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Stephen P Robertson

Showing results (51-60 of 146) with videos related to

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EMBO Molecular Medicine|August 23, 2023
Metformin rescues migratory deficits of cells derived from patients with periventricular heterotopiaCedric Bressan, Marta Snapyan, Marina Snapyan, et al.
European Journal of Clinical Investigation|August 31, 2024
The hinge-1 domain of Flna is not necessary for diverse physiological functions in miceEmma M Wade, Elizabeth A Goodin, Tim Morgan, et al.
Human Mutation|June 21, 2012
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanismsPhilippe M Campeau, James T Lu, Brian C Dawson, et al.
Genes|December 3, 2020
Deletion of Exon 1 in <i>AMER1</i> in Osteopathia Striata with Cranial SclerosisJingyi Mi, Padmini Parthasarathy, Benjamin J Halliday, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney syndromeMary J Gray, Chong Ae Kim, Debora Romeo Bertola, et al.
Journal of the Neurological Sciences|March 28, 2015
Congenital mirror movements: phenotypes associated with DCC and RAD51 mutationsElizabeth A Franz, Rachel Chiaroni-Clarke, Stephanie Woodrow, et al.
Frontiers in Cellular Neuroscience|March 30, 2018
Mob2 Insufficiency Disrupts Neuronal Migration in the Developing CortexAdam C O'Neill, Christina Kyrousi, Melanie Einsiedler, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Association of mutations in FLNA with craniosynostosisNathalie Fennell, Nicola Foulds, Diana S Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 29, 2011
RefilinB (FAM101B) targets filamin A to organize perinuclear actin networks and regulates nuclear shapeOlivia Gay, Benoît Gilquin, Fumihiko Nakamura, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 23, 2020
Fibulin-3 knockout mice demonstrate corneal dysfunction but maintain normal retinal integritySteffi Daniel, Marian Renwick, Viet Q Chau, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
EMBO Molecular Medicine|August 23, 2023
Metformin rescues migratory deficits of cells derived from patients with periventricular heterotopiaCedric Bressan, Marta Snapyan, Marina Snapyan, et al.
European Journal of Clinical Investigation|August 31, 2024
The hinge-1 domain of Flna is not necessary for diverse physiological functions in miceEmma M Wade, Elizabeth A Goodin, Tim Morgan, et al.
Human Mutation|June 21, 2012
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanismsPhilippe M Campeau, James T Lu, Brian C Dawson, et al.
Genes|December 3, 2020
Deletion of Exon 1 in <i>AMER1</i> in Osteopathia Striata with Cranial SclerosisJingyi Mi, Padmini Parthasarathy, Benjamin J Halliday, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney syndromeMary J Gray, Chong Ae Kim, Debora Romeo Bertola, et al.
Journal of the Neurological Sciences|March 28, 2015
Congenital mirror movements: phenotypes associated with DCC and RAD51 mutationsElizabeth A Franz, Rachel Chiaroni-Clarke, Stephanie Woodrow, et al.
Frontiers in Cellular Neuroscience|March 30, 2018
Mob2 Insufficiency Disrupts Neuronal Migration in the Developing CortexAdam C O'Neill, Christina Kyrousi, Melanie Einsiedler, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Association of mutations in FLNA with craniosynostosisNathalie Fennell, Nicola Foulds, Diana S Johnson, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 29, 2011
RefilinB (FAM101B) targets filamin A to organize perinuclear actin networks and regulates nuclear shapeOlivia Gay, Benoît Gilquin, Fumihiko Nakamura, et al.
Journal of Molecular Medicine (Berlin, Germany)|September 23, 2020
Fibulin-3 knockout mice demonstrate corneal dysfunction but maintain normal retinal integritySteffi Daniel, Marian Renwick, Viet Q Chau, et al.
Pageof 15