Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Arianna L. Smith"'
Autor:
Arianna L. Smith, Emmanuel Paul, Devin McGee, Ranuka Sinniah, Emily Flom, Devan Jackson-Humbles, Jack Harkema, Karen E. Racicot
Publikováno v:
Frontiers in Immunology, Vol 10 (2020)
Allergic asthma is a chronic pulmonary disorder fundamentally linked to immune dysfunction. Since the immune system begins developing in utero, prenatal exposures can affect immune programming and increase risk for diseases such as allergic asthma. C
Externí odkaz:
https://doaj.org/article/e636ab75bf604f85b92069817527bb2b
Autor:
Walid D. Fakhouri, Yunping Lei, Tamara Busch, Simon G. Gregory, Wei Yang, Richard H. Finnell, Arianna L. Smith, Edward Li, Alexander G. Bassuk, Gary M. Shaw, Huiping Zhu, Trevor Williams, Youssef A. Kousa, Tamer A. Mansour, Yang Chai, A. J. Agopian, Laura E. Mitchell, Akira Kinoshita, Brad A. Amendt, Elizabeth J. Leslie, Brian C. Schutte, Eric C. Liao, Xiao Li, Dhruv B. Sharma, Nicole K Patel, Raeuf Roushangar, Allison E. Ashley-Koch
Publikováno v:
Hum Mol Genet
Mutations in IRF6, TFAP2A and GRHL3 cause orofacial clefting syndromes in humans. However, Tfap2a and Grhl3 are also required for neurulation in mice. Here, we found that homeostasis of Irf6 is also required for development of the neural tube and ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbe0c76be9040181391af9fb105ce5b5
https://doi.org/10.1093/hmg/ddz010
https://doi.org/10.1093/hmg/ddz010
The placenta is a highly specialized organ that serves as the primary interface between the maternal environment and the fetus. One important placental function is to promote the development of maternal immune phenotypes that will prevent detrimental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb661c30dd6463de058819e964c0d0a8
https://doi.org/10.1016/b978-0-12-818508-7.00004-x
https://doi.org/10.1016/b978-0-12-818508-7.00004-x
Autor:
Paulomi Bole Aldo, Puja Bagri, M. Busse, Victoria Chase, Tanya Dimova, Jiahui Ding, Adrian Erlebacher, Jemma Evans, Binqing Fu, Nardhy Gomez-Lopez, Seth Guller, Satoshi Hayakawa, Michael J. Hickey, Charu Kaushic, Se Hoon Kim, Kaori Koga, Shihoko Komine-Aizawa, Keiichi Kumasawa, Ha-Yan Kwon, Ja-Young Kwon, Gendie E. Lash, Ai-Hua Liao, Hong Liu, Yong-Sun Maeng, Anthony J. Maxwell, Gil Mor, Kahinho P. Muyayalo, Fen Ning, Ivan Osokine, Yejin Park, Mickey V. Patel, Yifei Qi, Karen E. Racicot, Marta Rodríguez-García, Roberto Romero, Shigeru Saito, Lois A. Salamonsen, A. Schumacher, Zheng Shen, Naoya Shigeta, Arianna L. Smith, Kazuhide Takada, Tamara Tilburgs, Sayaka Tsuda, Noriko M. Tsuji, Haiming Wei, Shannon Whirledge, Charles R. Wira, Madeleine Wood, Yuan You, Emma Yu, A.C. Zenclussen, Yonghong Zhang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::339e37706d3af3ab1eaf1a8b24770bc9
https://doi.org/10.1016/b978-0-12-818508-7.09992-9
https://doi.org/10.1016/b978-0-12-818508-7.09992-9
Autor:
Devin McGee, Karen Racicot, Emily Flom, Ranuka Sinniah, Arianna L. Smith, Emmanuel Paul, Jack R. Harkema, Devan Jackson-Humbles
Publikováno v:
Frontiers in Immunology, Vol 10 (2020)
Frontiers in Immunology
Frontiers in Immunology
Allergic asthma is a chronic pulmonary disorder fundamentally linked to immune dysfunction. Since the immune system begins developing in utero, prenatal exposures can affect immune programming and increase risk for diseases such as allergic asthma. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44ced2d5ba8964907cd987003858ed6d
Problem Heightened maternal stress affects trophoblast function and increases risk for adverse pregnancy outcomes. Methods of Study Studies were performed using the first-trimester trophoblast cell line, Sw.71. Cytokines were quantified using qPCR an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26746a29d172378b86b4397d7120b473
https://europepmc.org/articles/PMC5833927/
https://europepmc.org/articles/PMC5833927/
Autor:
Nigel Paneth, Brooke L. Slawinski, Nicole M. Talge, Jean M. Kerver, Karen Racicot, Brooke Ingersoll, Arianna L. Smith, Alicynne Glazier
Publikováno v:
American Journal of Reproductive Immunology. 79:e12840
Problem Autism spectrum disorder (ASD) is one of the most commonly diagnosed neurodevelopmental disorders in the United States. While ASD can be significantly influenced by genetics, prenatal exposure to maternal infections has also been implicated i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::805ea4c3363d99250b8be216dea549ee
https://doi.org/10.1111/aji.12840
https://doi.org/10.1111/aji.12840
Autor:
Kate Fodor, Akira Kinoshita, Baoli Yang, Arianna L. Smith, Youssef A. Kousa, Brian C. Schutte
Publikováno v:
genesis. 55:e23038
Interferon Regulatory Factor 6 (IRF6) is a critical regulator of differentiation, proliferation and migration of keratinocytes. Mutations in IRF6 cause two autosomal dominant disorders characterized by cleft lip with or without cleft palate. In addit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ed2a73315960db46ac3efc8143b558a
https://doi.org/10.1002/dvg.23038
https://doi.org/10.1002/dvg.23038
Autor:
Peggi M. Angel, Britni Jacobs, Youssef A. Kousa, Richard M. Caprioli, Steven Goudy, Lawrence S. Prince, Veronica Mainini, Arianna L. Smith, Cynthia R. Hill, Brian C. Schutte, Scott Baldwin
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56270 (2013)
PLoS ONE
PLoS ONE
Interferon regulatory factor 6 (IRF6) encodes a highly conserved helix-turn-helix DNA binding protein and is a member of the interferon regulatory family of DNA transcription factors. Mutations in IRF6 lead to isolated and syndromic forms of cleft li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b34d7ad3e5d48638c748bff2656508c
https://doi.org/10.1371/journal.pone.0056270
https://doi.org/10.1371/journal.pone.0056270
Autor:
Steven Goudy, Peggi Angel, Britni Jacobs, Cynthia Hill, Veronica Mainini, Arianna L Smith, Youssef A Kousa, Richard Caprioli, Lawrence S Prince, Scott Baldwin, Brian C Schutte
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56270 (2013)
Interferon regulatory factor 6 (IRF6) encodes a highly conserved helix-turn-helix DNA binding protein and is a member of the interferon regulatory family of DNA transcription factors. Mutations in IRF6 lead to isolated and syndromic forms of cleft li
Externí odkaz:
https://doaj.org/article/c1d2ac7c32af420c8d9782a740c42130