ACCESSIBILITY OF INCLUSIVE PROVISIONS FOR STUDENTS WITH DISABILITIES TRANSITIONING INTO HIGHER EDUCATION IN THE UAE: AN INVESTIGATIVE STUDY by Alshehhi, Khawla

“…Statistical analysis and coding of the data revealed themes of PWDs readiness for the journey from high school to higher education highlighting needed provisions that can facilitate their transition to HEIs. …”
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Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi–Bickel Syndrome by Sanaa Sharari (12561952)

“…The intronic mutation did not affect the coding sequence of GLUT2, its expression, or glucose transport activity. …”

On the verge of colistin resistance. (c2019) by Alousi, Sahar

“…Plasmid encoded mcr-1 gene was screened through in silico PCR. …”
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Whole-genome Sequences of Multidrug-Resistant Escherichia coli by Khodor, Ragheed R.

“…To our knowledge, this is the first detection of blaNDM-6 encoding E. coli from Lebanon. Our study revealed the diversity within E. coli clinical isolates and the role of mobile elements in disseminating resistance determinants. …”
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Single-cell long noncoding RNA (lncRNA) transcriptome implicates MALAT1 in triple-negative breast cancer (TNBC) resistance to neoadjuvant chemotherapy by Hibah Shaath (5599658)

“…The differential analysis revealed upregulation of 202 and downregulation of 19 lncRNAs in the persistence group, including upregulation of five different transcripts encoding for the MALAT1 lncRNA. CRISPR/Cas9-mediated MALAT1 promoter deletion in BT-549 TNBC model enhanced sensitivity to paclitaxel and doxorubicin, suggesting a role for MALAT1 in conferring resistance. …”

Gene Expression Landscape of Chronic Myeloid Leukemia K562 Cells Overexpressing the Tumor Suppressor Gene PTPRG by Giulia Lombardi (3944720)

“…<div><p>This study concerns the analysis of the modulation of Chronic Myeloid Leukemia (CML) cell model K562 transcriptome following transfection with the tumor suppressor gene encoding for Protein Tyrosine Phosphatase Receptor Type G (PTPRG) and treatment with the tyrosine kinase inhibitor (TKI) Imatinib. …”

A depth-controlled and energy-efficient routing protocol for underwater wireless sensor networks by Umesh Kumar Lilhore (17727684)

“…In the proposed energy-efficient routing protocol, an existing genetic algorithm is enhanced by adding an encoding strategy, a crossover procedure, and an improved mutation operation that helps determine the nodes. …”

Comparative transcriptomics of primary cells in vertebrates by Tanvir Alam (638619)

“…Expression of genes with products involved in transcription, RNA processing, and transcriptional regulation was more likely to be conserved, while expression of genes encoding proteins involved in intercellular communication was more likely to have diverged during evolution. …”

The histone H2B Arg95 residue efficiently recruits the transcription factor Spt16 to mediate Ste5 expression of the pheromone response pathway by Abdallah Alhaj Sulaiman (17777421)

“…This mutant is defective in the expression of several genes belonging to the pheromone response pathway including STE5 encoding a scaffold protein that promotes the activation of downstream MAP kinases. …”

Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension by Ossama K. Abou Hassan (18618628)

“…Mutations in the gene encoding the eukaryotic translation initiation factor 2 alpha kinase 4 (EIF2AK4) have recently been linked to this particular subgroup of PH.…”

Functional Validation and Network-Based Prioritization of Key Transcriptional Factors of Diabetic Kidney Disease by Ikhlak Ahmed (6428939)

“…Further, we recognized a small but a closely connected set of these susceptibility genes enriched for podocyte differentiation, several of which were characterized as genes encoding critical transcriptional factors (TFs) involved in DN development and podocyte function. …”

A Novel Homozygous <i>MC2R</i> Variant Leading to Type-1 Familial Glucocorticoid Deficiency by Idris Mohammed (751020)

“…<h3>Context</h3><p dir="ltr">Type 1 familial glucocorticoid deficiency (FGD) (OMIM #607397) is a rare autosomal recessive disorder due to mutations in melanocortin-2-receptor (MC2R) gene encoding the G protein-coupled adrenocorticotropic (ACTH) transmembrane receptor.…”

Deep intronic ‘mutations’ cause hemophilia A by El Maarri, O.

“…In a small group of typical hemophilia A (HA) patients no mutations in the F8 coding sequence (cDNA) could be found. In the current study, we performed a systematic screening of genetic and non-genetic parameters associated with reduced FVIII:C levels in a group of mostly mild HA (only one moderate) patients with no detectable mutations in F8 cDNA. …”
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“Long term solutions for the self-reliance of Syrian paternally-orphaned institutionalized refugees by Sharabati, Nour

“…A deductive data analysis was implemented for the observations, interviews and documents, using a color-coding system that was based on priori codes from the reviewed literature. …”
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Sequence conservation and variability of imprinting in the Beckwith–Wiedemann syndrome gene cluster in human and mouse by El-Maarri, Osman

“…One of these clusters encompasses an additional gene coding for a homologue of the ribosomal protein L26. …”
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A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation by El Maarri, Osman

“…Of these, 24 were located in coding regions and 10 resulted in an amino acid change that may affect the corresponding DNMT protein structure or function. …”
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HistoMSC: Density and topology analysis for AI-based visual annotation of histopathology whole slide images by Zahoor Ahmad (358103)

“…Sparse nuclei-level annotations are then aggregated using kernel density estimation, followed by color-coding and isocontouring. This reduces visual clutter and provides per-pixel probabilities with respect to pathology taxonomies. …”

UniBFS: A novel uniform-solution-driven binary feature selection algorithm for high-dimensional data by Behrouz Ahadzadeh (19757022)

“…UniBFS exploits the inherent characteristic of binary algorithms-binary coding-to search the entire problem space for identifying relevant features while avoiding irrelevant ones. …”

EndMT Regulation by Small RNAs in Diabetes-Associated Fibrotic Conditions: Potential Link With Oxidative Stress by Roberta Giordo (299595)

“…Recent evidence suggests that small RNAs, in particular microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), are crucial mediators of EndMT. …”

Computational and Transcriptome Analyses Revealed Preferential Induction of Chemotaxis and Lipid Synthesis by SARS-CoV-2 by Hibah Shaath (5599658)

“…In this study, we analyzed RNA-seq transcriptome data from Calu-3 human lung epithelial cells infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) compared to five other viruses namely, severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East Respiratory Syndrome (SARS-MERS), influenzavirus A (FLUA), influenzavirus B (FLUB), and rhinovirus (RHINO) compared to mock-infected cells and characterized their coding and noncoding RNA transcriptional portraits. …”