Published in Genomics on December 07, 2005
Spot pattern of leopard Danio is caused by mutation in the zebrafish connexin41.8 gene. EMBO Rep (2006) 1.83
Connexin43 regulates joint location in zebrafish fins. Dev Biol (2008) 1.06
Gap junction-mediated electrical transmission: regulatory mechanisms and plasticity. Biochim Biophys Acta (2012) 1.06
Molecular and functional asymmetry at a vertebrate electrical synapse. Neuron (2013) 1.03
Biological and biophysical properties of vascular connexin channels. Int Rev Cell Mol Biol (2009) 0.98
Two distinct aquaporin 0s required for development and transparency of the zebrafish lens. Invest Ophthalmol Vis Sci (2010) 0.93
Cx23, a connexin with only four extracellular-loop cysteines, forms functional gap junction channels and hemichannels. FEBS Lett (2007) 0.92
Zebrafish early cardiac connexin, Cx36.7/Ecx, regulates myofibril orientation and heart morphogenesis by establishing Nkx2.5 expression. Proc Natl Acad Sci U S A (2008) 0.91
Regulation of cellular communication by signaling microdomains in the blood vessel wall. Pharmacol Rev (2014) 0.90
Gap junctions composed of connexins 41.8 and 39.4 are essential for colour pattern formation in zebrafish. Elife (2014) 0.89
A zebrafish model for Waardenburg syndrome type IV reveals diverse roles for Sox10 in the otic vesicle. Dis Model Mech (2008) 0.87
Calmodulin mediates the Ca2+-dependent regulation of Cx44 gap junctions. Biophys J (2009) 0.87
Determining how defects in connexin43 cause skeletal disease. Genesis (2012) 0.85
Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants. Neurobiol Dis (2008) 0.84
Hemichannel composition and electrical synaptic transmission: molecular diversity and its implications for electrical rectification. Front Cell Neurosci (2014) 0.83
Polyamine sensitivity of gap junctions is required for skin pattern formation in zebrafish. Sci Rep (2012) 0.83
Cx40.8, a Cx43-like protein, forms gap junction channels inefficiently and may require Cx43 for its association at the plasma membrane. FEBS Lett (2009) 0.81
Connexin 39.9 protein is necessary for coordinated activation of slow-twitch muscle and normal behavior in zebrafish. J Biol Chem (2011) 0.80
The Physiological Characterization of Connexin41.8 and Connexin39.4, Which Are Involved in the Striped Pattern Formation of Zebrafish. J Biol Chem (2015) 0.80
The Cx43-like connexin protein Cx40.8 is differentially localized during fin ontogeny and fin regeneration. PLoS One (2012) 0.79
Heterotypic gap junctions at glutamatergic mixed synapses are abundant in goldfish brain. Neuroscience (2014) 0.78
Connexin 35b expression in the spinal cord of Danio rerio embryos and larvae. J Comp Neurol (2014) 0.78
Phosphorylation in the C-terminus of the rat connexin46 (rCx46) and regulation of the conducting activity of the formed connexons. J Bioenerg Biomembr (2008) 0.78
Two Different Functions of Connexin43 Confer Two Different Bone Phenotypes in Zebrafish. J Biol Chem (2016) 0.77
The spatiotemporal expression of multiple coho salmon ovarian connexin genes and their hormonal regulation in vitro during oogenesis. Reprod Biol Endocrinol (2011) 0.76
Zebrafish cx30.3: identification and characterization of a gap junction gene highly expressed in the skin. Dev Dyn (2010) 0.75
Gap Junction in the Teleost Fish Lineage: Duplicated Connexins May Contribute to Skin Pattern Formation and Body Shape Determination. Front Cell Dev Biol (2017) 0.75
Specific connectivity between photoreceptors and horizontal cells in the zebrafish retina. J Neurophysiol (2016) 0.75
A genetic basis for molecular asymmetry at vertebrate electrical synapses. Elife (2017) 0.75
Dynamic trafficking and delivery of connexons to the plasma membrane and accretion to gap junctions in living cells. Proc Natl Acad Sci U S A (2002) 2.21
The role of erythropoietin in regulating angiogenesis. Dev Biol (2004) 1.66
Regulation of connexin biosynthesis, assembly, gap junction formation, and removal. Biochim Biophys Acta (2004) 1.60
Internalization of large double-membrane intercellular vesicles by a clathrin-dependent endocytic process. Mol Biol Cell (2006) 1.46
