Results 201 to 210 of about 21,628 (300)

Expression of connexins and pannexins in diseased human liver

, 2022
Kaat Leroy, Vânia Vilas‐Boas, Eva Gijbels, Bart Vanderborght, Lindsey Devisscher, Bruno Cogliati, Bert Van Den Bossche, Isabelle Colle, Mathieu Vinken   +8 more
openalex   +2 more sources

In situ structure of the human gap junction. [PDF]

Sci Adv
Eshriew E, Kumpula EP, Sah-Teli SK, Abettan A, Djurabekova A, Sharma V, Huiskonen JT.   +6 more
europepmc   +1 more source

Correction: Connexin 43 inhibitors reduce cell viability in glioblastoma and astrocyte co-culture systems [PDF]

Ali Genc, Berfin Uzunkaya, Gizem InetasYengin, Didem Tecimel, Altay Burak Dalan, Ömer Faruk Bayrak   +5 more
openalex   +1 more source

Gap junction protein connexin-43 interacts directly with microtubules [PDF]

, 2001
Ben N. G. Giepmans, Ingrid Verlaan, Trudi Hengeveld, Hans Janssen, Jero Calafat, Matthias M. Falk, Wouter H. Moolenaar   +6 more
openalex   +1 more source

The Interplay Between Periodontitis and Atrial Fibrillation: Inflammation as a Common Pathophysiological Bridge. [PDF]

Int J Mol Sci
Caprino F, Filardo A, Bria J, Coscarella I, Giudice A, Chiarella E, Di Vito A.   +6 more
europepmc   +1 more source

Connexin‐43 remodelling and arrhythmias: hemichannels as key drivers of cardiac dysfunction [PDF]

Priscila Araújo, Manuel F. Muñoz, Jonathan Quan, Jorge E. Contreras   +3 more
openalex   +1 more source

Connexins in Acquired Hearing Loss: Expanding Research Perspectives. [PDF]

Biomedicines
Huang S, Zhu J, Zhang J, Gong T, Fei Z, Chen P, Hou S, Yang J.   +7 more
europepmc   +1 more source

Apelin Ameliorates High Glucose-Induced Downregulation of Connexin 43 via AMPK-Dependent Pathway in Neonatal Rat Cardiomyocytes [PDF]

, 2018
Xiaoting Li, Lu Yu, Jing Gao, Xukun Bi, Juhong Zhang, Shiming Xu, Meihui Wang, Mengmeng Chen, Fuyu Qiu, Guosheng Fu   +9 more
openalex   +1 more source

Special Issue "Gap Junction Channels and Hemichannels in Health and Disease". [PDF]

Int J Mol Sci
Rijtano B, Bortolozzi M.
europepmc   +1 more source

A rare haplotype of the GJD3 gene segregating in familial Meniere’s disease interferes with connexin assembly [PDF]

Alba Escalera‐Balsera, Paula Robles-Bolívar, Alberto M. Parra‐Perez, Silvia Murillo-Cuesta, Han Chow Chua, Lourdes Rodríguez‐de la Rosa, Julio Contreras, Ewa Domarecka, Juan Carlos Amor‐Dorado, Andrés Soto-Varela, Isabel Varela‐Nieto, Agnieszka J. Szczepek, Alvaro Gallego‐Martinez, José A. López‐Escámez   +13 more
openalex   +1 more source