Effects of Rotational Symmetry Breaking in Polymer-coated Nanopores

Autor: Osmanovic, D., Kerr-Winter, M., Eccleston, R. C., Hoogenboom, B. W., Ford, I. J.

Publikováno v: Journal of Chemical Physics 142, 034901 (2015)

The statistical theory of polymers tethered around the inner surface of a cylindrical channel has traditionally employed the assumption that the equilibrium density of the polymers is independent of the azimuthal coordinate. However, simulations have

Externí odkaz: http://arxiv.org/abs/1501.07380

Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease.

Autor: Husain RA; Department of Neuropediatrics, Jena University Hospital, 07747 Jena, Germany.; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany., Jiao X; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA., Hennings JC; Institute of Human Genetics, Jena University Hospital, 07747 Jena, Germany., Giesecke J; Department of Anaesthesiology and Intensive Care Medicine, Jena University Hospital, Member of the Leibniz Center for Photonics in Infection Research (LPI), 07747 Jena, Germany., Palsule G; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA., Beck-Wödl S; Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany., Osmanović D; Institute of Human Genetics, Jena University Hospital, 07747 Jena, Germany., Bjørgo K; Department of Medical Genetics, Oslo University Hospital, 0424 Oslo, Norway., Mir A; Department of Biological Sciences, Faculty of Sciences, International Islamic University, Islamabad 44000, Pakistan., Ilyas M; Department of Biological Sciences, Faculty of Sciences, International Islamic University, Islamabad 44000, Pakistan., Abbasi SM; Department of Biological Sciences, Faculty of Sciences, International Islamic University, Islamabad 44000, Pakistan., Efthymiou S; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Dominik N; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Maroofian R; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Houlden H; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK., Rankin J; Department of Clinical Genetics, Royal Devon University Hospital, Exeter, EX1 2ED, UK., Pagnamenta AT; Oxford NIHR Biomedical Research Centre, Wellcome Centre for Human Genetics, Oxford, OX3 7BN, UK., Nashabat M; Medical Genomics Research Department, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia., Altwaijri W; Department of Pediatrics, Neurology Division, King Abdullah Specialist Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia., Alfadhel M; Medical Genomics Research Department, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; Genetics and Precision Medicine Department, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia., Umair M; Medical Genomics Research Department, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia., Khouj E; Department of Translational Genomics, Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia., Reardon W; Blackrock Clinic, Dublin, A94 E4X7, Ireland., El-Hattab AW; Department of Clinical Sciences, College of Medicine, University of Sharjah, 27272, Sharjah, United Arab Emirates.; Department of Pediatrics, University Hospital Sharjah, 72772, Sharjah, United Arab Emirates., Mekki M; Department of Pediatrics, University Hospital Sharjah, 72772, Sharjah, United Arab Emirates., Houge G; Department of Medical Genetics, Haukeland University Hospital, 5021 Bergen, Norway., Beetz C; Centogene GmbH, 18055 Rostock, Germany., Bauer P; Centogene GmbH, 18055 Rostock, Germany., Putoux A; Groupement Hospitalier Est, Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, 69677 Bron Cedex, France.; Équipe GENDEV, Centre de Recherche en Neurosciences de Lyon, Univ Lyon, Univ Lyon 1, INSERM U1028 CNRS UMR5292, 69008 Lyon, France., Lesca G; Groupement Hospitalier Est, Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, 69677 Bron Cedex, France.; Physiopathologie et Génétique du Neurone et du Muscle, Univ Lyon, Univ Lyon 1, CNRS, INSERM, UMR5261, U1315, Institut NeuroMyoGène, 69008 Lyon, France., Sanlaville D; Groupement Hospitalier Est, Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, 69677 Bron Cedex, France.; Physiopathologie et Génétique du Neurone et du Muscle, Univ Lyon, Univ Lyon 1, CNRS, INSERM, UMR5261, U1315, Institut NeuroMyoGène, 69008 Lyon, France., Alkuraya FS; Department of Translational Genomics, Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia., Taylor RW; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, NE1 4LP, UK., Mentzel HJ; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany.; Section of Pediatric Radiology, Department of Radiology, Jena University Hospital, 07747 Jena, Germany., Hübner CA; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany.; Institute of Human Genetics, Jena University Hospital, 07747 Jena, Germany., Huppke P; Department of Neuropediatrics, Jena University Hospital, 07747 Jena, Germany.; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany., Hart RP; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA., Haack TB; Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany., Kiledjian M; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA., Rubio I; Department of Anaesthesiology and Intensive Care Medicine, Jena University Hospital, Member of the Leibniz Center for Photonics in Infection Research (LPI), 07747 Jena, Germany.; Center for Sepsis Control and Care, Jena University Hospital, 07747 Jena, Germany.

Publikováno v: Brain : a journal of neurology [Brain] 2024 Apr 04; Vol. 147 (4), pp. 1197-1205.

Design principles of 3D epigenetic memory systems.

Autor: Owen JA; Department of Physics, Massachusetts Institute of Technology, Cambridge, MA, USA., Osmanović D; Department of Mechanical and Aeronautical Engineering, UCLA, Los Angeles, CA, USA., Mirny L; Department of Physics, Massachusetts Institute of Technology, Cambridge, MA, USA.

Publikováno v: Science (New York, N.Y.) [Science] 2023 Nov 17; Vol. 382 (6672), pp. eadg3053. Date of Electronic Publication: 2023 Nov 17.

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