Add to ORKG© 2015 Yee et al.Mutations in genes encoding cilia proteins cause human ciliopathies, diverse disorders affecting many tissues. Individual genes can be linked to ciliopathies with dramatically different phenotypes, suggesting that genetic modifiers may pa
Ciliopathies are inherited human disorders caused by both motile and non-motile cilia dysfunction th...
Primary cilia are microtubule-based “antennae-like” organelles extending from the apical surface of ...
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad ...
'Ciliopathies' are an emerging class of genetic multisystemic human disorders that are caused by a m...
Mutations in genes encoding cilia proteins cause human ciliopathies, diverse disorders affecting man...
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad ...
Ciliopathies, diseases that arise from defective ciliary function, afflict many tissues to various d...
Research of cilia has gained significant momentum in the last 15 years, as an increasing number of h...
Ciliopathies are a large group of human disorders caused by dysfunction of primary or motile cilia a...
Primary cilia are non-motile organelles associated with the cell cycle, which can be found in most v...
Primary cilia are microtubule-based organelles projecting from most epithelial cells in vertebrates,...
Primary cilia are microtubule-based organelles projecting from most epithelial cells in vertebrates,...
Soon, the genetic basis of most human Mendelian diseases will be solved. The next challenge will be ...
Mutations in genes encoding centriolar or ciliary proteins cause diseases collectively known as ‘cil...
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad ...
Ciliopathies are inherited human disorders caused by both motile and non-motile cilia dysfunction th...
Primary cilia are microtubule-based “antennae-like” organelles extending from the apical surface of ...
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad ...
'Ciliopathies' are an emerging class of genetic multisystemic human disorders that are caused by a m...
Mutations in genes encoding cilia proteins cause human ciliopathies, diverse disorders affecting man...
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad ...
Ciliopathies, diseases that arise from defective ciliary function, afflict many tissues to various d...
Research of cilia has gained significant momentum in the last 15 years, as an increasing number of h...
Ciliopathies are a large group of human disorders caused by dysfunction of primary or motile cilia a...
Primary cilia are non-motile organelles associated with the cell cycle, which can be found in most v...
Primary cilia are microtubule-based organelles projecting from most epithelial cells in vertebrates,...
Primary cilia are microtubule-based organelles projecting from most epithelial cells in vertebrates,...
Soon, the genetic basis of most human Mendelian diseases will be solved. The next challenge will be ...
Mutations in genes encoding centriolar or ciliary proteins cause diseases collectively known as ‘cil...
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad ...
Ciliopathies are inherited human disorders caused by both motile and non-motile cilia dysfunction th...
Primary cilia are microtubule-based “antennae-like” organelles extending from the apical surface of ...
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad ...