The role of the Atg1/ULK1 complex in autophagy regulation

TOR signaling in growth and metabolism

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p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

Bjørkøy, G., Lamark, T., Brech, A., Outzen, H., Perander, M., Øvervatn, A., Stenmark, H., & Johansen, T. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200507002 · Cited by 3,276

Defining the role of mTOR in cancer

Guertin, D. A., & Sabatini, D. M. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.05.008 · Cited by 2,833

Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

Ravikumar, B., Vacher, C., Berger, Z., Davies, J. E., Luo, S., Oroz, L. G., Scaravilli, F., Easton, D. F., Duden, R., O'Kane, C. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1362 · Cited by 2,347

Autophagosome formation: core machinery and adaptations

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Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice.

Komatsu, M., Waguri, S., Koike, M., Sou, Y.-S., Ueno, T., Hara, T., Mizushima, N., Iwata, J.-I., Ezaki, J., Murata, S., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.035 · Cited by 2,124

Nutrient-dependent mTORC1 Association with the ULK1–Atg13–FIP200 Complex Required for Autophagy

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ULK-Atg13-FIP200 Complexes Mediate mTOR Signaling to the Autophagy Machinery

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Autophagy: molecular machinery for self-eating

Yorimitsu, T., & Klionsky, D. J. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401765 · Cited by 1,566

ULK1·ATG13·FIP200 Complex Mediates mTOR Signaling and Is Essential for Autophagy

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Transcriptomic analysis reveals novel hub genes associated with astrocyte autophagy in intracerebral hemorrhage

Zheng, Y., Duan, C., Yu, H., Jiang, G., Shen, H., Li, H., Wang, Z., Zhou, X., Li, X., & He, M. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1433094 · Cited by 2

Inhibition of Unc-51-like-kinase is mitoprotective during Pseudomonas aeruginosa infection in corneal epithelial cells

Ramachandran, R. A., Titone, R., Abdallah, J. T., Rehman, M., Cao, M., Baniasadi, H. R., & Robertson, D. M. (2025) · mSphere · doi:10.1128/msphere.00537-24 · Cited by 2

Structural Insights into Autophagy in the AlphaFold Era

Maruyama, T., & Noda, N. N. (2025) · Journal of Molecular Biology · doi:10.1016/j.jmb.2025.169235 · Cited by 2

[Progress on association between autophagy and cancer].

Cao, J., & Xia, D. (2015) · PubMed Central · doi:10.3785/j.issn.1008-9292.2015.03.014 · Cited by 2

Vesicular trafficking in cellular responses to stress

Kepp, O., & Galluzzi, L. (2021) · Methods in cell biology · doi:10.1016/s0091-679x(21)00069-8 · Cited by 2

Autophagy and Toxins: A Matter of Life or Death

Mestre, M. B., & Colombo, M. I. (2013) · Current Molecular Medicine · doi:10.2174/156652413804810790 · Cited by 18

Lipid droplets-vacuoles interaction promotes lipophagy in the oleaginous diatom Fistulifera solaris

Tanaka, T., Moriya, S., Nonoyama, T., Maeda, Y., Kaha, M., Yoshino, T., Matsumoto, M., & Bowler, C. (2024) · Algal Research · doi:10.1016/j.algal.2024.103481 · Cited by 4

Autophagy: A Home Remodeler for Hepatitis C Virus

Hillaire, M. L. B., Décembre, É., & Dreux, M. (2014) · Wiley eBooks · doi:10.1002/9781118677551.ch7 · Cited by 2

Lc3i And Lc3ii As Autophagy Markers For The Development And Improvement Of Products And Techniques Used In Research

Williams, C. J. (2013) · Human Biology · Cited by 2

The G protein-Coupled Metabotropic Glutamate Receptor 1 controls neuronal macroautophagyPreprint

Donoso, M., Speranza, L., Kalinowska, M., Castillo, C., Sanctis, C. D., & Francesconi, A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.02.365783 · Cited by 2

