IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome
Aldahmesh, Mohammed A, Li, Yuanyuan, Alhashem, Amal, Anazi, Shams, Alkuraya, Hisham, Hashem, Mais, Awaji, Ali A, Sogaty, Sameera, Alkharashi, Abdullah, Alzahrani, Saeed, Al Hazzaa, Selwa A, Xiong, Yong, Kong, Shanshan, Sun, Zhaoxia, Alkuraya, Fowzan S
Published in Human molecular genetics (15.06.2014)
Published in Human molecular genetics (15.06.2014)
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The Influence of rs1859168 Polymorphism on Serum Expression of HOTTIP and Its Target miR-615-3p in Egyptian Patients with Breast Cancer
Abdelaleem, Omayma O., Shaker, Olfat G., AbdelHafez, Marwa N., Abdelghaffar, Noha K., Eid, Hanaa M., Zaidan, Mohamed, Khalefa, Abeer A., Ahmed, Naglaa A., Hemeda, Nada F., Zaki, Othman M., Awaji, Aeshah Ali A., Mohammed, Shereen R.
Published in Biomolecules (Basel, Switzerland) (14.05.2021)
Published in Biomolecules (Basel, Switzerland) (14.05.2021)
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Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy
Al-Hassnan, Zuhair N, Almesned, Abdulrahman, Tulbah, Sahar, Alakhfash, Ali, Alhadeq, Faten, Alruwaili, Nadiah, Alkorashy, Maarab, Alhashem, Amal, Alrashdan, Ahmad, Faqeih, Eissa, Alkhalifi, Salwa M, Al Humaidi, Zainab, Sogaty, Sameera, Azhari, Nawal, Bakhaider, Abdulrahman M, Al Asmari, Ali, Awaji, Ali, Albash, Buthaina, Alhabdan, Mohammed, Alghamdi, Malak A, Alshuaibi, Walaa, Al-Hassnan, Raghad Z, Alshenqiti, Abduljabbar, Alqahtani, Aisha, Shinwari, Zarghuna, Rbabeh, Monther, Takroni, Saud, Alomrani, Ahmed, Albert Brotons, Dimpna C, AlQwaee, Abdullah M, Almanea, Waleed, Alfadley, Fadel A, Alfayyadh, Majid, Alwadai, Abdullah
Published in Circulation. Genomic and precision medicine (01.10.2020)
Published in Circulation. Genomic and precision medicine (01.10.2020)
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Dilated cardiomyopathy associated with NRAP gene: a case series
Names, Abdellh, Tohary, Mohammed, Hadad, Basel, Alhazmi, Abdurahman, Alaksham, Hamad, Gohal, Hassan, Gosadi, Ghadah, Awaji, Ali, Jareebi, Mohammad
Published in Journal of Biochemical and Clinical Genetics (01.06.2023)
Published in Journal of Biochemical and Clinical Genetics (01.06.2023)
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Vitamin E for the Prevention of Contrast-Induced Nephropathy: A Systematic Review and Meta-Analysis
Awaji, Ahmed Ali, Bakhamees, Basel H, Alalshaikh, Nouf K, Albelwi, Nawaf M, AL-Zahrani, Mead M, Alshammari, Khalaf F, Almutairi, Shaden D, Siraj, Ilaf M, Aljaber, Taif N, Alnajdi, Raghad S, Al-Majnooni, Shatha S, Alserhani, Abdulaziz S
Published in Curēus (Palo Alto, CA) (26.06.2024)
Published in Curēus (Palo Alto, CA) (26.06.2024)
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Human ‘knockouts’ of CSF3 display severe congenital neutropenia
Khouj, Ebtissal, Marafi, Dana, Aljamal, Bayan, Hajiya, Anwar, Elshafie, Reem M., Hashem, Mais O., Abdulwahab, Firdous, Jaafar, Amal, Alshidi, Tarfa, Aboelanine, Ashraf H., Awaji, Ali, Alkuraya, Fowzan S.
Published in British journal of haematology (01.11.2023)
Published in British journal of haematology (01.11.2023)
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Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus
Alazami, Anas M, Hijazi, Hadia, Al-Dosari, Mohammed S, Shaheen, Ranad, Hashem, Amal, Aldahmesh, Mohammed A, Mohamed, Jawahir Y, Kentab, Amal, Salih, Mustafa A, Awaji, Ali, Masoodi, Tariq A, Alkuraya, Fowzan S
Published in Journal of medical genetics (01.07.2013)
Published in Journal of medical genetics (01.07.2013)
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Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans
Shaheen, Ranad, Al‐Owain, Mohammed, Faqeih, Eissa, Al‐Hashmi, Nadia, Awaji, Ali, Al‐Zayed, Zayed, Alkuraya, Fowzan S
Published in American journal of medical genetics. Part A (01.06.2011)
Published in American journal of medical genetics. Part A (01.06.2011)
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MONITORING OF CHRONIC SINUSITIS USING NASAL NITRIC OXIDE AS A MARKER OF SINUS HEALTH: A SYSTEMATIC REVIEW: Pharmaceutical Sciences - HEALTH
IBRAHIM KARIRI, KHALIL, MAJRASHI, KHALID AHMED, FAGEHI, AHMAD ALI ABDU, HAKAMI, KHALID ALI AWAJI, JABER HAKAMI, AYMAN MOHAMMED, HAMZI, NAWAR AHMED
Published in International journal of life science and pharma research (30.01.2019)
Published in International journal of life science and pharma research (30.01.2019)
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Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans
Shaheen, Ranad, Al-Owain, Mohammed, Faqeih, Eissa, Al-Hashmi, Nadia, Awaji, Ali, Al-Zayed, Zayed, Alkuraya, Fowzan S
Published in American Journal of Medical Genetics Part A (01.06.2011)
Published in American Journal of Medical Genetics Part A (01.06.2011)
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