Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Emma Wentworth Winchester"'
Autor:
Andrea Wilderman, Eva D’haene, Machteld Baetens, Tara N. Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sandra Janssens, Danny E. Miller, Miranda Galey, Kari M. Brown, Rolf W. Stottmann, Sarah Vergult, K. Nicole Weaver, Samantha A. Brugmann, Timothy C. Cox, Justin Cotney
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-23 (2024)
Abstract Craniofacial abnormalities account for approximately one third of birth defects. The regulatory programs that build the face require precisely controlled spatiotemporal gene expression, achieved through tissue-specific enhancers. Clusters of
Externí odkaz:
https://doaj.org/article/d8bfbb8f7d514cd7a8d154657d67b4ca
Autor:
Jeremie Oliver Piña, Resmi Raju, Daniela M. Roth, Emma Wentworth Winchester, Parna Chattaraj, Fahad Kidwai, Fabio R. Faucz, James Iben, Apratim Mitra, Kiersten Campbell, Gus Fridell, Caroline Esnault, Justin L. Cotney, Ryan K. Dale, Rena N. D’Souza
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract The terminal differentiation of osteoblasts and subsequent formation of bone marks an important phase in palate development that leads to the separation of the oral and nasal cavities. While the morphogenetic events preceding palatal osteoge
Externí odkaz:
https://doaj.org/article/6f572a2594494ecc86d33a6364a1b88c
Autor:
Tara N. Yankee, Sungryong Oh, Emma Wentworth Winchester, Andrea Wilderman, Kelsey Robinson, Tia Gordon, Jill A. Rosenfeld, Jennifer VanOudenhove, Daryl A. Scott, Elizabeth J. Leslie, Justin Cotney
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-23 (2023)
Abstract Craniofacial disorders arise in early pregnancy and are one of the most common congenital defects. To fully understand how craniofacial disorders arise, it is essential to characterize gene expression during the patterning of the craniofacia
Externí odkaz:
https://doaj.org/article/8fb52a1254b34d8ba4d504c9a78dcfc6
Publikováno v:
Frontiers in Dental Medicine, Vol 3 (2022)
Human odontogenic aberrations such as abnormal tooth number and delayed tooth eruption can occur as a symptom of rare syndromes or, more commonly, as nonsyndromic phenotypes. These phenotypes can require extensive and expensive dental treatment, posi
Externí odkaz:
https://doaj.org/article/1c3c3bb3d8e4442da9a816fd056eb1de
Autor:
Jeremie Oliver Piña, Daniela M. Roth, Resmi Raju, Emma Wentworth Winchester, Parna Chattaraj, Fahad Kidwai, Fabio R. Faucz, James Iben, Cameron Padilla, Justin L. Cotney, Rena N. D’Souza
Publikováno v:
bioRxiv
Cleft palate is a common craniofacial disorder involving multiple genetic and environmental predisposing factors. Currently, limited insight exists into the molecular mechanisms regulating osteogenic differentiation and patterning in the palate durin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11b8c3042ba24002182b0b1ae6f8e8d5
https://doi.org/10.1101/2023.05.16.541037
https://doi.org/10.1101/2023.05.16.541037
Dental malformations range from rare syndromes to common nonsyndromic phenotypes. These malformations can predispose individuals to dental disease, which can in turn affect systemic health. While many dental phenotypes are heritable, most cases have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab4d614282e23f90898f0c4339120292
https://doi.org/10.1101/2022.03.15.483501
https://doi.org/10.1101/2022.03.15.483501
Autor:
Andrea Wilderman, Eva D’haene, Machteld Baetens, Tara N. Yankee, Emma Wentworth Winchester, Nicole Glidden, Ellen Roets, Jo Van Dorpe, Sarah Vergult, Timothy C. Cox, Justin Cotney
Defects in embryonic patterning resulting in craniofacial abnormalities account for approximately 1/3 of birth defects. The regulatory programs that build and shape the face require precisely controlled spatiotemporal gene expression, achieved throug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b4ca502a6eea2605e2f8f2e36b8c3e3
https://doi.org/10.1101/2022.03.10.483852
https://doi.org/10.1101/2022.03.10.483852
Autor:
Tara N. Yankee, Andrea Wilderman, Emma Wentworth Winchester, Jennifer VanOudenhove, Justin Cotney
SummaryCraniofacial disorders are among the most common of all congenital defects. A majority of craniofacial development occurs early in pregnancy and to fully understand how craniofacial defects arise, it is essential to observe gene expression dur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::220201b00a98fa1e6b9fd6bc00af3c78
https://doi.org/10.1101/2022.02.28.482338
https://doi.org/10.1101/2022.02.28.482338