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Comparison of the McGrath® MAC video laryngoscope with direct Macintosh laryngoscopy for novice laryngoscopists in children without difficult intubation: A randomized controlled trialGiraudon, Antoine ; Bordes-Demolis, Maryline ; Blondeau, Barbara ; Sibai de Panthou, Nadia ; Ferrand, Nathan ; Bello, Maeva ; Dahlet, Victoria ; Semjen, François ; Biais, Matthieu ; Nouette-Gaulain, KarineAnaesthesia critical care & pain medicine, 2017-10, Vol.36 (5), p.261-265 [Periódico revisado por pares]France: Elsevier Masson SASTexto completo disponível |
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Obstetrical analgesiaDahl, VegardTidsskrift for den Norske Lægeforening, 2002-06, Vol.122 (17), p.1688-1690 [Periódico revisado por pares]NorwayTexto completo disponível |
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Material Type: Artigo
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Hypertension and insulin resistant models have divergent propensities to learned helpless behavior in rodentsEdwards, Emmeline ; King, Jean A ; Fray, JohnAmerican journal of hypertension, 2000-06, Vol.13 (6), p.659-665 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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Successful treatment of dihydropteridine reductase deficiency, with an interesting effect of 5‐hydroxytryptophan deficiency on sleep patternsLipson, A. H. ; Earl, J. W. ; Wilcken, B. ; Yu, J. S. ; O'Halloran, M. ; Cotton, R. G. H.Journal of inherited metabolic disease, 1991-01, Vol.14 (1), p.49-52 [Periódico revisado por pares]Dordrecht: Kluwer Academic PublishersTexto completo disponível |
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Loss of DNA methylation disrupts syncytiotrophoblast development: Proposed consequences of aberrant germline gene activationLea, Georgia ; Hanna, Courtney W.BioEssays, 2024-01, Vol.46 (1), p.e2300140-n/a [Periódico revisado por pares]United States: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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Mechanisms and function of de novo DNA methylation in placental development reveals an essential role for DNMT3BAndrews, Simon ; Krueger, Christel ; Mellado-Lopez, Maravillas ; Hemberger, Myriam ; Dean, Wendy ; Perez-Garcia, Vicente ; Hanna, Courtney WNature communications, 2023-01, Vol.14 (1), p.371-371, Article 371 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Repression of germline genes by PRC1.6 and SETDB1 in the early embryo precedes DNA methylation-mediated silencingMochizuki, Kentaro ; Sharif, Jafar ; Shirane, Kenjiro ; Uranishi, Kousuke ; Bogutz, Aaron B ; Janssen, Sanne M ; Suzuki, Ayumu ; Okuda, Akihiko ; Koseki, Haruhiko ; Lorincz, Matthew CNature communications, 2021-12, Vol.12 (1), p.7020-7020, Article 7020 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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A comparative methylome analysis reveals conservation and divergence of DNA methylation patterns and functions in vertebratesAl Adhami, Hala ; Bardet, Anaïs Flore ; Dumas, Michael ; Cleroux, Elouan ; Guibert, Sylvain ; Fauque, Patricia ; Acloque, Hervé ; Weber, MichaelBMC biology, 2022-03, Vol.20 (1), p.70-70, Article 70 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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Material Type: Artigo
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Soluble fms-like tyrosine kinase 1 promotes angiotensin II sensitivity in preeclampsiaBurke, Suzanne D ; Zsengellér, Zsuzsanna K ; Khankin, Eliyahu V ; Lo, Agnes S ; Rajakumar, Augustine ; DuPont, Jennifer J ; McCurley, Amy ; Moss, Mary E ; Zhang, Dongsheng ; Clark, Christopher D ; Wang, Alice ; Seely, Ellen W ; Kang, Peter M ; Stillman, Isaac E ; Jaffe, Iris Z ; Karumanchi, S AnanthThe Journal of clinical investigation, 2016-07, Vol.126 (7), p.2561-2574 [Periódico revisado por pares]United States: American Society for Clinical InvestigationTexto completo disponível |
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Material Type: Artigo
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SLC13A5 is the second gene associated with Kohlschütter–Tönz syndromeSchossig, Anna ; Bloch-Zupan, Agnès ; Lussi, Adrian ; Wolf, Nicole I ; Raskin, Salmo ; Cohen, Monika ; Giuliano, Fabienne ; Jurgens, Julie ; Krabichler, Birgit ; Koolen, David A ; de Macena Sobreira, Nara Lygia ; Maurer, Elisabeth ; Muller-Bolla, Michèle ; Penzien, Johann ; Zschocke, Johannes ; Kapferer-Seebacher, InesJournal of medical genetics, 2017-01, Vol.54 (1), p.54-62 [Periódico revisado por pares]England: BMJ Publishing Group LTDTexto completo disponível |