نتائج البحث - Boland, Anne
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A Novel Hypomorphic PDX1 Mutation Responsible for Permanent Neonatal Diabetes With Subclinical Exocrine Deficiency حسب Nicolino, Marc, Claiborn, Kathryn C., Senée, Valérie, Boland, Anne, Stoffers, Doris A., Julier, Cécile
منشور في 2010نص -
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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... حسب Mills, Scott D., Boland, Anne, Sory, Marie-Paule, van der Smissen, Patrick, Kerbourch, Corinne, Finlay, B. Brett, Cornelis, Guy R.
منشور في 1997نص -
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A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection حسب Pedergnana, Vincent, Gessain, Antoine, Tortevoye, Patricia, Byun, Minji, Bacq-Daian, Delphine, Boland, Anne, Casanova, Jean-Laurent, Abel, Laurent, Plancoulaine, Sabine
منشور في 2012نص -
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The Impact of Genetic Variations in ADORA2A in the Association between Caffeine Consumption and Sleep حسب Erblang, Mégane, Drogou, Catherine, Gomez-Merino, Danielle, Metlaine, Arnaud, Boland, Anne, Deleuze, Jean François, Thomas, Claire, Sauvet, Fabien, Chennaoui, Mounir
منشور في 2019نص -
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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... حسب Augière, Céline, Mégy, Simon, El Malti, Rajae, Boland, Anne, El Zein, Loubna, Verrier, Bernard, Mégarbané, André, Deleuze, Jean-François, Bouvagnet, Patrice
منشور في 2015نص -
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A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families حسب Veyssiere, Maëva, Perea, Javier, Michou, Laetitia, Boland, Anne, Caloustian, Christophe, Olaso, Robert, Deleuze, Jean-François, Cornelis, François, Petit-Teixeira, Elisabeth, Chaudru, Valérie
منشور في 2019نص -
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Genotyping on blood and buccal cells using loop-mediated isothermal amplification in healthy humans حسب Drogou, Catherine, Sauvet, Fabien, Erblang, Mégane, Detemmerman, Liselot, Derbois, Céline, Erkel, Marie Claire, Boland, Anne, Deleuze, Jean François, Gomez-Merino, Danielle, Chennaoui, Mounir
منشور في 2020نص -
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Temporal Gene Expression Profiles Reflect the Dynamics of Lymphoid Differentiation حسب Chalabi, Smahane, Legrand, Agnes, Michaels, Victoria, Palomares, Marie-Ange, Olaso, Robert, Boland, Anne, Deleuze, Jean-François, Ezine, Sophie, Battail, Christophe, Tronik-Le Roux, Diana
منشور في 2022نص -
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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 حسب 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
منشور في 2011نص -
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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 حسب 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
منشور في 2022نص -
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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 حسب 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
منشور في 2022نص -
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Bdf1 Bromodomains Are Essential for Meiosis and the Expression of Meiotic-Specific Genes حسب 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
منشور في 2017نص -
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A comparison of high-throughput SARS-CoV-2 sequencing methods from nasopharyngeal samples حسب 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
منشور في 2022نص -
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Genetic and Haplotypic Structure in 14 European and African Cattle Breeds حسب 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
منشور في 2007نص -
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A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1 حسب 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
منشور في 2018نص -
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Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A حسب 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
منشور في 2017نص -
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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning حسب 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
منشور في 2018نص