ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformations.

Autor: Laugwitz L; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.; Department of Neuropediatrics, Developmental Neurology and Social Pediatrics, University of Tübingen, Tübingen 72076, Germany., Cheng F; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany., Collins SC; Inserm UMR1231, Université de Bourgogne, Dijon Cedex 21070, France., Hustinx A; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany., Navarro N; Biogeosciences, UMR 6282 CNRS, EPHE, Université de Bourgogne, Dijon 2100, France.; EPHE, PSL University, Paris 75014, France., Welsch S; Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf 40225, Germany., Cox H; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham B15 2TG, UK., Hsieh TC; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany., Vijayananth A; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany., Buchert R; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany., Bender B; Diagnostic and Interventional Neuroradiology, Radiologic Clinics, University of Tübingen, Tübingen 72076, Germany., Efthymiou S; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK., Murphy D; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK., Zafar F; Pediatric Neurology, Children's Hospital, Multan 60000, Pakistan., Rana N; Pediatric Neurology, Children's Hospital, Multan 60000, Pakistan., Grasshoff U; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.; Center for Rare Disease, University of Tübingen, Tübingen 72072, Germany., Falb RJ; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany., Grimmel M; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany., Seibt A; Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf 40225, Germany., Zheng W; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany., Ghaedi H; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1985717443, Iran., Thirion M; Inserm UMR1231, Université de Bourgogne, Dijon Cedex 21070, France., Couette S; Biogeosciences, UMR 6282 CNRS, EPHE, Université de Bourgogne, Dijon 2100, France.; EPHE, PSL University, Paris 75014, France., Azizimalamiri R; Department of Pediatric Neurology, Golestan Medical, Educational, and Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz 6135715794, Iran., Sadeghian S; Department of Pediatric Neurology, Golestan Medical, Educational, and Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz 6135715794, Iran., Galehdari H; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz 6135783151, Iran., Zamani M; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz 6135783151, Iran.; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz 6155689467, Iran., Zeighami J; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz 6155689467, Iran., Sedaghat A; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz 6155689467, Iran.; Diabetes Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz 6135715794, Iran., Ramshe SM; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1985717443, Iran., Zare A; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran 1985717443, Iran., Alipoor B; Department of Laboratory Sciences, Faculty of Paramedicine, Yasuj University of Medical Sciences, Yasuj 7591741417, Iran., Klee D; Department of Pediatric Radiology, Medical Faculty, Institute of Radiology, Heinrich-Heine-University, Düsseldorf 40225, Germany., Sturm M; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.; Genomics England, Queen Mary University of London, London EC1M 6BQ, UK., Ossowski S; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.; NGS Competence Center Tübingen (NCCT), University of Tübingen, Tübingen 72076, Germany., Houlden H; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK., Riess O; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.; Center for Rare Disease, University of Tübingen, Tübingen 72072, Germany., Wieczorek D; Medical Faculty and University Hospital Düsseldorf, Institute of Human Genetics, Heinrich-Heine-University Düsseldorf, Düsseldorf 40225, Germany., Gavin R; West Midlands Regional Genetics Laboratory, Central and South Genomic Laboratory Hub, Birmingham B15 2TG, UK., Maroofian R; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London WC1N 3BG, UK., Krawitz P; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn 53127, Germany., Yalcin B; Inserm UMR1231, Université de Bourgogne, Dijon Cedex 21070, France., Distelmaier F; Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf 40225, Germany., Haack TB; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, 72076, Germany.; Center for Rare Disease, University of Tübingen, Tübingen 72072, Germany.

Publikováno v: Brain : a journal of neurology [Brain] 2024 Jul 05; Vol. 147 (7), pp. 2471-2482.

Circulating Levels of HOTAIR- lncRNA Are Associated with Disease Progression and Clinical Parameters in Type 2 Diabetes Patients.

Autor: Niknam N; Student Research Committee, Yasuj University of Medical Sciences, Yasuj, Iran., Nikooei S; Student Research Committee, Yasuj University of Medical Sciences, Yasuj, Iran., Ghasemi H; Department of Clinical Biochemistry, Abadan School of Medical Sciences, Abadan, Iran., Zadian SS; Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Goudarzi K; Department of Laboratory Sciences, Faculty of Paramedicine, Yasuj University of Medical Sciences, Yasuj, Iran., Ahmadi SM; Internal Medicine Department of Yasuj Medical School, Yasuj, Iran., Alipoor B; Department of Laboratory Sciences, Faculty of Paramedicine, Yasuj University of Medical Sciences, Yasuj, Iran.

Publikováno v: Reports of biochemistry & molecular biology [Rep Biochem Mol Biol] 2023 Oct; Vol. 12 (3), pp. 448-457.

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Circular RNAs in β-cell function and type 2 diabetes-related complications: a potential diagnostic and therapeutic approach.

Autor: Ghasemi H; Department of Clinical Biochemistry, Abadan Faculty of Medical Sciences, Abadan, Iran., Sabati Z; Student Research Committee, Abadan Faculty of Medical Sciences, Abadan, Iran., Ghaedi H; Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Salehi Z; Department of Radiation Sciences, Yasuj University of Medical Sciences, Yasuj, Iran., Alipoor B; Department of Laboratory Sciences, Faculty of Paramedicine, Yasuj University of Medical Sciences, Yasuj, Iran. behnam.alipour@yums.ac.ir.

Publikováno v: Molecular biology reports [Mol Biol Rep] 2019 Oct; Vol. 46 (5), pp. 5631-5643. Date of Electronic Publication: 2019 Jul 13.

Circulating mRNA and plasma levels of osteoprotegerin and receptor activator of NF-κB ligand in nonalcoholic fatty liver disease.

Autor: Nikseresht M; Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran., Azarmehr N; Student Research Committee, Yasuj University of Medical Sciences, Yasuj, Iran., Arya A; Internal medicine Department, Yasuj University of Medical Sciences, Yasuj, Iran., Alipoor B; Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran., Fadaei R; Sleep Disorders Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran., Khalvati B; Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran., Abidi H; Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran., Doustimotlagh AH; Medicinal Plants Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.; Department of Clinical Biochemistry, Faculty of Medicine, Yasuj University of Medical Sciences, Yasuj, Iran.

Publikováno v: Biotechnology and applied biochemistry [Biotechnol Appl Biochem] 2021 Dec; Vol. 68 (6), pp. 1243-1249. Date of Electronic Publication: 2020 Oct 15.