A developmental transition in growth control during zebrafish caudal fin development. Dev Biol (2006) 1.32
Specific amino-acid residues in the N-terminus and TM3 implicated in channel function and oligomerization compatibility of connexin43. J Cell Sci (2003) 1.27
Molecular reorganization of Cx43, Zo-1 and Src complexes during the endocytosis of gap junction plaques in response to a non-genomic carcinogen. J Cell Sci (2008) 1.25
Connexin43 (GJA1) is required in the population of dividing cells during fin regeneration. Dev Biol (2008) 1.22
Rapid evolution of cuticular hydrocarbons in a species radiation of acoustically diverse Hawaiian crickets (Gryllidae: trigonidiinae: Laupala). Evolution (2007) 1.11
Acute internalization of gap junctions in vascular endothelial cells in response to inflammatory mediator-induced G-protein coupled receptor activation. FEBS Lett (2008) 1.11
Double-membrane gap junction internalization requires the clathrin-mediated endocytic machinery. FEBS Lett (2008) 1.11
Zebrafish short fin mutations in connexin43 lead to aberrant gap junctional intercellular communication. FEBS Lett (2007) 1.08
Connexin43 regulates joint location in zebrafish fins. Dev Biol (2008) 1.06
Internalized gap junctions are degraded by autophagy. Autophagy (2012) 1.04
Proteins and mechanisms regulating gap-junction assembly, internalization, and degradation. Physiology (Bethesda) (2013) 1.03
Green-to-red photoconvertible fluorescent proteins: tracking cell and protein dynamics on standard wide-field mercury arc-based microscopes. BMC Cell Biol (2010) 1.02
Osteoblast maturation occurs in overlapping proximal-distal compartments during fin regeneration in zebrafish. Dev Dyn (2009) 0.99
Contributions of natural and sexual selection to the evolution of premating reproductive isolation: a research agenda. Trends Ecol Evol (2013) 0.98
Cx23, a connexin with only four extracellular-loop cysteines, forms functional gap junction channels and hemichannels. FEBS Lett (2007) 0.92
A genetic, deletion, physical, and human homology map of the long fin region on zebrafish linkage group 2. Genomics (2002) 0.88
Two tyrosine-based sorting signals in the Cx43 C-terminus cooperate to mediate gap junction endocytosis. Mol Biol Cell (2013) 0.87
E-cadherin differentially regulates the assembly of Connexin43 and Connexin32 into gap junctions in human squamous carcinoma cells. J Biol Chem (2010) 0.86
Assembly of connexin43 into gap junctions is regulated differentially by E-cadherin and N-cadherin in rat liver epithelial cells. Mol Biol Cell (2010) 0.86
Determining how defects in connexin43 cause skeletal disease. Genesis (2012) 0.85
Functional conservation between structurally diverse ribosomal proteins from Drosophila melanogaster and Saccharomyces cerevisiae: fly L23a can substitute for yeast L25 in ribosome assembly and function. Nucleic Acids Res (2007) 0.83
Male and female preference for conspecifics in a fish with male parental care (Percidae: Catonotus). Behav Processes (2010) 0.82
Cx40.8, a Cx43-like protein, forms gap junction channels inefficiently and may require Cx43 for its association at the plasma membrane. FEBS Lett (2009) 0.81
Fin-mutant female zebrafish (Danio rerio) exhibit differences in association preferences for male fin length. Behav Processes (2008) 0.80
Identification of an evx1-dependent joint-formation pathway during FIN regeneration. PLoS One (2013) 0.79
The Cx43-like connexin protein Cx40.8 is differentially localized during fin ontogeny and fin regeneration. PLoS One (2012) 0.79
Bone growth in zebrafish fins occurs via multiple pulses of cell proliferation. Dev Dyn (2007) 0.77
Further misconceptions about species recognition: a reply to Padian and Horner. Trends Ecol Evol (2013) 0.76
Differences in spectral sensitivity within and among species of darters (genus Etheostoma). Vision Res (2012) 0.76
Changes in sexual signals are greater than changes in ecological traits in a dichromatic group of fishes. Evolution (2014) 0.76
Nanoporosity significantly enhances the biological performance of engineered glass tissue scaffolds. Tissue Eng Part A (2013) 0.75