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M Chiara

Showing results (131-140 of 151) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|January 31, 2016
Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social DeficitsAdam W Oaks, Marta Zamarbide, Dimira E Tambunan, et al.
Annals of Neurology|May 4, 2010
Developmental and degenerative features in a complicated spastic paraplegiaM Chiara Manzini, Anna Rajab, Thomas M Maynard, et al.
Autophagy|January 7, 2017
Metabolic effects of fasting on human and mouse blood in vivoFederico Pietrocola, Yohann Demont, Francesca Castoldi, et al.
Human Molecular Genetics|June 14, 2014
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentationsStefania Di Costanzo, Anuradha Balasubramanian, Heather L Pond, et al.
Scientific Reports|July 26, 2024
Identification of kinase inhibitors as potential host-directed therapies for intracellular bacteriaRobin H G A van den Biggelaar, Kimberley V Walburg, Susan J F van den Eeden, et al.
Neurogenetics|July 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Nature Communications|January 6, 2016
Structure of the polyisoprenyl-phosphate glycosyltransferase GtrB and insights into the mechanism of catalysisChiara Ardiccioni, Oliver B Clarke, David Tomasek, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of <i>ATP8A2</i>-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Human Mutation|August 30, 2008
Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle EastM Chiara Manzini, Danielle Gleason, Bernard S Chang, et al.
Cell Reports|July 29, 2014
CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasisM Chiara Manzini, Lan Xiong, Ranad Shaheen, et al.
Pageof 16

Showing results (131-140 of 151) with videos related to

Sort By:
Pageof 16
Cerebral Cortex (New York, N.Y. : 1991)|January 31, 2016
Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social DeficitsAdam W Oaks, Marta Zamarbide, Dimira E Tambunan, et al.
Annals of Neurology|May 4, 2010
Developmental and degenerative features in a complicated spastic paraplegiaM Chiara Manzini, Anna Rajab, Thomas M Maynard, et al.
Autophagy|January 7, 2017
Metabolic effects of fasting on human and mouse blood in vivoFederico Pietrocola, Yohann Demont, Francesca Castoldi, et al.
Human Molecular Genetics|June 14, 2014
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentationsStefania Di Costanzo, Anuradha Balasubramanian, Heather L Pond, et al.
Scientific Reports|July 26, 2024
Identification of kinase inhibitors as potential host-directed therapies for intracellular bacteriaRobin H G A van den Biggelaar, Kimberley V Walburg, Susan J F van den Eeden, et al.
Neurogenetics|July 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Nature Communications|January 6, 2016
Structure of the polyisoprenyl-phosphate glycosyltransferase GtrB and insights into the mechanism of catalysisChiara Ardiccioni, Oliver B Clarke, David Tomasek, et al.
Medrxiv : the Preprint Server for Health Sciences|May 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of <i>ATP8A2</i>-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Human Mutation|August 30, 2008
Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle EastM Chiara Manzini, Danielle Gleason, Bernard S Chang, et al.
Cell Reports|July 29, 2014
CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasisM Chiara Manzini, Lan Xiong, Ranad Shaheen, et al.
Pageof 16