Circulating Tumour DNA Detection By The Urine-Informed Analysis Of Archival Serum Samples From Muscle-Invasive Bladder Cancer Patients.

Autor: BinHumaid FS; Bladder Cancer Research Centre, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK; Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Goel A; Bladder Cancer Research Centre, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK., Gordon NS; Bladder Cancer Research Centre, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK., Abbotts B; Bladder Cancer Research Centre, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK., Cheng KK; Institute of Applied Health Sciences, University of Birmingham, Birmingham, UK., Zeegers MP; University of Maastricht, Maastricht, The Netherlands., James ND; Institute of Cancer Research, London, UK., Altaweel WM; Department of Urology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Seyam RM; Department of Urology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Meyer BF; Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Arnold R; Bladder Cancer Research Centre, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK., Ward DG; Bladder Cancer Research Centre, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK., Bryan RT; Bladder Cancer Research Centre, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK. Electronic address: r.t.bryan@bham.ac.uk.

Publikováno v: European urology [Eur Urol] 2024 May; Vol. 85 (5), pp. 508-509. Date of Electronic Publication: 2024 Feb 01.

Novel Homozygous Variants of SLC13A5 Expand the Functional Heterogeneity of a Homogeneous Syndrome of Early Infantile Epileptic Encephalopathy.

Autor: Alsemari A; Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia. Electronic address: alsemari@kfshrc.edu.sa., Guzmán-Vega FJ; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia., Meyer BF; Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia; Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Computational Bioscience Research Centre (CBRC), Thuwal, Saudi Arabia., Arold ST; Saudi Human Genome Project, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.

Publikováno v: Pediatric neurology [Pediatr Neurol] 2024 Feb; Vol. 151, pp. 68-72. Date of Electronic Publication: 2023 Oct 19.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Wild-type S100A3 and S100A13 restore calcium homeostasis and mitigate mitochondrial dysregulation in pulmonary fibrosis patient-derived cells.

Autor: Al-Mutairy EA; Department of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; Department of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Al Qattan S; Department of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Khalid M; Department of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Al-Enazi AA; Department of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Al-Saif MM; BioMolecular Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Imtiaz F; Clinical Genomics, Center of Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Ramzan K; Clinical Genomics, Center of Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Raveendran V; Department of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Alaiya A; Stem Cell Therapy Program, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Meyer BF; Clinical Genomics, Center of Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Atamas SP; University of Maryland School of Medicine, Baltimore, MD, United States.; Baltimore VA Medical Center, Baltimore, MD, United States., Collison KS; Department of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Khabar KS; BioMolecular Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Hasday JD; University of Maryland School of Medicine, Baltimore, MD, United States.; Baltimore VA Medical Center, Baltimore, MD, United States., Al-Mohanna F; Department of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Publikováno v: Frontiers in cell and developmental biology [Front Cell Dev Biol] 2023 Nov 30; Vol. 11, pp. 1282868. Date of Electronic Publication: 2023 Nov 30 (Print Publication: 2023).

The clinical utility of rapid exome sequencing in a consanguineous population.

Autor: Monies D; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Goljan E; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Assoum M; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Albreacan M; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Binhumaid F; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Subhani S; Department of Computational Science, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Boureggah A; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Hashem M; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, MBC-26, PO Box 3354, Riyadh, 11211, Saudi Arabia., Abdulwahab F; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, MBC-26, PO Box 3354, Riyadh, 11211, Saudi Arabia., Abuyousef O; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, MBC-26, PO Box 3354, Riyadh, 11211, Saudi Arabia., Temsah MH; Department of Pediatrics, Pediatric Critical Care Unit, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia., Alsohime F; Department of Pediatrics, Pediatric Critical Care Unit, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia., Kelaher J; General Corporate Consultancy Department, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Abouelhoda M; Department of Computational Science, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. mabouelhoda@kfshrc.edu.sa., Meyer BF; Department of Clinical Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Alkuraya FS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, MBC-26, PO Box 3354, Riyadh, 11211, Saudi Arabia. falkuraya@kfshrc.edu.sa.

Publikováno v: Genome medicine [Genome Med] 2023 Jun 21; Vol. 15 (1), pp. 44. Date of Electronic Publication: 2023 Jun 21.