Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM1 gene
Zaouak, Anissa, Abdessalem, Ghaith, Mkaouar, Rahma, Messaoud, Olfa, Abdelhak, Sonia, Hammami, Houda, Fenniche, Samy
Published in International journal of dermatology (01.07.2019)
Published in International journal of dermatology (01.07.2019)
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Journal Article
Fgfr3 Is a Positive Regulator of Osteoblast Expansion and Differentiation During Zebrafish Skull Vault Development
Dambroise, Emilie, Ktorza, Ivan, Brombin, Alessandro, Abdessalem, Ghaith, Edouard, Joanne, Luka, Marine, Fiedler, Imke, Binder, Olivia, Pelle, Olivier, Patton, E Elizabeth, Busse, Björn, Menager, Mickaël, Sohm, Frederic, Legeai‐Mallet, Laurence
Published in Journal of bone and mineral research (01.09.2020)
Published in Journal of bone and mineral research (01.09.2020)
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Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family
Charfeddine, Cherine, Dallali, Hamza, Abdessalem, Ghaith, Ghedira, Kais, Hamdi, Yosr, Elouej, Sahar, Landoulsi, Zied, Delague, Valérie, Lagarde, Arnaud, Levy, Nicolas, El-Amraoui, Aziz, Boubaker, Mohamed Samir, Abdelhak, Sonia, Mokni, Mourad
Published in Journal of human genetics (01.04.2020)
Published in Journal of human genetics (01.04.2020)
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A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC26A4 gene
Sayeb, Marwa, Riahi, Zied, Laroussi, Nadia, Bonnet, Crystel, Romdhane, Lilia, Mkaouar, Rahma, Zaouak, Anissa, Marrakchi, Jihene, Abdessalem, Ghaith, Messaoud, Olfa, Bouchniba, Oussema, Ghilane, Nacer, Mokni, Mourad, Besbes, Ghazi, Yacoub‐Youssef, Houda, Petit, Christine, Abdelhak, Sonia
Published in International journal of dermatology (01.12.2019)
Published in International journal of dermatology (01.12.2019)
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Journal Article
A Comprehensive Map of the Monocyte-Derived Dendritic Cell Transcriptional Network Engaged upon Innate Sensing of HIV
Johnson, Jarrod S., De Veaux, Nicholas, Rives, Alexander W., Lahaye, Xavier, Lucas, Sasha Y., Perot, Brieuc P., Luka, Marine, Garcia-Paredes, Victor, Amon, Lynn M., Watters, Aaron, Abdessalem, Ghaith, Aderem, Alan, Manel, Nicolas, Littman, Dan R., Bonneau, Richard, Ménager, Mickaël M.
Published in Cell reports (Cambridge) (21.01.2020)
Published in Cell reports (Cambridge) (21.01.2020)
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Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved
Mezzi, Nessrine, Messaoud, Olfa, Mkaouar, Rahma, Zitouna, Nadia, Romdhane, Safa, Abdessalem, Ghaith, Charfeddine, Cherine, Maazoul, Faouzi, Ouerteni, Ines, Hamdi, Yosr, Zaouak, Anissa, Mrad, Ridha, Abdelhak, Sonia, Romdhane, Lilia
Published in Genes (19.11.2021)
Published in Genes (19.11.2021)
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Journal Article
Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM 1 gene
Zaouak, Anissa, Abdessalem, Ghaith, Mkaouar, Rahma, Messaoud, Olfa, Abdelhak, Sonia, Hammami, Houda, Fenniche, Samy
Published in International journal of dermatology (01.07.2019)
Published in International journal of dermatology (01.07.2019)
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Journal Article
Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus
Fassatoui, Meriem, Lopez-Siles, Mireia, Díaz-Rizzolo, Diana A, Jmel, Haifa, Naouali, Chokri, Abdessalem, Ghaith, Chikhaoui, Asma, Nadal, Belén, Jamoussi, Henda, Abid, Abdelmajid, Gomis, Ramon, Abdelhak, Sonia, Martinez-Medina, Margarita, Kefi, Rym
Published in Bioscience reports (28.06.2019)
Published in Bioscience reports (28.06.2019)
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Late-onset enteric virus infection associated with hepatitis (EVAH) in transplanted SCID patients
Riller, Quentin, Fourgeaud, Jacques, Bruneau, Julie, De Ravin, Suk See, Smith, Grace, Fusaro, Mathieu, Meriem, Samy, Magerus, Aude, Luka, Marine, Abdessalem, Ghaith, Lhermitte, Ludovic, Jamet, Anne, Six, Emmanuelle, Magnani, Alessandra, Castelle, Martin, Lévy, Romain, Lecuit, Mathilde M., Fournier, Benjamin, Winter, Sarah, Semeraro, Michaela, Pinto, Graziella, Abid, Hanène, Mahlaoui, Nizar, Cheikh, Nathalie, Florkin, Benoit, Frange, Pierre, Jeziorski, Eric, Suarez, Felipe, Sarrot-Reynauld, Françoise, Nouar, Dalila, Debray, Dominique, Lacaille, Florence, Picard, Capucine, Pérot, Philippe, Regnault, Béatrice, Da Rocha, Nicolas, de Cevins, Camille, Delage, Laure, Pérot, Brieuc P., Vinit, Angélique, Carbone, Francesco, Brunaud, Camille, Marchais, Manon, Stolzenberg, Marie-Claude, Asnafi, Vahid, Molina, Thierry, Rieux-Laucat, Frédéric, Notarangelo, Luigi D., Pittaluga, Stefania, Jais, Jean Philippe, Moshous, Despina, Blanche, Stephane, Malech, Harry, Eloit, Marc, Cavazzana, Marina, Fischer, Alain, Ménager, Mickaël M., Neven, Bénédicte
