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Developmental Neuroscience
|
May 26, 2023
Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder
Shah Rukh, Daniel W Meechan, Thomas M Maynard, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
June 6, 2014
Cortical interneurons require Jnk1 to enter and navigate the developing cerebral cortex
Abigail K Myers, Daniel W Meechan, Danielle R Adney, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
Daniel W Meechan, Eric S Tucker, Thomas M Maynard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 24, 2012
Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome
Daniel W Meechan, Eric S Tucker, Thomas M Maynard, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
December 3, 2014
Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation
Elizabeth M Paronett, Daniel W Meechan, Beverly A Karpinski, et al.
Human Molecular Genetics
|
October 19, 2012
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development
Thomas M Maynard, Deepak Gopalakrishna, Daniel W Meechan, et al.
Disease Models & Mechanisms
|
June 19, 2026
An antioxidant therapy elicits distinct transcriptome responses in 22q11-deleted upper layer cortical projection neurons
Shah Rukh, Daniel W Meechan, Abra Roberts, et al.
Biorxiv : the Preprint Server for Biology
|
December 19, 2025
Distinct cellular and transcriptional mechanisms mediate an antioxidant therapeutic response in 22q11-deleted upper layer cortical projection neurons
Shah Rukh, Daniel W Meechan, Abra Roberts, et al.
Progress in Neurobiology
|
April 14, 2015
Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development
Daniel W Meechan, Thomas M Maynard, Eric S Tucker, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 10, 2006
No evidence for parental imprinting of mouse 22q11 gene orthologs
Thomas M Maynard, Daniel W Meechan, Clifford C Heindel, et al.
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Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Developmental Neuroscience
|
May 26, 2023
Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder
Shah Rukh, Daniel W Meechan, Thomas M Maynard, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
June 6, 2014
Cortical interneurons require Jnk1 to enter and navigate the developing cerebral cortex
Abigail K Myers, Daniel W Meechan, Danielle R Adney, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
Daniel W Meechan, Eric S Tucker, Thomas M Maynard, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 24, 2012
Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome
Daniel W Meechan, Eric S Tucker, Thomas M Maynard, et al.
Cerebral Cortex (New York, N.Y. : 1991)
|
December 3, 2014
Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation
Elizabeth M Paronett, Daniel W Meechan, Beverly A Karpinski, et al.
Human Molecular Genetics
|
October 19, 2012
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development
Thomas M Maynard, Deepak Gopalakrishna, Daniel W Meechan, et al.
Disease Models & Mechanisms
|
June 19, 2026
An antioxidant therapy elicits distinct transcriptome responses in 22q11-deleted upper layer cortical projection neurons
Shah Rukh, Daniel W Meechan, Abra Roberts, et al.
Biorxiv : the Preprint Server for Biology
|
December 19, 2025
Distinct cellular and transcriptional mechanisms mediate an antioxidant therapeutic response in 22q11-deleted upper layer cortical projection neurons
Shah Rukh, Daniel W Meechan, Abra Roberts, et al.
Progress in Neurobiology
|
April 14, 2015
Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development
Daniel W Meechan, Thomas M Maynard, Eric S Tucker, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
August 10, 2006
No evidence for parental imprinting of mouse 22q11 gene orthologs
Thomas M Maynard, Daniel W Meechan, Clifford C Heindel, et al.
Page
of 2