BackgroundDYX1C1 (DNAAF4) and DCDC2 are two of the most replicated dyslexia candidate genes in genetic studies. They both have demonstrated roles in neuronal migration, in cilia growth and function and they both are cytoskeletal interactors. In addition, they both have been characterized as ciliopathy genes. However, their exact molecular functions are still incompletely described. Based on these known roles, we asked whether DYX1C1 and DCDC2 interact on the genetic and the protein level.ResultsHere, we report the physical protein-protein interaction of DYX1C1 and DCDC2 as well as their respective interactions with the centrosomal protein CPAP (CENPJ) on exogenous and endogenous levels in different cell models including brain organoids. In ...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder arising from dysmotility of cili...
Primary ciliary dyskinesia (PCD) is caused when defects of motile cilia lead to chronic airway infec...
Neural tube defects (NTDs) are severe malformations of the central nervous system caused by complex ...
Dyslexia is defined as an unexpected difficulty in reading despite normal intelligence, senses and ...
Dyx1c1 has been associated with dyslexia and neuronal migration in the developing neocortex. Unexpec...
DYX1C1, a susceptibility gene for dyslexia, encodes a tetratricopeptide repeat domain containing pro...
DYX1C1, DCDC2, and KIAA0319 are three of the most replicated dyslexia candidate genes (DCGs). Recent...
Linkage analysis has revealed a number of gene intervals conferring susceptibility to developmental ...
DCDC2 is one of the candidate susceptibility genes for dyslexia. It belongs to the superfamily of do...
DCDC2 is one of the candidate susceptibility genes for dyslexia. It belongs to the superfamily of do...
Cilia are highly conserved structures found from protozoa to mammals where they play essential physi...
Primary ciliary dyskinesia (PCD) is caused when defects of motile cilia lead to chronic airway infec...
Motile cilia and flagella are essential to many biological functions that require cellular or fluid ...
Dyslexia is a neurodevelopmental disorder that affects between 5% and 12% of school-aged children. ...
Cilia are essential for fertilization, respiratory clearance, cerebrospinal fluid circulation and es...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder arising from dysmotility of cili...
Primary ciliary dyskinesia (PCD) is caused when defects of motile cilia lead to chronic airway infec...
Neural tube defects (NTDs) are severe malformations of the central nervous system caused by complex ...
Dyslexia is defined as an unexpected difficulty in reading despite normal intelligence, senses and ...
Dyx1c1 has been associated with dyslexia and neuronal migration in the developing neocortex. Unexpec...
DYX1C1, a susceptibility gene for dyslexia, encodes a tetratricopeptide repeat domain containing pro...
DYX1C1, DCDC2, and KIAA0319 are three of the most replicated dyslexia candidate genes (DCGs). Recent...
Linkage analysis has revealed a number of gene intervals conferring susceptibility to developmental ...
DCDC2 is one of the candidate susceptibility genes for dyslexia. It belongs to the superfamily of do...
DCDC2 is one of the candidate susceptibility genes for dyslexia. It belongs to the superfamily of do...
Cilia are highly conserved structures found from protozoa to mammals where they play essential physi...
Primary ciliary dyskinesia (PCD) is caused when defects of motile cilia lead to chronic airway infec...
Motile cilia and flagella are essential to many biological functions that require cellular or fluid ...
Dyslexia is a neurodevelopmental disorder that affects between 5% and 12% of school-aged children. ...
Cilia are essential for fertilization, respiratory clearance, cerebrospinal fluid circulation and es...
Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder arising from dysmotility of cili...
Primary ciliary dyskinesia (PCD) is caused when defects of motile cilia lead to chronic airway infec...
Neural tube defects (NTDs) are severe malformations of the central nervous system caused by complex ...