Quantitation of autophagy in the pancreas at the tissue and cell levels

Iovanna, J. (2011) · doi:10.3998/panc.2010.13 · Cited by 2

Epigenetic Regulation of Mammalian Target of Rapamycin Debilitates Insulin Resistance Associated Alzheimer Disease Condition in RatsPreprint

Kakoty, V., Sarathlal, K. C., Dubey, S. K., Yang, C. H., & Taliyan, R. (2021) · Research Square · doi:10.21203/rs.3.rs-472911/v1 · Cited by 2

Correction: Inhibition of mTOR by Rapamycin Abolishes Cognitive Deficits and Reduces Amyloid-β Levels in a Mouse Model of Alzheimer's Disease

Spilman, P. R., Podlutskaya, N., Hart, M. J., Debnath, J., Gorostiza, O. F., Bredesen, D. E., Richardson, A., Strong, R., & Galván, V. (2011) · PLoS ONE · doi:10.1371/annotation/05c1b976-7eab-4154-808d-0526e604b8eb · Cited by 2

Correction: Inhibition of mTOR by Rapamycin Abolishes Cognitive Deficits and Reduces Amyloid-β Levels in a Mouse Model of Alzheimer's Disease

Spilman, P. R., Podlutskaya, N., Hart, M. J., Debnath, J., Gorostiza, O. F., Bredesen, D. E., Richardson, A. G., Strong, R., & Galván, V. (2011) · PLoS ONE · doi:10.1371/annotation/85294f34-4d64-4189-b4c8-b1d77c0b3908 · Cited by 2

Systematic Analysis of Autophagy Identifies Atg9 Vesicles as the Origin of the PhagophorePreprint

Broadbent, D. G., Barnaba, C., & Schmidt, J. C. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.03.502680 · Cited by 2

The triad interaction of ULK1, ATG13, and FIP200 is required for ULK complex formation and autophagyPreprint

Hama, Y., Fujioka, Y., Yamamoto, H., Mizushima, N., & Noda, N. N. (2024) · eLife · doi:10.7554/elife.101531.1 · Cited by 2

A Structural Approach into Drug Discovery Based on Autophagy

Kang, S., & Kim, D. (2021) · Life · doi:10.3390/life11060526 · Cited by 1

Lysosome Functioning as a Process that Slows Down Aging

Alekhin, V. A., Nazarova, S. F., Gizatullina, D., Lopatina, E. T., Kirpichnikov, M. P., Оstrovsky, М. А., Gordeliy, V., & Ilyinsky, N. S. (2025) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747824700387 · Cited by 1

Influence of oxidative stress on the activity of mTOR kinase in CD4+T lymphocytes in autoimmune thyroiditis

Burtseva, A. V., Tikhonova, A. O., Afanasyeva, Z. A., & Abramova, Z. I. (2025) · Medical Immunology (Russia) · doi:10.15789/1563-0625-ioo-3141 · Cited by 1

Natural chromones targeting autophagy signalling pathways as potential anticancer interventions: a systematic review

Shamsudin, N. F., Nawi, A. R. M., Jantan, I., Salim, E., Abdullah, M. A., Chia, S. L., Saad, N., Imran, S., Leong, S. W., Nainu, F., et al. (2025) · Results in Chemistry · doi:10.1016/j.rechem.2025.102601 · Cited by 1

Retinitis Pigmentosa‐Associated Gene TRIM49 Regulates ULK1‐Mediated Autophagy and Photoreceptor Phagocytosis by the Retinal Pigment Epithelium

Yi, Z., Wen, C., Du, H., Wang, Y., Chen, S., Liu, J., Zhang, S., Wang, J., Xiao, X., Li, S., et al. (2025) · Advanced Science · doi:10.1002/advs.202512305 · Cited by 2

The Role of Autophagy during Nontuberculous Mycobacterial Infection

Kim, Y. J., Sapkota, A., Lee, B., Park, E., & Jo, E. (2025) · Journal of Bacteriology and Virology · doi:10.4167/jbv.2025.55.3.205 · Cited by 1

