Signalling to translation: how signal transduction pathways control the protein synthetic machinery

Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex

Sarbassov, D. D., Guertin, D. A., Ali, S. M., & Sabatini, D. M. (2005) · Science · doi:10.1126/science.1106148 · Cited by 6,216

TOR signaling in growth and metabolism

Wullschleger, S., Loewith, R., & Hall, M. N. (2006) · Cell · doi:10.1016/j.cell.2006.01.016 · Cited by 5,787

TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival

Inoki, K., Zhu, T., & Guan, K.-L. (2003) · Cell · doi:10.1016/s0092-8674(03)00929-2 · Cited by 3,914

Regulated Translation Initiation Controls Stress-Induced Gene Expression in Mammalian Cells

Harding, H. P., Novoa, I., Zhang, Y., Zeng, H., Wek, R. C., Schapira, M., & Ron, D. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00108-8 · Cited by 3,344

ERK and p38 MAPK-Activated Protein Kinases: a Family of Protein Kinases with Diverse Biological Functions

Roux, P. P., & Blenis, J. (2004) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.68.2.320-344.2004 · Cited by 2,540

Prolonged Rapamycin Treatment Inhibits mTORC2 Assembly and Akt/PKB

Sarbassov, D. D., Ali, S. M., Sengupta, S., Sheen, J.-H., Hsu, P. P., Bagley, A. F., Markhard, A. L., & Sabatini, D. M. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.03.029 · Cited by 2,365

eIF4 Initiation Factors: Effectors of mRNA Recruitment to Ribosomes and Regulators of Translation

Gingras, A., Raught, B., & Sonenberg, N. (1999) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.68.1.913 · Cited by 2,103

Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive

Jacinto, E., Loewith, R., Schmidt, A., Lin, S., Rüegg, M. A., Hall, A., & Hall, M. N. (2004) · Nature Cell Biology · doi:10.1038/ncb1183 · Cited by 2,097

Absence of S6K1 protects against age- and diet-induced obesity while enhancing insulin sensitivity

Um, S. H., Frigerio, F., Watanabe, M., Picard, F., Joaquin, M., Sticker, M., Fumagalli, S., Allegrini, P. R., Kozma, S. C., Auwerx, J., et al. (2004) · Nature · doi:10.1038/nature02866 · Cited by 1,677

Growing roles for the mTOR pathway

Sarbassov, D. D., Ali, S. M., & Sabatini, D. M. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.09.009 · Cited by 1,590

Circadian activities of the brain MNK‐eIF4E signalling axis contribute to diurnal rhythms of some cognitive functions

Liu, D., Li, J., Lin, H., Lorsung, E., Le, N., Singla, R., Mishra, A., Fukunaga, R., & Cao, R. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15678 · Cited by 20

Bi-polarized translation of ascidian maternal mRNA determinant pem-1 associated with regulators of the translation machinery on cortical Endoplasmic Reticulum (cER)

Paix, A., Nguyen, P. N. L., & Sardet, C. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.06.019 · Cited by 20

Role of the ERK1/2 Signaling Pathway in the Replication of Junín and Tacaribe Viruses

Brunetti, J. E., Foscaldi, S., Quintana, V. M., Scolaro, L. A., López, N., & Castilla, V. (2018) · Viruses · doi:10.3390/v10040199 · Cited by 20

Glutamate-dependent phosphorylation of the mammalian target of rapamycin (mTOR) in Bergmann glial cells

Zepeda, R. C., Barrera, I., Castelán, F., Suárez‐Pozos, E., Melgarejo, Y., González-Mejía, M. E., Hernández‐Kelly, L. C., López‐Bayghen, E., Aguilera, J., & Ortega, A. (2009) · Neurochemistry International · doi:10.1016/j.neuint.2009.03.011 · Cited by 20

Down-regulation of CHERP inhibits neuroblastoma cell proliferation and induces apoptosis through ER stress induction

