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Andrew DiStasio

Showing results (1-10 of 6) with videos related to

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Developmental Biology|November 17, 2019
Nubp2 is required for cranial neural crest survival in the mouseAndrew DiStasio, David Paulding, Praneet Chaturvedi, et al.
Developmental Biology|May 1, 2014
A gene expression atlas of early craniofacial developmentEric W Brunskill, Andrew S Potter, Andrew Distasio, et al.
Genesis (New York, N.Y. : 2000)|October 31, 2018
Using human sequencing to guide craniofacial researchRyan P Liegel, Erin Finnerty, Lauren Blizzard, et al.
Plos One|September 3, 2015
Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 ExpressionStefanie Jeruschke, Kay Jeruschke, Andrew DiStasio, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
<i>NUBP2</i> deficiency disrupts the centrosome-check point in the brain and causes primary microcephalyRebekah Rushforth, Hanan E Shamseldin, Nicole Costantino, et al.
Human Molecular Genetics|October 17, 2017
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephalyAndrew DiStasio, Ashley Driver, Kristen Sund, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Developmental Biology|November 17, 2019
Nubp2 is required for cranial neural crest survival in the mouseAndrew DiStasio, David Paulding, Praneet Chaturvedi, et al.
Developmental Biology|May 1, 2014
A gene expression atlas of early craniofacial developmentEric W Brunskill, Andrew S Potter, Andrew Distasio, et al.
Genesis (New York, N.Y. : 2000)|October 31, 2018
Using human sequencing to guide craniofacial researchRyan P Liegel, Erin Finnerty, Lauren Blizzard, et al.
Plos One|September 3, 2015
Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 ExpressionStefanie Jeruschke, Kay Jeruschke, Andrew DiStasio, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
<i>NUBP2</i> deficiency disrupts the centrosome-check point in the brain and causes primary microcephalyRebekah Rushforth, Hanan E Shamseldin, Nicole Costantino, et al.
Human Molecular Genetics|October 17, 2017
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephalyAndrew DiStasio, Ashley Driver, Kristen Sund, et al.
Pageof 1