Autophagy in emerging and highly concerned severe zoonotic infectious diseases

Qi, Y., Wang, L., Wu, S., Meng, C., Chu, Y., Yin, Y., & Jiao, H. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1761571 · Cited by 1

Lactic Acid Bacteria with Probiotic Potential Regulating Macrophages: Mechanisms, Regulatory Features, and Clinical Applications

Mai, Z., Wang, B., Hu, Q., Jia, Z., Wang, J., Liu, B. Y., & Ge, J. (2026) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-026-10979-y · Cited by 1

Adaptive crosstalk between polyamine metabolism, translation, and autophagy sustains energy homeostasis in mammals during starvation: a scoping review

Karimi, K., Roberts, S. C., Carter, N. S., Hofer, S. J., & Karimi, R. (2026) · Amino Acids · doi:10.1007/s00726-026-03512-6 · Cited by 1

Autophagy-related protein 1 orchestrates autophagy initiation and feedback degradation in Alternaria alternata

Choo, C. Y. L., Lu, H.-Y., Chung, K.-R., & Wu, P. (2026) · BMC Microbiology · doi:10.1186/s12866-026-05075-8 · Cited by 1

Roles of autophagy in brain homeostasis and disease

Kim, H., Wickstead, E. S., Zhou, X., Choi, I., & Yue, Z. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02426-6 · Cited by 1

Autophagy in Glioma Cells

Ciechomska, I. A., Ellert‐Miklaszewska, A., & Kaminska, B. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1431-5_5 · Cited by 1

Dynamic regulation of neutrophil activation, migration and death

Itakura, A. (2013) · doi:10.6083/m43t9f7z · Cited by 1

Lymphangioleiomyomatosis (LAM)

Steagall, W. K., Glasgow, C. G., Pacheco–Rodriguez, G., & Moss, J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802733-2.00021-9 · Cited by 1

Regulation of Autophagy by the Heat Shock Factor 1-Mediated Stress Response Pathway

Watanabe, Y., & Tanaka, M. (2018) · Heat shock proteins · doi:10.1007/978-3-319-90725-3_9 · Cited by 1

Role of VPS34 Complexes in Starvation-Induced Autophagy

Sinha, S. C., Li, Y., Mukhopadhyay, S., Wyatt, S., & Dasanna, S. (2019) · Springer eBooks · doi:10.1007/978-3-319-55387-0_94 · Cited by 1

Exploring New Strategies to Monitor Autophagy and Related Cell Death Pathways Using Raman Spectroscopy

Isabelle, M. (2013) · Journal of Cancer Research and Therapeutic Oncology · doi:10.17303/jcrto.2013.103 · Cited by 1

Atg1/ULK1 complex in autophagy process and regulation

Bhol, C. S., & Bhutia, S. K. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-90142-0.00003-7 · Cited by 1

Role of P53 Mediated Molecular Regulation in Starvation-Induced Autophagy in HCT-116 and HT-29 Colorectal Carcinoma Cells

Wang, J., Liu, Y., Cai, J., Yang, X., Xiong, Z., Zou, D., Jiao, D., Xu, K., Wei, H., & Zhao, H. (2023) · Biology Bulletin · doi:10.1134/s1062359023602823 · Cited by 1

The Influence of Stress and Binge-Patterned Alcohol Drinking on Mouse Skeletal Muscle Protein Synthesis and Degradation Pathways

Reed, C. H., Tystahl, A. C., Eo, H., Buhr, T. J., Bauer, E. E., Lee, J. H., Clark, P., & Valentine, R. J. (2024) · Biomolecules · doi:10.3390/biom14050527 · Cited by 2

Autophagy and Reactive Oxygen Species in Cancer: An Introduction

Kumar, P., Ruchitha, C., Gowtham, A., & Kaundal, R. K. (2024) · Cancer drug discovery and develogment/Cancer drug discovery and development · doi:10.1007/978-3-031-66421-2_1 · Cited by 1

Prostate Cancer, Apoptosis, Autophagy and Ferroptosis: Cell Death Mechanisms and Their Cross-talk