Zhang, D., Wang, F., Pang, Y., Ke, X., Zhu, S., Zhao, E., Zhang, K., Chen, L., & Cui, H. (2017) · Oncotarget · doi:10.18632/oncotarget.20898 · Cited by 19

Identification of unique key genes and miRNAs in latent tuberculosis infection by network analysis

Lin, Y., Zhang, Y., Yu, H., Tian, R., Wang, G., & Li, F. (2019) · Molecular Immunology · doi:10.1016/j.molimm.2019.04.032 · Cited by 19

Tissue-specific regulation of S6K1 by insulin in chickens divergently selected for growth

Duchêne, S., Cailleau-Audouin, E., Berri, C., Dupont, J., & Tesseraud, S. (2008) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2007.12.008 · Cited by 20

Exploration of low temperature microRNA function in an anoxia tolerant vertebrate ectotherm, the red eared slider turtle ( Trachemys scripta elegans )

Biggar, K. K., & Storey, K. B. (2016) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2016.09.008 · Cited by 20

Glutamate-Dependent Translational Control in Cultured Bergmann Glia Cells: eIF2α Phosphorylation

Flores‐Méndez, M., Martínez‐Lozada, Z., Monroy, H., Hernández‐Kelly, L. C., Barrera, I., & Ortega, A. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1024-1 · Cited by 18

The Insulin-like Growth Factor-1 Axis and its Potential as a Therapeutic Target in Central Nervous System (CNS) Disorders

Bibollet‐Bahena, O., Cui, Q., & Almazán, G. (2009) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/187152409788452108 · Cited by 18

Differential mTOR and ERK pathway utilization by effector CD4 T cells suggests combinatorial drug therapy of arthritis

Lin, J. T., Stein, E. A., Wong, M. T., Kalpathy, K. J., Su, L., Utz, P. J., Robinson, W. H., & Fathman, C. G. (2011) · Clinical Immunology · doi:10.1016/j.clim.2011.09.008 · Cited by 17

Long-acting insulins alter milk composition and metabolism of lactating dairy cows

Winkelman, L. A., & Overton, T. R. (2013) · Journal of Dairy Science · doi:10.3168/jds.2012-6498 · Cited by 18

Programmed Cell Death 4 ( PDCD 4): A Novel Player in Ethanol‐Mediated Suppression of Protein Translation in Primary Cortical Neurons and Developing Cerebral Cortex

Narasimhan, M., Rathinam, M., Riar, A. K., Patel, D., Mummidi, S., Yang, H., Colburn, N. H., Henderson, G. I., & Mahimainathan, L. (2012) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2012.01850.x · Cited by 19

Cyclic mechanical load causes global translational arrest in articular chondrocytes: a process which is partially dependent upon PKR phosphorylation

Lomas, C., Tang, X., Chanalaris, A., Saklatvala, J., & Vincent, T. L. (2011) · European Cells and Materials · doi:10.22203/ecm.v022a14 · Cited by 17

Interplay between steroid hormone activation of the unfolded protein response and nuclear receptor action

Zheng, X., Andruska, N. D., Yu, L., Mao, C., Kim, J. E., Livezey, M. R., Helferich, W. G., & Shapiro, D. J. (2016) · Steroids · doi:10.1016/j.steroids.2016.03.014 · Cited by 18

Proteomic and Phosphoproteomic Changes Induced by Prolonged Activation of Human Eosinophils with IL-3

Esnault, S. J., Hebert, A. S., Jarjour, N. N., Coon, J. J., & Mosher, D. F. (2018) · Journal of Proteome Research · doi:10.1021/acs.jproteome.8b00057 · Cited by 18

Potent Antineoplastic Effects of Combined PI3Kα–MNK Inhibition in Medulloblastoma

