Most cited biochemistry, genetics and molecular biology papers
- Verified
Evidence for adenylate cyclase as a scaffold protein for Ras2–Ira interaction in Saccharomyces cerevisie
Colombo, S., Paiardi, C., Pardons, K., Winderickx, J., & Martegani, E. (2014) · Cellular Signalling
Protein Kinase Regulation and GTPase SignalingFungal and yeast genetics research
Cited by 9
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Arylamine N-acetyltransferase 1 activity is regulated by the protein acetylation status
Salazar-González, R. A., Doll, M. A., & Hein, D. W. (2022) · Frontiers in Pharmacology
Histone Deacetylase Inhibitors ResearchPharmacogenetics and Drug Metabolism
Cited by 9
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Expression of S100A2 and S100P in human eccrine sweat glands and their application in differentiating secretory coil-like from duct-like structures in the 3D reconstituted eccrine sweat spheroids
Li, H., Zhang, M., Chen, L., Zhang, B., & Zhang, C. (2017) · Journal of Molecular Histology
S100 Proteins and AnnexinsCancer and Skin Lesions
Cited by 9
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Characterisation of high throughput screening outputs for small molecule degrader discovery
Bell, L. E., Bardelle, C., Packer, M. J., Kastl, J., Holdgate, G. A., & Davies, G. (2024) · SLAS Discovery
Protein Degradation and InhibitorsUbiquitin and proteasome pathways
Cited by 9
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PLD1 regulates Xenopus convergent extension movements by mediating Frizzled7 endocytosis for Wnt/PCP signal activation
Lee, H., Lee, S. J., Kim, G.-H., Yeo, I., & Han, J.-K. (2016) · Developmental Biology
Wnt/β-catenin signaling in development and cancerDevelopmental Biology and Gene Regulation
Cited by 9
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Exosomal miR-21-5p from glioma associated mesenchymal stem cells promotes the progression and glycolysis of glioblastoma via PDHA1
Zhang, Y., Lv, P., Zhang, Q., Xiang, W., Jiang, X., Guo, Z., & Zhang, T. (2025) · Scientific Reports
Extracellular vesicles in diseaseCancer, Hypoxia, and Metabolism
Cited by 9
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The hypoxia-sensor carbonic anhydrase IX affects macrophage metabolism, but is not a suitable biomarker for human cardiovascular disease
Demandt, J. A. F., Dubois, L. J., van Kuijk, K., Zaťovičová, M., Jin, H., Parkkila, S., van der Laan, S. W., Jelenska, L., Mees, B. M. E., Reutelingsperger, C. P. M., et al. (2021) · Scientific Reports
Enzyme function and inhibitionAtherosclerosis and Cardiovascular Diseases
Cited by 9
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Neuronal Morphogenesis: Golgi Outposts, Acentrosomal Microtubule Nucleation, and Dendritic Branching
Lewis, T. L., & Polleux, F. (2012) · Neuron
Microtubule and mitosis dynamicsNeurogenesis and neuroplasticity mechanisms
Cited by 9
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Implications of past and present genetic connectivity for management of the saltwater crocodile (Crocodylus porosus)
Lloyd‐Jones, L. R., Brien, M. L., Feutry, P., Lawrence, E., Beri, P., Booth, S., Coulson, S., Baylis, S. M., Villiers, K., Taplin, L. E., et al. (2023) · Evolutionary Applications
Genetic diversity and population structureWildlife Ecology and Conservation
Cited by 9
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The causal nature of the association between resting pulse in late adolescence and risk for internalizing and externalizing disorders: a co-relative analysis in a national male Swedish sample
Kendler, K. S., Lönn, S. L., Sundquist, J., & Sundquist, K. (2021) · Psychological Medicine
Genetic Associations and EpidemiologyChild and Adolescent Psychosocial and Emotional Development
Cited by 9
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Reproducible and flexible simulation experiments with ML-Rules and SESSL
Warnke, T., Helms, T., & Uhrmacher, A. M. (2018) · Bioinformatics
Gene Regulatory Network AnalysisScientific Computing and Data Management
Cited by 9
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Genomewide interaction and enrichment analysis on antidepressant response
Antypa, N., Drago, A., & Serretti, A. (2014) · Psychological Medicine
Genetic Associations and EpidemiologyTreatment of Major Depression
Cited by 9
