Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Neil Miller"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101753- (2024)
Externí odkaz:
https://doaj.org/article/ed86e929edbc40a390de6c328ddc16b7
Autor:
Damla Senol Cali, Thomas Anantharaman, Martin Muggli, Samer Al-Saffar, Charles Schoonover, Neil Miller
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101761- (2024)
Externí odkaz:
https://doaj.org/article/ffa627455b6a43bd86a7289da187b148
Autor:
Daniel Saul, Sam Dougaparsad, Megan Roytman, Westley Sherman, Soheil Shams, Shalini Verma, Neil Miller
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100597- (2023)
Externí odkaz:
https://doaj.org/article/bd6b9eb4251b42c296c01161be050ade
Autor:
Jennifer Crow, Glenson Samuel, Emily Farrow, Margaret Gibson, Jefferey Johnston, Erin Guest, Neil Miller, Dong Pei, Devin Koestler, Harsh Pathak, Xiaobo Liang, Cooper Mangels, Andrew K Godwin
Publikováno v:
Biomarker Insights, Vol 17 (2022)
Objective: Ewing Sarcoma Family of Tumors (ESFT) are a highly aggressive pediatric bone and soft tissue malignancy with poor outcomes in the refractory and recurrent setting. Over 90% of Ewing Sarcoma (ES) tumors are driven by the pathognomonic EWS-E
Externí odkaz:
https://doaj.org/article/39a4540fb45c44d9b9dd3f9070920ef8
Publikováno v:
Cancer Reports, Vol 5, Iss 10, Pp n/a-n/a (2022)
Abstract Background In malignancy, eosinophils have been shown to play an important role in the tumour micro‐environment. Increasingly, development of eosinophilia with immune checkpoint inhibitor (ICI) use is thought to be predictive of prognosis
Externí odkaz:
https://doaj.org/article/3f76d5676bfc4c358730d5adfe2f3e2a
Autor:
Chen-Shan Chin, Justin Wagner, Qiandong Zeng, Erik Garrison, Shilpa Garg, Arkarachai Fungtammasan, Mikko Rautiainen, Sergey Aganezov, Melanie Kirsche, Samantha Zarate, Michael C. Schatz, Chunlin Xiao, William J. Rowell, Charles Markello, Jesse Farek, Fritz J. Sedlazeck, Vikas Bansal, Byunggil Yoo, Neil Miller, Xin Zhou, Andrew Carroll, Alvaro Martinez Barrio, Marc Salit, Tobias Marschall, Alexander T. Dilthey, Justin M. Zook
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Accurate, phased assemblies are a key tool in understanding the human genome, particularly in highly polymorphic regions like the medically important MHC. Here the authors provide an assembly-based benchmark for this difficult-to-characterize region.
Externí odkaz:
https://doaj.org/article/5e9e6d5734354b4a86ef752be8c0d26e
Autor:
Carla Dippenaar, Hitoshi Shimbo, Kazunobu Okon, Neil Miller, Elizabeth Joubert, Tadashi Yoshida, Dalene de Beer
Publikováno v:
Separations, Vol 9, Iss 10, p 278 (2022)
Anti-allergic activity was previously demonstrated for extracts of Cyclopia subternata Vogel plant material, containing substantial amounts of xanthones, benzophenones, dihydrochalcones, flavanones and flavones. Fractionation of a hot water extract o
Externí odkaz:
https://doaj.org/article/76dda8ca24474c1584aca277777b94d6
Publikováno v:
Journal of Functional Foods, Vol 48, Iss , Pp 400-409 (2018)
Limiting aspalathin degradation during spray-drying of green rooibos extract (GRE) is crucial to produce a functional food ingredient with antidiabetic properties. Retention of aspalathin in a GRE-inulin mixture (1:1, m/m) was not affected by process
Externí odkaz:
https://doaj.org/article/2b67531a3c3b4931b3107b6f84336076
Autor:
Maxime Cadieux-Dion, Nicole P. Safina, Kendra Engleman, Carol Saunders, Elena Repnikova, Nikita Raje, Kristi Canty, Emily Farrow, Neil Miller, Lee Zellmer, Isabelle Thiffault
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Ectodermal dysplasias (ED) are a group of diseases that affects the development or function of the teeth, hair, nails and exocrine and sebaceous glands. One type of ED, ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
Externí odkaz:
https://doaj.org/article/b2506092c6044442b77579414d9b560b
Autor:
Isabelle Thiffault, Britton Zuccarelli, Holly Welsh, Xuan Yuan, Emily Farrow, Lee Zellmer, Neil Miller, Sarah Soden, Ahmed Abdelmoity, Robert A. Brodsky, Carol Saunders
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
Abstract Background Defects in the human glycosylphosphatidylinositol anchor biosynthetic pathway are associated with inherited glycosylphosphatidylinositol (GPI)-deficiencies characterized by a broad range of clinical phenotypes including multiple c
Externí odkaz:
https://doaj.org/article/62e2ea1ee7c143b8a7a53e166b7fbad7