP branch of insulin signalling pathway to mitigate human poly(Q) disorders in Drosophila disease models

Tandon, S., & Sarkar, S. (2023) · Nutritional Neuroscience · doi:10.1080/1028415x.2023.2253028 · Cited by 1

Tissue‐specific expression differences in Ras‐related GTP‐binding proteins in male rats

Kincheloe, G. N., Roberson, P. A., Jefferson, L. S., & Kimball, S. R. (2024) · Physiological Reports · doi:10.14814/phy2.15928

Role of L-glutamine in the regulation of rat Sertoli cell proliferation by FSH

Centola, C. L., Dasso, M. E., Riera, M. F., Meroni, S. B., & Galardo, M. N. (2024) · Reproduction · doi:10.1530/rep-24-0177 · Cited by 1

Leveraging single-cell and multi-omics approaches to identify MTOR-centered deubiquitination signatures in esophageal cancer therapy

Tian, K., Yao, Z., & Pan, D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1490623 · Cited by 1

Crosstalk between metabolites and myeloid cell biology

Goldspiel, B. P., Haggadone, M. D., Shin, S., & Bailis, W. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-15447-8.00003-9 · Cited by 1

PI3K-Akt-mTOR Signaling in Cancer and Cancer Therapeutics

Chopra, S. S., & Cantley, L. C. (2016) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-319-34211-5_1 · Cited by 1

Mechanistic Target of Rapamycin

McKee-Muir, O. C., & Russell, R. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00009-3 · Cited by 2

Cancer Metabolomics 2018

de Pinho, P. G., Carvalho, M. C., & Pinto, J. (2019) · MDPI eBooks · doi:10.3390/books978-3-03921-346-7 · Cited by 1

Macronutrient Deprivation: Biological Mechanisms and Effects on Early Neurodevelopment

(2016) · CRC Press eBooks · doi:10.1201/9781315372402-3 · Cited by 1

Disruption of Branched-Chain Amino Acid Catabolism Impairs Rat Myoblast Survival and Differentiation

Dhanani, Z. (2016) · YorkSpace (York University) · Cited by 1

Glutamine Synthetase-1 induces autophagy-lysosomal degradation of huntingtin aggregates and ameliorates animal motility in a Drosophila model for Huntington’s diseasePreprint

Vernizzi, L., Paiardi, C., Licata, G., Vitali, T., Santarelli, S., Raneli, M., Manelli, V., Rizzetto, M., Gioria, M., Pasini, M. E., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/618629 · Cited by 1

Glutamine metabolism and interactions with mechanistic target of rapamycin complex 1 in porcine preimplantation embryos

Chen, P. R. (2021) · doi:10.32469/10355/90986 · Cited by 1

Malonyl-CoA is an ancient physiological ATP-competitive mTORC1 inhibitorPreprint

Nicastro, R., Brohée, L., Alba, J., Nüchel, J., Figlia, G., Kipschull, S., Gollwitzer, P., Romero‐Pozuelo, J., Fernandes, S., Lamprakis, A. A., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.06.515351 · Cited by 1

Dietary Selenium Yeast Requirement and the Effect of Selenium Yeast on Skeletal Muscle Protein Deposition in Largemouth Bass (Micropterus Salmoides)Preprint

Wei, D., Qin, M., Liao, C., Chen, F., Yu, H., & Zhang, X. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4873845 · Cited by 1

Bcl-2 protein Noxa is required for metabolic reprogramming to glutamine dependence and for apoptosis in stimulated human CD8 + T cellsPreprint

Yang, T., Sharma, H., Benson, J. M., Valente, W. J., LaRue, R. S., Webber, B. R., Moriarity, B. S., Pennell, C. A., Jameson, S. C., & Kelekar, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.08.692849 · Cited by 1

Reconstructing The S. Cerevisiae Growth Control Network In Stress Conditions

Worley, J. (2015) · UA Campus Repository (The University of Arizona)

A Systems Approach for Dissecting Integrated Signaling Pathways: TORC1 and Ras/PKA Regulation of Glucose Induced Growth Control in S. cerevisiae

Kunkel, J. G. (2015) · UA Campus Repository (The University of Arizona)

The impact of mTOR, TFEB and Bid on non-alcoholic fatty liver disease and metabolic syndrome

Zhang, H. (2015) · IUScholarWorks (Indiana University) · doi:10.7912/c2/1939

Efeitos da suplementação com glutamina e/ou do treinamento físico resistido nas vias de sinalização da síntese e degradação de proteínas no músculo esquelético de ratos.

