Bilaketaren emaitzak - Alyafee, Yusra

Synthesis of protein-coated biocompatible methotrexate-loaded PLA-PEG-PLA nanoparticles for breast cancer treatment nork Massadeh, Salam, Alaamery, Manal, Al-Qatanani, Shatha, Alarifi, Saqer, Bawazeer, Shahad, Alyafee, Yusra

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A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia nork Alhamoudi, Kheloud M., Bhat, Javaid, Nashabat, Marwan, Alharbi, Masheal, Alyafee, Yusra, Asiri, Abdulaziz, Umair, Muhammad, Alfadhel, Majid

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Identification of the TTC26 Splice Variant in a Novel Complex Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations nork Alfadhel, Majid, Umair, Muhammad, Almuzzaini, Bader, Asiri, Abdulaziz, Al Tuwaijri, Abeer, Alhamoudi, Khaloud, Alyafee, Yusra, Al-Owain, Mohammed

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Preparation of anastrozole loaded PEG-PLA nanoparticles: evaluation of apoptotic response of breast cancer cell lines nork Alyafee, Yusra A, Alaamery, Manal, Bawazeer, Shahad, Almutairi, Mansour S, Alghamdi, Badr, Alomran, Nawaf, Sheereen, Atia, Daghestani, Maha, Massadeh, Salam

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Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia nork Alyafee, Yusra, Alam, Qamre, Tuwaijri, Abeer Al, Umair, Muhammad, Haddad, Shahad, Alharbi, Meshael, Alrabiah, Hayat, Al-Ghuraibi, Maha, Al-Showaier, Sahar, Alfadhel, Majid

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Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay nork Asiri, Abdulaziz, Aloyouni, Essra, Umair, Muhammad, Alyafee, Yusra, Al Tuwaijri, Abeer, Alhamoudi, Kheloud M., Almuzzaini, Bader, Al Baz, Abeer, Alwadaani, Deemah, Nashabat, Marwan, Alfadhel, Majid

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Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia nork Alyafee, Yusra, Al Tuwaijri, Abeer, Alam, Qamre, Umair, Muhammad, Haddad, Shahad, Alharbi, Mashael, Ballow, Maryam, Al Drees, Mohammed, AlAbdulrahman, Abdulkareem, Al Khaldi, Aziza, Alfadhel, Majid

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Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish nork Umair, Muhammad, Farooq Khan, Muhammad, Aldrees, Mohammed, Nashabat, Marwan, Alhamoudi, Kheloud M., Bilal, Muhammad, Alyafee, Yusra, Al Tuwaijri, Abeer, Aldarwish, Manar, Al-Rumayyan, Ahmed, Alkhalaf, Hamad, Wadaan, Mohammad A. M., Alfadhel, Majid

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EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay nork Umair, Muhammad, Ballow, Mariam, Asiri, Abdulaziz, Alyafee, Yusra, al Tuwaijri, Abeer, Alhamoudi, Kheloud M., Aloraini, Taghrid, Abdelhakim, Marwa, Althagafi, Azza Thamer, Kafkas, Senay, Alsubaie, Lamia, Alrifai, Muhammad Talal, Hoehndorf, Robert, Alfares, Ahmed, Alfadhel, Majid

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Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect: Expanding the Molecular and Ph... nork Asiri, Abdulaziz, Alwadaani, Deemah, Umair, Muhammad, Alhamoudi, Kheloud M., Almuhanna, Mohammed H., Nasir, Abdul, Alrfaei, Bahauddeen M., Al Tuwaijri, Abeer, Barhoumi, Tlili, Alyafee, Yusra, Almuzzaini, Bader, Aldrees, Mohammed, Ballow, Mariam, Alayyar, Latifah, Al Abdulrahman, Abdulkareem, Alhaidan, Yazeid, Al Ghasham, Nahlah, Al-Ajaji, Sulaiman, Alsalamah, Mohammad, Al Suwairi, Wafa, Alfadhel, Majid

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