Search Results - "Sobahy, Turki"
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CACSV: a computational web-sever that provides classification for cancer somatic genetic variants from different tissues
Published in BMC bioinformatics (15-03-2023)“…Understanding the role and function of genetic variants is extremely important when analyzing and interpreting a myriad of human disease processes. For cancer…”
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AllelePred: A Simple Allele Frequencies Ensemble Predictor for Different Single Nucleotide Variants
Published in IEEE/ACM transactions on computational biology and bioinformatics (01-01-2023)“…Background & Objective: Genomic medicine stands to be revolutionized by understanding single nucleotide variants (SNVs) and their expression in single-gene…”
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Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden
Published in Genetics in medicine (01-12-2016)“…Most autosomal recessive diseases are rare, but they collectively account for a substantial proportion of disease burden, especially in consanguineous…”
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Clinically actionable cancer somatic variants (CACSV): a tumor interpreted dataset for analytical workflows
Published in BMC medical genomics (25-04-2022)“…The recent development and enormous application of parallel sequencing technology in oncology has produced immense amounts of cell-specific genetic…”
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The role of BRCA1/2 in hereditary and familial breast and ovarian cancers
Published in Molecular genetics & genomic medicine (01-09-2019)“…Background BRCA1/2 pathogenic variants have become associated with familial breast and ovarian cancers, and hereditary cancer‐predisposition syndrome. With…”
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SARS-COV-2 Triggers the Development of Class I and Class II HLA Antibodies in Recovered Convalescent Plasma Donors
Published in Intervirology (04-04-2022)“…Various studies have shown that SARS-CoV-2 is a highly immunogenic virus. It is known that different types of immunogenic viral pathogens could trigger the…”
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Biweekly cetuximab in combination with capecitabine and oxaliplatin (XELOX) or irinotecan (XELIRI) in the first-line and second-line treatment of patients with RAS wild-type metastatic colorectal cancer
Published in Ecancermedicalscience (15-12-2022)“…Oral capecitabine in combination with intravenous oxaliplatin (XELOX) or irinotecan (XELIRI) are acceptable substitutions to fully intravenous regimens…”
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Quantitative DNA analysis of very low-level hepatitis B viremic patients reporting to the gastroenterology clinic
Published in Saudi medical journal (01-02-2011)“…To examine data on very low-level viremic hepatitis B virus (HBV) infections in patients reporting to a gastroenterology clinic, and to investigate methods to…”
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Synthesis and antitumorigenesis effect of novel 2-amino -3-cyano pyridine derivatives containing sulfonamide moiety against breast cancer
Published in Journal of molecular structure (05-04-2024)“…•Novel 2-amino-3-cyano pyridine derivatives containing sulphonamide were synthesized.•Spectroscopic tools characterized the structures of the synthesized…”
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Abstract P4-09-13: Spectrum analysis of the inherited mutations of BRCA1/-2 genes that associated with high risk breast cancer in Saudi population
Published in Cancer research (Chicago, Ill.) (15-02-2020)“…Background: Breast cancer (BC) is the most common prevalent cancer among female worldwide, despite the advances in molecular biology. In Saudi Arabia, the…”
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Prognostic and predictive biomarkers for clear cell renal cell carcinoma utilizing next generation sequencing
Published in Journal of clinical oncology (20-05-2019)“…Abstract only e16070 Background: The management of the clear cell renal cell carcinoma (cc-RCC) has evolved over the past decade. Clinical patients’ and tumor…”
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Abstract 3372: Mutations of mismatch repair genes in Her2 overexpressed breast cancer
Published in Cancer research (Chicago, Ill.) (01-07-2018)“…The importance of Mismatch Repair (MMR) in therapeutic selection is an area of recent research. Minority of unselected breast tumors exhibit mutations…”
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Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia, cross section hospital base study
Published in Journal of the neurological sciences (15-03-2022)“…To retrospectively report prVEPs in SPG11 ARHSP-TCC. ARHSPTCC is characterized by a thin corpus callosum, progressive spastic paraparesis, cognitive…”
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