Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
RJ Ferland, TJ Cherry, PO Preware… - Journal of …, 2003 - Wiley Online Library
Foxp2 and Foxp1 are recently identified members of the Fox family of winged‐helix/forkhead
transcription factor genes. A recent study has found that mutations in human FOXP2 …
transcription factor genes. A recent study has found that mutations in human FOXP2 …
International multicentre review of perioperative management and outcome for catecholamine-producing tumours
…, M Yamakage, JA Miller, TJ Cherry… - Journal of British …, 2020 - academic.oup.com
Background Surgery for catecholamine-producing tumours can be complicated by
intraoperative and postoperative haemodynamic instability. Several perioperative management …
intraoperative and postoperative haemodynamic instability. Several perioperative management …
Early asymmetry of gene transcription in embryonic human left and right cerebral cortex
…, C Patoine, A Abu-Khalil, J Visvader, E Sum, TJ Cherry… - Science, 2005 - science.org
The human left and right cerebral hemispheres are anatomically and functionally asymmetric.
To test whether human cortical asymmetry has a molecular basis, we studied gene …
To test whether human cortical asymmetry has a molecular basis, we studied gene …
Development and diversification of retinal amacrine interneurons at single cell resolution
TJ Cherry, JM Trimarchi, MB Stadler… - Proceedings of the …, 2009 - National Acad Sciences
The vertebrate retina uses diverse neuronal cell types arrayed into complex neural circuits to
extract, process, and relay information from the visual scene to the higher order processing …
extract, process, and relay information from the visual scene to the higher order processing …
[PDF][PDF] Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina
Gene regulatory networks (GRNs), consisting of transcription factors and their target sites,
control neurogenesis and cell-fate specification in the developing central nervous system. In …
control neurogenesis and cell-fate specification in the developing central nervous system. In …
NeuroD factors regulate cell fate and neurite stratification in the developing retina
TJ Cherry, S Wang, I Bormuth, M Schwab… - Journal of …, 2011 - Soc Neuroscience
Members of the basic helix-loop-helix (bHLH) family of transcription factors have been shown
to control critical aspects of development in many tissues. To identify bHLH genes that …
to control critical aspects of development in many tissues. To identify bHLH genes that …
[PDF][PDF] MEF2D drives photoreceptor development through a genome-wide competition for tissue-specific enhancers
MM Andzelm, TJ Cherry, DA Harmin, AC Boeke, C Lee… - Neuron, 2015 - cell.com
Organismal development requires the precise coordination of genetic programs to regulate
cell fate and function. MEF2 transcription factors (TFs) play essential roles in this process but …
cell fate and function. MEF2 transcription factors (TFs) play essential roles in this process but …
Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging
SK Bonney, LT Sullivan, TJ Cherry… - Journal of Cerebral …, 2022 - journals.sagepub.com
Perivascular fibroblasts (PVFs) are recognized for their pro-fibrotic role in many central
nervous system disorders. Like mural cells, PVFs surround blood vessels and express Pdgfrβ. …
nervous system disorders. Like mural cells, PVFs surround blood vessels and express Pdgfrβ. …
Mapping the cis-regulatory architecture of the human retina reveals noncoding genetic variation in disease
TJ Cherry, MG Yang, DA Harmin… - Proceedings of the …, 2020 - National Acad Sciences
The interplay of transcription factors and cis-regulatory elements (CREs) orchestrates the
dynamic and diverse genetic programs that assemble the human central nervous system (CNS…
dynamic and diverse genetic programs that assemble the human central nervous system (CNS…
[HTML][HTML] Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
Purpose Part of the hidden genetic variation in heterogeneous genetic conditions such as
inherited retinal diseases (IRDs) can be explained by copy-number variations (CNVs). Here, …
inherited retinal diseases (IRDs) can be explained by copy-number variations (CNVs). Here, …