Distinct behavior of connexin56 and connexin46 gap junctional channels can be predicted from the behavior of their hemi-gap-junctional channels.

Por Ebihara, L, Berthoud, V M, Beyer, E C
Publicado em 1995

Functional Role of the Carboxyl Terminal Domain of Human Connexin 50 in Gap Junctional Channels

Por Xu, X., Berthoud, V.M., Beyer, E.C., Ebihara, L.
Publicado em 2002

Phosphorylation of connexin43 gap junction protein in uninfected and Rous sarcoma virus-transformed mammalian fibroblasts.

Por Crow, D S, Beyer, E C, Paul, D L, Kobe, S S, Lau, A F
Publicado em 1990

Heterotypic docking of Cx43 and Cx45 connexons blocks fast voltage gating of Cx43.

Por Elenes, S, Martinez, A D, Delmar, M, Beyer, E C, Moreno, A P
Publicado em 2001

Co-expression of lens fiber connexins modifies hemi-gap-junctional channel behavior.

Por Ebihara, L, Xu, X, Oberti, C, Beyer, E C, Berthoud, V M
Publicado em 1999

Connexin43 mediates direct intercellular communication in human osteoblastic cell networks.

Por Civitelli, R, Beyer, E C, Warlow, P M, Robertson, A J, Geist, S T, Steinberg, T H
Publicado em 1993

Connexin37 forms high conductance gap junction channels with subconductance state activity and selective dye and ionic permeabilities.

Por Veenstra, R D, Wang, H Z, Beyer, E C, Ramanan, S V, Brink, P R
Publicado em 1994

The extent of heterocellular communication mediated by gap junctions is predictive of bystander tumor cytotoxicity in vitro.

Por Fick, J, Barker, F G, Dazin, P, Westphale, E M, Beyer, E C, Israel, M A
Publicado em 1995

Molecular cloning and functional expression of human connexin37, an endothelial cell gap junction protein.

Por Reed, K E, Westphale, E M, Larson, D M, Wang, H Z, Veenstra, R D, Beyer, E C
Publicado em 1993

Slow ventricular conduction in mice heterozygous for a connexin43 null mutation.

Por Guerrero, P A, Schuessler, R B, Davis, L M, Beyer, E C, Johnson, C M, Yamada, K A, Saffitz, J E
Publicado em 1997

A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts

Por Arora, A, Minogue, P J, Liu, X, Addison, P K, Russel-Eggitt, I, Webster, A R, Hunt, D M, Ebihara, L, Beyer, E C, Berthoud, V M, Moore, A T
Publicado em 2007

A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract

Por Arora, A, Minogue, P J, Liu, X, Reddy, M A, Ainsworth, J R, Bhattacharya, S S, Webster, A R, Hunt, D M, Ebihara, L, Moore, A T, Beyer, E C, Berthoud, V M
Publicado em 2006