TITLE: A Systematic Evaluation of Endurance Impairments: The Reversible and Irreversible Components

Autor: K. J. Dias

Publikováno v: Cardiopulmonary Physical Therapy Journal. 20:41

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::917bb4c1e6733a84ff7c23923708ff02
https://doi.org/10.1097/01823246-200920040-00048

Profiling nonhuman primate germline RNA to understand the legacy of early life stress.

Autor: Morin, Elyse L.^1,2 (AUTHOR), Garza, Kristie M.^1,2,3,4 (AUTHOR), Aoued, Hadj^1,2 (AUTHOR), Sannigrahi, Soma^1,2 (AUTHOR), Siebert, Erin R.¹ (AUTHOR), Howell, Brittany R.^1,2,5,6 (AUTHOR), Walum, Hasse¹ (AUTHOR), Sanchez, Mar M.^1,2 (AUTHOR), Dias, Brian G.^1,2 (AUTHOR) bdias@chla.usc.edu

Publikováno v: Journal of Experimental Zoology: Part A Ecological & Integrative Physiology. Jan2022, Vol. 337 Issue 1, p15-23. 9p.

Blepharophimosis with intellectual disability and Helsmoortel-Van Der Aa Syndrome share episignature and phenotype.

Autor: Sarli C; Department of Translational Medicine, Federico II University of Naples, Naples, Italy., van der Laan L; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands., Reilly J; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada., Trajkova S; Department of Medical Sciences, University of Torino, Turin, Italy.; Molecular Biotechnology Center 'Guido Tarone', University of Turin, Turin, Italy., Carli D; Department of Medical Sciences, University of Torino, Turin, Italy., Brusco A; Department of Medical Sciences, University of Torino, Turin, Italy.; Medical Genetics Unit, Città della Salute e della Scienza University Hospital, Turin, Italy.; Department of Neurosciences Rita Levi-Montalcini, University of Turin, Turin, Italy., Levy MA; Verspeeten Clinical Genome Centre, London Health Science Centre, London, Ontario, Canada., Relator R; Verspeeten Clinical Genome Centre, London Health Science Centre, London, Ontario, Canada., Kerkhof J; Verspeeten Clinical Genome Centre, London Health Science Centre, London, Ontario, Canada., McConkey H; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.; Verspeeten Clinical Genome Centre, London Health Science Centre, London, Ontario, Canada., Tedder ML; Greenwood Genetic Center, Greenwood, South Carolina, USA., Skinner C; Greenwood Genetic Center, Greenwood, South Carolina, USA., Alders M; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands., Henneman P; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands., Hennekam RCM; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands., Ciaccio C; Department of Pediatric Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., D'Arrigo S; Department of Pediatric Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy., Vitobello A; Department of Genetics, UNICAEN, Caen University Hospital, Normandy University, Caen, France., Faivre L; Université de Bourgogne, Inserm U1231, Equipe GAD, Dijon, France.; CHU Dijon Bourgogne, Centre de Génétique, Centre de Référence Maladies Rares 'Anomalies du Développement et Syndromes Malformatifs', FHU-TRANSLDAD, Dijon, France., Weber S; Service de Génétique, CHU de Caen-Normandie, Caen, France.; Service de Neurologie, CHU de Caen-Normandie, Caen, France., Vincent-Devulder A; Department of Genetics, UNICAEN, Caen University Hospital, Normandy University, Caen, France., Perrin L; Department of Genetics, UNICAEN, Caen University Hospital, Normandy University, Caen, France., Bourgois A; Department of Genetics, UNICAEN, Caen University Hospital, Normandy University, Caen, France., Yamamoto T; Division of Gene Medicine, Graduate School of Medical Science, Tokyo Women's Medical University, Tokyo, Japan., Metcalfe K; Manchester Centre for Genomic Medicine, St Mary's Hospital, Health Innovation Manchester, Manchester University Foundation NHS Trust, Manchester, UK.; Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK., Zollino M; Institute of Genomic Medicine, Department of Life Sciences and Public Health, 'Sacro Cuore' Catholic University of Rome, Rome, Italy.; Medical Genetics Unit, Foundation IRCCS AOU Policlinico 'A. Gemelli', Rome, Italy., Kini U; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK., Oliveira D; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal., Sousa SB; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal., Williams D; Department of Clinical Genetics, Birmingham Women's & Children's NHS Foundation Trust, Birmingham, UK., Cappuccio G; Department of Translational Medicine, Federico II University of Naples, Naples, Italy., Sadikovic B; Department of Human Genetics, Amsterdam Reproduction & Development Research Institute, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.; Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.; Verspeeten Clinical Genome Centre, London Health Science Centre, London, Ontario, Canada., Brunetti-Pierri N; Department of Translational Medicine, Federico II University of Naples, Naples, Italy.; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.; Scuola Superiore Meridionale (SSM, School of Advanced Studies), Genomics and Experimental Medicine Program, University of Naples Federico II, Naples, Italy.

Publikováno v: American journal of medical genetics. Part C, Seminars in medical genetics [Am J Med Genet C Semin Med Genet] 2024 Dec; Vol. 196 (4), pp. e32089. Date of Electronic Publication: 2024 Jun 17.

Is Psychopathy a Mental Disorder or an Adaptation? Evidence From a Meta-Analysis of the Association Between Psychopathy and Handedness.

Autor: Pullman, Lesleigh E.¹ (AUTHOR), Refaie, Nabhan² (AUTHOR), Lalumière, Martin L.¹ (AUTHOR), Krupp, DB³ (AUTHOR) dbkrupp@saltlab.org

Publikováno v: Evolutionary Psychology. Oct2021, Vol. 19 Issue 4, p1-17. 17p.

Exploring a paradox: Psychopathy, Morality and Organisational Citizenship Behaviour.

Autor: Kirrane, Melrona¹ (AUTHOR) Melrona.kirrane@dcu.ie, Farqan, Adeela (AUTHOR), Cloak, Emer (AUTHOR)

Publikováno v: Journal of Business Ethics. Jun2024, p1-20.