Most cited biochemistry, genetics and molecular biology papers
- Verified
Exercise Metabolism and Adaptation in Skeletal Muscle
Smith, J. A. B., Murach, K. A., Dyar, K. A., & Zierath, J. R. (2023) · Nature Reviews Molecular Cell Biology
Muscle Physiology and DisordersCardiovascular and exercise physiology
Cited by 342
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Messenger RNA Turnover in Eukaryotes: Pathways and Enzymes
Meyer, S., Temme, C., & Wahle, E. (2004) · Critical Reviews in Biochemistry and Molecular Biology
RNA Research and SplicingRNA regulation and disease
Cited by 342
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Lipid rafts, cholesterol, and the brain
Korade, Z., & Kenworthy, A. K. (2008) · Neuropharmacology
Lipid Membrane Structure and BehaviorCaveolin-1 and cellular processes
Cited by 342
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Fast and accurate long-range phasing in a UK Biobank cohort
Loh, P.-R., Palamara, P. F., & Price, A. L. (2016) · Nature Genetics
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 342
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Dietary Restriction Benefits Learning and Motor Performance of Aged Mice
Ingram, D. K., Weindruch, R., Spangler, E. L., Freeman, J. R., & Walford, R. L. (1987) · Journal of Gerontology
Genetics, Aging, and Longevity in Model OrganismsDietary Effects on Health
Cited by 342
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Inflammaging as a Major Characteristic of Old People: Can It Be Prevented or Cured?
Franceschi, C. (2008) · Nutrition Reviews
Genetics, Aging, and Longevity in Model OrganismsImmune Response and Inflammation
Cited by 342
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Roles of NapF, NapG and NapH, subunits of the Escherichia coli periplasmic nitrate reductase, in ubiquinol oxidation: Roles of NapF, G and H in ubiquinol oxidation in E. coli
Brondijk, T. H. C., Fiegen, D., Richardson, D. J., & Cole, J. A. (2002) · Molecular Microbiology
Bacterial Genetics and BiotechnologyMetalloenzymes and iron-sulfur proteins
Cited by 342
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Linking β-Catenin to Androgen-signaling Pathway
Yang, F., Li, X., Sharma, M., Sasaki, C. Y., Longo, D. L., Lim, B., & Sun, Z. (2002) · Journal of Biological Chemistry
Prostate Cancer Treatment and ResearchWnt/β-catenin signaling in development and cancer
Cited by 342
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Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice
Tyynismaa, H., Mjosund, K. P., Wanrooij, S., Lappalainen, I., Ylikallio, E., Jalanko, A., Spelbrink, J. N., Paetau, A., & Suomalainen, A. (2005) · Proceedings of the National Academy of Sciences
Mitochondrial Function and PathologyMetabolism and Genetic Disorders
Cited by 342
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Solution structure of the N-terminal zinc binding domain of HIV-1 integrase
Cai, M., Zheng, R., Caffrey, M., Craigie, R., Clore, G. M., & Gronenborn, A. M. (1997) · Nature Structural Biology
Protein Structure and DynamicsHIV/AIDS drug development and treatment
Cited by 342
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A mitochondrial bioenergetic etiology of disease
Wallace, D. C. (2013) · Journal of Clinical Investigation
Mitochondrial Function and PathologyMetabolism and Genetic Disorders
Cited by 342
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The role of Nrf2 signaling in counteracting neurodegenerative diseases
Dinkova‐Kostova, A. T., Kostov, R. V., & Kazantsev, A. G. (2018) · The FEBS Journal
Genomics, phytochemicals, and oxidative stressNuclear Receptors and Signaling
Cited by 342
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Prime, Repair, Restore: The Active Role of Chromatin in the DNA Damage Response
Soria, G., Polo, S. E., & Almouzni, G. (2012) · Molecular Cell
DNA Repair MechanismsGenomics and Chromatin Dynamics
Cited by 342
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Peripheral-type benzodiazepine receptor: structure and function of a cholesterol-binding protein in steroid and bile acid biosynthesis
Lacapère, J.-J., & Papadopoulos, V. (2003) · Steroids
Cholesterol and Lipid MetabolismLipid Membrane Structure and Behavior
Cited by 342
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Regulation of Metabolism by Hypoxia-Inducible Factor 1
Semenza, G. L. (2011) · Cold Spring Harbor Symposia on Quantitative Biology
Cancer, Hypoxia, and MetabolismMetabolism, Diabetes, and Cancer
Cited by 342
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Dial 9–1–1 for DNA damage: the Rad9–Hus1–Rad1 (9–1–1) clamp complex
Parrilla-Castellar, E. R., Arlander, S. J. H., & Karnitz, L. (2004) · DNA Repair
DNA Repair MechanismsCancer-related Molecular Pathways
Cited by 342
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TGF-beta in CAF-mediated tumor growth and metastasis
Calon, A., Tauriello, D. V. F., & Batlle, E. (2014) · Seminars in Cancer Biology
TGF-β signaling in diseasesCancer Cells and Metastasis
Cited by 342
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Prolonged increase in insulin-stimulated glucose transport in muscle after exercise
Cartee, G. D., Young, D. A., Sleeper, M. D., Zierath, J., Wallberg-Henriksson, H., & Holloszy, J. O. (1989) · American Journal of Physiology-Endocrinology and Metabolism
Metabolism, Diabetes, and CancerMuscle metabolism and nutrition
Cited by 342
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Impaired TFEB-Mediated Lysosome Biogenesis and Autophagy Promote Chronic Ethanol-Induced Liver Injury and Steatosis in Mice
Chao, X., Wang, S., Zhao, K., Li, Y., Williams, J. A., Li, T., Chavan, H., Krishnamurthy, P., He, X. C., Li, L., et al. (2018) · Gastroenterology
Autophagy in Disease and TherapyAlcohol Consumption and Health Effects
Cited by 342
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Nitrite reductase activity is a novel function of mammalian mitochondria
Kozlov, A. V., Staniek, K., & Nohl, H. (1999) · FEBS Letters
Mitochondrial Function and PathologyNitric Oxide and Endothelin Effects
Cited by 342
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Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II)
Fujita, E., Kouroku, Y., Isoai, A., Kumagai, H., Misutani, A., Matsuda, C., Hayashi, Y. K., & Momoi, T. (2007) · Human Molecular Genetics
Endoplasmic Reticulum Stress and DiseaseMuscle Physiology and Disorders
Cited by 342
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Decline with age of the respiratory chain activity in human skeletal muscle
Boffoli, D., Scacco, S. C., Vergari, R., Solarino, G., Santacroce, G., & Papa, S. (1994) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Mitochondrial Function and PathologyMuscle Physiology and Disorders
Cited by 341
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A role for the Perlman syndrome exonuclease Dis3l2 in the Lin28–let-7 pathway
Chang, H.-M., Triboulet, R., Thornton, J. E., & Gregory, R. I. (2013) · Nature
MicroRNA in disease regulationRNA regulation and disease
Cited by 341
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The chemokine growth-regulated oncogene 1 (Gro-1) links RAS signaling to the senescence of stromal fibroblasts and ovarian tumorigenesis
Yang, G., Rosen, D. G., Zhang, Z., Bast, R. C., Mills, G. B., Colacino, J. A., Mercado-Uribe, I., & Liu, J. (2006) · Proceedings of the National Academy of Sciences
Telomeres, Telomerase, and SenescenceOvarian cancer diagnosis and treatment
Cited by 341
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