Search Results - "El‐Harouni, Ashraf A."

Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches by Shaik, Noor Ahmad, Nasser, Khalidah, Mohammed, Arif, Mujalli, Abdulrahman, Obaid, Ahmad A, El-Harouni, Ashraf A, Elango, Ramu, Banaganapalli, Babajan

“…Asthma is a life-threatening and chronic inflammatory lung disease that is posing a true global health challenge. The genetic basis of the disease is fairly…”
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Pluripotent Stem Cell‐Derived Hematopoietic Progenitors Are Unable to Downregulate Key Epithelial‐Mesenchymal Transition‐Associated miRNAs by Meader, Ellie, Barta, Tomas, Melguizo‐Sanchis, Dario, Tilgner, Katarzyna, Montaner, David, El‐Harouni, Ashraf A., Armstrong, Lyle, Lako, Majlinda

“…Hematopoietic stem cells derived from pluripotent stem cells could be used as an alternative to bone marrow transplants. Deriving these has been a long‐term…”
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Distribution of CYP2C8 and CYP2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study by Rao, Durga Koteswara, Murthy, Dwaraknath K, Shaik, Nazia Sultana, Banaganapalli, Babajan, Konda, Kumaraswami, Rao, Hanmantha P, Ganti, Eswar, Ahmed Awan, Zuhair, A El‐Harouni, Ashraf, Elango, Ramu, Ali Khan, Imran, Shaik, Noor Ahmad

“…Summary The CYP2C8 and CYP2C9 are two major isoforms of the cytochrome P450 enzyme family, which is involved in drug response, detoxification, and disease…”
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iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors by Melguizo-Sanchis, Dario, Xu, Yaobo, Taheem, Dheraj, Yu, Min, Tilgner, Katarzyna, Barta, Tomas, Gassner, Katja, Anyfantis, George, Wan, Tengfei, Elango, Ramu, Alharthi, Sameer, El-Harouni, Ashraf A., Przyborski, Stefan, Adam, Soheir, Saretzki, Gabriele, Samarasinghe, Sujith, Armstrong, Lyle, Lako, Majlinda

“…Aplastic Anemia (AA) is a bone marrow failure (BMF) disorder, resulting in bone marrow hypocellularity and peripheral pancytopenia. Severe aplastic anemia…”
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Review of literature: genes related to postaxial polydactyly by Verma, Prashant Kumar, El-Harouni, Ashraf A

“…Postaxial polydactyly (PAP) is one of the commonest congenital malformations and usually is associated to several syndromes. There is no primary…”
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Molecular prenatal diagnosis of autosomal recessive childhood spinal muscular atrophies (SMAs) by Essawi, Mona L., Al-Attribi, Ghada M., Gaber, Khaled R., El-Harouni, Ashraf A.

“…Autosomal recessive childhood spinal muscular atrophy (SMAs) is the second most common neuromuscular disorder and a common cause of infant disability and…”
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First Comprehensive In Silico Analysis of the Functional and Structural Consequences of SNPs in Human GalNAc-T1 Gene by Ali Mohamoud, Hussein Sheikh, Manwar Hussain, Muhammad Ramzan, El-Harouni, Ashraf A., Shaik, Noor Ahmad, Qasmi, Zaheer Ulhaq, Merican, Amir Feisal, Baig, Mukhtiar, Anwar, Yasir, Asfour, Hani, Bundajji, Nabil S., al-Aama, Jumana Yousuf

“…GalNAc-T1, a key candidate of GalNac-transferases genes family that is involved in mucin-type O-linked glycosylation pathway, is expressed in most biological…”
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Congenital heart defects in Down syndrome patients from western Saudi Arabia by Al-Aama, Jumana Y, Bondagji, Nabeel S, El-Harouni, Ashraf A

“…To characterize congenital heart defects in individuals with Down syndrome (DS) in the Western Region of Saudi Arabia, and compare with studies from other…”
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Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches by Noor Ahmad Shaik, Khalidah Nasser, Arif Mohammed, Abdulrahman Mujalli, Ahmad A. Obaid, Ashraf A. El‐Harouni, Ramu Elango, Babajan Banaganapalli

“…Asthma is a life-threatening and chronic inflammatory lung disease that is posing a true global health challenge. The genetic basis of the disease is fairly…”
Get full text

Distribution of CYP 2C8 and CYP 2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study by Rao, Durga Koteswara, Murthy, Dwaraknath K, Shaik, Nazia Sultana, Banaganapalli, Babajan, Konda, Kumaraswami, Rao, Hanmantha P, Ganti, Eswar, Ahmed Awan, Zuhair, A El‐Harouni, Ashraf, Elango, Ramu, Ali Khan, Imran, Shaik, Noor Ahmad

“…The CYP 2C8 and CYP 2C9 are two major isoforms of the cytochrome P450 enzyme family, which is involved in drug response, detoxification, and disease…”
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Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies by EFFAT, Laila K, EL-HAROUNI, Ashraf A, AMRA, Khalda S, EL-MINISI, Tarik I, MEGUID, Nagwa Abdel, EL-AWADY, Mostafa

“…Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are allelic disorders caused by mutations within the dystrophin gene. Our study has…”
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