Eckerdt, F., Bell, J. B., Beauchamp, E. M., Clymer, J. R., Blyth, G. T., Kościuczuk, E. M., Ma, Q., Chen, D. Z., Horbinski, C., Goldman, S., et al. (2019) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-18-1193 · Cited by 17

l ‐Serine deficiency caused by genetic P hgdh deletion leads to robust induction of 4E‐ BP 1 and subsequent repression of translation initiation in the developing central nervous system

Sayano, T., Kawakami, Y., Kusada, W., Suzuki, T., Kawano, Y., Watanabe, A., Takashima, K., Arimoto, Y., Esaki, K., Wada, A., et al. (2013) · FEBS Journal · doi:10.1111/febs.12146 · Cited by 17

An investigation of nutrient-dependent mRNA translation in Drosophila larvae

Nagarajan, S., & Grewal, S. (2014) · Biology Open · doi:10.1242/bio.20149407 · Cited by 19

Energy sensor AMPK gamma regulates translation via phosphatase PPP6C independent of AMPK alpha

Zhou, Q., Hao, B., Cao, X., Gao, L., Yu, Z., Zhao, Y., Zhu, M., Zhong, G., Chi, F., Dai, X., et al. (2022) · Molecular Cell · doi:10.1016/j.molcel.2022.10.030 · Cited by 16

Regulation of the cardiomyocyte transcriptome vs translatome by endothelin-1 and insulin: translational regulation of 5' terminal oligopyrimidine tract (TOP) mRNAs by insulin

Markou, T., Marshall, A. K., Cullingford, T. E., Tham, E. L., Sugden, P. H., & Clerk, A. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-343 · Cited by 16

Muscle Atrophy in Cancer

Yang, J., Cao, R. Y., Li, Q. X., & Zhu, F. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1435-3_15 · Cited by 16

Global and Gene-Specific Translational Regulation in Rat Lung Development

Otulakowski, G., Duan, W., & O'Brodovich, H. M. (2008) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0284oc · Cited by 16

Effects of neonatal MK-801 treatment on p70S6K-S6/eIF4B signal pathways and protein translation in the frontal cortex of the developing rat brain.

Kim, S. H., Park, H. G., Kim, H. S., Ahn, Y., & Kim, Y. S. (2010) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145709991192 · Cited by 15

Structural changes, increased hypoxia, and oxidative DNA damage in placenta due to maternal smokeless tobacco use

Kumar, S. N., Bastia, B., Borgohain, D., Agrawal, U., Raisuddin, S., & Jain, A. K. (2021) · Birth Defects Research · doi:10.1002/bdr2.1941 · Cited by 15

Dysregulation of epithelial Na+ absorption induced by inhibition of the kinases TORC1 and TORC2

Mansley, M. K., & Wilson, S. M. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.01003.x · Cited by 14

Chromium(III) Triggers the DNA-Damaged Checkpoint of the Cell Cycle and Induces a Functional Increase of 4E-BP

Bouffant, R. L., Mulner‐Lorillon, O., Morales, J., Cormier, P., & Bellé, R. (2008) · Chemical Research in Toxicology · doi:10.1021/tx700244h · Cited by 15

Overcoming resistance to rapalogs in gliomas by combinatory therapies

Grzmil, M., & Hemmings, B. A. (2013) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2013.01.041 · Cited by 15

Differentiation-Induced Post-Transcriptional Control of B7-H1 in Human Trophoblast Cells

Holets, L. M., Carletti, M. Z., Kshirsagar, S., Christenson, L. K., & Petroff, M. G. (2008) · Placenta · doi:10.1016/j.placenta.2008.10.001 · Cited by 15

Heat shock protein 70 promotes coxsackievirus B3 translation initiation and elongation via Akt-mTORC1 pathway depending on activation of p70S6K and Cdc2

Wang, F., Qiu, Y., Zhang, H. M., Hanson, P., Ye, X., Zhao, G., Xie, R., Tong, L., & Yang, D. (2017) · Cellular Microbiology · doi:10.1111/cmi.12725 · Cited by 15

