Downregulation of MGMT expression by targeted editing of DNA methylation enhances temozolomide sensitivity in glioblastoma
Han, Xinyu, Abdallah, Mohammed O.E., Breuer, Peter, Stahl, Fabian, Bakhit, Yousuf, Potthoff, Anna-Laura, Pregler, Barbara E.F., Schneider, Matthias, Waha, Andreas, Wüllner, Ullrich, Evert, Bernd O.
Published in Neoplasia (New York, N.Y.) (01.10.2023)
Published in Neoplasia (New York, N.Y.) (01.10.2023)
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Novel variants causing megalencephalic leukodystrophy in Sudanese families
Amin, Mutaz, Vignal, Cedric, Hamed, Ahlam A A, Mohammed, Inaam N, Elseed, Maha A, Drunat, Severine, Babai, Arwa, Eltaraifee, Esraa, Elbadi, Iman, Abubaker, Rayan, Mustafa, Doaa, Yahia, Ashraf, Koko, Mahmoud, Osman, Melka, Bakhit, Yousuf, Elshafea, Azza, Alsiddig, Mohamed, Haroun, Sahwah, Lelay, Gurvan, Elsayed, Liena E O, Ahmed, Ammar E, Boespflug-Tanguy, Odile, Dorboz, Imen
Published in Journal of human genetics (01.03.2022)
Published in Journal of human genetics (01.03.2022)
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Journal Article
Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment
Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A, Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H Y, Kniper, Marlies
Published in BMC ear, nose and throat disorders (21.05.2018)
Published in BMC ear, nose and throat disorders (21.05.2018)
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Journal Article
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
Koko, Mahmoud, Elseed, Maha A, Mohammed, Inaam N, Hamed, Ahlam A, Abd Allah, Amal S I, Yahia, Ashraf, Siddig, Rayan A, Altmüller, Janine, Toliat, Mohammad Reza, Elmahdi, Esra O, Amin, Mutaz, Ahmed, Elhami A, Eltazi, Isra Z M, Elmugadam, Fatima A, Abdelgadir, Wasma A, Eltaraifee, Esraa, Ibrahim, Mohamed O M, Ali, Nabila M H, Malik, Hiba M, Babai, Arwa M, Bakhit, Yousuf H, Nürnberg, Peter, Ibrahim, Muntaser E, Salih, Mustafa A, Schubert, Julian, Elsayed, Liena E O, Lerche, Holger
Published in European journal of human genetics : EJHG (05.02.2024)
Published in European journal of human genetics : EJHG (05.02.2024)
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Journal Article
Methylation of alpha-synuclein in a Sudanese cohort
Bakhit, Yousuf, Schmitt, Ina, Hamed, Ahlam, Ibrahim, Etedal Ahmed A., Mohamed, Inaam N., El-Sadig, Sarah M., Elseed, Maha A., Alebeed, Mohamed A., Shaheen, Mutaz T., Ibrahim, Mohamed O., Elhassan, Ali A., Eltom, Khalid, Ali, Hiba A., Ibrahim, Yousuf A., Almak, Murad E., Abubaker, Rayan, Ahmed, Mohamed Anwer, Abugrain, Ahmed A., Elrasheed, Salma M., Omar, Mawia A., Almahal, Mohamed A., MohamedSharif, Abubaker A., Tahir, Mohamed Y., Malik, Sawazen M., Eldirdiri, Hazim S., Khidir, Reem J., Mohamed, Malaz T., Abdalla, Abdelmohaymin, Omer, Farouk Yassen, Elsayed, Liena E.O., Babikir, Haydar El Hadi, Bukhari, Elfateh Abd-Allah, Seidi, Osheik, Wüllner, Ullrich
Published in Parkinsonism & related disorders (01.08.2022)
Published in Parkinsonism & related disorders (01.08.2022)
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Journal Article
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
