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1541por Peebles, Karen C., Tan, Isabella, Butlin, Mark, Collins, Felicity, Tofts, Louise, Avolio, Alberto P., Pacey, Verity“…Orthostatic intolerance (OI) is frequently reported in young women with generalized hypermobility spectrum disorder (G‐HSD) and hypermobile EDS (hEDS). …”
Publicado 2022
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1542“…OI-exo-delivered hierarchical mesoporous bioactive glass (MBG) scaffold effectively promote in vivo bone formation in aging rat cranial defect model. …”
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1543por Lapointe, Andrew P., Ware, Ashley L., Duszynski, Chris C., Stang, Antonia, Yeates, Keith Owen, Dunn, Jeff F.“…This novel pilot study examined differences in cerebral hemodynamics, as measured using functional near-infrared spectroscopy (fNIRS), and its association with diffusion tensor imaging (DTI) metrics in children with mTBI or mild orthopedic injury (OI) to address these gaps. Children 8.00–16.99 years of age with mTBI (n = 9) or OI (n = 6) were recruited in a pediatric emergency department, where acute injury characteristics were assessed. …”
Publicado 2023
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1544“…Osteogenesis imperfecta (OI) is a disease caused by mutations in different genes resulting in mild, severe, or lethal forms. …”
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1545“…Herein, we fused induced pluripotent stem cell-derived endothelial cell (iEC) membrane together with M1 type macrophage membrane to construct a hybrid membrane (iEC-M) camouflaged 4OI nanovesicles (4OI@iEC-M). Furthermore, bioinspired nanovesicles 4OI@iEC-M are incorporated into the injectable, multifunctional gelatin methacryloyl hydrogels for diabetic wound repair and regeneration. …”
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1546“…Early embryonic loss was 6.7% points lower for cows inseminated at a stronger OI (OI = 3) compared to at a weaker OI (OI = 2, P = 0.006). …”
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1547por Schäfer, Guido, Hoffmann, Christian, Arasteh, Keikawus, Schürmann, Dirk, Stephan, Christoph, Jensen, Björn, Stoll, Matthias, Bogner, Johannes R., Faetkenheuer, Gerd, Rockstroh, Jürgen, Klinker, Hartwig, Härter, Georg, Stöhr, Albrecht, Degen, Olaf, Freiwald, Eric, Hüfner, Anja, Jordan, Sabine, Schulze zur Wiesch, Julian, Addo, Marylyn, Lohse, Ansgar W., van Lunzen, Jan, Schmiedel, Stefan“…Patients were randomized into an immediate therapy arm (starting antiretroviral therapy (ART) within 7 days after initiation of OI treatment) versus a deferred arm (starting ART after completing the OI-therapy). …”
Publicado 2019
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1548por He, Ruyuan, Liu, Bohao, Xiong, Rui, Geng, Boxin, Meng, Heng, Lin, Weichen, Hao, Bo, Zhang, Lin, Wang, Wei, Jiang, Wenyang, Li, Ning, Geng, Qing“…The silence of Nrf2 abolished the inhibition of ferroptosis from 4-OI in THP-1 cells. Additionally, the protection of 4-OI for ALI was abolished in Nrf2-knockout mice. …”
Publicado 2022
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1549por Sohail, Aaqib, Iqbal, Azeem A., Sahini, Nishika, Chen, Fangfang, Tantawy, Mohamed, Waqas, Syed F.H., Winterhoff, Moritz, Ebensen, Thomas, Schultz, Kristin, Geffers, Robert, Schughart, Klaus, Preusse, Matthias, Shehata, Mahmoud, Bähre, Heike, Pils, Marina C., Guzman, Carlos A., Mostafa, Ahmed, Pleschka, Stephan, Falk, Christine, Michelucci, Alessandro, Pessler, Frank“…We evaluated effects of endogenous itaconate and exogenous application of itaconate and its variants dimethyl- and 4-octyl-itaconate (DI, 4OI) on host responses to influenza A virus (IAV). …”
Publicado 2022
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1550por Duran, Ivan, Zieba, Jennifer, Csukasi, Fabiana, Martin, Jorge H., Wachtell, Davis, Barad, Maya, Dawson, Brian, Fafilek, Bohumil, Jacobsen, Christina M., Ambrose, Catherine G., Cohn, Daniel H., Krejci, Pavel, Lee, Brendan H., Krakow, Deborah“…Osteogenesis imperfecta (OI) is a genetically heterogenous disorder most often due to heterozygosity for mutations in the type I procollagen genes, COL1A1 or COL1A2. …”
Publicado 2022
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1551por Rosca, Ovidiu, Bumbu, Bogdan Andrei, Ancusa, Oana, Talpos, Serban, Urechescu, Horatiu, Ursoniu, Sorin, Bloanca, Vlad, Pricop, Marius“…Background and Objectives: Odontogenic infections (OI) represent a frequent cause of dental and maxillo-facial interventions, mostly due to late presentations or misdiagnosed complications. …”
Publicado 2022
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1552por Chen, Peikai, Tan, Zhijia, Qiu, Anmei, Yin, Shijie, Zhou, Yapeng, Dong, Zhongxin, Qiu, Yan, Xu, Jichun, Li, Kangsen, Dong, Lina, Shek, Hiu Tung, Liu, Jingwen, Yeung, Eric H. K., Gao, Bo, Cheung, Kenneth Man Chee, To, Michael Kai-Tsun“…BACKGROUND: Osteogenesis imperfecta (OI) is a rare congenital disorder of the skeletal system, inflicting debilitating physical and psychological distress on patients and caregivers. …”
Publicado 2022
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1553por Kodama, Yoshihiko, Meiri, Satoru, Asada, Tomoko, Matsuyama, Misayo, Makino, Shinya, Iwai, Minayo, Yamaguchi, Masatoshi, Moritake, Hiroshi“…Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by brittle bones. …”
Publicado 2023
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1554“…Osteogenesis imperfecta (OI) is generally caused by a dominant mutation in Collagen I, encoded by the genes COL1A1 and COL1A2. …”
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1555“…Both heterotopic pregnancy and spontaneous twinning are frequent after OI, this combination although extremely rare must be kept in mind. …”
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1556por Monti, Elena, Mottes, Monica, Fraschini, Paolo, Brunelli, PierCarlo, Forlino, Antonella, Venturi, Giacomo, Doro, Francesco, Perlini, Silvia, Cavarzere, Paolo, Antoniazzi, Franco“…Osteogenesis imperfecta (OI) is the most common bone genetic disorder and it is characterized by bone brittleness and various degrees of growth disorder. …”
Publicado 2010
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1557“…One monoester ligand in Ti(2)(OiPr)(6)(μ(2)-OOC-C(6)H(4)-COOiPr)(η(1)-OOC-C(6)H(4)-COOiPr)(iPrOH) is bridging and the other is η(1)-coordinated. …”
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1558“…Osteogenesis imperfecta (OI) is a heterogeneous disorder of connective tissue that manifests mainly as skeletal deformity and bone fragility. …”
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1559“…[Results] There were significant differences in items in the SFT, except for the respiratory item, between the OI group and the NOI group. There were significant differences in all items on the SWAL-QOL, except for the sleep item, between the OI group and the NOI group. …”
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1560por Sa-ngasoongsong, Paphon, Saisongcroh, Tanyawat, Angsanuntsukh, Chanika, Woratanarat, Patarawan, Mulpruek, Pornchai“…Osteogenesis imperfecta (OI) is a rare inherited connective tissue disorder caused by mutation of collagen which results in a wide spectrum of clinical manifestations including long bone fragility fractures and deformities. …”
Publicado 2017
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