Daniel P. S. Osborn

发表

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

Andrew C. Nelson, S. Hughes, F. Wardle, 2020, Development.

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

Ryan Marshall, Daniel P. S. Osborn, 2016, Cilia.

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

H. May-Simera, P. Beales, M. Kai, 2010, Developmental biology.

Heat shock induces rapid resorption of primary cilia

C. Thompson, M. Knight, P. Beales, 2012, Development.

Heat shock induces rapid resorption of primary cilia

C. Thompson, M. Knight, P. Beales, 2012, Journal of cell science.

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

R. Schüle, R. Boostani, T. Schwarzmayr, 2019, Nature Communications.

Vestigial-like-2b (VITO-1b) and Tead-3a (Tef-5a) expression in zebrafish skeletal muscle, brain and notochord.

C. Mann, S. Hughes, Daniel P. S. Osborn, 2007, Gene expression patterns : GEP.

Evaluation of zebrafish kidney function using a fluorescent clearance assay.

P. Beales, S. Christou-Savina, Daniel P. S. Osborn, 2015, Journal of visualized experiments : JoVE.

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

P. Rigby, J. Carvajal, S. Hughes, 2007, Gene expression patterns : GEP.

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

S. Hughes, Gianluca Tettamanti, C. Hammond, 2007, Developmental biology.

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

S. Hughes, Y. Hinits, Daniel P. S. Osborn, 2011, Developmental biology.

Loss of FTO Antagonises Wnt Signaling and Leads to Developmental Defects Associated with Ciliopathies

R. Cox, D. Stemple, I. Barroso, 2014, PloS one.

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

R. Hennekam, A. Latos-Bieleńska, H. Ropers, 2010, American journal of human genetics.

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

J. Badano, P. Beales, M. Graña, 2012, Human Genetics.

Basal body stability and ciliogenesis requires the conserved component Poc1

P. Beales, T. Giddings, C. Pearson, 2009, The Journal of cell biology.

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

S. Hughes, Y. Hinits, Daniel P. S. Osborn, 2009, Development.

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

Cheol‐Hee Kim, Hyung-Goo Kim, T. Raivio, 2017, EMBO reports.

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

Cheol‐Hee Kim, Hyung-Goo Kim, T. Raivio, 2017, bioRxiv.

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

H. Peeters, M. Bitner-Glindzicz, R. Hennekam, 2011, Nature Genetics.

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

N. Katsanis, J. Badano, P. Beales, 2013, Human molecular genetics.

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

Andrew C. Nelson, S. Hughes, F. Wardle, 2019, Development.

A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B, located within the Turner syndrome critical interval, causes idiopathic scoliosis

D. Jenkins, M. Seda, Daniel P. S. Osborn, 2018 .

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

J. Badano, P. Beales, M. Graña, 2012, Human Genetics.

Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

R. Hennekam, A. Latos-Bieleńska, H. Ropers, 2022 .

Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3

Joshua S. Clayton, N. Laing, H. Galehdari, 2020, Genetics in Medicine.

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

S. Hughes, Y. Hinits, Daniel P. S. Osborn, 2011, Developmental biology.

A Technique for Studying Glomerular Filtration Integrity in the Zebrafish Pronephros.

Daniel P. S. Osborn, M. Kolatsi-Joannou, 2020, Methods in molecular biology.