Hasil Pencarian - Mohammad El-khateeb

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  1. 1
    Effect of combined G6PD deficiency and diabetes on protein oxidation and lipid peroxidation

    Effect of combined G6PD deficiency and diabetes on protein oxidation and lipid peroxidation oleh Naif S. Karadsheh, Nisreen A. Quttaineh, Salem N. Karadsheh, Mohammad El-Khateeb

    Diterbitkan 2021-12-01
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  2. 2
    Dyslipidemia among patients with type 2 diabetes in Jordan: Prevalence, pattern, and associated factors

    Dyslipidemia among patients with type 2 diabetes in Jordan: Prevalence, pattern, and associated factors oleh Dana Hyassat, Saba Al-Saeksaek, Duha Naji, Awn Mahasneh, Yousef Khader, Mousa Abujbara, Mohammad El-Khateeb, Kamel Ajlouni

    Diterbitkan 2022-11-01
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  3. 3
    Assessment of the Zooplankton Community and Water Quality in an Artificial Freshwater Lake from a Semi-Arid Area (Irbid, Jordan)

    Assessment of the Zooplankton Community and Water Quality in an Artificial Freshwater Lake from a Semi-Arid Area (Irbid, Jordan) oleh Wassim Guermazi, Mohammad El-khateeb, Muna Abu-Dalo, Ikbel Sallemi, Bashar Al-Rahahleh, Amira Rekik, Genuario Belmonte, Habib Ayadi, Neila Annabi-Trabelsi

    Diterbitkan 2023-08-01
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  4. 4
    FAM20A mutations can cause enamel-renal syndrome (ERS).

    FAM20A mutations can cause enamel-renal syndrome (ERS). oleh Shih-Kai Wang, Parissa Aref, Yuanyuan Hu, Rachel N Milkovich, James P Simmer, Mohammad El-Khateeb, Hinda Daggag, Zaid H Baqain, Jan C-C Hu

    Diterbitkan 2013-01-01
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  5. 5
    Synthesis, Characterization, Computational and Biological Activity of Some Schiff Bases and Their Fe, Cu and Zn Complexes

    Synthesis, Characterization, Computational and Biological Activity of Some Schiff Bases and Their Fe, Cu and Zn Complexes oleh Tareq M. A. Al-Shboul, Mohammad El-khateeb, Zaid H. Obeidat, Taher S. Ababneh, Suha S. Al-Tarawneh, Mazhar S. Al Zoubi, Walhan Alshaer, Anas Abu Seni, Taqwa Qasem, Hayato Moriyama, Yukihiro Yoshida, Hiroshi Kitagawa, Taghreed M. A. Jazzazi

    Diterbitkan 2022-08-01
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  6. 6
    A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability

    A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability oleh Poh Hui Chia, Franklin Lei Zhong, Shinsuke Niwa, Carine Bonnard, Kagistia Hana Utami, Ruizhu Zeng, Hane Lee, Ascia Eskin, Stanley F Nelson, William H Xie, Samah Al-Tawalbeh, Mohammad El-Khateeb, Mohammad Shboul, Mahmoud A Pouladi, Mohammed Al-Raqad, Bruno Reversade

    Diterbitkan 2018-05-01
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  7. 7
    A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing

    A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing oleh Nasrinsadat Nabavizadeh, Annkatrin Bressin, Mohammad Shboul, Ricardo Moreno Traspas, Poh Hui Chia, Carine Bonnard, Emmanuelle Szenker‐Ravi, Burak Sarıbaş, Emmanuel Beillard, Umut Altunoglu, Zohreh Hojati, Scott Drutman, Susanne Freier, Mohammad El‐Khateeb, Rajaa Fathallah, Jean‐Laurent Casanova, Wesam Soror, Alaa Arafat, Nathalie Escande‐Beillard, Andreas Mayer, Bruno Reversade

    Diterbitkan 2023-02-01
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  8. 8
    INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex

    INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex oleh Lauren G. Mascibroda, Mohammad Shboul, Nathan D. Elrod, Laurence Colleaux, Hanan Hamamy, Kai-Lieh Huang, Natoya Peart, Moirangthem Kiran Singh, Hane Lee, Barry Merriman, Jeanne N. Jodoin, Poojitha Sitaram, Laura A. Lee, Raja Fathalla, Baeth Al-Rawashdeh, Osama Ababneh, Mohammad El-Khateeb, Nathalie Escande-Beillard, Stanley F. Nelson, Yixuan Wu, Liang Tong, Linda J. Kenney, Sudipto Roy, William K. Russell, Jeanne Amiel, Bruno Reversade, Eric J. Wagner

    Diterbitkan 2022-10-01
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