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Stephen LA (2013)
Failure of centrosome migration causes a loss of motile cilia in talpid(3) mutants.
in Developmental dynamics : an official publication of the American Association of Anatomists
Wann AK (2012)
Primary cilia mediate mechanotransduction through control of ATP-induced Ca2+ signaling in compressed chondrocytes.
in FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Lucas JS (2012)
Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD.
in Human mutation
Herrera J (2022)
The UIP honeycomb airway cells are the site of mucin biogenesis with deranged cilia
Stephen L (2013)
Failure of centrosome migration causes a loss of motile cilia in talpid 3 mutants
in Developmental Dynamics
Haward F (2021)
Nucleo-cytoplasmic shuttling of splicing factor SRSF1 is required for development and cilia function.
in eLife
Haward F (2020)
Nucleo-cytoplasmic shuttling of splicing factor SRSF1 is required for development and cilia function
Quidwai T (2020)
A WDR35-dependent coatomer transports ciliary membrane proteins from the Golgi to the cilia
Haward F (2021)
Nucleo-cytoplasmic shuttling of splicing factor SRSF1 is required for development and cilia function.
in eLife
Meng H (2023)
YAP activation inhibits inflammatory signalling and cartilage breakdown associated with reduced primary cilia expression.
in Osteoarthritis and cartilage
Wheway G (2014)
The role of primary cilia in the development and disease of the retina.
in Organogenesis
Bergen DJM (2017)
The Golgi matrix protein giantin is required for normal cilia function in zebrafish.
in Biology open
Bergen DJM (2017)
The Golgi matrix protein giantin is required for normal cilia function in zebrafish.
in Biology open
Martinez-Heredia V (2023)
Absence of the primary cilia formation gene Talpid3 impairs muscle stem cell function.
in Communications biology
Bergen DJM (2017)
The Golgi matrix protein giantin is required for normal cilia function in zebrafish.
in Biology open
Avolio R (2018)
Protein Syndesmos is a novel RNA-binding protein that regulates primary cilia formation.
in Nucleic acids research
Thompson CL (2017)
Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signalling.
in European cells & materials
Martinez-Heredia V (2023)
Absence of the primary cilia formation gene Talpid3 impairs muscle stem cell function.
in Communications biology
Martinez-Heredia V (2023)
Absence of the primary cilia formation gene Talpid3 impairs muscle stem cell function.
in Communications biology
Avolio R (2018)
Protein Syndesmos is a novel RNA-binding protein that regulates primary cilia formation.
in Nucleic acids research
Thompson CL (2017)
Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signalling.
in European cells & materials
Bakey Z (2023)
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans.
in medRxiv : the preprint server for health sciences
Hasenpusch-Theil K (2021)
The Multifaceted Roles of Primary Cilia in the Development of the Cerebral Cortex.
in Frontiers in cell and developmental biology
Bergen D (2017)
The Golgi matrix protein giantin is required for normal cilia function in zebrafish
Quidwai T (2021)
A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia
in eLife
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