List of works - Daniel Osborn

A novel 9 kDa phosphoprotein is a component of the primary cilium and interacts with polycystin-1.

scientific article published on 16 November 2012

A novel role for the obesity-associated gene FTO in ciliogenesis and Wnt signalling

article

Basal body stability and ciliogenesis requires the conserved component Poc1

scientific article

Bbs8, together with the planar cell polarity protein Vangl2, is required to establish left-right asymmetry in zebrafish.

scientific article published on 17 July 2010

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

scientific article published on 21 October 2019

Cdkn1c drives muscle differentiation through a positive feedback loop with Myod.

scientific article

Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndrome

scientific article

Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene

scientific article

Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations

scientific article published on February 2009

Evaluation of zebrafish kidney function using a fluorescent clearance assay

scientific article

Fgf-driven Tbx protein activities directly induce myf5 and myod to initiate zebrafish myogenesis

scientific article published on 28 April 2020

Heat shock induces rapid resorption of primary cilia

scientific article published on 20 June 2012

Heat-shock induces rapid resorption of primary cilia

Mrf4 (myf6) is dynamically expressed in differentiated zebrafish skeletal muscle.

scientific article published on 15 June 2007

Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome

scientific article

Signals and myogenic regulatory factors restrict pax3 and pax7 expression to dermomyotome-like tissue in zebrafish.

scientific article

The Bardet-Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex

scientific article published on 31 May 2013

WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

scientific article published on 20 December 2017

Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function

scientific article

List of works by Daniel Osborn

A novel 9 kDa phosphoprotein is a component of the primary cilium and interacts with polycystin-1.

A novel role for the obesity-associated gene FTO in ciliogenesis and Wnt signalling

Basal body stability and ciliogenesis requires the conserved component Poc1

Bbs8, together with the planar cell polarity protein Vangl2, is required to establish left-right asymmetry in zebrafish.

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia

Cdkn1c drives muscle differentiation through a positive feedback loop with Myod.

Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndrome

Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene

Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations

Evaluation of zebrafish kidney function using a fluorescent clearance assay

Fgf-driven Tbx protein activities directly induce myf5 and myod to initiate zebrafish myogenesis

Heat shock induces rapid resorption of primary cilia

Heat-shock induces rapid resorption of primary cilia

Mrf4 (myf6) is dynamically expressed in differentiated zebrafish skeletal muscle.

Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome

Signals and myogenic regulatory factors restrict pax3 and pax7 expression to dermomyotome-like tissue in zebrafish.

The Bardet-Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex

WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

Zebrafish: a vertebrate tool for studying basal body biogenesis, structure, and function