Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Michael S Chung"'
Publikováno v:
Open Biology, Vol 10, Iss 9 (2020)
Prader-Willi syndrome (PWS) is caused by the loss of function of the paternally inherited 15q11-q13 locus. This region is governed by genomic imprinting, a phenomenon in which genes are expressed exclusively from one parental allele. The genomic impr
Externí odkaz:
https://doaj.org/article/8f60d06192414a5ab3ae32c3b55eb6ee
Autor:
Jeffrey P. Kanne, Constantine A. Raptis, Travis S. Henry, Christopher M. Walker, Peter D. Filev, Michael S Chung, Kaitlin M Marquis, Fernando Uliana Kay, Subba R. Digumarthy, Seth Kligerman, Alan M Ropp, Jonathan H. Chung, Kristen Pope, Tan-Lucien H. Mohammed, Daniel Vargas, Jacob W. Sechrist
Publikováno v:
Chest. 160:1492-1511
Background e-Cigarette or vaping-induced lung injury (EVALI) causes a spectrum of CT lung injury patterns. Relative frequencies and associations with vaping behavior are unknown. Research Question What are the frequencies of imaging findings and CT p
Autor:
Dea Gorka, Noelle D. Germain, Clémence M Dupont-Thibert, Stormy J. Chamberlain, Michael S Chung, Christopher E Stoddard, Marc Lalande, Leann Crandall, Heather Glatt-Deeley, Justin Cotney, Maéva Langouët, Clarisse Orniacki
Publikováno v:
Hum Mol Genet
Prader-Willi syndrome (PWS) is characterized by neonatal hypotonia, developmental delay, and hyperphagia/obesity. This disorder is caused by the absence of paternally-expressed gene products from chromosome 15q11-q13. We previously demonstrated that
Autor:
Michael S Chung, William E Gioia, Yong Wang, David F. Yankelevitz, Artit C. Jirapatnakul, Yeqing Zhu, Rowena Yip, Claudia I. Henschke
Publikováno v:
European Radiology. 30:2658-2668
To evaluate risk factors for prevalence and progression of aortic valve calcification (AVC) in lung cancer screening participants and also to assess the sensitivity and reliability of visual AVCs on low-dose CT (LDCT) for predicting aortic stenosis (
Autor:
Scott R. Kennedy, Alan J. Herr, Thu H. B. Tran, Ian T. Dowsett, Mitchell B. Lee, Niloufar Ghodsian, Anh B. Diep, Michael G. Kiflezghi, Michael S. Chung, Daniel T. Carr, Katherine A. Grayden, Anna Bode, Thao T Tang, Priya A. Uppal, Daniel E. L. Promislow, Ngoc Han Tran, Brian M. Wasko, Sarah G. Stanton, Yordanos C. Elala, Michael Hope, Matt Kaeberlein
Publikováno v:
Proceedings of the National Academy of Sciences. 116:3062-3071
Mutations accumulate within somatic cells and have been proposed to contribute to aging. It is unclear what level of mutation burden may be required to consistently reduce cellular lifespan. Human cancers driven by a mutator phenotype represent an in
Autor:
Aditi Mathur, Adam Bernheim, Michael S. Chung, Sakshi Dua, Maria L. Padilla, Mary Beth Beasley, Antonios Charokopos
Publikováno v:
American journal of respiratory and critical care medicine. 203(4)
Autor:
Seulah Choi, Danielle Toussie, Adam Jacobi, Jun Yeop Lee, Adam Bernheim, Corey Eber, Ariana Mills, Jennifer M. Watchmaker, Mark Finkelstein, Daryl Goldman, Michael S. Chung, Alex Sher, Robert A. Lookstein
Publikováno v:
Academic Emergency Medicine
Early detection of acute pulmonary embolism (PE) in patients with SARS‐CoV‐2 infection is integral to the clinical management of these patients. Many recently published studies have evaluated incidence of PE in hospitalized patients with COVID‐
Publikováno v:
Open Biology
Open Biology, Vol 10, Iss 9 (2020)
Open Biology, Vol 10, Iss 9 (2020)
Prader-Willi syndrome (PWS) is caused by the loss of function of the paternally inherited 15q11-q13 locus. This region is governed by genomic imprinting, a phenomenon in which genes are expressed exclusively from one parental allele. The genomic impr
Autor:
Maéva Langouët, Michael S. Chung, Christopher E Stoddard, Erin Banda, Marc Lalande, Leann Crandall, Heather Glatt-Deeley, Elodie Mathieux, Clémence M Dupont-Thibert
Publikováno v:
Human Molecular Genetics. 27:505-515
Prader-Willi syndrome (PWS) is characterized by neonatal hypotonia, developmental delay and hyperphagia/obesity and is caused by the absence of paternal contribution to chromosome 15q11-q13. Using induced pluripotent stem cell (iPSC) models of PWS, w
Autor:
Zahi A. Fayad, Mark Finkelstein, Mario A. Cedillo, Adam Jacobi, Danielle Toussie, Adam Bernheim, Young Joon Kwon, Benjamin S. Glicksberg, Anthony Costa, Nicholas Voutsinas, Samuel Z. Maron, Yogesh Sean Gupta, Eric K. Oermann, Corey Eber, Michael S. Chung, Sayan Manna
Publikováno v:
Radiology. Artificial Intelligence
“Just Accepted” papers have undergone full peer review and have been accepted for publication in Radiology: Artificial Intelligence. This article will undergo copyediting, layout, and proof review before it is published in its final version. Plea