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Investigative Ophthalmology & Visual Science
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April 25, 2017
Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
Suzanne M Michalak, Mary C Whitman, Jong G Park, et al.
Development (Cambridge, England)
|
August 17, 2023
Loss of Twist1 and balanced retinoic acid signaling from the meninges causes cortical folding in mice
Matt J Matrongolo, Khue-Tu Ho-Nguyen, Manav Jain, et al.
Frontiers in Molecular Neuroscience
|
May 29, 2026
Caffeine attenuates cisplatin induced microglial reactivity and cognitive dysfunction
Alfredo Oliveros, Ivan Loncar, Marwan Mostafa, et al.
Neuron
|
January 31, 2017
Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes
Amit Agarwal, Pei-Hsun Wu, Ethan G Hughes, et al.
Biorxiv : the Preprint Server for Biology
|
October 9, 2023
Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice
Matt J Matrongolo, Phillip S Ang, Junbing Wu, et al.
The Journal of Clinical Investigation
|
November 2, 2023
Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice
Matt J Matrongolo, Phillip S Ang, Junbing Wu, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
The clinical spectrum of homozygous HOXA1 mutations
Thomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.
Developmental Cell
|
August 29, 2017
Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura
Max A Tischfield, Caroline D Robson, Nicole M Gilette, et al.
Nature Genetics
|
September 13, 2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
Max A Tischfield, Thomas M Bosley, Mustafa A M Salih, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2015
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development
Mary C Whitman, Caroline Andrews, Wai-Man Chan, et al.
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of 3
Search research articles
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Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
Investigative Ophthalmology & Visual Science
|
April 25, 2017
Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle
Suzanne M Michalak, Mary C Whitman, Jong G Park, et al.
Development (Cambridge, England)
|
August 17, 2023
Loss of Twist1 and balanced retinoic acid signaling from the meninges causes cortical folding in mice
Matt J Matrongolo, Khue-Tu Ho-Nguyen, Manav Jain, et al.
Frontiers in Molecular Neuroscience
|
May 29, 2026
Caffeine attenuates cisplatin induced microglial reactivity and cognitive dysfunction
Alfredo Oliveros, Ivan Loncar, Marwan Mostafa, et al.
Neuron
|
January 31, 2017
Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes
Amit Agarwal, Pei-Hsun Wu, Ethan G Hughes, et al.
Biorxiv : the Preprint Server for Biology
|
October 9, 2023
Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice
Matt J Matrongolo, Phillip S Ang, Junbing Wu, et al.
The Journal of Clinical Investigation
|
November 2, 2023
Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice
Matt J Matrongolo, Phillip S Ang, Junbing Wu, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
The clinical spectrum of homozygous HOXA1 mutations
Thomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.
Developmental Cell
|
August 29, 2017
Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura
Max A Tischfield, Caroline D Robson, Nicole M Gilette, et al.
Nature Genetics
|
September 13, 2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
Max A Tischfield, Thomas M Bosley, Mustafa A M Salih, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2015
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development
Mary C Whitman, Caroline Andrews, Wai-Man Chan, et al.
Page
of 3