Search Results - "Awan, Ahmed Zuhier"

Assessment of Knowledge of Monkeypox Viral Infection among the General Population in Saudi Arabia by Alshahrani, Najim Z, Alzahrani, Faris, Alarifi, Abdullah M, Algethami, Mohammed R, Alhumam, Maathir Naser, Ayied, Hatim Abdullah Mohammed, Awan, Ahmed Zuhier, Almutairi, Abdullah Faisal, Bamakhrama, Saeed Abdullah, Almushari, Budur Saad, Sah, Ranjit

“…Monkeypox is re-emerging and spreading over the world, posing a serious threat to human life, especially in non-endemic countries, including Saudi Arabia. Due…”
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Molecular insights into the coding region mutations of low‐density lipoprotein receptor adaptor protein 1 (LDLRAP1) linked to familial hypercholesterolemia by Shaik, Noor A., Al‐Qahtani, Faten, Nasser, Khalidah, Jamil, Kaiser, Alrayes, Nuha Mohammad, Elango, Ramu, Awan, Zuhier Ahmed, Banaganapalli, Babajan

“…Background Familial hypercholesterolemia (FH) is a lipid disorder caused by pathogenic mutations in LDLRAP1 gene. The present study has aimed to deepen our…”
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A Comparison between Eight Formulas for the Estimation of Plasma Low-Density Lipoprotein Cholesterol in the Saudi Arabian Population by Zuhier Ahmed Awan, Dena Abdulbadea Nuwaylati

“…CONTEXT: Low-density lipoprotein cholesterol (LDL-C) is the classical target in cardiovascular (CV) disease management and is usually estimated by Friedewald's…”
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Etodolac Fortified Sodium Deoxycholate Stabilized Zein Nanoplatforms for Augmented Repositioning Profile in Human Hepatocellular Carcinoma: Assessment of Bioaccessibility, Anti-Proliferation, Pro-Apoptosis and Oxidant Potentials in HepG2 Cells by Kammoun, Ahmed K, Hegazy, Maha A, Khedr, Alaa, Awan, Zuhier Ahmed, Khayat, Maan T, Al-Sawahli, Majid Mohammad

“…This work aimed to enhance the purposing profile of Etodolac (ETD) in Human Hepatocellular Carcinoma (HCC) HepG2 cells using sodium deoxycholate stabilized…”
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Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen by Awan, Zuhier Ahmed, Rashidi, Omran M., Al-Shehri, Bandar Ali, Jamil, Kaiser, Elango, Ramu, Al-Aama, Jumana Y., Hegele, Robert A., Banaganapalli, Babajan, Shaik, Noor A.

“…Familial hypercholesterolemia (FH), a well-known lipid disease caused by inherited genetic defects in cholesterol uptake and metabolism is underdiagnosed in…”
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Structural characterization and conformational dynamics of alpha-1 antitrypsin pathogenic variants causing alpha-1-antitrypsin deficiency by Shaik, Noor Ahmad, Saud Al-Saud, Najla Bint, Abdulhamid Aljuhani, Thamer, Jamil, Kaiser, Alnuman, Huda, Aljeaid, Deema, Sultana, Nasreen, El-Harouni, Ashraf AbdulRahman, Awan, Zuhier Ahmed, Elango, Ramu, Banaganapalli, Babajan

“…Alpha-1 antitrypsin deficiency (A1ATD) is a progressive lung disease caused by inherited pathogenic variants in the gene. However, their actual role in…”
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Low resolution protein mapping and KB-R7943 drug-protein molecular interaction analysis of long-QT syndrome linked KCNH2 mutations by Ahmed Awan, Zuhier, Bima, Abdulhadi, Rashidi, Omran M., Jamil, Kaiser, Khan, Imran A., Almukadi, Haifa S., Bilgrami, Anwar L., Ahmad Shaik, Noor, Banaganapalli, Babajan

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Multilevel systems biology analysis of lung transcriptomics data identifies key miRNAs and potential miRNA target genes for SARS-CoV-2 infection by Banaganapalli, Babajan, Al-Rayes, Nuha, Awan, Zuhier Ahmed, Alsulaimany, Faten A., Alamri, Abdulhakeem S., Elango, Ramu, Malik, Md Zubbair, Shaik, Noor A.

“…The spread of a novel severe acute respiratory syndrome corona virus 2 (SARS-CoV-2) has affected both the public health and the global economy. The current…”
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Spectral signal processing approaches for selective quantification of the recently FDA approved brand-new combination of Vaborbactam and Meropenem; for conformity assessment of bulk and batch release by Awan, Zuhier Ahmed, Hegazy, Maha A., Kammoun, Ahmed K.

“…Vaborbactam (VBR) and Meropenem (MRP) is a recently approved combination for treatment of complicated urinary tract infection (cUTI). Three different signal…”
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Structural and Molecular Interaction Studies on Familial Hypercholesterolemia Causative PCSK9 Functional Domain Mutations Reveals Binding Affinity Alterations with LDLR by Awan, Zuhier Ahmed, Bahattab, Rawabi, Kutbi, Hussam Ibrahim, Noor, Ahmad Omar Jamal, Al-Nasser, Marzog S., Shaik, Noor Ahmad, Banaganapalli, Babajan

“…Familial hypercholesterolemia (FH) is a metabolic disease caused by the inherited pathogenic mutations in PCSK9 gene. This study has evaluated the potential of…”
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Interpreting the Mechanism of APOE (p.Leu167del) Mutation in the Incidence of Familial Hypercholesterolemia; An In-silico Approach by Rashidi, Omran Mohammed, H Nazar, Fatima Amanullah, Alama, Mohamed Nabil, Awan, Zuhier Ahmed

“…Apolipoprotein E (APOE) gene is a ligand protein in humans which mediates the metabolism of cholesterol by binding to the low-density lipoprotein receptor…”
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