Published in Journal of allergy and clinical immunology (01.06.2023)
Published in Journal of allergy and clinical immunology (01.06.2023)
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A monocyte/dendritic cell molecular signature of SARS-CoV-2-related multisystem inflammatory syndrome in children with severe myocarditis
de Cevins, Camille, Luka, Marine, Smith, Nikaïa, Meynier, Sonia, Magérus, Aude, Carbone, Francesco, García-Paredes, Víctor, Barnabei, Laura, Batignes, Maxime, Boullé, Alexandre, Stolzenberg, Marie-Claude, Pérot, Brieuc P., Charbit, Bruno, Fali, Tinhinane, Pirabakaran, Vithura, Sorin, Boris, Riller, Quentin, Abdessalem, Ghaith, Beretta, Maxime, Grzelak, Ludivine, Goncalves, Pedro, Di Santo, James P., Mouquet, Hugo, Schwartz, Olivier, Zarhrate, Mohammed, Parisot, Mélanie, Bole-Feysot, Christine, Masson, Cécile, Cagnard, Nicolas, Corneau, Aurélien, Brunaud, Camille, Zhang, Shen-Ying, Casanova, Jean-Laurent, Bader-Meunier, Brigitte, Haroche, Julien, Melki, Isabelle, Lorrot, Mathie, Oualha, Mehdi, Moulin, Florence, Bonnet, Damien, Belhadjer, Zahra, Leruez, Marianne, Allali, Slimane, Gras-Leguen, Christèle, de Pontual, Loïc, Fischer, Alain, Duffy, Darragh, Rieux-Laucat, Fredéric, Toubiana, Julie, Ménager, Mickaël M.
Published in Med (New York, N.Y. : Online) (10.09.2021)
Published in Med (New York, N.Y. : Online) (10.09.2021)
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Journal Article
A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene
Sayeb, Marwa, Riahi, Zied, Laroussi, Nadia, Bonnet, Crystel, Romdhane, Lilia, Mkaouar, Rahma, Zaouak, Anissa, Marrakchi, Jihene, Abdessalem, Ghaith, Messaoud, Olfa, Bouchniba, Oussema, Ghilane, Nacer, Mokni, Mourad, Besbes, Ghazi, Yacoub‐Youssef, Houda, Petit, Christine, Abdelhak, Sonia
Published in International journal of dermatology (01.12.2019)
Published in International journal of dermatology (01.12.2019)
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Journal Article
A monocyte/dendritic cell molecular signature of SARS-CoV2-related multisystem inflammatory syndrome in children (MIS-C) with severe myocarditis
De Cevins, Camille, Luka, Marine, Smith, Nikaïa, Meynier, Sonia, Magérus, Aude, Carbone, Francesco, García-Paredes, Víctor, Barnabei, Laura, Batignes, Maxime, Boullé, Alexandre, Stolzenberg, Marie-Claude, Pérot, Brieuc P, Charbit, Bruno, Tinhinane Fali, Pirabarakan, Vithura, Sorin, Boris, Riller, Quentin, Ghaith Abdessalem, Beretta, Maxime, Grzelak, Ludivine, Goncalves, Pedro, Di Santo, James P, Mouquet, Hugo, Schwartz, Olivier, Zarhrate, Mohammed, Parisot, Mélanie, Bole-Feysot, Christine, Masson, Cécile, Cagnard, Nicolas, Corneau, Aurélien, Bruneau, Camille, Shen-Ying, Zhang, Jean-Laurent Casanova, Brigitte Bader Meunier, Haroche, Julien, Melki, Isabelle, Mathie Lorrot, Oualha, Mehdi, Moulin, Florence, Bonnet, Damien, Belhadjer, Zahra, Leruez, Marianne, Allali, Slimane, Christèle Gras Leguen, Loïc De Pontual, Pediatric-Biocovid Study Group, Fischer, Alain, Duffy, Darragh, Laucat, Fredéric Rieux, Toubiana, Julie, Ménager, Mickaël M
Published in bioRxiv (23.02.2021)
Published in bioRxiv (23.02.2021)
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Paper
Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM1 gene
Zaouak, Anissa, Abdessalem, Ghaith, Mkaouar, Rahma, Messaoud, Olfa, Abdelhak, Sonia, Hammami, Houda, Fenniche, Samy
Published in International journal of dermatology (01.07.2019)
Published in International journal of dermatology (01.07.2019)
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Report
FGFR3 is a positive regulator of osteoblast expansion and differentiation during zebrafish skull vault development
Dambroise, Emilie, Ktorza, Ivan, Brombin, Alessandro, Ghaith Abdessalem, Edouard, Joanne, Luka, Marine, Fiedler, Imke, Binder, Olivia, Pelle, Olivier, Patton, Elizabeth, Busse, Bjorn, Menager, Mickael, Sohm, Frederic, Legeai-Mallet, Laurence
Published in bioRxiv (02.01.2020)
Published in bioRxiv (02.01.2020)
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