Rodrigues, C. (2015) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2015.tde-07122015-184843

Regulation of Hepatic Metabolism by the Mechanistic Target of Rapamycin

Lamming, D. W. (2015) · Springer eBooks · doi:10.1007/978-3-319-25065-6_3

Computer simulation of a large-scale signalling network regulating translation Initiation in the mammalian cell.

Taylor, D. W. (2017) · Surrey Research Insight Open Access (The University of Surrey)

The role of glutamine in the regulation of mTOR signalling in pancreatic β-cells

Alghanim, G. (2017) · Leicester Research Archive (University of Leicester)

Avaliação do controle da expressão gênica de citocinas pró inflamatórias mediado pela IL-10. Participação da IL-10 na modulação da resposta inflamatória exercida pela glutamina e na restrição alimentar

de Oliveira, D. C. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.9.2017.tde-16112017-174159

A participação da autofagia na regulação da célula-tronco hemopoética em camundongos knockouts para Atg7 e transglutaminase 2

Beltran, J. S. D. O. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.9.2018.tde-16082018-144356

Molecular Mechanisms of Postmeal Regulation of Muscle Anabolism

Bacquer, O. L. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-810422-4.00003-8

Crosstalk between mTORC1 and cAMP Signaling

Guan, K. (2015)

Investigating the role of amino acid transporter LAT3/SLC43A1 in prostate cancer

Zhang, K. (2019) · The Sydney eScholarship Repository (The University of Sydney)

Studies on Differentiation Mechanisms of Epithelial Cells in the Digestive System

杉山, 昌., & Sugiyama, M. (2018) · Institutional Repositories DataBase (IRDB) · doi:10.15068/00152275

Impact of Rapamycin on Genome Organization

Pickering, J. (2018) · HARVEST (University of Saskatchewan)

Dietary Protein and Muscle in Aging People

Cesari, M., & Marzetti, E. (2018) · MDPI eBooks · doi:10.3390/books978-3-03897-458-1

Tumor starvation by deprivation of glutamine and aspartate

Fried, R., Carlton, R. M., & Fried, D. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-824013-7.00008-0

Multi-omics characterization of pancreatic neuroendocrine neoplasms

Yang, C. F. K. (2021) · Summit (Simon Fraser University)

Влияние органических солей лития на содержание белков Akt/mTOR-сигнального пути в мононуклеарах периферической крови больных биполярным аффективным расстройством

Losenkov, I. S., Plotnikov, E. V., Epimakhova, E. V., Boiko, A. S., & Ivanova, S. А. (2021) · Сибирский вестник психиатрии и наркологии · doi:10.26617/1810-3111-2021-3(112)-30-38

Pengaruh Penerapan Keselamatan dan Kesehatan Kerja (K3) dan Kondisi Kelayakan Bengkel Terhadap Prestasi Belajar Peserta Didik pada Bengkel Pemesinan SMK Negeri 3 Boyolangu Kabupaten Tulungagung

Wibowo, A. (2014) · SKRIPSI Jurusan Teknik Mesin - Fakultas Teknik UM

Faculty Opinions recommendation of mTOR at the nexus of nutrition, growth, ageing and disease.

Ferguson, S. M. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737205281.793574661

Faculty Opinions recommendation of Rap1-GTPases control mTORC1 activity by coordinating lysosome organization with amino acid availability.

Proud, C. G. (2021) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737582213.793585692

Implicações de variantes bialélicas de perda de função no gene TBCK, no transporte de vesículas de células progenitoras neurais derivadas de células-tronco pluripotentes induzidas

Suzuki, Â. M. (2021) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2021.tde-09122021-143412

Unravelling novel functions of the MTOR network across subcellular compartments

Sandoval, M. C. (2022) · University of Groningen research database (University of Groningen / Centre for Information Technology) · doi:10.33612/diss.208570309

Integrins and Cell Metabolism: An Intimate Relationship Impacting Cancer

Ata, R., & Antonescu, C. N. (2021) · doi:10.32920/14639496

Mitogenic and Metabolic signals regulate mTOR complex 1 function to control GSK3β nuclear program

Bautista, S. J. (2021) · doi:10.32920/ryerson.14654061.v1 · Cited by 1

Faculty Opinions recommendation of Signaling networks in immunometabolism.

