Results 201 to 210 of about 75,295 (332)

Potassium‐Dependent Coupling of Retinal Astrocyte Light Response to Müller Glia

Glia, Volume 73, Issue 7, Page 1520-1534, July 2025.
Main Points Astrocytes depolarize to light ON and OFF like Müller glia. The astrocyte light response is due to potassium influx. Retinal macroglial current‐voltage responses exhibit rectification which changes with repeated stimulation. ABSTRACT Astrocytes throughout the central nervous system mediate a variety of functions to support proper tissue ...
Joseph Matthew Holden, Andrew M. Boal, Lauren Katie Wareham, David John Calkins   +3 more
wiley   +1 more source

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

, 1998
DA Scott, ML Kraft, Rivka Carmi, A. Ramesh, Khalil Elbedour, Yael Yairi, C. R. Srikumari Srisailapathy, S. Rosengren, AF Markham, Mueller Rf, Nicholas Lench, Guy Van Camp, Richard J. Smith, Val C. Sheffield   +13 more
openalex   +1 more source

A simple RT-PCR-based strategy for screening connexin identity [PDF]

, 1999
Marcia Urban, Renato Rozental, David C. Spray   +2 more
openalex   +1 more source

Specialized Pro‐Resolving Mediators as Emerging Players in Cardioprotection: From Inflammation Resolution to Therapeutic Potential

Acta Physiologica, Volume 241, Issue 7, July 2025.
ABSTRACT Aim Timely myocardial reperfusion is essential for restoring blood flow to post‐ischemic tissue, thereby reducing cardiac injury and limiting infarct size. However, this process can paradoxically result in additional, irreversible myocardial damage, known as myocardial ischemia–reperfusion injury (MIRI).
Anna De Bartolo, Naomi Romeo, Tommaso Angelone, Carmine Rocca   +3 more
wiley   +1 more source

Connexin hemichannels and cell-cell channels: comparison of properties [PDF]

, 2000
Vytas K. Verselis, E. Brady Trexler, Feliksas F. Bukauskas   +2 more
openalex   +1 more source

High‐throughput screening identifies bazedoxifene as a potential therapeutic for dysferlin‐deficient limb girdle muscular dystrophy

British Journal of Pharmacology, Volume 182, Issue 13, Page 2930-2949, July 2025.
Abstract Background and Purpose Limb‐girdle muscular dystrophy R2 (LGMD R2) is a rare genetic disorder characterised by progressive weakness and wasting of proximal muscles. LGMD R2 is caused by the loss of function of dysferlin, a transmembrane protein crucial for plasma membrane repair in skeletal muscles.
Celine Bruge, Nathalie Bourg, Emilie Pellier, Johana Tournois, Jerome Polentes, Manon Benabides, Noella Grossi, Anne Bigot, Anthony Brureau, Isabelle Richard, Xavier Nissan   +10 more
wiley   +1 more source

Connexin mimetic peptides reversibly inhibit Ca²⁺signaling through gap junctions in airway cells [PDF]

, 2000
Scott Boitano, William Evans
openalex   +1 more source

Immune cell dynamics in heart failure: implicated mechanisms and therapeutic targets

ESC Heart Failure, Volume 12, Issue 3, Page 1739-1758, June 2025.
Abstract The relationship between heart failure (HF) and immune activation has garnered significant interest. Studies highlight the critical role of inflammation in HF, affecting cardiac structure and function. Despite promising anti‐inflammatory therapies, clinical trials have faced challenges, indicating an incomplete understanding of immune ...
Gen Li, Wu He, Dao Wen Wang
wiley   +1 more source

Human diseases associated with connexin mutations.

Biochimica et Biophysica Acta - Biomembranes, 2018
M. Srinivas, V. Verselis, T. W. White
semanticscholar   +1 more source

The molecular basis of selective permeability of connexins is complex and includes both size and charge [PDF]

, 2000
Bruce J. Nicholson, Paul A. Weber, Fengli Cao, Hao-Chen Chang, Paul D. Lampe, Gary S. Goldberg   +5 more
openalex   +1 more source