Ras Suppresses TXNIP Expression by Restricting Ribosome Translocation

Ye, Z., & Ayer, D. E. (2018) · Molecular and Cellular Biology · doi:10.1128/mcb.00178-18 · Cited by 15

The Plateau in Muscle Growth with Resistance Training: An Exploration of Possible Mechanisms

Kataoka, R., Hammert, W. B., Yamada, Y., Song, J. S., Seffrin, A., Kang, A., Spitz, R. W., Wong, V. H. Y., & Loenneke, J. P. (2023) · Sports Medicine · doi:10.1007/s40279-023-01932-y · Cited by 17

2D-DIGE screening of high-productive CHO cells under glucose limitation—Basic changes in the proteome equipment and hints for epigenetic effects

Wingens, M., Gätgens, J., Schmidt, A., Albaum, S. P., Büntemeyer, H., Noll, T., & Hoffrogge, R. (2015) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2015.01.005 · Cited by 15

Intracellular NF-HEV/IL-33 harbors essential roles in Ras-induced cellular transformation by contributing to cyclin D1 protein synthesis

Ohta, S., Tago, K., Funakoshi‐Tago, M., Matsugi, J., & Yanagisawa, K. (2016) · Cellular Signalling · doi:10.1016/j.cellsig.2016.04.013 · Cited by 14

Heat stress-induced changes in skeletal muscle: Heat shock proteins and cell signaling transduction

Naıto, H., Yoshihara, T., Kakigi, R., Ichinoseki‐Sekine, N., & Tsuzuki, T. (2012) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.1.125 · Cited by 14

Hepatic translation control in the late-gestation fetal rat

Gruppuso, P. A., Tsai, S., Boylan, J. M., & Sanders, J. A. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00091.2008 · Cited by 14

Analysis of RPS15aE, an Isoform of a Plant-Specific Evolutionarily Distinct Ribosomal Protein in Arabidopsis thaliana, Reveals its Potential Role as a Growth Regulator

Szick-Miranda, K., Zanial, A. S., Zanial, A. S., Abidayo, S., & Slater, K. L. C. (2009) · Plant Molecular Biology Reporter · doi:10.1007/s11105-009-0148-6 · Cited by 14

Physiological and Molecular Adaptations to Strength Training

Ahtiainen, J. P. (2018) · Springer eBooks · doi:10.1007/978-3-319-75547-2_5 · Cited by 16

Genes related to heat tolerance in cattle—a review

Zeng, L., Qu, K., Zhang, J., Huang, B., & Lei, C. (2023) · Animal Biotechnology · doi:10.1080/10495398.2022.2047995 · Cited by 13

The Mechanisms of Muscle Mass and Strength Increase during Strength Training

Lysenko, E. A., Виноградова, О. Л., & Popov, D. V. (2021) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093021040104 · Cited by 17

Review: Influence of postabsorptive metabolism on essential amino acid partitioning in lactating dairy cows

Cant, J. P., Reyes, G. C., & Seymour, D. J. (2022) · animal · doi:10.1016/j.animal.2022.100573 · Cited by 13

The eEF2 kinase coordinates the DNA damage response to cisplatin by supporting p53 activation

Lim, J. K. M., Samiei, A., Delaidelli, A., de Santis, J. O., Brinkmann, V., Carnie, C. J., Radiloff, D. R., Hruby, L., Kahler, A., Cran, J., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06891-4 · Cited by 13

The prohibitin-binding compound fluorizoline affects multiple components of the translational machinery and inhibits protein synthesis

Jin, X., Xie, J., Zabolocki, M., Wang, X., Jiang, T., Wang, D., Désaubry, L., Bardy, C., & Proud, C. G. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.012979 · Cited by 13

Akt (protein kinase B) isoform phosphorylation and signaling downstream of mTOR (mammalian target of rapamycin) in denervated atrophic and hypertrophic mouse skeletal muscle

