Statins Induce Locomotion and Muscular Phenotypes in Drosophila melanogaster That Are Reminiscent of Human Myopathy: Evidence for the Role of the Chloride Channel Inhibition in the... von Al-Sabri, Mohamed H, Behare, Neha, Alsehli, Ahmed M, Berkins, Samuel, Arora, Aadeya, Antoniou, Eirini, Moysiadou, Eleni I, Anantha-Krishnan, Sowmya, Cosmen, Patricia D, Vikner, Johanna, Moulin, Thiago C, Ammar, Nourhene, Boukhatmi, Hadi, Clemensson, Laura E, Rask-Andersen, Mathias, Mwinyi, Jessica, Williams, Michael J, Fredriksson, Robert, Schiöth, Helgi B

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Studying Muscle Transcriptional Dynamics at Single-molecule Scales in Drosophila von Leroux, Emma, Ammar, Nourhene, Moinet, Savannah, Pecot, Thierry, Boukhatmi, Hadi

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Statins Induce Locomotion and Muscular Phenotypes in IDrosophila melanogaster/I That Are Reminiscent of Human Myopathy: Evidence for the Role of the Chloride Channel Inhibition in... von Al-Sabri, Mohamed H, Behare, Neha, Alsehli, Ahmed M, Berkins, Samuel, Arora, Aadeya, Antoniou, Eirini, Moysiadou, Eleni I, Anantha-Krishnan, Sowmya, Cosmen, Patricia D, Vikner, Johanna, Moulin, Thiago C, Ammar, Nourhene, Boukhatmi, Hadi, Clemensson, Laura E, Rask-Andersen, Mathias, Mwinyi, Jessica, Williams, Michael J, Fredriksson, Robert, Schiöth, Helgi B

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Statins Induce Locomotion and Muscular Phenotypes in Drosophila melanogaster That Are Reminiscent of Human Myopathy : Evidence for the Role of the Chloride Channel Inhibition in th... von Al-Sabri, Mohamed H, Behare, Neha, Alsehli, Ahmed M, Berkins, Samuel, Arora, Aadeya, Antoniou, Eirini, Moysiadou, Eleni I, Anantha-Krishnan, Sowmya, Cosmen, Patricia D, Vikner, Johanna, Moulin, Thiago C, Ammar, Nourhene, Boukhatmi, Hadi, Clemensson, Laura E, Rask-Andersen, Mathias, Mwinyi, Jessica, Williams, Michael J, Fredriksson, Robert, Schiöth, Helgi B

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Allium roseum L. volatile compounds profile and antioxydant activity for chemotype discrimination – Case study of the wild plant of Sfax (Tunisia) von Zouari, Sami, Ketata, Mouna, Boudhrioua, Nourhene, Ammar, Emna

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First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and comp... von Ghorbel, Rania, Ghorbel, Raouia, Rouissi, Aida, Fendri-Kriaa, Nourhene, Ben Salah, Ghada, Belguith, Neila, Ammar-Keskes, Leila, Gouider-Khouja, Neziha, Fakhfakh, Faiza

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Clinical, Molecular, and Computational Analysis in Patients With a Novel Double Mutation and a New Synonymous Variant in MeCP2: Report of the First Missense Mutation Within the AT-... von Kharrat, Marwa, Kamoun, Yosra, Kamoun, Fatma, Ellouze, Emna, Maalej, Marwa, Fendri-Kriaa, Nourhene, Ammar-Keskes, Leila, Belghith, Neila, Gargouri, Ali, Triki, Chahnez, Fakhfakh, Faiza

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Phenotypic variability in two infants sharing the same MECP2 mutation: evidence of chromosomal rearrangements and high sister-chromatid exchange levels in Rett syndrome von Kharrat, Marwa, Hsairi, Ines, Doukali, Hajer, Fendri-Kriaa, Nourhene, Kammoun, Hassen, Ammar-keskes, Leila, Triki, Chahnez, Fakhfakh, Faiza

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Implication de l’hyperhomocystéinémie dans les accidents vasculaires cérébraux ischémiques von Samet, Sana, Khayati, Nourhene, Ammar, Mariem, Moussa, Amira, Asma, Omezzine, Amor, Sana Ben, Bouslama, Ali

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