Výsledky vyhledávání - "Na'ama Avitzur"

Perceptions of Genetic Testing: A Mixed-Methods Study of Patients with Pulmonary Fibrosis and Their First-Degree Relatives

Autor: Amanda Grant-Orser, Na’ama Avitzur, Julie Morisset, Charlene D. Fell, Kerri A. Johannson

Publikováno v: Annals of the American Thoracic Society. 19:1305-1312

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::870fce93a13cc454cf7d434b0b18b941
https://doi.org/10.1513/annalsats.202111-1300oc

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Relative environmental and social disadvantage in patients with idiopathic pulmonary fibrosis

Autor: Na'ama Avitzur, Elizabeth M Noth, Mubasiru Lamidi, Steven D Nathan, Harold R Collard, Alison M DeDent, Neeta Thakur, Kerri A Johannson

Publikováno v: Thorax. 77(12)

BackgroundAir pollution exposure is associated with disease severity, progression and mortality in patients with idiopathic pulmonary fibrosis (IPF). Combined impacts of environmental and socioeconomic factors on outcomes in patients with IPF are unk

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2fee7706fc3846d6cbf1ad8080e0cd0
https://pubmed.ncbi.nlm.nih.gov/34949724

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3D myocardial deformation analysis from cine MRI as a marker of amyloid protein burden in cardiac amyloidosis: validation versus T1 mapping

Autor: Yoko Mikami, Kelvin Chow, Reis Hansen, James A. White, Alessandro Satriano, Muhammad Sarim Afzal, Na’ama Avitzur, Nowell M. Fine, Jacqueline Flewitt, Gary Dobko, Carmen P Lydell, Andrew G Howarth, Mariam Narous

Publikováno v: The international journal of cardiovascular imaging. 34(12)

Cardiac amyloidosis (CA) is a significant contributor to heart failure with preserved ejection fraction and is appreciating expanding therapeutic options. Non-invasive tools aimed at accurate identification and surveillance of therapeutic response ar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7467b77e2aba7c40d81e428bbb7a893a
https://pubmed.ncbi.nlm.nih.gov/30014362

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Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

Autor: Adam, Shlien, Brittany B, Campbell, Richard, de Borja, Ludmil B, Alexandrov, Daniele, Merico, David, Wedge, Peter, Van Loo, Patrick S, Tarpey, Paul, Coupland, Sam, Behjati, Aaron, Pollett, Tatiana, Lipman, Abolfazl, Heidari, Shriya, Deshmukh, Na'ama, Avitzur, Bettina, Meier, Moritz, Gerstung, Ye, Hong, Diana M, Merino, Manasa, Ramakrishna, Marc, Remke, Roland, Arnold, Gagan B, Panigrahi, Neha P, Thakkar, Karl P, Hodel, Erin E, Henninger, A Yasemin, Göksenin, Doua, Bakry, George S, Charames, Harriet, Druker, Jordan, Lerner-Ellis, Matthew, Mistry, Rina, Dvir, Ronald, Grant, Ronit, Elhasid, Roula, Farah, Glenn P, Taylor, Paul C, Nathan, Sarah, Alexander, Shay, Ben-Shachar, Simon C, Ling, Steven, Gallinger, Shlomi, Constantini, Peter, Dirks, Annie, Huang, Stephen W, Scherer, Richard G, Grundy, Carol, Durno, Melyssa, Aronson, Anton, Gartner, M Stephen, Meyn, Michael D, Taylor, Zachary F, Pursell, Christopher E, Pearson, David, Malkin, P Andrew, Futreal, Michael R, Stratton, Eric, Bouffet, Cynthia, Hawkins, Peter J, Campbell, Uri, Tabori

Publikováno v: Nature Genetics. 47:257-262

DNA replication-associated mutations are repaired by two components: polymerase proofreading and mismatch repair. The mutation consequences of disruption to both repair components in humans are not well studied. We sequenced cancer genomes from child

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2872d9f4b6d4f6a48ba693ff41bee84f
https://doi.org/10.1038/ng.3202

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