Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ashley E Siegel"'
Autor:
Pratik Koirala, PhD, Ziyu Chen, MD, PhD, Mengfan Wu, MD, Samerender Nagam Hunamantharao, PhD, Ashley E. Siegel, MD, David Maridas, PhD, Vicki Rosen, PhD, Shailesh Agarwal, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss S4, Pp 3-3 (2024)
Externí odkaz:
https://doaj.org/article/9e1d26e08afe4330a240b0bf1d90384e
Autor:
Millie A Ferrés, Diana W Bianchi, Ashley E Siegel, Roderick T Bronson, Gordon S Huggins, Faycal Guedj
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0168009 (2016)
The Ts1Cje model of Down syndrome is of particular interest for perinatal studies because affected males are fertile. This permits affected pups to be carried in wild-type females, which is similar to human pregnancies. Here we describe the early nat
Externí odkaz:
https://doaj.org/article/e7453e6f014f4bdeb403b72d32197a98
Publikováno v:
Case Reports in Plastic Surgery & Hand Surgery
Here, we describe single case review of a 14-year-old female who presented with an angiofibroma on the right nipple areolar complex, which was treated successfully with debulking and CO2 laser. After 8 months of follow up, there has still been no rec
Autor:
Fatimah Alsebaa, Lauren J. Massingham, Diana W. Bianchi, Umadevi Tantravahi, Faycal Guedj, Ashley E Siegel, Jeroen L. A. Pennings
Publikováno v:
Am J Hum Genet
Human fetuses with trisomy 21 (T21) have atypical brain development that is apparent sonographically in the second trimester. Prenatal diagnosis provides a potential opportunity to begin treatment in utero. We hypothesize that by analyzing and integr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f13b5dfd471e00118483e488182fba9d
http://hdl.handle.net/10029/624466
http://hdl.handle.net/10029/624466
Humans with Down syndrome (DS) exhibit hippocampal learning deficits in the Cambridge Neuropsychological Test Automated Battery (CANTAB). Here we translated the CANTAB Visual Discrimination (VD) and Extinction tasks to investigate hippocampal learnin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d11e56e75023207f35268292ff35a84
https://doi.org/10.1101/2020.07.21.214106
https://doi.org/10.1101/2020.07.21.214106
Publikováno v:
Cureus
It has been well documented that female sex is a significant risk factor for the development of various autoimmune diseases. While the reason for this has been debated, one well-regarded theory is that increased estrogen and decreased testosterone pl
Autor:
Diana W. Bianchi, Ashley E Siegel, Nadine M. Aziz, Faycal Guedj, Jeroen L. A. Pennings, Jose Luis Olmos-Serrano, Tarik F. Haydar
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 11, Iss 6 (2018)
Disease Models & Mechanisms, Vol 11, Iss 6 (2018)
Down syndrome (DS) results from triplication of human chromosome 21. Neuropathological hallmarks of DS include atypical central nervous system development that manifests prenatally and extends throughout life. As a result, individuals with DS exhibit
Autor:
Diana W. Bianchi, Umadevi Tantravahi, Lauren J. Massingham, Ashley E. Siegel, Heather C. Wick, Faycal Guedj, Jeroen L. A. Pennings
Publikováno v:
Scientific Reports
Anatomical and functional brain abnormalities begin during fetal life in Down syndrome (DS). We hypothesize that novel prenatal treatments can be identified by targeting signaling pathways that are consistently perturbed in cell types/tissues obtaine
Autor:
Faycal Guedj, Diana W. Bianchi, Roderick T. Bronson, Ashley E. Siegel, Millie A. Ferres, Gordon S. Huggins
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 12, p e0168009 (2016)
PLoS ONE, Vol 11, Iss 12, p e0168009 (2016)
Background The Ts1Cje model of Down syndrome is of particular interest for perinatal studies because affected males are fertile. This permits affected pups to be carried in wild-type females, which is similar to human pregnancies. Here we describe th
Autor:
Harrison, Andrea1
Publikováno v:
ILSA Journal of International & Comparative Law. Summer2018, Vol. 24 Issue 3, p647-687. 41p.