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OpenAlex Citation Counts

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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:

Cytosolic Ca2+ Modulates Golgi Structure Through PKCα-Mediated GRASP55 Phosphorylation
Stephen Ireland, Saiprasad Ramnarayanan, Mingzhou Fu, et al.
iScience (2020) Vol. 23, Iss. 3, pp. 100952-100952
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

Golgi Metal Ion Homeostasis in Human Health and Diseases
Jie Li, Yanzhuang Wang
Cells (2022) Vol. 11, Iss. 2, pp. 289-289
Open Access | Times Cited: 38
Nonredundant Roles of GRASP55 and GRASP65 in the Golgi Apparatus and Beyond
Xiaoyan Zhang, Yanzhuang Wang
Trends in Biochemical Sciences (2020) Vol. 45, Iss. 12, pp. 1065-1079
Open Access | Times Cited: 57
Adaptation of the Golgi Apparatus in Cancer Cell Invasion and Metastasis
Sarah Bui, Isabel Mejia, Begoña Díaz, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 53
SARS-CoV-2 remodels the Golgi apparatus to facilitate viral assembly and secretion
Jianchao Zhang, Andrew A. Kennedy, Daniel Macedo de Melo Jorge, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 25
Palmitoylation-Dependent Small-Molecule Fluorescent Probes for Live-Cell Golgi Imaging
Shunsuke Sawada, Masaru Yoshikawa, Keita Tsutsui, et al.
ACS Chemical Biology (2023) Vol. 18, Iss. 5, pp. 1047-1053
Closed Access | Times Cited: 11
Targeting CDK1 inhibits Golgi apparatus stress-mediated neuroinflammation and neuronal apoptosis after intracerebral hemorrhage by modulating GRASP55 phosphorylation
Xiaobo Zhang, Ming Yang, Feifei Jiang, et al.
Cellular Signalling (2025), pp. 111835-111835
Closed Access
Golgi’s Role in the Development of Possible New Therapies in Cancer
Dragos-Bogdan Vlad, David-Ioan Dumitrascu, A Dumitraşcu
Cells (2023) Vol. 12, Iss. 11, pp. 1499-1499
Open Access | Times Cited: 10
Ca2+ regulation of constitutive vesicle trafficking
John Sargeant, Jesse Hay
Faculty Reviews (2022) Vol. 11
Open Access | Times Cited: 15
Jaw1/LRMP is associated with the maintenance of Golgi ribbon structure
Wataru Okumura, Kazuko Tadahira, Takuma Kozono, et al.
The Journal of Biochemistry (2023) Vol. 173, Iss. 5, pp. 383-392
Closed Access | Times Cited: 9
Morphological alterations of the neuronal Golgi apparatus upon seizures
Anna Skupien, Andrzej A. Szczepankiewicz, Andrzej Rysz, et al.
Neuropathology and Applied Neurobiology (2023) Vol. 49, Iss. 5
Open Access | Times Cited: 7
Requirement of a functional ion channel for Sindbis virus glycoprotein transport, CPV-II formation, and efficient virus budding
Zeinab El Masri, Vashi Negi, Richard Kühn, et al.
PLoS Pathogens (2022) Vol. 18, Iss. 10, pp. e1010892-e1010892
Open Access | Times Cited: 11
Split but merge: Golgi fragmentation in physiological and pathological conditions
Pelin Zobaroğlu-Özer, Gamze Bora
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access | Times Cited: 2
Ceramide-1-phosphate is a regulator of Golgi structure and is co-opted by the obligate intracellular bacterial pathogen Anaplasma phagocytophilum
Curtis B. Read, Anika N. Ali, Daniel Stephenson, et al.
mBio (2024) Vol. 15, Iss. 4
Open Access | Times Cited: 2
Emerging Evidence of Golgi Stress Signaling for Neuropathies
Remina Shirai, Junji Yamauchi
Neurology International (2024) Vol. 16, Iss. 2, pp. 334-348
Open Access | Times Cited: 2
Cellular Organelle-Related Transcriptomic Profile Abnormalities in Neuronopathic Types of Mucopolysaccharidosis: A Comparison with Other Neurodegenerative Diseases
Karolina Wiśniewska, Lidia Gaffke, Magdalena Żabińska, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 3, pp. 2678-2700
Open Access | Times Cited: 2
ALG-2 and peflin regulate COPII targeting and secretion in response to calcium signaling
John Sargeant, Danette Kowal Seiler, Tucker Costain, et al.
Journal of Biological Chemistry (2021) Vol. 297, Iss. 6, pp. 101393-101393
Open Access | Times Cited: 15
The exquisite structural biophysics of the Golgi Reassembly and Stacking Proteins
Luís F.S. Mendes, Natália A. Fontana, S. Thirupathi Reddy, et al.
International Journal of Biological Macromolecules (2020) Vol. 164, pp. 3632-3644
Closed Access | Times Cited: 16
Metalloglycobiology: The power of metals in regulating glycosylation
Zoé Durin, Marine Houdou, Dominique Legrand, et al.
Biochimica et Biophysica Acta (BBA) - General Subjects (2023) Vol. 1867, Iss. 9, pp. 130412-130412
Open Access | Times Cited: 5
Hydrogen peroxide induces Arl1 degradation and impairs Golgi-mediated trafficking
Stephen Ireland, Haoran Huang, Jianchao Zhang, et al.
Molecular Biology of the Cell (2020) Vol. 31, Iss. 17, pp. 1931-1942
Open Access | Times Cited: 14
Golgi defect as a major contributor to lysosomal dysfunction
Sarah Reem Akaaboune, Yanzhuang Wang
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 1
Biogenesis of specialized lysosomes in differentiated keratinocytes relies on close apposition with the Golgi apparatus
Sarmistha Mahanty, Ptissam Bergam, Vivek Belapurkar, et al.
Cell Death and Disease (2024) Vol. 15, Iss. 7
Open Access | Times Cited: 1
Mitotic phosphorylation inhibits the Golgi mannosidase MAN1A1
Shijiao Huang, Yoshimi Haga, Jie Li, et al.
Cell Reports (2022) Vol. 41, Iss. 8, pp. 111679-111679
Open Access | Times Cited: 6
Structure modeling hints at a granular organization of the Golgi ribbon
Karen M. Page, Jessica J. McCormack, Mafalda Lopes da Silva, et al.
BMC Biology (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 5
Unraveling the Multifaceted Role of the Golgi Apparatus: Insights into Neuronal Plasticity, Development, Neurogenesis, Alzheimer’s Disease, and SARS-CoV-2 Interactions
Corneliu Toader, Lucian Eva, Razvan-Adrian Covache-Busuioc, et al.
Brain Sciences (2023) Vol. 13, Iss. 10, pp. 1363-1363
Open Access | Times Cited: 2
CHOP upregulation and dysregulation of the mature form of the SNAT2 amino acid transporter in the placentas from small for gestational age newborns
Emma Barroso, Marta Díaz, Ana Cristina Reguera, et al.
Cell Communication and Signaling (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 2
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