Hashemi, M., Hosseini, A. S., Monjezi, S., Hasany, S., Binaei, S., Nejat, M., Melyani, H., Bashandeh, N., Matinahmadi, A., Zayani, Z., et al. (2024) · Springer eBooks · doi:10.1007/978-981-97-4612-5_4 · Cited by 1

The Role of Autophagy in Drug Resistance and Potential for Therapeutic Targeting

Rangwala, R. A., & Amaravadi, R. K. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5847-0_4 · Cited by 1

Circadian Clocks and mTOR Signaling

Gupta, R., & Kondratov, R. V. (2017) · Healthy ageing and longevity · doi:10.1007/978-3-319-64543-8_9 · Cited by 1

Control of basal autophagy rate by vacuolar peduncle

Bourouis, M., Mondin, M., Dussert, A., & Léopold, P. (2019) · PLoS ONE · doi:10.1371/journal.pone.0209759 · Cited by 1

Future Strategies in Management of Diabetes Mellitus: A Brief Report

Singh, A. P., & Kumar, A. (2019) · International Journal of Medical Reviews and Case Reports · doi:10.5455/ijmrcr.management-diabetes-mellitus · Cited by 1

Vesicle Trafficking, Autophagy and Nanoparticles: A Brief Review

Li, T., & Yang, M. (2019) · Current Nanomedicine · doi:10.2174/2468187309666190906114325 · Cited by 1

Autophagy: A new insight into pathogenesis and treatment possibilities in age-related macular degeneration

Kubicka‐Trząska, A., Karska‐Basta, I., & Żuber-Łaskawiec, K. (2020) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/01.3001.0014.2495 · Cited by 1

Regulation of Tumor Suppressor Par-4 by Ceramide

Galadari, S., Cheratta, A. R., & Thayyullathil, F. (2022) · Springer eBooks · doi:10.1007/978-3-030-73572-2_10 · Cited by 1

Autophagy in Mammalian Development and Differentiation

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Drosophila BEACH domain autophagic adaptor blue cheese shuttles between vesicle populations and is required for an early step in autophagyPreprint

Sim, J. P. L., Osborne, K. A., García, I. A., Matysik, A. S., & Kraut, R. S. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/084434 · Cited by 1

The ULK1-FBXW5-SEC23B nexus controls autophagyPreprint

Jeong, Y., Simoneschi, D., Keegan, S., Melville, D., Adler, N. S., Saraf, A. P., Florens, L. A., Washburn, M. P., Cavasotto, C. N., Fenyö, D., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/441923 · 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

Type One Protein Phosphatase Regulates Fixed-Carbon Starvation-Induced Autophagy by Dephosphorylating ATG13a to Facilitate ATG1a-ATG13a Formation in ArabidopsisPreprint

Wang, Q., & Hou, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.10.487768 · Cited by 1

The Nutrient Sensor mTORC1 Regulates Insulin Secretion by Modulating ß-cell Autophagy

Israeli, T., Riahi, Y., Garzon, P., Louzada, R. A. N., Werneck‐de‐Castro, J. P., Blandino-Rosano, M., Yeroslaviz-Stolper, R., Kadosh, L., Tornovsky-Babeay, S., Hacker, G., et al. (2021) · doi:10.2337/figshare.17099846 · Cited by 1

Cdc14 Spatiotemporally Regulates Rim4-mRNA Complex Assembly and Stability During MeiosisPreprint

Zhang, R., Feng, W., Qian, S., Li, S., & Wang, F. (2022) · SSRN Electronic Journal · doi:10.1101/2022.12.22.521673 · Cited by 1

The triad interaction of ULK1, ATG13, and FIP200 is required for ULK complex formation and autophagyPreprint

Hama, Y., Fujioka, Y., Yamamoto, H., Mizushima, N., & Noda, N. N. (2025) · eLife · doi:10.7554/elife.101531.2 · Cited by 1

Modulation of Autophagy as a Novel Cancer Therapeutic Strategy

Cui, J., & Shen, H. (2013) · Humana Press eBooks · doi:10.1007/978-1-62703-456-2_10

Regulation of autophagy and mTOR during Semliki Forest virus infection

Eng, K. E. (2012) · Figshare

Aspectos celulares e moleculares das glândulas salivares e do corpo gorduroso de Rhynchosciara americana durante o desenvolvimento.

