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Item type:Publication, Thymectomy for non-thymomatous myasthenia gravis(2013) ;Gabriel Cea ;Michael Benatar ;Renato J VerdugoRodrigo A Salinas2Scopus© Citations 45 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Editorial: Free Fatty Acids as Signaling Molecules: Role of Free Fatty Acid Receptors and CD36(2022) ;Carlos Puebla ;Eugenia Morselli ;Naim Akhtar KhanScopus© Citations 6 1 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Exome Sequencing Identifies Genetic Variants Associated with Extreme Manifestations of the Cardiovascular Phenotype in Marfan Syndrome(2022) ;Yanireth Jimenez ;Cesar Paulsen ;Eduardo Turner ;Sebastian IturraOscar Cuevas<jats:p>Marfan Syndrome (MFS) is an autosomal dominant condition caused by variants in the fibrillin-1 (FBN1) gene. Cardinal features of MFS include ectopia lentis (EL), musculoskeletal features and aortic root aneurysm and dissection. Although dissection of the ascending aorta is the main cause of mortality in MFS, the clinical course differs considerably in age of onset and severity, even among individuals who share the same causative variant, suggesting the existence of additional genetic variants that modify the severity of the cardiovascular phenotype in MFS. We recruited MFS patients and classified them into severe (n = 8) or mild aortic phenotype (n = 14) according to age of presentation of the first aorta-related incident. We used Exome Sequencing to identify the genetic variants associated with the severity of aortic manifestations and we performed linkage analysis where suitable. We found five genes associated with severe aortic phenotype and three genes that could be protective for this phenotype in MFS. These genes regulate components of the extracellular matrix, TGFβ pathway and other signaling pathways that are involved in the maintenance of the ECM or angiogenesis. Further studies will be required to understand the functional effect of these variants and explore novel, personalized risk management and, potentially, therapies for these patients.</jats:p>37Scopus© Citations 4 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Receptors involved in dexketoprofen analgesia in murine visceral pain(2020) ;V Noriega ;F Sierralta ;P Poblete ;N ArandaR Sotomayor-Zárate52Scopus© Citations 2 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Lineage-specific events underlie aortic root aneurysm pathogenesis in Loeys-Dietz syndrome(2019) ;Elena Gallo MacFarlane ;Sarah J. Parker ;Joseph Y. Shin ;Shira G. ZieglerTyler J. CreamerScopus© Citations 91 1 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Multiplexed (18-Plex) Measurement of Signaling Targets and Cytotoxic T Cells in Trastuzumab-Treated Patients using Imaging Mass Cytometry(2019); ;Jonathan Patsenker ;Kelly P. Stanton ;Franz Villarroel-EspindolaAmanda Esch<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Purpose:</jats:title> <jats:p>Imaging mass cytometry (IMC) uses metal-conjugated antibodies to provide multidimensional, objective measurement of protein targets. We used this high-throughput platform to perform an 18-plex assessment of HER2 ICD/ECD, cytotoxic T-cell infiltration and other structural and signaling proteins in a cohort of patients treated with trastuzumab to discover associations with trastuzumab benefit.</jats:p> </jats:sec> <jats:sec> <jats:title>Experimental Design:</jats:title> <jats:p>An antibody panel for detection of 18 targets (pan-cytokeratin, HER2 ICD, HER2 ECD, CD8, vimentin, cytokeratin 7, β-catenin, HER3, MET, EGFR, ERK 1–2, MEK 1–2, PTEN, PI3K p110 α, Akt, mTOR, Ki67, and Histone H3) was used with a selection of trastuzumab-treated patients from the Hellenic Cooperative Oncology Group 10/05 trial (n = 180), and identified a case–control series.</jats:p> </jats:sec> <jats:sec> <jats:title>Results:</jats:title> <jats:p>Patients that recurred after adjuvant treatment with trastuzumab trended toward a decreased fraction of HER2 ECD pixels over threshold compared with cases without recurrence (P = 0.057). After exclusion of the lowest HER2 expressers, 5-year recurrence events were associated with reduced total extracellular domain (ECD)/intracellular domain (ICD) ratio intensity in tumor (P = 0.044). These observations are consistent with our previous work using quantitative immunofluorescence, but represent the proof on identical cell content. We also describe the association of the ECD of HER2 with CD8 T-cell infiltration on the same slide.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions:</jats:title> <jats:p>The proximity of CD8 cells as a function of the expression of the ECD of HER2 provides further evidence for the role of the immune system in the mechanism of action of trastuzumab.</jats:p> </jats:sec>14Scopus© Citations 45 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Epithelial HMGB1 Delays Skin Wound Healing and Drives Tumor Initiation by Priming Neutrophils for NET Formation(2019) ;Esther Hoste ;Christian Maueröder ;Lisette van Hove ;Leen CatrysseHanna-Kaisa Vikkula17Scopus© Citations 66