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Mohammed Al-Dosari

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Chemicals & Drugs

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Sequence Analysis, DNA

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Publications

TOP 3
Salma Awad; Dilek Colak; Mohammed S Al-Dosari; Fowzan S Alkuraya; Nadya Al-Yacoub; Mustafa A Salih; Coralie Poizat
Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis.
Mohammed S Al-Dosari; Amal Al-Hemidan; Nouran Adly; Buthainah Albash; Mohammed Al-Owain; Wesam Kurdi; Tariq A Masoodi; Maha Tulbah; Fowzan S Alkuraya
Mutation in MPDZ causes severe congenital hydrocephalus.
Fahad Al-Jenoobi; Khalid M Alkharfy; Abdullah M Al-Mohizea; Saleh Al-Muhsen; Khawla M Bagulb; Rabih Halwani; Mohammad Khalid Parvez; Amal M Alghamdi; Mohammed S Al-Dosari
CYP2C19 genetic polymorphism in Saudi Arabians.

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All Publications

2013: Salma Awad; Dilek Colak; Mohammed S Al-Dosari; Fowzan S Alkuraya; Nadya Al-Yacoub; Mustafa A Salih; Coralie Poizat
Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis.
Human molecular genetics 2013;22(11):2200-13.
2013: Mohammed S Al-Dosari; Amal Al-Hemidan; Nouran Adly; Buthainah Albash; Mohammed Al-Owain; Wesam Kurdi; Tariq A Masoodi; Maha Tulbah; Fowzan S Alkuraya
Mutation in MPDZ causes severe congenital hydrocephalus.
Journal of medical genetics 2013;50(1):54-8.
2013: Fahad Al-Jenoobi; Khalid M Alkharfy; Abdullah M Al-Mohizea; Saleh Al-Muhsen; Khawla M Bagulb; Rabih Halwani; Mohammad Khalid Parvez; Amal M Alghamdi; Mohammed S Al-Dosari
CYP2C19 genetic polymorphism in Saudi Arabians.
Basic & clinical pharmacology & toxicology 2013;112(1):50-4.
2012: Mohammed Al-Owain; Taghreed Shuaib; Asma Sunker; Mohammed S Al-Dosari; Fowzan S Alkuraya
Identification of a novel ZNF469 mutation in a large family with Ehlers-Danlos phenotype.
Gene 2012;511(2):447-50.
2012: Abdullah M Al-Mohizea; Saleh Al-Muhsen; Khawla M Bagulb; Rabih Halwani; M Khalid Parvez; Mohammad Khalid Parvez; Amal M Alghamdi; Fahad Al-Jenoobi; Khalid M Alkharfy; Mohammed S Al-Dosari
Genetic variability and haplotype profile of MDR1 in Saudi Arabian males.
Molecular biology reports 2012;39(12):10293-301.
2012: Ranad Shaheen; Hanan E Shamseldin; Asma Sunker; Nouran Adly; Mohammed S Al-Dosari; Muneera Al-Husain; Futwan Al-Mohanna; Muneera J Alshammari; Tarfa Al-Sheddi; Eissa Faqeih; Sean G Megason; Ramil R Noche; Fowzan S Alkuraya
POC1A truncation mutation causes a ciliopathy in humans characterized by primordial dwarfism.
American journal of human genetics 2012;91(2):330-6.
2012: Mohammed S Al-Dosari; Mohammed A Alghofely; Muneera Al-Shammari; Ahmad Boukai; Eissa Faqeih; Ranad Shaheen; Fowzan S Alkuraya
3M syndrome: an easily recognizable yet underdiagnosed cause of proportionate short stature.
The Journal of pediatrics 2012;161(1):139-45.e1.
2012: Hanif Khalak; Brian Meyer; Dorota Monies; Khushnooda Ramzan; Ranad Shaheen; Hanan Shamseldin; Salma Majid Majid; Leen Abu-Safieh; Nada Abu-Dhaim; Anas Alazami; Mohammed Aldahmesh; Mohammed S Al-Dosari; Mohammed S Al-Hamed; Latifa Al-Jbali; Abeer Almostafa; May Al-Rashed; Nada Al-Tassan; Fatema Alzahrani; Batoul Baz; Samya Hagos; Mais Hashem; Faiqa Imtiaz; Namik Kaya; Fowzan S Alkuraya
