Mediation of most atypical effects by species homologues of the β3‐adrenoceptor von Blin, Nathalie, Nahmias, Clara, Drumare, Marie F., Strosberg, A. Donny

Volltext

Mediation of most atypical effects by species homologues of the beta 3-adrenoceptor von Blin, N, Nahmias, C, Drumare, M F, Strosberg, A D

Volltext

Peanut allergens are rapidly transferred in human breast milk and can prevent sensitization in mice von Bernard, H, Ah-Leung, S, Drumare, M-F, Feraudet-Tarisse, C, Verhasselt, V, Wal, J-M, Créminon, C, Adel-Patient, K

Volltext

Goat's milk allergy without cow's milk allergy: suppression of non-cross-reactive epitopes on caprine β-casein von Hazebrouck, S., Ah-Leung, S., Bidat, E., Paty, E., Drumare, M.-F., Tilleul, S., Adel-Patient, K., Wal, J.-M., Bernard, H.

Volltext

Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants von Poncet, Anaïs F, Grunewald, Olivier, Vaclavik, Veronika, Meunier, Isabelle, Drumare, Isabelle, Pelletier, Valérie, Bocquet, Béatrice, Todorova, Margarita G, Le Moing, Anne-Gaëlle, Devos, Aurore, Schorderet, Daniel F, Jobic, Florence, Defoort-Dhellemmes, Sabine, Dollfus, Hélène, Smirnov, Vasily M, Dhaenens, Claire-Marie

Volltext

Enzyme immunoassay for a urinary metabolite of 4-hydroxynonenal as a marker of lipid peroxidation von Guéraud, Françoise, Peiro, Géraldine, Bernard, Hervé, Alary, Jacques, Créminon, Christophe, Debrauwer, Laurent, Rathahao, Estelle, Drumare, Marie-Françoise, Canlet, Cécile, Wal, Jean-Michel, Bories, Georges

Volltext

TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Kohl, Susanne, Leroy, Bart P., Munier, Francis L., Guillonneau, Xavier, Mohand-Saïd, Saddek, Bujakowska, Kinga, Nandrot, Emeline F., Lorenz, Birgit, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Bernd, Antje, Antonio, Aline, Moskova-Doumanova, Veselina, Lancelot, Marie-Elise, Poloschek, Charlotte M., Drumare, Isabelle, Defoort-Dhellemmes, Sabine, Wissinger, Bernd, Léveillard, Thierry, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Berger, Wolfgang, Jacobson, Samuel G., Zrenner, Eberhart, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

Volltext

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D., Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G., Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

Volltext

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M, Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D, Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P, Munier, Francis L, Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B, Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P, Schorderet, Daniel F, De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G, Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W, Meire, Francoise, Prescott, Katrina, de Ravel de l'Argentière, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina

Volltext

Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M, Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D, Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P, Munier, Francis L, Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B, Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P, Schorderet, Daniel F, De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G, Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W, Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina

Volltext

Genomic cloning and species-specific properties of the recombinant canine β3-adrenoceptor von LENZEN, G, PIETRI-ROUXEL, F, DRUMARE, M.-F, AMIARD, A, GUILLOT, S, ARCHIMBAULT, P, STROSBERG, A. D

Volltext

Long Term Phorbol Ester Treatment Down-regulates the -Adrenergic Receptor in 3T3-F442A Adipocytes von Bruno Fève, France Piétri-Rouxel, Khadija El Hadri, Marie-Franoise Drumare, A. Donny Strosberg

Volltext