Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Emily Curl"'
Autor:
Hanna Pulaski, Shraddha S Mehta, Laryssa C Manigat, Stephanie Kaufman, Hypatia Hou, ILKe Nalbantoglu, Xuchen Zhang, Emily Curl, Ross Taliano, Tae Hun Kim, Michael Torbenson, Jonathan N Glickman, Murray B Resnick, Neel Patel, Cristin E Taylor, Pierre Bedossa, Michael C Montalto, Andrew H Beck, Katy E Wack
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 10, Iss 5, Pp n/a-n/a (2024)
Abstract The gold standard for enrollment and endpoint assessment in metabolic dysfunction‐associated steatosis clinical trials is histologic assessment of a liver biopsy performed on glass slides. However, obtaining the evaluations from several ex
Externí odkaz:
https://doaj.org/article/eb1dc91a8f284aa1a624e1e8e3395dbb
Autor:
Brenda J. Hoffman, Victoria J. Findlay, Ernest Ramsay Camp, Emily Curl, Yun Zhu, Cynthia Timmers, Cindy Wang, Elizabeth G. Hill, Graham W. Warren, Ashley W. Cross, Scott A. Becker, David N. Lewin, Harinarayanan Janakiraman
Publikováno v:
International journal of cancerReferences. 147(5)
Progress in rectal cancer therapy has been hindered by the lack of effective disease-specific preclinical models that account for the unique molecular profile and biology of rectal cancer. Thus, we developed complementary patient-derived xenograft (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe84448313ab6dd26d201297ba71d9c6
https://pubmed.ncbi.nlm.nih.gov/31989583
https://pubmed.ncbi.nlm.nih.gov/31989583
Autor:
Ellen C. Riemer, Emily Curl
Publikováno v:
European Heart Journal: Case Reports
Background Caseous calcification of the mitral annulus (CCMA) is a very rare variant of mitral annular calcification, which is typically asymptomatic but can manifest as a cardiac tumour, abscess, or in the form of mitral valve dysfunction. Case summ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb832eb2a80b82f842ef4a114c743b1e
https://doi.org/10.1093/ehjcr/yty124
https://doi.org/10.1093/ehjcr/yty124
Publikováno v:
Blood. 132:5031-5031
Background: Von Willebrand disease (vWD) is the most common inherited bleeding disorder worldwide. Genetic mutations in the von Willebrand gene may result in either quantitative (Types 1 and 3 vWD) or qualitative defects (Type 2 vWD) of von Willebran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c0ede33b040b0cc245e10d0d6c86629
https://doi.org/10.1182/blood-2018-99-112976
https://doi.org/10.1182/blood-2018-99-112976