Zobrazeno 1 - 10
of 197
pro vyhledávání: '"Mark A. Roth"'
Autor:
Daniel I. Sullivan, Mao Jiang, Angela M. Hinchie, Mark G. Roth, Harinath Bahudhanapati, Mehdi Nouraie, Jie Liu, John F. McDyer, Rama K. Mallampalli, Yingze Zhang, Daniel J. Kass, Toren Finkel, Jonathan K. Alder
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Cellular senescence due to telomere dysfunction has been hypothesized to play a role in age-associated diseases including idiopathic pulmonary fibrosis (IPF). It has been postulated that paracrine mediators originating from senescent alveolar epithel
Externí odkaz:
https://doaj.org/article/0cd55ce4a07c4a47bf85b736b8a2dc7f
Autor:
István Édes, Andrew S.P. Sharp, Neal G. Uren, Michael A Insko, János Tomcsányi, Shahzad Munir, Leong L. Ng, Ben Haber, Azfar Zaman, Keith M. Channon, Mario J. Garcia, Géza Lupkovics, Keith G. Oldroyd, David Adlam, John Irving, Piotr Musialek, Róbert Gábor Kiss, Hussain Contractor, Stephen Hill, Mark B. Roth, Simon Tulloch, Paweł Ptaszyński, P A Quinn, Lori Siegel, Cheerag Shirodaria, Joseph B. Selvanayagam, Maciej Zarębiński, Gergely Nagy, Joanna Szachniewicz
Publikováno v:
International Journal of Cardiology. 347:1-7
Background Ischemia-reperfusion injury remains a major clinical problem in patients with ST-elevation myocardial infarction (STEMI), leading to myocardial damage despite early reperfusion by primary percutaneous coronary intervention (PPCI). There ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc51fe3cc83f33c2c5e0dac1946ba39e
https://doi.org/10.1016/j.ijcard.2021.11.016
https://doi.org/10.1016/j.ijcard.2021.11.016
Autor:
Erica A. Siebrasse, Diana V. Pastrana, Nang L. Nguyen, Annie Wang, Mark J. Roth, Steven M. Holland, Alexandra F. Freeman, John McDyer, Christopher B. Buck, David Wang
Publikováno v:
Emerging Infectious Diseases, Vol 21, Iss 1, Pp 103-106 (2015)
We detected WU polyomavirus (WUPyV) in a bronchoalveolar lavage sample from lungs transplanted into a recipient with Job syndrome by using immunoassays specific for the WUPyV viral protein 1. Co-staining for an epithelial cell marker identified most
Externí odkaz:
https://doaj.org/article/a6640139372e43cd8a324ec876411243
Autor:
David M, Kwiatkowski, Molly K, Ball, Fabio J, Savorgnan, Catherine K, Allan, Joseph A, Dearani, Mark D, Roth, Rachel Z, Roth, Kristen S, Sexson, James S, Tweddell, Patricia K, Williams, Jill E, Zender, Victor Y, Levy
Publikováno v:
Pediatrics. 150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d806f22513cefc5428beb54d0fed43c2
https://doi.org/10.1542/peds.2022-056415d
https://doi.org/10.1542/peds.2022-056415d
Autor:
Jason N. Pitt, Eduardo Chavez, Kathryn M. Provencher, Michelle Chen, Christina Tran, Jennifer Tran, Karen Huang, Anuj Vaid, Marian L Abadir, Naheed Arang, Scott F. Leiser, Mark B. Roth, Matt Kaeberlein
Genetic activation of the hypoxia response robustly extends lifespan inC. elegans, while environmental hypoxia shows more limited benefit. Here we describe an intermittent hypoxia therapy (IHT) able to double the lifespan of wildtype worms. The lifes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bea23dfe18600b7c63a172ec482a52c
https://doi.org/10.1101/2022.10.13.512140
https://doi.org/10.1101/2022.10.13.512140
Autor:
Avi Z Rosenberg, Michael D Armani, Patricia A Fetsch, Liqiang Xi, Tina Thu Pham, Mark Raffeld, Yun Chen, Neil O'Flaherty, Rebecca Stussman, Adele R Blackler, Qiang Du, Jeffrey C Hanson, Mark J Roth, Armando C Filie, Michael H Roh, Michael R Emmert-Buck, Jason D Hipp, Michael A Tangrea
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0151775 (2016)
Precision medicine promises to enhance patient treatment through the use of emerging molecular technologies, including genomics, transcriptomics, and proteomics. However, current tools in surgical pathology lack the capability to efficiently isolate
Externí odkaz:
https://doaj.org/article/a5a3d2f27a6042f5bd9aff365f3ddd55
Autor:
Mark J. Roth, Gwen Murphy, Jin-Hu Fan, Christian C. Abnet, Shaoming Wang, Sanford M. Dawsey, Philip R. Taylor, You-Lin Qiao
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 28:2022-2029
Background: Autoimmune gastritis is understudied and possibly associated with gastric noncardia adenocarcinoma (GNCA) and esophageal squamous cell carcinoma (ESCC) in Western populations when it presents as pernicious anemia. Methods: A nested case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2800309fbcb9185c65a7c2e10c328606
https://doi.org/10.1158/1055-9965.epi-19-0512
https://doi.org/10.1158/1055-9965.epi-19-0512
Publikováno v:
Sensors, Vol 18, Iss 3, p 880 (2018)
Assessing climate-related ecological changes across spatiotemporal scales meaningful to resource managers is challenging because no one method reliably produces essential data at both fine and broad scales. We recently confronted such challenges whil
Externí odkaz:
https://doaj.org/article/8cd58dbcc3734af1a352dc390959e419
Autor:
Tanupriya Agrawal, Liqiang Xi, Winnifred Navarro, Mark Raffeld, Snehal B. Patel, Mark J. Roth, Joanna Klubo‐Gwiezdzinska, Armando C. Filie
Publikováno v:
Cytopathology : official journal of the British Society for Clinical CytologyREFERENCES. 33(3)
Molecular testing for genetic alterations in thyroid neoplasms, including BRAF V600E (BRAF) mutation, are often applied to thyroid aspirates falling into the Bethesda System for Reporting Thyroid Cytopathology indeterminate categories. Current method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90f06c80c69ff927cc6afbe27006440a
https://pubmed.ncbi.nlm.nih.gov/34957617
https://pubmed.ncbi.nlm.nih.gov/34957617
Autor:
Blythe Durbin-Johnson, Flora Tassone, Mark S. Roth, Diego Cadavid, Randi J Hagerman, Lucienne Ronco
Publikováno v:
Diagnostics (Basel, Switzerland), vol 11, iss 10
Diagnostics
Volume 11
Issue 10
Diagnostics, Vol 11, Iss 1780, p 1780 (2021)
Diagnostics
Volume 11
Issue 10
Diagnostics, Vol 11, Iss 1780, p 1780 (2021)
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability. FXS is an X-linked, neurodevelopmental disorder caused by a CGG trinucleotide repeat expansion in the 5′ untranslated region (UTR) of the Fragile X Mental Retard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3b663ff81bd04ee89d6612a93656fcf
https://escholarship.org/uc/item/2jw4n34p
https://escholarship.org/uc/item/2jw4n34p