检索结果 - Boland, Anne

Role of YopP in Suppression of Tumor Necrosis Factor Alpha Release by Macrophages during Yersinia Infection 由 Boland, Anne, Cornelis, Guy R.

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Quantitative Microbial Risk Assessment Models for Consumption of Raw Vegetables Irrigated with Reclaimed Water 由 Hamilton, Andrew J., Stagnitti, Frank, Premier, Robert, Boland, Anne-Maree, Hale, Glenn

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A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency 由 Nicolino, Marc, Claiborn, Kathryn C., Senée, Valérie, Boland, Anne, Stoffers, Doris A., Julier, Cécile

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The Virulence Plasmid of Yersinia, an Antihost Genome 由 Cornelis, Guy R., Boland, Anne, Boyd, Aoife P., Geuijen, Cecile, Iriarte, Maite, Neyt, Cécile, Sory, Marie-Paule, Stainier, Isabelle

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Yersinia enterocolitica induces apoptosis in macrophages by a process requiring functional type III secretion and translocation mechanisms and involving YopP, presumably acting a... 由 Mills, Scott D., Boland, Anne, Sory, Marie-Paule, van der Smissen, Patrick, Kerbourch, Corinne, Finlay, B. Brett, Cornelis, Guy R.

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A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection 由 Pedergnana, Vincent, Gessain, Antoine, Tortevoye, Patricia, Byun, Minji, Bacq-Daian, Delphine, Boland, Anne, Casanova, Jean-Laurent, Abel, Laurent, Plancoulaine, Sabine

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The Impact of Genetic Variations in ADORA2A in the Association between Caffeine Consumption and Sleep 由 Erblang, Mégane, Drogou, Catherine, Gomez-Merino, Danielle, Metlaine, Arnaud, Boland, Anne, Deleuze, Jean François, Thomas, Claire, Sauvet, Fabien, Chennaoui, Mounir

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A Novel Alpha Cardiac Actin (ACTC1) Mutation Mapping to a Domain in Close Contact with Myosin Heavy Chain Leads to a Variety of Congenital Heart Defects, Arrhythmia and Possibly Mi... 由 Augière, Céline, Mégy, Simon, El Malti, Rajae, Boland, Anne, El Zein, Loubna, Verrier, Bernard, Mégarbané, André, Deleuze, Jean-François, Bouvagnet, Patrice

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A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families 由 Veyssiere, Maëva, Perea, Javier, Michou, Laetitia, Boland, Anne, Caloustian, Christophe, Olaso, Robert, Deleuze, Jean-François, Cornelis, François, Petit-Teixeira, Elisabeth, Chaudru, Valérie

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Genotyping on blood and buccal cells using loop-mediated isothermal amplification in healthy humans 由 Drogou, Catherine, Sauvet, Fabien, Erblang, Mégane, Detemmerman, Liselot, Derbois, Céline, Erkel, Marie Claire, Boland, Anne, Deleuze, Jean François, Gomez-Merino, Danielle, Chennaoui, Mounir

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Temporal Gene Expression Profiles Reflect the Dynamics of Lymphoid Differentiation 由 Chalabi, Smahane, Legrand, Agnes, Michaels, Victoria, Palomares, Marie-Ange, Olaso, Robert, Boland, Anne, Deleuze, Jean-François, Ezine, Sophie, Battail, Christophe, Tronik-Le Roux, Diana

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Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD 由 Saint-Pierre, Aude, Kaufman, Jean-Marc, Ostertag, Agnes, Cohen-Solal, Martine, Boland, Anne, Toye, Kaatje, Zelenika, Diana, Lathrop, Mark, de Vernejoul, Marie-Christine, Martinez, Maria

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Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes 由 Schramm, Catherine, Charbonnier, Camille, Zaréa, Aline, Lacour, Morgane, Wallon, David, Boland, Anne, Deleuze, Jean-François, Olaso, Robert, Alarcon, Flora, Campion, Dominique, Nuel, Grégory, Nicolas, Gaël

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Publisher Correction: Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes 由 Schramm, Catherine, Charbonnier, Camille, Zaréa, Aline, Lacour, Morgane, Wallon, David, Boland, Anne, Deleuze, Jean-François, Olaso, Robert, Alarcon, Flora, Campion, Dominique, Nuel, Grégory, Nicolas, Gaël

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Bdf1 Bromodomains Are Essential for Meiosis and the Expression of Meiotic-Specific Genes 由 García-Oliver, Encar, Ramus, Claire, Perot, Jonathan, Arlotto, Marie, Champleboux, Morgane, Mietton, Flore, Battail, Christophe, Boland, Anne, Deleuze, Jean-François, Ferro, Myriam, Couté, Yohann, Govin, Jérôme

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A comparison of high-throughput SARS-CoV-2 sequencing methods from nasopharyngeal samples 由 Gerber, Zuzana, Daviaud, Christian, Delafoy, Damien, Sandron, Florian, Alidjinou, Enagnon Kazali, Mercier, Jonathan, Gerber, Sylvain, Meyer, Vincent, Boland, Anne, Bocket, Laurence, Olaso, Robert, Deleuze, Jean-François

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Genetic and Haplotypic Structure in 14 European and African Cattle Breeds 由 Gautier, Mathieu, Faraut, Thomas, Moazami-Goudarzi, Katayoun, Navratil, Vincent, Foglio, Mario, Grohs, Cécile, Boland, Anne, Garnier, Jean-Guillaume, Boichard, Didier, Lathrop, G. Mark, Gut, Ivo G., Eggen, André

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A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1 由 AME van der Beek, Nadine, Nelson, Isabelle, Froissart, Roseline, Levade, Thierry, Garcia, Virginie, Lacene, Emmanuelle, Boland, Anne, Masson, Cécile, Romero, Norma B., Stojkovic, Tanya, Bonne, Gisèle, Béhin, Anthony

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Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A 由 Mercier, Sandra, Lornage, Xavière, Malfatti, Edoardo, Marcorelles, Pascale, Letournel, Franck, Boscher, Cécile, Caillaux, Gaëlle, Magot, Armelle, Böhm, Johann, Boland, Anne, Deleuze, Jean-François, Romero, Norma, Péréon, Yann, Laporte, Jocelyn

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning 由 Laugel-Haushalter, Virginie, Morkmued, Supawich, Stoetzel, Corinne, Geoffroy, Véronique, Muller, Jean, Boland, Anne, Deleuze, Jean-François, Chennen, Kirsley, Pitiphat, Waranuch, Dollfus, Hélène, Niederreither, Karen, Bloch-Zupan, Agnès, Pungchanchaikul, Patimaporn

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