檢索結果 - Almuzzaini, Bader

A novel interstitial deletion of chromosome 2q21.1‐q23.3: Case report and literature review 由 Almuzzaini, Bader, Alatwi, Nasser S., Alsaif, Saif, Al Balwi, Mohammed A.

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Nuclear myosin 1 contributes to a chromatin landscape compatible with RNA polymerase II transcription activation 由 Almuzzaini, Bader, Sarshad, Aishe A., Farrants, Ann-Kristin Östlund, Percipalle, Piergiorgio

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Can First-Dose Therapeutic Drug Monitoring Predict the Steady State Area Under the Blood Concentration-Time Curve of Busulfan in Pediatric Patients Undergoing Hematopoietic Stem Ce... 由 Alsultan, Abdullah, Albassam, Ahmed A., Alturki, Abdullah, Alsultan, Abdulrahman, Essa, Mohammed, Almuzzaini, Bader, Alfadhel, Salman

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

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Herbal melanin induces interleukin-1β secretion and production by human THP-1 monocytes via Toll-like receptor 2 and p38 MAPK activation 由 El-Obeid, Adila, Yahya, Wesam Bin, Almuzzaini, Bader, Tuwaijri, Abeer Al, Najdi, Maria, Hassib, Adil, Matou-Nasri, Sabine

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The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohort 由 Al Ammari, Maha, AlBalwi, Mohammed, Sultana, Khizra, Alabdulkareem, Ibrahim B., Almuzzaini, Bader, Almakhlafi, Nada S., Aldrees, Mohammed, Alghamdi, Jahad

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Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation Sequencing 由 Rashid, Mamoon, Alasiri, Abdulrahman, Al Balwi, Mohammad A., Alkhaldi, Aziza, Alsuhaibani, Ahmed, Alsultan, Abdulrahman, Alharbi, Talal, Alomair, Lamya, Almuzzaini, Bader

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Nuclear Wiskott–Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells 由 Kuznetsov, Nikolai V., Almuzzaini, Bader, Kritikou, Joanna S., Baptista, Marisa A. P., Oliveira, Mariana M. S., Keszei, Marton, Snapper, Scott B., Percipalle, Piergiorgio, Westerberg, Lisa S.

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Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay 由 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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Discovery of a novel potentially transforming somatic mutation in CSF2RB gene in breast cancer 由 Rashid, Mamoon, Ali, Rizwan, Almuzzaini, Bader, Song, Hao, AlHallaj, Alshaimaa, Abdulkarim, Al Abdulrahman, Mohamed Baz, Omar, Al Zahrani, Hajar, Mustafa Sabeena, Muhammed, Alharbi, Wardah, Hussein, Mohamed, Boudjelal, Mohamed

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Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profiling 由 Matou-Nasri, Sabine, Najdi, Maria, AlSaud, Nouran Abu, Alhaidan, Yazeid, Al-Eidi, Hamad, Alatar, Ghada, AlWadaani, Deemah, Trivilegio, Thadeo, AlSubait, Arwa, AlTuwaijri, Abeer, Abudawood, Manal, Almuzzaini, Bader

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Epidemiology of cancer in Saudi Arabia thru 2010–2019: a systematic review with constrained meta-analysis 由 Alqahtani, Wedad Saeed, Almufareh, Nawaf Abdulrahman, Domiaty, Dalia Mostafa, Albasher, Gadah, Alduwish, Manal Abduallah, Alkhalaf, Huda, Almuzzaini, Bader, AL-marshidy, Salma Sanhaat, Alfraihi, Rgya, Elasbali, Abdelbaset Mohamed, Ahmed, Hussain Gadelkarim, Almutlaq, Bassam Ahmed

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Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer Panel 由 Almuzzaini, Bader, Alghamdi, Jahad, Alomani, Alhanouf, AlGhamdi, Saleh, Alsharm, Abdullah A., Alshieban, Saeed, Sayed, Ahood, Alhejaily, Abdulmohsen G., Aljaser, Feda S., Abudawood, Manal, Almajed, Faisal, Samman, Abdulhadi, Balwi, Mohammed A. Al, Aziz, Mohammad Azhar

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Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality 由 Alghamdi, Jahad, Alaamery, Manal, Barhoumi, Tlili, Rashid, Mamoon, Alajmi, Hala, Aljasser, Nasser, Alhendi, Yaseen, Alkhalaf, Hind, Alqahtani, Hanadi, Algablan, Omer, Alshaya, Abdulraham I., Tashkandi, Nabiha, Massadeh, Salam, Almuzzaini, Bader, Ehaideb, Salleh N., Bosaeed, Mohammad, Ayoub, Kamal, Yezli, Saber, Khan, Anas, Alaskar, Ahmed, Bouchama, Abderrezak

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Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening 由 Alfadhel, Majid, Umair, Muhammad, Almuzzaini, Bader, Alsaif, Saif, AlMohaimeed, Sulaiman A., Almashary, Maher A., Alharbi, Wardah, Alayyar, Latifah, Alasiri, Abdulrahman, Ballow, Mariam, AlAbdulrahman, Abdulkareem, Alaujan, Monira, Nashabat, Marwan, Al‐Odaib, Ali, Altwaijri, Waleed, Al‐Rumayyan, Ahmed, Alrifai, Muhammad T., Alfares, Ahmed, AlBalwi, Mohammed, Tabarki, Brahim

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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... 由 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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