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Developmental Biology
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November 17, 2019
Nubp2 is required for cranial neural crest survival in the mouse
Andrew DiStasio, David Paulding, Praneet Chaturvedi, et al.
Developmental Biology
|
May 1, 2014
A gene expression atlas of early craniofacial development
Eric W Brunskill, Andrew S Potter, Andrew Distasio, et al.
Genesis (New York, N.Y. : 2000)
|
October 31, 2018
Using human sequencing to guide craniofacial research
Ryan P Liegel, Erin Finnerty, Lauren Blizzard, et al.
Plos One
|
September 3, 2015
Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 Expression
Stefanie 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 microcephaly
Rebekah Rushforth, Hanan E Shamseldin, Nicole Costantino, et al.
Human Molecular Genetics
|
October 17, 2017
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly
Andrew DiStasio, Ashley Driver, Kristen Sund, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Developmental Biology
|
November 17, 2019
Nubp2 is required for cranial neural crest survival in the mouse
Andrew DiStasio, David Paulding, Praneet Chaturvedi, et al.
Developmental Biology
|
May 1, 2014
A gene expression atlas of early craniofacial development
Eric W Brunskill, Andrew S Potter, Andrew Distasio, et al.
Genesis (New York, N.Y. : 2000)
|
October 31, 2018
Using human sequencing to guide craniofacial research
Ryan P Liegel, Erin Finnerty, Lauren Blizzard, et al.
Plos One
|
September 3, 2015
Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 Expression
Stefanie 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 microcephaly
Rebekah Rushforth, Hanan E Shamseldin, Nicole Costantino, et al.
Human Molecular Genetics
|
October 17, 2017
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly
Andrew DiStasio, Ashley Driver, Kristen Sund, et al.
Page
of 1