Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Sunit Dutta"'
Autor:
Holly Hardy, James GD Prendergast, Aara Patel, Sunit Dutta, Violeta Trejo-Reveles, Hannah Kroeger, Andrea R Yung, Lisa V Goodrich, Brian Brooks, Jane C Sowden, Joe Rainger
Publikováno v:
eLife, Vol 8 (2019)
Epithelial fusion underlies many vital organogenic processes during embryogenesis. Disruptions to these cause a significant number of human birth defects, including ocular coloboma. We provide robust spatial-temporal staging and unique anatomical det
Externí odkaz:
https://doaj.org/article/954b152a5b0d453aa0310ee5b9f00758
Autor:
Holly E Babcock, Sunit Dutta, Ramakrishna P Alur, Chad Brocker, Vasilis Vasiliou, Susan Vitale, Mones Abu-Asab, Brian P Brooks
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e101782 (2014)
Uveal coloboma is a potentially blinding congenital ocular malformation caused by failure of the optic fissure to close during development. Although mutations in numerous genes have been described, these account for a minority of cases, complicating
Externí odkaz:
https://doaj.org/article/e830525ea41f45949613332e50f1e6e4
Publikováno v:
3rd Asia Pacific Meeting on Near Surface Geoscience & Engineering.
Publikováno v:
Journal of Neurochemistry. 146:47-62
Gestational alcohol exposure causes a range of neuropsychological disorders by modulating neurodevelopmental genes and proteins. The extent of damage depends on the stage of the embryo as well as dosage, duration and frequency of exposure. Here, we i
Autor:
Holly Hardy, Joe Rainger, Violeta Trejo-Reveles, Aara Patel, Sunit Dutta, Lisa V. Goodrich, Andrea R. Yung, Jane C. Sowden, James Prendergast, Brian P. Brooks, Hannah Kroeger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d28cc776e475783cb5f0ec4fc01fcf72
https://doi.org/10.7554/elife.43877.026
https://doi.org/10.7554/elife.43877.026
Autor:
Sunit Dutta, Violeta Trejo-Reveles, Andrea R. Yung, Aara Patel, Jane C. Sowden, Lisa V. Goodrich, Joe Rainger, Hannah Kroeger, Brian P. Brooks, Holly Hardy, James Prendergast
Epithelial fusion underlies many vital organogenic processes during embryogenesis. Disruptions to these cause a significant number of human birth defects, including ocular coloboma. We provide robust spatial-temporal staging and unique anatomical det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5af338dde73e1d086b298450c10c7ee1
https://doi.org/10.1101/477729
https://doi.org/10.1101/477729
Publikováno v:
Stem Cells. 34:334-345
Neural crest cells (NCC) are a population of epithelial cells that arise from the dorsal tube and undergo epithelial-mesenchymal transition (EMT) eventually generating tissues from peripheral nervous system, melanocytes, craniofacial cartilage, and b
Autor:
Igor B. Dawid, Xiaodong Jiao, Jacob D. Brown, Peter J. Munson, J. Fielding Hejtmancik, Ramakrishna P. Alur, Amana L. Akhtar, Kapil Bharti, Brian P. Brooks, Jeffrey M. Gross, Ighovie F. Onojafe, Robert F. Bonner, Wai-Yee Chan, Sunit Dutta
Publikováno v:
Proceedings of the National Academy of Sciences. 106:1462-1467
The gene networks underlying closure of the optic fissure during vertebrate eye development are poorly understood. Here, we profile global gene expression during optic fissure closure using laser capture microdissected (LCM) tissue from the margins o
Autor:
Ramakrishna P. Alur, Sunit Dutta, Abdel G. Elkahloun, Shahila Sriskanda, Elangovan Boobalan, Brian P. Brooks
Publikováno v:
Developmental biology. 406(2)
The formation of cilia is a fundamental developmental process affecting diverse functions such as cellular signaling, tissue morphogenesis and body patterning. However, the mechanisms of ciliogenesis during vertebrate development are not fully unders
Autor:
Susan Vitale, Chad Brocker, Mones Abu-Asab, Brian P. Brooks, Sunit Dutta, Vasilis Vasiliou, Holly E. Babcock, Ramakrishna P. Alur
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e101782 (2014)
PLoS ONE
PLoS ONE
Uveal coloboma is a potentially blinding congenital ocular malformation caused by failure of the optic fissure to close during development. Although mutations in numerous genes have been described, these account for a minority of cases, complicating