Search Results - "Bucher, Stephanie"

How to Be Unfaithful to Eurocentrism: A Spanglish Decolonial Critique to Knowledge Gentrification, Captivity and Storycide in Qualitative Research by polanco, marcela, Hanson, Nathan, Hernandez, Camila, Le Feber, Tirzah, Medina, Sonia, Old Bucher, Stephanie, Rivera, Eva, Rodriguez, Ione, Vela, Elizabeth, Velasco, Brandi, Le Feber, Jackolyn

“…From a position of academic activism, we critique the longstanding dominance del production of knowledge that solely implicates fidelity to Eurocentric…”
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Manufacturing and characterization of a recombinant adeno-associated virus type 8 reference standard material by Ayuso, Eduard, Blouin, Véronique, Lock, Martin, McGorray, Susan, Leon, Xavier, Alvira, Mauricio R, Auricchio, Alberto, Bucher, Stephanie, Chtarto, Abdelwahed, Clark, K Reed, Darmon, Christophe, Doria, Monica, Fountain, Will, Gao, Guangping, Gao, Kai, Giacca, Mauro, Kleinschmidt, Juergen, Leuchs, Barbara, Melas, Catherine, Mizukami, Hiroaki, Müller, Marcus, Noordman, Yvet, Bockstael, Olivier, Ozawa, Keiya, Pythoud, Catherine, Sumaroka, Marina, Surosky, Richard, Tenenbaum, Liliane, van der Linden, Inge, Weins, Brigitte, Wright, J Fraser, Zhang, Xinhua, Zentilin, Lorena, Bosch, Fatima, Snyder, Richard O, Moullier, Philippe

“…Abstract Gene therapy approaches using recombinant adeno-associated virus serotype 2 (rAAV2) and serotype 8 (rAAV8) have achieved significant clinical…”
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Changes in the accessibility of the HIV-1 Integrase C-terminus in the presence of cellular proteins by Benkhelifa-Ziyyat, Sofia, Bucher, Stéphanie, Zanta-Boussif, Maria-Antonietta, Pasquet, Julie, Danos, Olivier

“…Following entry, uncoating, and reverse transcription, a number of cellular proteins become associated with the human immunodeficiency virus type 1 (HIV-1)…”
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A Deficiency in Dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl α3-Glucosyltransferase Defines a New Subtype of Congenital Disorders of Glycosylation by Chantret, Isabelle, Dancourt, Julia, Dupré, Thierry, Delenda, Christophe, Bucher, Stéphanie, Vuillaumier-Barrot, Sandrine, Ogier de Baulny, Hélène, Peletan, Céline, Danos, Olivier, Seta, Nathalie, Durand, Geneviève, Oriol, Rafael, Codogno, Patrice, Moore, Stuart E.H.

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How to Be Unfaithful to Eurocentrism: A Spanglish1 Decolonial Critique to Knowledge Gentrification, Captivity and Storycide in Qualitative Research by Polanco, Marcela, Hanson, Nathan D, Hernández, Camila, Feber, Tirzah Le, Medina, Sonia, Bucher, Stephanie Old, Rivera, Eva I, Rodriguez, Ione, Vela, Elizabeth, Velasco, Brandi, Feber, Jackolyn Le

“…From a position of academic activism, we critique the longstanding dominance del production of knowledge that solely implicates fidelity to Eurocentric…”
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Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients by Le Guiner, Caroline, Montus, Marie, Servais, Laurent, Cherel, Yan, Francois, Virginie, Thibaud, Jean-Laurent, Wary, Claire, Matot, Béatrice, Larcher, Thibaut, Guigand, Lydie, Dutilleul, Maeva, Domenger, Claire, Allais, Marine, Beuvin, Maud, Moraux, Amélie, Le Duff, Johanne, Devaux, Marie, Jaulin, Nicolas, Guilbaud, Mickaël, Latournerie, Virginie, Veron, Philippe, Boutin, Sylvie, Leborgne, Christian, Desgue, Diana, Deschamps, Jack-Yves, Moullec, Sophie, Fromes, Yves, Vulin, Adeline, Smith, Richard H, Laroudie, Nicolas, Barnay-Toutain, Frédéric, Rivière, Christel, Bucher, Stéphanie, Le, Thanh-Hoa, Delaunay, Nicolas, Gasmi, Mehdi, Kotin, Robert M, Bonne, Gisèle, Adjali, Oumeya, Masurier, Carole, Hogrel, Jean-Yves, Carlier, Pierre, Moullier, Philippe, Voit, Thomas

“…Duchenne muscular dystrophy (DMD) is a severe muscle-wasting disorder caused by mutations in the dystrophin gene, without curative treatment yet available. Our…”
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Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl Mannosyltransferase by Chantret, Isabelle, Dupré, Thierry, Delenda, Christophe, Bucher, Stéphanie, Dancourt, Julia, Barnier, Anne, Charollais, Aude, Heron, Delphine, Bader-Meunier, Brigitte, Danos, Olivier, Seta, Nathalie, Durand, Geneviève, Oriol, Rafael, Codogno, Patrice, Moore, Stuart E.H.

“…Type I congenital disorders of glycosylation (CDG I) are diseases presenting multisystemic lesions including central and peripheral nervous system deficits…”
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A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation by Chantret, Isabelle, Dancourt, Julia, Dupré, Thierry, Delenda, Christophe, Bucher, Stéphanie, Vuillaumier-Barrot, Sandrine, Ogier de Baulny, Hélène, Peletan, Celine, Danos, Olivier, Seta, Nathalie, Durand, Geneviève, Oriol, Rafael, Codogno, Patrice, Moore, Stuart E H

“…The underlying causes of type I congenital disorders of glycosylation (CDG I) have been shown to be mutations in genes encoding proteins involved in the…”
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