Norrby, M., Evertsson, K., Fjällström, A.-K., Svensson, A. C., & Tågerud, S. (2012) · Journal of Molecular Signaling · doi:10.1186/1750-2187-7-7 · Cited by 13

The Mechanisms of Insulin Action

White, M. F., & Copps, K. D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-18907-1.00033-0 · Cited by 12

Signaling responses to high and moderate load strength exercise in trained muscle

Lysenko, E. A., Popov, D. V., Vepkhvadze, T. F., Sharova, A. P., & Vinogradova, O. L. (2019) · Physiological Reports · doi:10.14814/phy2.14100 · Cited by 12

An Alternative Mechanism of Eukaryotic Translation Initiation

Morley, S., & Coldwell, M. J. (2008) · Science Signaling · doi:10.1126/scisignal.125pe32 · Cited by 13

Disease-modifying pharmacological treatments of type 1 diabetes: Molecular mechanisms, target checkpoints, and possible combinatorial treatments

Kosheleva, L., Koshelev, D., Lagunas‐Rangel, F. A., Levit, S., Rabinovitch, A., & Schiöth, H. B. (2025) · Pharmacological Reviews · doi:10.1016/j.pharmr.2025.100044 · Cited by 12

Differential mRNA Translation in Medicago truncatula Accessions with Contrasting Responses to Ozone-Induced Oxidative Stress

Puckette, M. C., Iyer, N. J., Tang, Y., Dai, X., Zhao, P. X., & Mahalingam, R. (2011) · Molecular Plant · doi:10.1093/mp/ssr069 · Cited by 12

Activation of a GPCR leads to eIF4G phosphorylation at the 5′ cap and to IRES-dependent translation

Leon, K. E., Boulo, T., Musnier, A., Morales, J., Gauthier, C., Dupuy, L., Heyne, S., Backofen, R., Poupon, A., Cormier, P., et al. (2014) · Journal of Molecular Endocrinology · doi:10.1530/jme-14-0009 · Cited by 12

Effects of time of day on resistance exercise-induced anabolic signaling in skeletal muscle

Sedliak, M., Zeman, M., Buzgó, G., Cvečka, J., Hamar, D., Laczo, E., Zelko, A., Okuliarová, M., Raastad, T., Nilsen, T. S., et al. (2012) · Biological Rhythm Research · doi:10.1080/09291016.2012.740314 · Cited by 14

Role of Amino Acids and Peptides in the Molecular Signaling in Skeletal Muscle after Resistance Exercise

Koopman, R. (2007) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.17.s1.s47 · Cited by 12

G Protein-Coupled Receptors As Regulators of Localized Translation: The Forgotten Pathway?

Trefier, A., Pellissier, L. P., Musnier, A., Reiter, É., Guillou, F., & Crépieux, P. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00017 · Cited by 10

Short communication: Supplementing lysine and methionine in a lactation diet containing a high concentration of wet corn gluten feed did not alter milk protein yield

Mullins, C. R., Weber, D., Block, E., Smith, J. F., Brouk, M. J., & Bradford, B. J. (2013) · Journal of Dairy Science · doi:10.3168/jds.2013-6755 · Cited by 11

Protein Translation and Signaling in Human Eosinophils

Esnault, S. J., Shen, Z.-J., & Malter, J. S. (2017) · Frontiers in Medicine · doi:10.3389/fmed.2017.00150 · Cited by 12

Effect of Paraquat-Induced Oxidative Stress on Insulin Regulation of Insulin-Like Growth Factor-Binding Protein-1 Gene Expression

Kimura, K., Katsumata, Y., Ozawa, T., Tawara, S., Igarashi, K., Cho, Y., Shibata, N., Hakuno, F., Takahashi, S., & Takenaka, A. (2010) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.09-97 · Cited by 11

PEITC-mediated inhibition of mRNA translation is associated with both inhibition of mTORC1 and increased eIF2α phosphorylation in established cell lines and primary human leukemia cells

