Search Results - "Mollin, Michelle"

Second Report of Chronic Granulomatous Disease in Jordan: Clinical and Genetic Description of 31 Patients From 21 Different Families, Including Families From Lybia and Iraq by Bakri, Faris Ghalib, Mollin, Michelle, Beaumel, Sylvain, Vigne, Bénédicte, Roux-Buisson, Nathalie, Al-Wahadneh, Adel Mohammed, Alzyoud, Raed Mohammed, Hayajneh, Wail Ahmad, Daoud, Ammar Khaled, Shukair, Mohammed Elian Abu, Karadshe, Mansour Fuad, Sarhan, Mahmoud Mohammad, Al-Ramahi, Jamal Ahmad Wadi, Fauré, Julien, Rendu, John, Stasia, Marie Jose

“…Chronic granulomatous Disease (CGD) is a rare innate immunodeficiency disorder caused by mutations in one of the six genes ( , and /EROS) encoding the…”
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NOX4 is the main NADPH oxidase involved in the early stages of hematopoietic differentiation from human induced pluripotent stem cells by Brault, Julie, Vigne, Bénédicte, Meunier, Mathieu, Beaumel, Sylvain, Mollin, Michelle, Park, Sophie, Stasia, Marie José

“…Reactive oxygen species (ROS) produced in hematopoietic stem cells (HSCs) are involved in the balance between quiescence, self-renewal, proliferation and…”
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Clinical, functional and genetic characterization of 16 patients suffering from chronic granulomatous disease variants – identification of 11 novel mutations in CYBB by Mollin, M., Beaumel, S., Vigne, B., Brault, J., Roux‐Buisson, N., Rendu, J., Barlogis, V., Catho, G., Dumeril, C., Fouyssac, F., Monnier, D., Gandemer, V., Revest, M., Brion, J.‐P., Bost‐Bru, C., Jeziorski, E., Eitenschenck, L., Jarrasse, C., Drillon Haus, S., Houachée‐Chardin, M., Hancart, M., Michel, G., Bertrand, Y., Plantaz, D., Kelecic, J., Traberg, R., Kainulainen, L., Fauré, J., Fieschi, F., Stasia, M. J.

“…Sixteen CGD cases were clinically, functionally and genetically characterized and classified as suffering from different variant forms (X910, X91− or X91+)…”
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Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease – Identification of Eight Novel Mutations in CYBB and NCF2 Genes by Martel, Cécile, Mollin, Michelle, Beaumel, Sylvain, Brion, Jean Paul, Coutton, Charles, Satre, Véronique, Vieville, Gaëlle, Callanan, Mary, Lefebvre, Christine, Salmon, Alexandra, Pagnier, Anne, Plantaz, Dominique, Bost-Bru, Cécile, Eitenschenck, Laurence, Durieu, Isabelle, Floret, Daniel, Galambrun, Claire, Chambost, Hervé, Michel, Gérard, Stephan, Jean-Louis, Hermine, Olivier, Blanche, Stéphane, Blot, Nathalie, Rubié, Hervé, Pouessel, Guillaume, Drillon-Haus, Stephanie, Conrad, Bernard, Posfay-Barbe, Klara M., Havlicekova, Zuzana, Voskresenky-Baricic, Tamara, Jadranka, Kelecic, Arriazu, Maria Cristina, Garcia, Luis Alberto, Mansour, Lamia Sfaihi Ben, Bordigoni, Pierre, Stasia, Marie José

“…Chronic granulomatous disease is an inherited disorder in which phagocytes lack a functional NADPH oxidase and cannot produce superoxide anions. The most…”
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Erratum to: Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease—Identification of Eight Novel Mutations in CYBB and NCF2 Genes by Martel, Cécile, Mollin, Michelle, Beaumel, Sylvain, Brion, Jean Paul, Coutton, Charles, Satre, Véronique, Vieville, Gaëlle, Callanan, Mary, Lefebvre, Christine, Salmon, Alexandra, Pagnier, Anne, Plantaz, Dominique, Bost-Bru, Cécile, Eitenschenck, Laurence, Durieu, Isabelle, Floret, Daniel, Galambrun, Claire, Chambost, Hervé, Michel, Gérard, Stephan, Jean-Louis, Hermine, Olivier, Blanche, Stéphane, Blot, Nathalie, Rubié, Hervé, Pouessel, Guillaume, Drillon-Haus, Stephanie, Conrad, Bernard, Posfay-Barbe, Klara M., Havlicekova, Zuzana, Voskresenky-Baricic, Tamara, Jadranka, Kelecic, Arriazu, Maria Cristina, Garcia, Luis Alberto, Sfaihi, Lamia Ben Mansour, Bordigoni, Pierre, Stasia, Marie José

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