Zobrazeno 1 - 10
of 125
pro vyhledávání: '"L. Everson"'
Autor:
Yonit A. Addissie, Paul Kruszka, Angela Troia, Zoë C. Wong, Joshua L. Everson, Beth A. Kozel, Robert J. Lipinski, Kristen M. C. Malecki, Maximilian Muenke
Publikováno v:
Environmental Health, Vol 19, Iss 1, Pp 1-13 (2020)
Abstract Background Pesticide exposure during susceptible windows and at certain doses are linked to numerous birth defects. Early experimental evidence suggests an association between active ingredients in pesticides and holoprosencephaly (HPE), the
Externí odkaz:
https://doaj.org/article/b860ee5ed34445d3aacaebfce021f2d1
Autor:
Jeremy L. Everson, Darbi R. Jones, Amy K. Taylor, Barb J. Rutan, Timothy D. Leeds, Kate E. Langwig, Andrew R. Wargo, Gregory D. Wiens
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Infectious hematopoietic necrosis virus (IHNV) and Flavobacterium psychrophilum are major pathogens of farmed rainbow trout. Improved control strategies are desired but the influence of on-farm environmental factors that lead to disease outbreaks rem
Externí odkaz:
https://doaj.org/article/1a72582197274b09992d97c889fc0ffd
Autor:
Matthew T. McLaughlin, Miranda R. Sun, Tyler G. Beames, Austin C. Steward, Joshua W. M. Theisen, Hannah M. Chung, Joshua L. Everson, Ivan P. Moskowitz, Michael D. Sheets, Robert J. Lipinski
Publikováno v:
Developmental Dynamics. 252:483-494
Frem1 has been linked to human face shape variation, dysmorphology, and malformation, but little is known about its regulation and biological role in facial development.During midfacial morphogenesis in mice, we observed Frem1 expression in the embry
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-11 (2018)
Abstract Background The evolutionarily conserved Sonic Hedgehog (Shh) signaling pathway is essential for embryogenesis and orofacial development. SHH ligand secreted from the surface ectoderm activates pathway activity in the underlying cranial neura
Externí odkaz:
https://doaj.org/article/115bfc797eab4171b305fc43de2ce4a5
Autor:
Galen W. Heyne, Joshua L. Everson, Lydia J. Ansen-Wilson, Cal G. Melberg, Dustin M. Fink, Kia F. Parins, Padydeh Doroodchi, Caden M. Ulschmid, Robert J. Lipinski
Publikováno v:
Disease Models & Mechanisms, Vol 9, Iss 11, Pp 1307-1315 (2016)
Holoprosencephaly (HPE) is a common and severe human developmental abnormality marked by malformations of the forebrain and face. Although several genetic mutations have been linked to HPE, phenotypic outcomes range dramatically, and most cases canno
Externí odkaz:
https://doaj.org/article/5a807d1f7f5f49e4b86b88fa9ece4960
Autor:
Joshua L. Everson, Johann K. Eberhart
Publikováno v:
Current Topics in Developmental Biology ISBN: 9780128201572
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4371fea4720065cbae815aef93ed0b2d
https://doi.org/10.1016/bs.ctdb.2022.10.003
https://doi.org/10.1016/bs.ctdb.2022.10.003
Publikováno v:
Birth defects researchREFERENCES.
Losses and malformations of cranial neural crest cell (cNCC) derivatives are a hallmark of several common brain and face malformations. Nevertheless, the etiology of these cNCC defects remains unknown for many cases, suggesting a complex basis involv
Autor:
Matthew T. McLaughlin, Miranda R. Sun, Tyler G. Beames, Austin C. Steward, Joshua W. M. Theisen, Hannah M. Chung, Joshua L. Everson, Ivan P. Moskowitz, Michael D. Sheets, Robert J. Lipinski
The Frem/Fras family of extracellular matrix proteins has been linked to human face shape variation and malformation, but little is known about their regulation and biological roles in facial development. During midfacial morphogenesis in mice, we ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f5adb2ba963ac5b5be74e69a26aaace
https://doi.org/10.1101/2022.07.16.500318
https://doi.org/10.1101/2022.07.16.500318
Autor:
Beth A. Kozel, Paul Kruszka, Maximilian Muenke, Zoë C. Wong, Robert J. Lipinski, Kristen Malecki, Joshua L. Everson, Angela Troia, Yonit A. Addissie
Publikováno v:
Birth Defects Res
BACKGROUND: Holoprosencephaly is the most common malformation of the forebrain (1 in 250 embryos) with severe consequences for fetal and child development. This study evaluates nongenetic factors associated with holoprosencephaly risk, severity, and