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Daniel P S Osborn

Showing results (11-20 of 19) with videos related to

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Human Molecular Genetics|June 4, 2013
The Bardet-Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complexMagdalena Cardenas-Rodriguez, Florencia Irigoín, Daniel P S Osborn, et al.
Development (Cambridge, England)|April 30, 2020
Fgf-driven Tbx protein activities directly induce <i>myf5</i> and <i>myod</i> to initiate zebrafish myogenesisDaniel P S Osborn, Kuoyu Li, Stephen J Cutty, et al.
Journal of Cell Science|June 22, 2012
Heat shock induces rapid resorption of primary ciliaNatalia V Prodromou, Clare L Thompson, Daniel P S Osborn, et al.
Plos One|February 8, 2014
Loss of FTO antagonises Wnt signaling and leads to developmental defects associated with ciliopathiesDaniel P S Osborn, Rosa Maria Roccasecca, Fiona McMurray, et al.
Human Molecular Genetics|September 15, 2018
Bi-allelic mutations in MYL1 cause a severe congenital myopathyGianina Ravenscroft, Irina T Zaharieva, Carlo A Bortolotti, et al.
Nature Genetics|January 25, 2011
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndromeCaroline Rooryck, Anna Diaz-Font, Daniel P S Osborn, et al.
Human Molecular Genetics|February 5, 2019
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24Carola Hedberg-Oldfors, Alexandra Abramsson, Daniel P S Osborn, et al.
American Journal of Human Genetics|February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and DystroglycanopathyDaniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Nature Communications|October 23, 2019
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegiaMatias Wagner, Daniel P S Osborn, Ina Gehweiler, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Human Molecular Genetics|June 4, 2013
The Bardet-Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complexMagdalena Cardenas-Rodriguez, Florencia Irigoín, Daniel P S Osborn, et al.
Development (Cambridge, England)|April 30, 2020
Fgf-driven Tbx protein activities directly induce <i>myf5</i> and <i>myod</i> to initiate zebrafish myogenesisDaniel P S Osborn, Kuoyu Li, Stephen J Cutty, et al.
Journal of Cell Science|June 22, 2012
Heat shock induces rapid resorption of primary ciliaNatalia V Prodromou, Clare L Thompson, Daniel P S Osborn, et al.
Plos One|February 8, 2014
Loss of FTO antagonises Wnt signaling and leads to developmental defects associated with ciliopathiesDaniel P S Osborn, Rosa Maria Roccasecca, Fiona McMurray, et al.
Human Molecular Genetics|September 15, 2018
Bi-allelic mutations in MYL1 cause a severe congenital myopathyGianina Ravenscroft, Irina T Zaharieva, Carlo A Bortolotti, et al.
Nature Genetics|January 25, 2011
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndromeCaroline Rooryck, Anna Diaz-Font, Daniel P S Osborn, et al.
Human Molecular Genetics|February 5, 2019
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24Carola Hedberg-Oldfors, Alexandra Abramsson, Daniel P S Osborn, et al.
American Journal of Human Genetics|February 14, 2017
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and DystroglycanopathyDaniel P S Osborn, Heather L Pond, Neda Mazaheri, et al.
Nature Communications|October 23, 2019
Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegiaMatias Wagner, Daniel P S Osborn, Ina Gehweiler, et al.
Pageof 2