AbstractMechanisms that regulate the size and shape of bony structures are largely unknown. The molecular identification of the fin length mutant short fin (sof), which causes defects in the length of bony fin ray segments, may provide insights regarding the regulation of bone growth. In this report, we demonstrate that the sof phenotype is caused by mutations in the connexin43 (cx43) gene. This conclusion is supported by genetic mapping, reduced expression of cx43 in the original sof allele (sofb123), identification of missense mutations in three ENU-induced alleles, and by demonstration of partially abrogated cx43 function in sofb123 embryos. Expression of cx43 was identified in cells flanking the germinal region of newly growing segments...
<div><p>Skeletal development is a tightly regulated process and requires proper communication betwee...
For many years bone research has been mainly performed in mice, chicken, cell culture systems, or hu...
AbstractSystematic identification of skeletal dysplasias in model vertebrates provides insight into ...
AbstractMechanisms that regulate the size and shape of bony structures are largely unknown. The mole...
AbstractMutations in the zebrafish connexin43 (cx43) gene cause the short fin phenotype, indicating ...
AbstractIn zebrafish, mutations in the gap junction gene connexin43 lead to short bony fin ray segme...
AbstractJoints are essential for skeletal form and function, yet their development remains poorly un...
The zebrafish fin is composed of multiple bony fin rays. Each fin ray is comprised of multiple segme...
Skeletal morphogenesis is a complex process through which bones grow to their correct size and shape...
<div><p>Cell–cell communication, facilitating the exchange of small metabolites, ions and second mes...
AbstractGap junctions are proteinaceous channels that reside at the plasma membrane and permit the e...
Joints are essential for skeletal flexibly and form, yet the process underlying joint morphogenesis ...
AbstractMechanisms that regulate the growth and form of the vertebrate skeleton are largely unknown....
Research on the genetic mechanisms underlying human skeletal development and disease have largely re...
<div><p>Connexins (Cx) are the subunits of gap junctions, membraneous protein channels that permit t...
<div><p>Skeletal development is a tightly regulated process and requires proper communication betwee...
For many years bone research has been mainly performed in mice, chicken, cell culture systems, or hu...
AbstractSystematic identification of skeletal dysplasias in model vertebrates provides insight into ...
AbstractMechanisms that regulate the size and shape of bony structures are largely unknown. The mole...
AbstractMutations in the zebrafish connexin43 (cx43) gene cause the short fin phenotype, indicating ...
AbstractIn zebrafish, mutations in the gap junction gene connexin43 lead to short bony fin ray segme...
AbstractJoints are essential for skeletal form and function, yet their development remains poorly un...
The zebrafish fin is composed of multiple bony fin rays. Each fin ray is comprised of multiple segme...
Skeletal morphogenesis is a complex process through which bones grow to their correct size and shape...
<div><p>Cell–cell communication, facilitating the exchange of small metabolites, ions and second mes...
AbstractGap junctions are proteinaceous channels that reside at the plasma membrane and permit the e...
Joints are essential for skeletal flexibly and form, yet the process underlying joint morphogenesis ...
AbstractMechanisms that regulate the growth and form of the vertebrate skeleton are largely unknown....
Research on the genetic mechanisms underlying human skeletal development and disease have largely re...
<div><p>Connexins (Cx) are the subunits of gap junctions, membraneous protein channels that permit t...
<div><p>Skeletal development is a tightly regulated process and requires proper communication betwee...
For many years bone research has been mainly performed in mice, chicken, cell culture systems, or hu...
AbstractSystematic identification of skeletal dysplasias in model vertebrates provides insight into ...