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9-Nitrocamptothecin as second line chemotherapy for men with progressive, metastatic, hormone refractory prostate cancer: Results of the CALGB 99901
Amin, A., Halabi, S., Gelmann, E. P., Stadler, W., Vogelzang, N., & Small, E. (2004) · Urologic Oncology: Seminars and Original Investigations
Prostate Cancer Treatment and ResearchCancer therapeutics and mechanisms
Cited by 9
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Role of Sug1, a 19S proteasome ATPase, in the transcription of MHC I and the atypical MHC II molecules, HLA-DM and HLA-DO
Inostroza-Nieves, Y., Venkatraman, P., & Zavala-Ruiz, Z. (2012) · Immunology Letters
Genomics and Chromatin DynamicsUbiquitin and proteasome pathways
Cited by 9
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The first case of a patient with de novo partial distal 16q tetrasomy and a data's review
Kucharczyk, M., Kochański, A., Jezela‐Stanek, A., Kugaudo, M., Sielska‐Rotblum, D., Gutkowska, A., & Krajewska‐Walasek, M. (2014) · American Journal of Medical Genetics Part A
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 9
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1H-NMR Spectroscopy Shows Cellular Uptake of HEPES Buffer by Human Cell Lines-An Effect to Be Considered in Cell Culture Experiments
Depping, R., & Seeger, K. (2019) · Analytical and Bioanalytical Chemistry
Metabolomics and Mass Spectrometry StudiesAdvanced NMR Techniques and Applications
Cited by 9
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Multiplex gene editing by CRISPR-Cpf1 through autonomous processing of a single crRNA array
Zetsche, B., Heidenreich, M., Mohanraju, P., Fedorova, I., Kneppers, J., DeGennaro, E. M., Winblad, N., Choudhury, S. R., Abudayyeh, O. O., Gootenberg, J. S., et al. (2016) · bioRxiv (Cold Spring Harbor Laboratory)
CRISPR and Genetic EngineeringRNA regulation and disease
Cited by 9
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Longitudinal report of child with de novo 16p11.2 triplication
Wallace, A. S., Hudac, C. M., Steinman, K. J., Peterson, J. L., DesChamps, T. D., Duyzend, M. H., Nuttle, X., Eichler, E. E., & Bernier, R. A. (2018) · Clinical Case Reports
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 9
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Developing Colorimetric and Luminescence-Based High-Throughput Screening Platforms for Monitoring the GTPase Activity of Ferrous Iron Transport Protein B (FeoB)
Veloria, J., Shin, M., Devkota, A. K., Payne, S. M., Cho, E. J., & Dalby, K. N. (2019) · SLAS Discovery
Bacterial Genetics and Biotechnologybioluminescence and chemiluminescence research
Cited by 9
- Verified
Coordination of Two Genomes by Mitochondrial Translational Plasticity
Rampelt, H., & Pfanner, N. (2016) · Cell
Mitochondrial Function and PathologyRNA and protein synthesis mechanisms
Cited by 9
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Dual Role of Dysfunctional Asc-1 Transporter in Distinct Human Pathologies, Human Startle Disease, and Developmental Delay
Drehmann, P., Milanos, S., Schaefer, N., Kasaragod, V. B., Herterich, S., Holzbach-Eberle, U., Harvey, R. J., & Villmann, C. (2023) · eneuro
Amino Acid Enzymes and MetabolismNeuroscience and Neuropharmacology Research
Cited by 9
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Serum microRNA‐501‐3p is a potential diagnostic tool for detecting mild cognitive impairment: Ehime genome study
Toyama, K., Spin, J. M., Tsao, P. S., Maruyama, K., Osawa, H., Mogi, M., & Takata, Y. (2023) · Journal of Neurochemistry
MicroRNA in disease regulationDementia and Cognitive Impairment Research
Cited by 9
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A RUNX/AML‐binding motif residing in a novel 13‐bp DNA palindrome may determine the expression of the proximal promoter of the human uPA gene
KOPF, E., & MISKIN, R. (2005) · Journal of Thrombosis and Haemostasis
Genomics and Chromatin DynamicsProtease and Inhibitor Mechanisms
Cited by 9
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Machine learning and multi-omics data reveal driver gene-based molecular subtypes in hepatocellular carcinoma for precision treatment
Wang, M., Yan, X., Dong, Y., Li, X., & Gao, B. (2024) · PLOS Computational Biology
Cancer Genomics and DiagnosticsHepatocellular Carcinoma Treatment and Prognosis
Cited by 9
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