Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Nucleic acid actions on abnormal protein aggregation, phase transitions and phase separation
Jerson L. Silva, Tuane C. R. G. Vieira, Yraima Cordeiro, et al.
Current Opinion in Structural Biology (2022) Vol. 73, pp. 102346-102346
Closed Access | Times Cited: 22

Showing 22 citing articles:

Targeting Biomolecular Condensation and Protein Aggregation against Cancer
Jerson L. Silva, Débora Foguel, Vı́tor F. Ferreira, et al.
Chemical Reviews (2023) Vol. 123, Iss. 14, pp. 9094-9138
Closed Access | Times Cited: 35
p53 Isoforms as Cancer Biomarkers and Therapeutic Targets
Liuqun Zhao, Suparna Sanyal
Cancers (2022) Vol. 14, Iss. 13, pp. 3145-3145
Open Access | Times Cited: 29
The regulation of liquid‐liquid phase separated condensates containing nucleic acids
Zhuojun Dai, Xiaorong Yang
FEBS Journal (2023) Vol. 291, Iss. 11, pp. 2320-2331
Open Access | Times Cited: 17
Oncogenic p53 triggers amyloid aggregation of p63 and p73 liquid droplets
Elaine C. Petronilho, Guilherme C. de Andrade, Gileno dos S. de Sousa, et al.
Communications Chemistry (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 5
A sePARate phase? Poly(ADP-ribose) versus RNA in the organization of biomolecular condensates
Elizaveta E. Alemasova, Olga I. Lavrik
Nucleic Acids Research (2022) Vol. 50, Iss. 19, pp. 10817-10838
Open Access | Times Cited: 14
Excess PrPC inhibits muscle cell differentiation via miRNA-enhanced liquid–liquid phase separation implicated in myopathy
Jing Tao, Yanping Zeng, Bin Dai, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 8
Protein of a thousand faces: The tumor-suppressive and oncogenic responses of p53
Mayra A. Marques, Guilherme C. de Andrade, Jerson L. Silva, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 12
Multiscale simulations reveal the driving forces of p53C phase separation accelerated by oncogenic mutations
Yawei Yu, Qian Liu, Jiyuan Zeng, et al.
Chemical Science (2024) Vol. 15, Iss. 32, pp. 12806-12818
Open Access | Times Cited: 2
The chameleonic behavior of p53 in health and disease: the transition from a client to an aberrant condensate scaffold in cancer
Mayra A. Marques, Guilherme A. P. de Oliveira, Jerson L. Silva
Essays in Biochemistry (2022) Vol. 66, Iss. 7, pp. 1023-1033
Closed Access | Times Cited: 10
Poly(ADP-ribose) in Condensates: The PARtnership of Phase Separation and Site-Specific Interactions
Elizaveta E. Alemasova, Olga I. Lavrik
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 14075-14075
Open Access | Times Cited: 8
Phase-separated ParB enforces diverse DNA compaction modes and stabilizes the parS-centered partition complex
Yilin Zhao, Lijuan Guo, Jiaojiao Hu, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 14, pp. 8385-8398
Open Access | Times Cited: 1
PrP meets alpha‐synuclein: Molecular mechanisms and implications for disease
Tuane C. R. G. Vieira, Caroline A. Barros, Renato Domingues, et al.
Journal of Neurochemistry (2023) Vol. 168, Iss. 8, pp. 1625-1639
Open Access | Times Cited: 3
(Dys)functional insights into nucleic acids and RNA-binding proteins modulation of the prion protein and α-synuclein phase separation
Yraima Cordeiro, Maria Heloisa O. Freire, Adalgisa Felippe Wiecikowski, et al.
Biophysical Reviews (2023) Vol. 15, Iss. 4, pp. 577-589
Closed Access | Times Cited: 2
Mutant p53 Induces Amyloid Aggregation in p63 and p73 Liquid Droplets: Mechanistic Insights into Oncogenic Phase Transitions
Jerson L. Silva, Elaine C. Petronilho, Guilherme de Andrade, et al.
Research Square (Research Square) (2024)
Open Access
Oncogenic Phase Transitions: How Mutant p53 Drives Amyloid Formation in p63 and p73 Liquid Droplets
Elaine C. Petronilho, Guilherme C. de Andrade, Gileno dos S. de Sousa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Unfolding Mechanism and Fibril Formation Propensity of Human Prion Protein in the Presence of Molecular Crowding Agents
Manoj Madheswaran, Nataliia Ventserova, Gianluca D’Abrosca, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 18, pp. 9916-9916
Open Access
Protein condensates unfold G‐quadruplex resembling a helicase activity.
Liang Luo, Shixia Ji, Qiong Wu, et al.
ChemBioChem (2024)
Closed Access
Liquid-liquid phase separation in viral infection: from the occurrence and function to treatment potentials
Zheng Cao, Yanhua Yang, Simeng Zhang, et al.
Colloids and Surfaces B Biointerfaces (2024) Vol. 246, pp. 114385-114385
Closed Access
Amyloids. Evolutionary Past and Biotechnological Future
O. V. Nevzglyadova, Е. В. Михайлова, Soĭdla Tr
Cell and Tissue Biology (2024) Vol. 18, Iss. 6, pp. 587-601
Closed Access
Molecular Mechanisms Underlying Alzheimer’s and Parkinson’s Disease and the Possibility of Their Neutralization
O. V. Nevzglyadova, Е. В. Михайлова, Soĭdla Tr
Cell and Tissue Biology (2023) Vol. 17, Iss. 6, pp. 593-607
Closed Access | Times Cited: 1
Molecular Mechanisms Underlying Alzheimer’s and Parkinson’s Diseases and the Potential Possibility of their Neutralization
O. V. Nevzglyadova, Е. В. Михайлова, Soĭdla Tr
Tsitologiya (2023) Vol. 65, Iss. 4, pp. 323-338
Closed Access | Times Cited: 1
Excess PrPCinhibits muscle cell differentiation via miRNA-enhanced liquid–liquid phase separation implicated in myopathy
Jing Tao, Yanping Zeng, Bin Dai, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
Page 1

Scroll to top