Two co‐inherited novel SNPs in the MC4R gene related to live body weight and hormonal assays in Awassi and Arabi sheep breeds of Iraq

od Al‐Thuwaini, Tahreer M., Al‐Shuhaib, Mohammed Baqur S., Lepretre, Frederic, Dawud, Halla Hassan
Izdano u Vet Med Sci (2020)

VE-statin, an endothelial repressor of smooth muscle cell migration

od Soncin, Fabrice, Mattot, Virginie, Lionneton, Frédéric, Spruyt, Nathalie, Lepretre, Frédéric, Begue, Agnès, Stehelin, Dominique
Izdano 2003

Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn’s Disease Patients

od Choteau, Laura, Vasseur, Francis, Lepretre, Frederic, Figeac, Martin, Gower-Rousseau, Corine, Dubuquoy, Laurent, Poulain, Daniel, Colombel, Jean-Frederic, Sendid, Boualem, Jawhara, Samir
Izdano u Sci Rep (2016)

Corrigendum: Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn’s Disease Patients

od Choteau, Laura, Vasseur, Francis, Lepretre, Frederic, Figeac, Martin, Gower-Rousseau, Corine, Dubuquoy, Laurent, Poulain, Daniel, Colombel, Jean-Frederic, Sendid, Boualem, Jawhara, Samir
Izdano u Sci Rep (2016)

Isolation and characterization of two canine melanoma cell lines: new models for comparative oncology

od Segaoula, Zacharie, Primot, Aline, Lepretre, Frederic, Hedan, Benoit, Bouchaert, Emmanuel, Minier, Kevin, Marescaux, Laurent, Serres, François, Galiègue-Zouitina, Sylvie, André, Catherine, Quesnel, Bruno, Thuru, Xavier, Tierny, Dominique
Izdano u BMC Cancer (2018)

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independ...

od Vionnet, Nathalie, Hani, El Habib, Dupont, Sophie, Gallina, Sophie, Francke, Stephan, Dotte, Sébastien, De Matos, Frédérique, Durand, Emmanuelle, Leprêtre, Frédéric, Lecoeur, Cécile, Gallina, Philippe, Zekiri, Lirije, Dina, Christian, Froguel, Philippe
Izdano 2000

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

od Chartier-Harlin, Marie-Christine, Dachsel, Justus C., Vilariño-Güell, Carles, Lincoln, Sarah J., Leprêtre, Frédéric, Hulihan, Mary M., Kachergus, Jennifer, Milnerwood, Austen J., Tapia, Lucia, Song, Mee-Sook, Le Rhun, Emilie, Mutez, Eugénie, Larvor, Lydie, Duflot, Aurélie, Vanbesien-Mailliot, Christel, Kreisler, Alexandre, Ross, Owen A., Nishioka, Kenya, Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Melrose, Heather L., Behrouz, Bahareh, Keeling, Brett H., Bacon, Justin A., Hentati, Emna, Williams, Lindsey, Yanagiya, Akiko, Sonenberg, Nahum, Lockhart, Paul J., Zubair, Abba C., Uitti, Ryan J., Aasly, Jan O., Krygowska-Wajs, Anna, Opala, Grzegorz, Wszolek, Zbigniew K., Frigerio, Roberta, Maraganore, Demetrius M., Gosal, David, Lynch, Tim, Hutchinson, Michael, Bentivoglio, Anna Rita, Valente, Enza Maria, Nichols, William C., Pankratz, Nathan, Foroud, Tatiana, Gibson, Rachel A., Hentati, Faycal, Dickson, Dennis W., Destée, Alain, Farrer, Matthew J.
Izdano 2011