Amin, Mutaz, Vignal, Cedric, Hamed, Ahlam A. A., Mohammed, Inaam N., Elseed, Maha A., Abubaker, Rayan, Bakhit, Yousuf, Babai, Arwa, Elbadi, Eman, Eltaraifee, Esraa, Mustafa, Doua, Yahia, Ashraf, Osman, Melka, Koko, Mahmoud, Mustafa, Mohamed, Alsiddig, Mohamed, Haroun, Sahwah, Elshafea, Azza, Drunat, Severine, Elsayed, Liena E. O., Ahmed, Ammar E., Boespflug-Tanguy, Odile, Dorboz, Imen
Published in Frontiers in genetics (02.06.2022)
Published in Frontiers in genetics (02.06.2022)
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Journal Article
Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment
Kaheel, Hazem, Breß, Andreas, Hassan, Mohamed A., Shah, Aftab Ali, Amin, Mutaz, Bakhit, Yousuf H. Y., Kniper, Marlies
Published in Genetics Research International (01.01.2017)
Published in Genetics Research International (01.01.2017)
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Journal Article
PLA2G6‐associated late‐onset parkinsonism in a Sudanese family
Bakhit, Yousuf, Tesson, Christelle, Ibrahim, Mohamed O., Eltom, Khalid, Eltazi, Isra, Elsayed, Liena E.O., Lesage, Suzanne, Seidi, Osheik, Corvol, Jean‐Christophe, Wüllner, Ullrich
Published in Annals of clinical and translational neurology (01.06.2023)
Published in Annals of clinical and translational neurology (01.06.2023)
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Journal Article
In Silico Analysis of SNPs in PARK2 and PINK1 Genes That Potentially Cause Autosomal Recessive Parkinson Disease
Bakhit, Yousuf Hasan Yousuf, Ibrahim, Mohamed Osama Mirghani, Amin, Mutaz, Mirghani, Yousra Abdelazim, Hassan, Mohamed Ahmed Salih
Published in Advances in bioinformatics (2016)
Published in Advances in bioinformatics (2016)
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Journal Article
Intrafamilial and interfamilial heterogeneity of PINK1-associated Parkinson's disease in Sudan
Bakhit, Yousuf, Ibrahim, Mohamed O., Tesson, Christelle, Elhassan, Ali A., Ahmed, Mohamed Anwer, Alebeed, Mohamed A., Elrasheed, Salma M., Omar, Mawia A., Abubaker, Rayan, Eltom, Khalid, Shaheen, Mutaz T., Ibrahim, Yousuf A., Almak, Murad E., Ali, Hiba A., Abugrain, Ahmed A., Almahal, Mohamed A., MohamedSharif, Abubaker A., Tahir, Mohamed Y., Malik, Sawazen M., Eldirdiri Abdelrahman, Hazim, Khidir, Reem J., Mohamed, Malaz T., Abdalla, Abdelmohaymin, Elsayed, Liena E.O., Lesage, Suzanne, Corvol, Jean-Christophe, Seidi, Osheik, Wüllner, Ullrich
Published in Parkinsonism & related disorders (01.06.2023)
Published in Parkinsonism & related disorders (01.06.2023)
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Journal Article
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
Amin, Mutaz, Vignal, Cedric, Hamed, Ahlam A A, Mohammed, Inaam N, Elseed, Maha A, Abubaker, Rayan, Bakhit, Yousuf, Babai, Arwa, Elbadi, Eman, Eltaraifee, Esraa, Mustafa, Doua, Yahia, Ashraf, Osman, Melka, Koko, Mahmoud, Mustafa, Mohamed, Alsiddig, Mohamed, Haroun, Sahwah, Elshafea, Azza, Drunat, Severine, Elsayed, Liena E O, Ahmed, Ammar E, Boespflug-Tanguy, Odile, Dorboz, Imen
Published in Frontiers in genetics (01.01.2022)
Published in Frontiers in genetics (01.01.2022)
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