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by Monies, Dorota and Abouelhoda, Mohammed and Assoum, Mirna and Moghrabi, Nabil and Rafiullah, Rafiullah and Almontashiri, Naif and Alowain, Mohammed and Alzaidan, Hamad and Alsayed, Moeen and Subhani, Shazia and Cupler, Edward and Faden, Maha and Alhashem, Amal and Qari, Alya and Chedrawi, Aziza and Aldhalaan, Hisham and Kurdi, Wesam and Khan, Sameena and Rahbeeni, Zuhair and Alotaibi, Maha and Goljan, Ewa and Elbardisy, Hadeel and ElKalioby, Mohamed and Shah, Zeeshan and Alruwaili, Hibah and Jaafar, Amal and Albar, Ranad and Akilan, Asma and Tayeb, Hamsa and Tahir, Asma and Fawzy, Mohammed and Nasr, Mohammed and Makki, Shaza and Alfaifi, Abdullah and Akleh, Hanna and Yamani, Suad and Bubshait, Dalal and Mahnashi, Mohammed and Basha, Talal and Alsagheir, Afaf and Abu Khaled, Musad and Alsaleem, Khalid and Almugbel, Maisoon and Badawi, Manal and Bashiri, Fahad and Bohlega, Saeed and Sulaiman, Raashida and Tous, Ehab and Ahmed, Syed and Algoufi, Talal and Al-Mousa, Hamoud and Alaki, Emadia and Alhumaidi, Susan and Althagafi, Malak and Alghamdi, Hadeel and Alghamdi, Malak and Sahly, Ahmed and Nahrir, Shapar and Al-Ahmari, Ali and Alkuraya, Hisham and Alkuraya, Fowzan S and Almehaidib, Ali and Abanemai, Mohammed and Alsohaibaini, Fahad and Alsaud, Bandar and Arnaout, Rand and Abdel-Salam, Ghada M.H and Aldhekri, Hasan and AlKhater, Suzan and Alqadi, Khalid and Alsabban, Essam and Alshareef, Turki and Awartani, Khalid and Banjar, Hanaa and Alsahan, Nada and Abosoudah, Ibraheem and Alashwal, Abdullah and Aldekhail, Wajeeh and Alhajjar, Sami and Al-Mayouf, Sulaiman and Alsemari, Abdulaziz and Alshuaibi, Walaa and Altala, Saeed and Altalhi, Abdulhadi and Baz, Salah and Hamad, Muddathir and Abalkhail, Tariq and Alenazi, Badi and Alkaff, Alya and Almohareb, Fahad and Al Mutairi, Fuad and Alsaleh, Mona and Alsonbul, Abdullah and Alzelaye, Somaya and Bahzad, Shakir and Manee, Abdulaziz Bin and Jarrad, Ola and Meriki, Neama and Albeirouti, Bassem and Alqasmi, Amal and ...
The American Journal of Human Genetics, ISSN 0002-9297, 06/2019, Volume 104, Issue 6, pp. 1182 - 1201
We report the results of clinical exome sequencing (CES) on >2,200 previously unpublished Saudi families as a first-tier test. The predominance of... 
knockout | clinical genomics | hybrid phenotype | phenotypic expansion | multilocus phenotypes | fetal malformation | autozygome | genomics-first | exome | gonadal mosaicism | expanded carrier screening | candidate genes | first-tier | prenatal | dual diagnosis
Journal Article
Biomedicine & Pharmacotherapy, ISSN 0753-3322, 04/2019, Volume 112, pp. 108584 - 108584
Stem cell therapy represents a promising therapeutic avenue for cardiac disorders, including heart failure. Although stem cell transplantation showed... 
Heart failure | Homing | NaHS | Neovascularization | Differentiation | Stem cell | MEDICINE, RESEARCH & EXPERIMENTAL | HOMEOSTASIS | MYOCARDIAL-INFARCTION | CARDIOMYOCYTES | ISOPROTERENOL | TRANSPLANTATION | REPAIR | CARDIAC-HYPERTROPHY | NITRIC-OXIDE | PHARMACOLOGY & PHARMACY | GROWTH-FACTOR | EXPRESSION
Journal Article
Journal of the Egyptian Womenʼs Dermatologic Society, ISSN 1687-1537, 01/2018, Volume 15, Issue 1, pp. 23 - 29
BACKGROUNDBasal cell carcinomas (BCC) produce large varieties of matrix metalloproteinases (MMPs). MMP induction occurs as a consequence of acute ultraviolet... 
matrix metalloproteinases, basal cell carcinoma | undifferentiated | differentiated | safety margin | Basal cell carcinoma | Proteases | Physiological aspects | Development and progression | Genetic aspects | Research | Gene expression
Journal Article
Annals of Hematology, ISSN 0939-5555, 8/2014, Volume 93, Issue 8, pp. 1313 - 1318
Matrix metalloproteinases (MMPs) are zinc-dependent endopeptidases capable of extracellular matrix degradation. MMP2 is the key molecule that control invasion,... 
