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:
KCTD1 is a new modulator of the KCASH family of Hedgehog suppressors
A. Di Fiore, Sara Bellardinelli, Luciano Pirone, et al.
Neoplasia (2023) Vol. 43, pp. 100926-100926
Open Access | Times Cited: 8
A. Di Fiore, Sara Bellardinelli, Luciano Pirone, et al.
Neoplasia (2023) Vol. 43, pp. 100926-100926
Open Access | Times Cited: 8
Showing 8 citing articles:
A Comprehensive Analysis of the Structural Recognition between KCTD Proteins and Cullin 3
Nicole Balasco, Luciana Esposito, Giovanni Smaldone, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1881-1881
Open Access | Times Cited: 4
Nicole Balasco, Luciana Esposito, Giovanni Smaldone, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1881-1881
Open Access | Times Cited: 4
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies
Cholaporn Ruangchan, Chumpol Ngamphiw, Annop Krasaesin, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5179-5179
Open Access | Times Cited: 4
Cholaporn Ruangchan, Chumpol Ngamphiw, Annop Krasaesin, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5179-5179
Open Access | Times Cited: 4
Colorectal cancer in Lynch syndrome families: consequences of gene germline mutations and the gut microbiota
Xuexin Wang, Zhijun Zheng, Dongliang Yu, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Xuexin Wang, Zhijun Zheng, Dongliang Yu, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Aplasia Cutis Congenita Pathomechanisms Reveal Key Regulators of Skin and Skin Appendage Morphogenesis
Alexander G. Marneros
Journal of Investigative Dermatology (2024) Vol. 144, Iss. 11, pp. 2399-2405
Closed Access | Times Cited: 1
Alexander G. Marneros
Journal of Investigative Dermatology (2024) Vol. 144, Iss. 11, pp. 2399-2405
Closed Access | Times Cited: 1
Structural studies of KCTD1 and its disease-causing mutant P20S provide insights into the protein function and misfunction
Nicole Balasco, Alessia Ruggiero, Giovanni Smaldone, et al.
International Journal of Biological Macromolecules (2024) Vol. 277, pp. 134390-134390
Open Access | Times Cited: 1
Nicole Balasco, Alessia Ruggiero, Giovanni Smaldone, et al.
International Journal of Biological Macromolecules (2024) Vol. 277, pp. 134390-134390
Open Access | Times Cited: 1
Structural studies of KCTD1 and its disease-causing mutant P20S provide insights into the protein function and misfunction
Nicole Balasco, Alessia Ruggiero, Giovanni Smaldone, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Nicole Balasco, Alessia Ruggiero, Giovanni Smaldone, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
The Proteasome and Cul3-Dependent Protein Ubiquitination Is Required for Gli Protein-Mediated Activation of Gene Expression in the Hedgehog Pathway
Tomasz Uśpieński, Paweł Niewiadomski
Cells (2024) Vol. 13, Iss. 17, pp. 1496-1496
Open Access
Tomasz Uśpieński, Paweł Niewiadomski
Cells (2024) Vol. 13, Iss. 17, pp. 1496-1496
Open Access
SMURF1 and SMURF2 directly target GLI1 for ubiquitination and proteasome-dependent degradation
F Bordin, Gloria Terriaca, Adriano Apostolico, et al.
Cell Death Discovery (2024) Vol. 10, Iss. 1
Open Access
F Bordin, Gloria Terriaca, Adriano Apostolico, et al.
Cell Death Discovery (2024) Vol. 10, Iss. 1
Open Access
