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Peter D Currie

Showing results (61-70 of 113) with videos related to

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Disease Models & Mechanisms|October 8, 2014
Loss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathyJoachim Berger, Hakan Tarakci, Silke Berger, et al.
Plos One|January 5, 2012
Zebrafish prox1b mutants develop a lymphatic vasculature, and prox1b does not specifically mark lymphatic endothelial cellsShijie Tao, Merlijn Witte, Robert J Bryson-Richardson, et al.
Disease Models & Mechanisms|August 30, 2020
Machine learning discriminates a movement disorder in a zebrafish model of Parkinson's diseaseGideon L Hughes, Michael A Lones, Matthew Bedder, et al.
Development (Cambridge, England)|April 27, 2019
Muscle precursor cell movements in zebrafish are dynamic and require Six family genesJared C Talbot, Emily M Teets, Dhanushika Ratnayake, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 1, 2012
Fgf-dependent glial cell bridges facilitate spinal cord regeneration in zebrafishYona Goldshmit, Tamar E Sztal, Patricia R Jusuf, et al.
Molecular and Cellular Neurosciences|May 5, 2015
Rapamycin increases neuronal survival, reduces inflammation and astrocyte proliferation after spinal cord injuryYona Goldshmit, Sivan Kanner, Maria Zacs, et al.
Developmental Cell|February 6, 2007
Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryoGeorgina E Hollway, Robert J Bryson-Richardson, Silke Berger, et al.
Development (Cambridge, England)|October 24, 2003
Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryoDavid I Bassett, Robert J Bryson-Richardson, David F Daggett, et al.
Genomics|March 7, 2003
The structure and evolution of the melanocortin and MCH receptors in fish and mammalsDarren W Logan, Robert J Bryson-Richardson, Kayleene E Pagán, et al.
Cell Reports|January 11, 2018
In Vivo Function of the Chaperonin TRiC in α-Actin Folding during Sarcomere AssemblyJoachim Berger, Silke Berger, Mei Li, et al.
Pageof 12

Showing results (61-70 of 113) with videos related to

Sort By:
Pageof 12
Disease Models & Mechanisms|October 8, 2014
Loss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathyJoachim Berger, Hakan Tarakci, Silke Berger, et al.
Plos One|January 5, 2012
Zebrafish prox1b mutants develop a lymphatic vasculature, and prox1b does not specifically mark lymphatic endothelial cellsShijie Tao, Merlijn Witte, Robert J Bryson-Richardson, et al.
Disease Models & Mechanisms|August 30, 2020
Machine learning discriminates a movement disorder in a zebrafish model of Parkinson's diseaseGideon L Hughes, Michael A Lones, Matthew Bedder, et al.
Development (Cambridge, England)|April 27, 2019
Muscle precursor cell movements in zebrafish are dynamic and require Six family genesJared C Talbot, Emily M Teets, Dhanushika Ratnayake, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 1, 2012
Fgf-dependent glial cell bridges facilitate spinal cord regeneration in zebrafishYona Goldshmit, Tamar E Sztal, Patricia R Jusuf, et al.
Molecular and Cellular Neurosciences|May 5, 2015
Rapamycin increases neuronal survival, reduces inflammation and astrocyte proliferation after spinal cord injuryYona Goldshmit, Sivan Kanner, Maria Zacs, et al.
Developmental Cell|February 6, 2007
Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryoGeorgina E Hollway, Robert J Bryson-Richardson, Silke Berger, et al.
Development (Cambridge, England)|October 24, 2003
Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryoDavid I Bassett, Robert J Bryson-Richardson, David F Daggett, et al.
Genomics|March 7, 2003
The structure and evolution of the melanocortin and MCH receptors in fish and mammalsDarren W Logan, Robert J Bryson-Richardson, Kayleene E Pagán, et al.
Cell Reports|January 11, 2018
In Vivo Function of the Chaperonin TRiC in α-Actin Folding during Sarcomere AssemblyJoachim Berger, Silke Berger, Mei Li, et al.
Pageof 12