Autozygome maps dispensable DNA and reveals potential selective bias against nullizygosity.
Genetics in medicine : official journal of the American College of Medical Genetics 2012;14(5):515-9.
2012: M S El-Said; Mohammed S Al-Dosari; M G El-Gazzar; Moustafa M Ghorab
Synthesis, anticancer activity and radiosensitizing evaluation of some new 2-pyridone derivatives.
Arzneimittel-Forschung 2012;62(3):149-56.
2012: Mohammed S Al-Dosari
In vitro and in vivo antioxidant activity of alfalfa (Medicago sativa L.) on carbon tetrachloride intoxicated rats.
The American journal of Chinese medicine 2012;40(4):779-93.
2011: Fowzan S Alkuraya; Xuyu Cai; Carina Emery; Ganeshwaran H Mochida; Mohammed S Al-Dosari; Jillian M Felie; R Sean Hill; Brenda J Barry; Jennifer N Partlow; Generoso G Gascon; Amal Kentab; mohammed m jan; Ranad Shaheen; Yuanyi Feng; Christopher Walsh
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected].
American journal of human genetics 2011;88(5):536-47.
2011: Mansour S Al-Said; Moustafa M Ghorab; Mohammed S Al-Dosari; Mostafa M Hamed
Synthesis and in vitro anticancer evaluation of some novel hexahydroquinoline derivatives having a benzenesulfonamide moiety.
European journal of medicinal chemistry 2011;46(1):201-7.
2010: Mohammed S Al-Dosari; Ranad Shaheen; Dilek Colak; Fowzan S Alkuraya
Novel CENPJ mutation causes Seckel syndrome.
Journal of medical genetics 2010;47(6):411-4.
2010: Mohammed S Al-Dosari; Fowzan S Alkuraya
Trichorhinophalangeal syndrome: Report of a novel familial TRPS1 mutation.
Clinical dysmorphology 2010;19(2):98-100.
2010: Mohammed S Al-Dosari
The effectiveness of ethanolic extract of Amaranthus tricolor L.: A natural hepatoprotective agent.
The American journal of Chinese medicine 2010;38(6):1051-64.
2010: Mohammed S Al-Dosari; M Almazyad; L Al-Ebdi; J Y Mohamed; Saad Al-Dahmash; Hassan Al-Dhibi; Eman Al-Kahtani; Shahira Al-turkmani; Hisham Alkuraya; B D Hall; Fowzan S Alkuraya
Ocular manifestations of branchio-oculo-facial syndrome: report of a novel mutation and review of the literature.
Molecular vision 2010;16():813-8.
2009: Mohammed S Al-Dosari; Xiang Gao
Nonviral gene delivery: principle, limitations, and recent progress.
The AAPS journal 2009;11(4):671-81.
2008: Mohammed S Al-Dosari; Saleh Al-Muhsen; Ayman Al-Jazaeri; Julia Mayerle; Martin Zenker; Fowzan S Alkuraya
Johanson-Blizzard syndrome: report of a novel mutation and severe liver involvement.
American journal of medical genetics. Part A 2008;146A(14):1875-9.
2006: Mohammed S Al-Dosari; Guisheng Zhang; Joseph E Knapp; Dexi Liu
Direct assessment of promoter activity of human cytochrome p450 genes using optimized transfection in vitro and in vivo.
Bioscience reports 2006;26(3):217-29.
2006: Mohammed S Al-Dosari; Joseph E Knapp; Dexi Liu
Activation of human CYP2C9 promoter and regulation by CAR and PXR in mouse liver.
Molecular pharmaceutics 2006;3(3):322-8.
2006: Mohammed S Al-Dosari; Guisheng Zhang; Joseph E Knapp; Dexi Liu
Evaluation of viral and mammalian promoters for driving transgene expression in mouse liver.
Biochemical and biophysical research communications 2006;339(2):673-8.
2005: Mohammed S Al-Dosari; Joseph E Knapp; Dexi Liu
Hydrodynamic delivery.
Advances in genetics 2005;54():65-82.