Yeomans, A., Lemm, E. A., Wilmore, S., Cavell, B. E., Valle‐Argos, B., Krysov, S. V., Sánchéz‐Hidalgo, M., Leonard, E., Willis, A. E., Forconi, F., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.11655 · Cited by 11

Nitric oxide mediates NMDA-induced persistent inhibition of protein synthesis through dephosphorylation of eukaryotic initiation factor 4E-binding protein 1 and eukaryotic initiation factor 4G proteolysis

Petegnief, V., Font-Nieves, M., Martín, M. E., Salinas, M., & Planas, A. M. (2008) · Biochemical Journal · doi:10.1042/bj20071060 · Cited by 11

The eIF3a translational control axis in the Wnt/β-catenin signaling pathway and colon tumorigenesis

Dong, Z., Ojha, A., Barlow, L., Luo, L., Liu, J., & Zhang, J. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.217303 · Cited by 10

Manipulation of mRNA translation elongation influences the fragmentation of a biotherapeutic Fc‐fusion protein produced in CHO cells

Knight, T. J., Povey, J. F., Vito, D., Mohindra, A., Jaques, C. M., & Smales, C. M. (2022) · Biotechnology and Bioengineering · doi:10.1002/bit.28230 · Cited by 11

Dissociation of eIF4E-Binding Protein 2 (4E-BP2) from eIF4E Independent of Thr37/Thr46 Phosphorylation in the Ischemic Stress Response

Ayuso, M. I., Martínez‐Alonso, E., Salvador, N., Bonová, P., Regidor, I., & Alcázar, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0121958 · Cited by 10

Mechanisms of kidney repair by human mesenchymal stromal cells after ischemia: A comprehensive view using label‐free MS E

da Costa, M. R., Pizzatti, L., Lindoso, R. S., Sant’Anna, J. F., Rocher, B. D., Abdelhay, E. S. F. W., & Vieyra, A. R. (2014) · PROTEOMICS · doi:10.1002/pmic.201300084 · Cited by 10

The mGluR Theory of Fragile X: From Mice to Men

Stoppel, L. J., Osterweil, E. K., & Bear, M. F. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804461-2.00009-3 · Cited by 9

Identification of a new isoform of eEF2 whose phosphorylation is required for completion of cell division in sea urchin embryos

Bellé, R., Pluchon, P.-F., Cormier, P., & Mulner‐Lorillon, O. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.12.015 · Cited by 10

Down-regulation of Sprouty2 via p38 MAPK plays a key role in the induction of cellular apoptosis by tumor necrosis factor-α

Ding, W., & Warburton, D. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.08.037 · Cited by 10

Cholesteryl Glucoside Stimulates Activation of Protein Kinase B/Akt in the Motor Neuron-Derived NSC34 Cell Line.

Ly, P. T. T., Pelech, S., & Shaw, C. A. (2008) · PubMed · Cited by 9

Supplementing conjugated and non-conjugated L-methionine and acetate alters expression patterns ofCSN2, proteins and metabolites related to protein synthesis in bovine mammary cells

Jeon, S. W., Conejos, J. R. V., Kim, J., Kim, M., Lee, J., Lee, B.-S., Park, J.-S., Moon, J.-O., Lee, J., & Lee, H. (2020) · Journal of Dairy Research · doi:10.1017/s0022029919000979 · Cited by 9

Ciliary neurotrophic factor signaling in the rat orbitofrontal cortex ameliorates stress-induced deficits in reversal learning

Girotti, M., Silva, J. D., George, C. M., & Morilak, D. A. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107791 · Cited by 8

Rapid elevation of sodium transport through insulin is mediated by AKT in alveolar cells

Mattes, C., Laube, M., & Thome, U. H. (2014) · Physiological Reports · doi:10.1002/phy2.269 · Cited by 9