Kane, L. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737610223.793578145

mTORC1: Upstream and Downstream

Yao, Y., & Inoki, K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00182-6

https://elsevier.proofcentral.com/en-us/landing-page.html?token=baf280639f2773e07701834b1c13daInhibition of spermatogenesis by hypoxia is mediated by V-ATPase via the JNK/c-Jun pathway in mice

Yin, J., He, W., Zhang, M., He, W., Zhang, G., & Ni, B. J. (2023) · Reproductive Biology · doi:10.1016/j.repbio.2023.100761

Amino Acids and Their Derivatives in Oncology: A Review

Нефёдов, Л. И. (2023) · Лабораторная диагностика Восточная Европа · doi:10.34883/pi.2023.12.1.008

Mecanismo bioquímico de los cánceres: Una revisión del linfoma

Centeno, D. H., García, C. S., Solano, T. M., & Madrigal, M. G. (2023) · Revista de la Facultad de Medicina de la Universidad de lberoamérica · doi:10.54376/rcmui.v2i2.104

Leucine alleviates cytokine storm syndrome by regulating macrophage polarization via the mTORC1/LXRα signaling pathwayPreprint

Yan, H., Liu, Y., Li, X., Yu, B., He, J., Mao, X., Yu, J., Huang, Z., Luo, Y., Luo, J., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.21.546014

Underpinning the role of phospholipase D as a therapeutic target in cancer

Gopal, P. K., Mukherjee, K., & Das, A. K. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-95697-0.00005-4

Leucine alleviates cytokine storm syndrome by regulating macrophage polarization via the mTORC1/LXRα signaling pathwayPreprint

Yan, H., Liu, Y., Li, X., Yu, B., He, J., Mao, X., Yu, J., Huang, Z., Luo, Y., Luo, J., et al. (2023) · eLife · doi:10.7554/elife.89750.1

A evolução tumoral durante a gravidez

Oliveira, M. D. M. S. (2021) · doi:10.47749/t/unicamp.2021.1233741

Leucine alleviates cytokine storm syndrome by regulating macrophage polarization via the mTORC1/LXRα signaling pathwayPreprint

Yan, H., Liu, Y., Li, X., Yu, B., He, J., Mao, X., Yu, J., Huang, Z., Luo, Y., Luo, J., et al. (2023) · eLife · doi:10.7554/elife.89750.2

The nutrient-sensing Rag-GTPase complex in B cells controls humoral immunity via TFEB/TFE3-dependent mitochondrial fitnessPreprint

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Additional file 1 of Glutamine involvement in nitrogen regulation of cellulase production in fungi

Pang, A., Zhang, F., Hu, X. Y., Luo, Y., Wang, H., Durrani, S., Wu, F., Li, B., Zhou, Z., Lu, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16807775

Additional file 6 of Glutamine involvement in nitrogen regulation of cellulase production in fungi

Pang, A., Zhang, F., Hu, X. Y., Luo, Y., Wang, H., Durrani, S., Wu, F., Li, B., Zhou, Z., Lu, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16807790

Additional file 5 of Glutamine involvement in nitrogen regulation of cellulase production in fungi

Pang, A., Zhang, F., Hu, X. Y., Luo, Y., Wang, H., Durrani, S., Wu, F., Li, B., Zhou, Z., Lu, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16807787

Additional file 4 of Glutamine involvement in nitrogen regulation of cellulase production in fungi

Pang, A., Zhang, F., Hu, X. Y., Luo, Y., Wang, H., Durrani, S., Wu, F., Li, B., Zhou, Z., Lu, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16807784

Additional file 2 of Glutamine involvement in nitrogen regulation of cellulase production in fungi

Pang, A., Zhang, F., Hu, X. Y., Luo, Y., Wang, H., Durrani, S., Wu, F., Li, B., Zhou, Z., Lu, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16807778

Additional file 3 of Glutamine involvement in nitrogen regulation of cellulase production in fungi

Pang, A., Zhang, F., Hu, X. Y., Luo, Y., Wang, H., Durrani, S., Wu, F., Li, B., Zhou, Z., Lu, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16807781

Additional file 7 of Glutamine involvement in nitrogen regulation of cellulase production in fungi

Pang, A., Zhang, F., Hu, X. Y., Luo, Y., Wang, H., Durrani, S., Wu, F., Li, B., Zhou, Z., Lu, Z., et al. (2021) · Figshare · doi:10.6084/m9.figshare.16807793

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