Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Desire M. Buckley"'
Autor:
Alfire Sidik, Groves Dixon, Desire M. Buckley, Hannah G. Kirby, Shuge Sun, Johann K. Eberhart
Publikováno v:
BMC Biology, Vol 19, Iss 1, Pp 1-18 (2021)
Abstract Background Gene-environment interactions are likely to underlie most human birth defects. The most common known environmental contributor to birth defects is prenatal alcohol exposure. Fetal alcohol spectrum disorders (FASD) describe the ful
Externí odkaz:
https://doaj.org/article/a592c15870db4880a94181c1d34e8337
Publikováno v:
Journal of Developmental Biology, Vol 8, Iss 9, p 9 (2020)
Journal of Developmental Biology
Volume 8
Issue 2
Journal of Developmental Biology
Volume 8
Issue 2
The molecular mechanisms regulating neurogenesis involve the control of gene expression by transcription factors. Gbx1 and Gbx2, two members of the Gbx family of homeodomain-containing transcription factors, are known for their essential roles in cen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1fcbd20f3c902eb75e678d9828126b8
https://www.mdpi.com/2221-3759/8/2/9
https://www.mdpi.com/2221-3759/8/2/9
Publikováno v:
Biochem Cell Biol
The term fetal alcohol spectrum disorder (FASD) refers to the entire suite of deleterious outcomes resulting from embryonic exposure to alcohol. Along with other reviews in this special issue, we provide insight into how animal models, specifically t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfbf4848158fabb152b7fc0c62d5c281
https://doi.org/10.1139/bcb-2017-0122
https://doi.org/10.1139/bcb-2017-0122
Publikováno v:
Birth defects research. 111(12)
BACKGROUND: A cardinal feature of prenatal ethanol exposure is CNS damage, resulting in a continuum of neurological and behavioral impairments that are described by the term Fetal Alcohol Spectrum Disorders (FASD). FASDs are variable and depend on se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d2eeead21ca8ff2cc4452385d8288fc
https://pubmed.ncbi.nlm.nih.gov/30793540
https://pubmed.ncbi.nlm.nih.gov/30793540
Autor:
Megan M. Krogman, Christian L. Lorson, Michael L. Garcia, Ferrill F. Rose, Hansjörg Rindt, Spencer M. Vale, Desire M. Buckley
Publikováno v:
Neuromuscular Disorders. 22:277-285
Spinal Muscular Atrophy (SMA) is a devastating neurodegenerative disease and is a leading genetic cause of infantile death. SMA is caused by the homozygous loss of Survival Motor Neuron-1 (SMN1). The presence of a nearly identical copy gene called SM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cd437dedc670b62ac61fe4ca1039cf1
https://doi.org/10.1016/j.nmd.2011.10.012
https://doi.org/10.1016/j.nmd.2011.10.012
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 2, p e56214 (2013)
PLoS ONE, Vol 8, Iss 2, p e56214 (2013)
The Gbx class of homeobox genes encodes DNA binding transcription factors involved in regulation of embryonic central nervous system (CNS) development. Gbx1 is dynamically expressed within spinal neuron progenitor pools and becomes restricted to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab494f1f031cf75ce3ac29223fbb649
http://europepmc.org/articles/PMC3572027
http://europepmc.org/articles/PMC3572027
Autor:
David A. Roeseler, Doris K. Wu, Samuel T. Waters, Desire M. Buckley, Dong Xu, Shrikesh Sachdev, Trupti Joshi, Mark Hannink
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e47366 (2012)
PLoS ONE
PLoS ONE
Gbx2 encodes a DNA-binding transcription factor that plays pivotal roles during embryogenesis. Gain-and loss-of-function studies in several vertebrate species have demonstrated a requirement for Gbx2 in development of the anterior hindbrain, spinal c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a5bdf0a0d6e0a41bf3c4c022ea1fb65
http://europepmc.org/articles/PMC3493575?pdf=render
http://europepmc.org/articles/PMC3493575?pdf=render