Genes and proteins: Dogmas in decline

Newman, S. A., & Bhat, R. (2007) · Journal of Biosciences · doi:10.1007/s12038-007-0104-2 · Cited by 9

Surviving Metabolic Stress: Of Mice (Squirrels) and Men

Hait, W. N., Versele, M., & Yang, J. (2014) · Cancer Discovery · doi:10.1158/2159-8290.cd-14-0114 · Cited by 8

Activation of SsoPK4, an Archaeal eIF2α Kinase Homolog, by Oxidized CoA

Ray, W., Potters, M., Haile, J. D., & Kennelly, P. J. (2015) · Proteomes · doi:10.3390/proteomes3020089 · Cited by 8

The muscle‐hypertrophic effect of clenbuterol is additive to the hypertrophic effect of myostatin suppression

Kim, K. H., Kim, Y. S., & Yang, J. (2011) · Muscle & Nerve · doi:10.1002/mus.21950 · Cited by 9

Post-Transcriptional Regulation of Alpha One Antitrypsin by a Proteasome Inhibitor

Rao, L., Xu, Y., Reineke, L. C., Bhattacharya, A., Tyryshkin, A., Shin, J.-N., & Eissa, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124318 · Cited by 8

Lysine Depletion during Different Feeding Phases: Effects on Growth Performances and Meat Quality of Broiler Chickens

Soglia, F., Zampiga, M., Baldi, G., Malila, Y., Thanatsang, K. V., Srimarut, Y., Tatiyaborworntham, N., Unger, O., Klamchuen, A., Laghi, L., et al. (2021) · Animals · doi:10.3390/ani11061499 · Cited by 8

Translational Control by Amino Acids and Energy

Thedieck, K., & Hall, M. N. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374145-5.00274-6 · Cited by 8

Células gliales y actividad sináptica: control traduccional del acople metabólico

Bayghen, E. L., & Ortega, A. (2010) · Revista de Neurología · doi:10.33588/rn.5010.2010190 · Cited by 8

Environmental enrichment improves social isolation-induced memory impairment: The possible role of ITSN1-Reelin-AMPA receptor signaling pathway

Sowndharya, S., & Rajan, K. E. (2024) · PLoS ONE · doi:10.1371/journal.pone.0294354 · Cited by 7

Understanding the regulation of protein synthesis under stress conditions

Irshad, I. U., & Sharma, A. K. (2024) · Biophysical Journal · doi:10.1016/j.bpj.2024.09.014 · Cited by 10

Translational Up-Regulation and High-Level Protein Expression from Plasmid Vectors by mTOR Activation via Different Pathways in PC3 and 293T Cells

Karyala, P., Namsa, N. D., & Chilakalapudi, D. R. (2010) · PLoS ONE · doi:10.1371/journal.pone.0014408 · Cited by 7

Targeting mTORC1 Activity to Improve Efficacy of Radioligand Therapy in Cancer

Grzmil, M., Wiesmann, F., Schibli, R., & Béhé, M. P. (2022) · Cancers · doi:10.3390/cancers15010017 · Cited by 9

Complexity in Organismal Evolution

Newman, S. A. (2011) · Elsevier eBooks · doi:10.1016/b978-0-444-52076-0.50012-2 · Cited by 7

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Toward Multiscale Modeling of Molecular and Biochemical Events Occurring at Fertilization Time in Sea Urchins

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Lovastatin effect in rat neuroblasts of the CNS: inhibition of cap‐dependent translation

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Themed section: molecular pharmacology of GPCRs

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Acute Exposure to SiO2 Nanoparticles Affects Protein Synthesis in Bergmann Glia Cells

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Cloning and functional analysis of goat glucose transporter 4

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Phosphorylation of elongation factor and its kinase expression in Rat m. soleus under early stage of hindlimb unloading

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Molecular mechanisms of mTOR-mediated translational control

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Control of the translational machinery in mammalian cells

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Signaling Pathways Involved in the Regulation of mRNA Translation

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