Brandão, A. D. S. (2011) · doi:10.11606/t.87.2011.tde-04052011-153224

The relationship between HIF-1α and autophagy activity in the hypoxic environment of breast cancer

Mills, J. (2013) · SUNScholar (Stellenbosch University)

Autophagy in Critical Illness

Aneja, R. K., Au, A. K., Pang, D., & Clark, R. S. B. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801033-4.00011-4

Atg9 cycling: The molecular mechanisms of anterograde and retrograde Atg9 trafficking

van der Burgh, A. W. (2011) · Utrecht University Repository (Utrecht University)

Exploring New Strategies to Monitor Autophagy and Related Cell Death Pathways Using Raman Spectroscopy

Lum, J. J. (2013) · Journal of Cancer Research and Therapeutic Oncology · doi:10.17303/jcrto.2013.1.103 · Cited by 1

Signal Transduction Regulation of Autophagy

Wong, P., & Jiang, X. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6561-4_4

The in vitro effects of Herpes simplex virus and Rubella virus on autophagy

Pásztor, K. (2014) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.2342

Modulação da autofagia hipotalâmica em camundongos alimentados com dieta hiperlipídica

Araújo, M. P. D. O. (2013) · doi:10.47749/t/unicamp.2013.917754

The role of alpha-synuclein phosphorylation in synucleinopathies

Basso, E. (2014) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

The study of Drosophila melanogaster blue cheese (bchs) function in the involvement of autophagy in neurodegenerative disorders

Sim, J. P. L. (2014) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/64797

DISTINCT FUNCTIONS OF AUTOPHAGY KINASES ULK1 AND ULK2 IN ADIPOGENESIS AND ADIPOCYTE METABOLISM

Ro, S. (2011) · University of Minnesota Digital Conservancy (University of Minnesota)

mTOR Pathway in Renal Cell Carcinoma

Santoni, M., & Massari, F. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802733-2.00026-8 · Cited by 1

The Role of Autophagy in Immunity and Autoimmune Diseases / Uloga Autofagije U Imunskom Odgovoru I Autoimunskim Bolestima

Marković, B. S., Vucicevic, L. M., Bojić, S., & Volarević, V. (2014) · Serbian Journal of Experimental and Clinical Research · doi:10.2478/sjecr-2014-0028

Investigation into the effects and mechanisms of rapamycin treatment in two mouse models of Complex I-deficient neurological pathology

Yanos, M. E. (2014) · ResearchWorks at the University of Washington (University of Washington)

The Involvement of Reactive Oxygen Species in Autophagy Regulation by Amino Acids

Angcajas, A. B., & アンカハス, ア. バ. (2014) · Institutional Repositories DataBase (IRDB)

The influence of ageing and culture conditions on limbal epithelial cells

Hallam, D. (2015)

ULK1 and JNK are involved in mitophagy incurred by LRRK2 G2019S expression ESEARCH ARTICLE R

Zhu, Y., Wang, C., Yu, M. Y., Cui, J., Liu, L., & Xu, Z. (2013)

The role of autophagy in clearance of protein aggregates

Isakson, P. (2011) · NORA - Norwegian Open Research Archives

animalsin skeletal muscle of apoptosis-deficient Denervation-induced mitochondrial dysfunction and

Vainshtein, A., Carter, H. N., & Zhang, Y. (2016)

Pathogenic Role of Autophagy in Rheumatic Diseases

Choi, Y. J., & Yoo, W. (2016) · Journal of Rheumatic Diseases · doi:10.4078/jrd.2016.23.4.202

Bacterial infection, immune responses, and autophagy in lutzomyia longipalpis sand flies

Heerman, M. C. (2016) · K-State Research Exchange (Kansas State University)