B-NHL | MMP2 −735C/T | Medicine & Public Health | Hematology | Egypt | Oncology | MMP2 −1306C/T
Journal Article
Experimental and Clinical Transplantation, ISSN 1304-0855, 06/2016, Volume 14, Issue 3, pp. 271 - 275
Objectives: The study objective was to investigate the predictability and risk factors for the development of new-onset type 2 diabetes mellitus after... 
Risk | NODAT | Saudi | IMPACT | RENAL-ALLOGRAFT RECIPIENTS | KIDNEY-TRANSPLANTATION | GLUCOSE | ARABIA | PREDICTION | CYCLOSPORINE | TRANSPLANTATION | T?p
Journal Article
Egyptian Journal of Chest Diseases and Tuberculosis, ISSN 0422-7638, 07/2015, Volume 64, Issue 3, pp. 693 - 701
Improving the outcome of mechanically ventilated patients remains a mission we all strive to achieve. To provide baseline information for epidemiological... 
Invasive and noninvasive mechanical ventilation
Journal Article
INTERNATIONAL JOURNAL OF DERMATOLOGY, ISSN 0011-9059, 06/2009, Volume 48, Issue 6, pp. 584 - 587
Background Genetic polymorphisms of the androgen receptor (AR) gene have been studied in male androgenetic alopecia (AGA); however, little is known about gene... 
MALE PATTERN BALDNESS | POLYMORPHISM | DERMATOLOGY | Genetic Predisposition to Disease | Premenopause | Gene Frequency | Humans | Egypt | Exons - genetics | Genotype | Case-Control Studies | Receptors, Androgen - genetics | Alopecia - genetics | Polymorphism, Restriction Fragment Length | Sex Factors | Adult | Female
Journal Article
Indian Journal of Dermatology, ISSN 0019-5154, 11/2011, Volume 56, Issue 6, pp. 673 - 677
Most atopic dermatitis (AD) patients have elevated serum immunoglobulin E (IgE). Impaired folic acid (FA) metabolism was found to reduce the intracellular... 
folic acid | Atopic dermatitis | IgE | Care and treatment | Immunoglobulin E | Physiological aspects | Genetic aspects | Diagnosis | Research | Health aspects | Folic acid | Dermatology | Dermatitis | Vitamin B | Original
Journal Article
International Journal of Dermatology, ISSN 0011-9059, 2009, Volume 48, Issue 6, pp. 584 - 587
Genetic polymorphisms of the androgen receptor (AR) gene have been studied in male androgenetic alopecia (AGA); however, little is known about gene... 
Genetic research | Alopecia | Baldness | Population genetics | Analysis | Index Medicus
Journal Article
The Advocate, 11/2007
  Most importantly, he has made the flame of freedom burn ever brighter and our remembrance of, and respect for, our military heroes ever stronger. [...] as... 
Newspaper Article
Journal Article
Journal of Drug Delivery Science and Technology, ISSN 1773-2247, 08/2019, Volume 52, p. 83
Journal Article
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2018, Volume 20, Issue 4, pp. 420 - 427
Purpose: The application of genomic sequencing to investigate unexplained death during early human development, a form of lethality likely enriched for severe... 
embryonic lethality | genomic autopsy | ETIOLOGY | VARIANTS | GENETICS & HEREDITY | MUTATIONS | IDENTIFICATION | DISCOVERY | Index Medicus
Journal Article
Genetics in Medicine, ISSN 1098-3600, 03/2019, Volume 21, Issue 3, pp. 736 - 742
Purpose: Establishing links between Mendelian phenotypes and genes enables the proper interpretation of variants therein. Autozygome, a rich source of... 
candidate genes | ACMG guidelines | variant interpretation | CLINICAL VALIDITY | ASSOCIATIONS | LANDSCAPE | DISORDERS | DISCOVERY | INTELLECTUAL DISABILITY | EXOME SEQUENCING REVEALS | GENOMICS | GENETICS & HEREDITY | TRANSFER-RNA | MUTATIONS | Disease | Genomics | Index Medicus
Journal Article