Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.

Autor: Alrayes N; Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Mallah BA; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Issa NM; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Human Genetics, Medical Research Institute, Alexandria University, Egypt., Banaganapalli B; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Ahmad Shaik N; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Nasser KK; Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Alshehri BA; Laboratory Department, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Bhuiyan ZA; Laboratoire de Génétique Moléculaire, Service de Génétique Médicale, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland., Bdier AY; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia. Electronic address: nanabdeir@yahoo.com., Al-Aama JY; Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia. Electronic address: jalama@kau.edu.sa.

Publikováno v: Gene [Gene] 2023 Jan 30; Vol. 851, pp. 146909. Date of Electronic Publication: 2022 Sep 23.

Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.

Autor: Yang C; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Xu Y; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Yu M; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Lee D; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Alharti S; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Hellen N; NHLI, Faculty of Medicine, Imperial College London, London, UK., Ahmad Shaik N; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Banaganapalli B; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Sheikh Ali Mohamoud H; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Elango R; Princess Al Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Saudi Arabia., Przyborski S; Department of Bioscience, Durham University, Durham, UK., Tenin G; Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK., Williams S; Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK., O'Sullivan J; The Newcastle upon Tyne NHS Hospital, UK., Al-Radi OO; Department of Surgery, King Abdulaziz University, Saudi Arabia., Atta J; Department of Surgery, King Abdulaziz University, Saudi Arabia., Harding SE; NHLI, Faculty of Medicine, Imperial College London, London, UK., Keavney B; Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK., Lako M; Institute of Genetic Medicine, Newcastle University, Newcastle, UK., Armstrong L; Institute of Genetic Medicine, Newcastle University, Newcastle, UK.

Publikováno v: Human molecular genetics [Hum Mol Genet] 2017 Aug 15; Vol. 26 (16), pp. 3031-3045.

Identification of Plasma Exosomes hsa_circ_0001360 and hsa_circ_0000038 as Key Biomarkers of Coronary Heart Disease.

Autor: Zhang, Wan¹ (AUTHOR), Cui, Jiasen¹ (AUTHOR), Li, Li¹ (AUTHOR), Zhu, Ting² (AUTHOR), Guo, Zhenyu² (AUTHOR)

Publikováno v: Cardiology Research & Practice. 3/26/2024, Vol. 2024, p1-10. 10p.

Artificial Intelligence in Cardiology and Atherosclerosis in the Context of Precision Medicine: A Scoping Review.

Autor: Kolaszyńska, Oliwia, Lorkowski, Jacek

Publikováno v: Applied Bionics & Biomechanics; 4/30/2024, Vol. 2024, p1-17, 17p

Current advances in human-induced pluripotent stem cell-based models and therapeutic approaches for congenital heart disease.

Autor: Cao M; Department of Neonatology, The First Hospital of China Medical University, Shenyang, 110001, Liaoning, China., Liu Y; Department of Pediatrics, The First Hospital of China Medical University, No.155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning, China., Sun Y; Department of Pediatrics, The First Hospital of China Medical University, No.155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning, China., Han R; Department of Pediatrics, The First Hospital of China Medical University, No.155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning, China., Jiang H; Department of Pediatrics, The First Hospital of China Medical University, No.155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning, China. jianghongkun007@163.com.

Publikováno v: Molecular and cellular biochemistry [Mol Cell Biochem] 2024 Apr 18. Date of Electronic Publication: 2024 Apr 18.