Trauma, Regulated Cell Death, and Inflammation

Fan, J., & Fan, L. (2016) · Springer eBooks · doi:10.1007/978-981-10-2425-2_16

Analysis of the apoptotic threshold at the onset of embryonic differentiation

Nieto, S. (2015) · Spiral (Imperial College London) · doi:10.25560/43929

Second Messenger-mediated Regulation of Autophagy

Shahnazari, S. (2012) · TSpace (University of Toronto)

Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells

Chen, C. (2016) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)

Interactions of L. monocytogenes with Host Cellular Defenses

Lam, G. Y. (2012) · TSpace (University of Toronto)

MCL-1 - Guardian of the Ovarian Reserve: Characterization of the Contribution of MCL-1 to Oocyte Survival

Omari, S. (2014) · TSpace (University of Toronto)

Structure and Function of Atg101-Atg13 HORMA Heterodimer: Insight into Mammalian Autophagy Initiation

SUZUKI, H., & Noda, N. N. (2015) · Nihon Kessho Gakkaishi · doi:10.5940/jcrsj.57.324

Estudio de la ruta de la autofagia en carcinoma de endometrio esporádico

Prieto, M. F. (2016) · doi:10.14201/gredos.132924

Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand Induces Autophagic Protein Cleavage in Melanoma Cells

You, M., Nguyen, D. M., Feun, L. G., Kuo, M. T., Wangpaichitr, M., Wu, C., & Savaraj, N. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00025-1

Dissecting the Physiological Roles of ULK1/2 in the Mouse Brain

Wang, B. (2016) · doi:10.21007/etd.cghs.2016.0419

Targeting Unselective Autophagy of Cellular Aggregates

Seneci, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801944-3.00004-7

Unselective Disposal of Cellular Aggregates

Seneci, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800186-8.00004-3

Mechanisms Regulating Target Selection and Degradation by Selective Autophagy

Kamber, R. A. (2016) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)

GRh1-dependent unconventional protein secretion

Bruns, C. (2013) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Role of VPS34 Complexes in Starvation-Induced Autophagy

Sinha, S. C., Li, Y., Mukhopadhyay, S., Wyatt, S., & Dasanna, S. (2017) · Springer eBooks · doi:10.1007/978-3-319-40007-5_94-1

Synthesis of L68Q mutant cystatin C. Aggregation and autophagy in HEK293T cells

Hákonarson, E. E. (2015)

Inactivation of Magel2 in a mouse model of Prader-Willi Syndrome alters autophagy in the hypothalamus and impairs muscle function

Kamaludin, A. A. (2016) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3cr5np7z

Controle de qualidade de proteína na disfunção/atrofia muscular esquelética: papel do receptor β2-adrenérgico.

Campos, J. C. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2018.tde-22022018-141618

Could Antibiotics Be Therapeutic Agents in Alzheimer’s Disease?

Gómez, O., Pintado, C., Rodríguez-Pérez, M., & Burgos‐Ramos, E. (2019) · Frontiers in clinical drug research. Alzheimer disorders · doi:10.2174/9789811401893119080005

Endothelial PKA targets ATG16L1 to regulate angiogenesis by limiting autophagyPreprint

Zhao, X., Nedvetsky, P. I., Vion, A.-C., Popp, O., Zühlke, K., Dittmar, G. A. G., Klußmann, E., & Gerhardt, H. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/573683

A Minimum-Labeling Approach for Reconstructing Protein Networks across Multiple ConditionsPreprint

Mazza, A., Gat‐Viks, I., Farhan, H., & Sharan, R. (2013) · arXiv (Cornell University) · doi:10.48550/arxiv.1307.7803

HIV Tat and Morphine-induced Neurodegeneration in a Beclin 1 Hemizygous Mouse Model

Lapierre, J. (2018) · FIU - Digital Commons (Florida International University) · doi:10.25148/etd.fidc007019

Avaliação de um novo candidato a fármaco para o tratamento do carcinoma de pulmão de células não pequenas

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LEVELS OF FREE PLASMA AMINO ACIDS UNDER ACUTE NORMOBARIC HYPOXIA IN VOLUNTEERS IN FASTED AND POSTPRANDIAL STATES

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