Pyrazine emission by a tropical firefly: An example of chemical aposematism?

Autor: Fredric V. Vencl, Catalina Estrada, Rachel A. Page, Kristina J. Ottens, Ximena E. Bernal, Sarah Candler, Marjorie M. Dixon

Publikováno v: Biotropica. 48:645-655

Although famous for photic courtship displays, fireflies (Coleoptera: Lampyridae) are also notable for emitting strong odors when molested. The identity of volatile emissions and their possible role, along with photic signals, as aposematic warnings

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bf2c7cb2b9215a12c710be2e26f31e57
https://doi.org/10.1111/btp.12336

Risks of multimodal signaling: bat predators attend to dynamic motion in frog sexual displays

Autor: Michael J. Ryan, Rachel A. Page, Ryan C. Taylor, Marjorie M. Dixon, Wouter Halfwerk, Patricia L. Jones, Kristina J. Ottens

Publikováno v: Journal of Experimental Biology, 217(17), 3038-3044. Company of Biologists Ltd
Halfwerk, W, Dixon, M M, Ottens, K J, Taylor, R C, Ryan, M J, Page, R A & Jones, P L 2014, ' Risks of multimodal signaling: bat predators attend to dynamic motion in frog sexual displays ', Journal of Experimental Biology, vol. 217, no. 17, pp. 3038-3044 . https://doi.org/10.1242/jeb.107482

Many sexual displays contain multiple components that are received through a variety of sensory modalities. Primary and secondary signal components can interact to induce novel receiver responses and become targets of sexual selection as complex sign

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebe05049b310e3471091a0534c837c4e
https://research.vu.nl/en/publications/44f971fb-9a11-4a7a-950b-5d21938342e6

BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening.

Autor: Tangeraas T; Paediatric and Adolescent Medicine, Oslo University Hospital, 0424 Oslo, Norway.; European Reference Network for Hereditary Metabolic Diseases (MetabERN)., Constante JR; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Neurometabolic Unit and Synaptic Metabolism Laboratory, Department of Neurology, Sant Joan de Déu Hospital, IPR, Barcelona 08950, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid 28029, Spain., Backe PH; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Department of Medical Biochemistry, Oslo University Hospital-Rikshospitalet, PO Box 4950 Nydalen, OUS HF Rikshospitalet, 0424 Oslo, Norway.; Department of Microbiology, Clinic for Diagnostics and Intervention, Oslo University Hospital, Rikshospitalet, Nydalen, N-0424 Oslo, Norway., Oyarzábal A; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Neurometabolic Unit and Synaptic Metabolism Laboratory, Department of Neurology, Sant Joan de Déu Hospital, IPR, Barcelona 08950, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid 28029, Spain., Neugebauer J; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Department of Pediatric Gastroenterology, Nephrology and Metabolic Medicine, Charité-Universitätsmedizin Berlin, Berlin 13353, Germany.; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, Berlin 13353, Germany., Weinhold N; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Department of Pediatric Gastroenterology, Nephrology and Metabolic Medicine, Charité-Universitätsmedizin Berlin, Berlin 13353, Germany.; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, Berlin 13353, Germany., Boemer F; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Biochemical Genetics Laboratory, Human Genetics, CHU of Liege, University of Liège, Liège 4000, Belgium., Debray FG; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Department of Human Genetics, CHU of Liege, University of Liège, Liège 4000, Belgium., Ozturk-Hism B; Department of Pediatric Metabolic Diseases, Marmara University School of Medicine, Istanbul 34854, Turkey., Evren G; Department of Medical Genetics, University of Harran, 63000 Sanliurfa, Turkey., Tuba EF; Department of Pediatric Metabolism, Ankara University School of Medicine, 06100 Ankara, Turkey., Ummuhan O; Department of Pediatric Metabolism, Ankara University School of Medicine, 06100 Ankara, Turkey., Footitt E; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Department of Metabolic Medicine, Great Ormond Street Hospital for Children, London WC1N 3JH, UK.; NIHR Great Ormond Street Hospital Biomedical Research Centre (NIHR GOSH BRC), London WC1N 3JH, UK., Davison J; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Department of Metabolic Medicine, Great Ormond Street Hospital for Children, London WC1N 3JH, UK.; NIHR Great Ormond Street Hospital Biomedical Research Centre (NIHR GOSH BRC), London WC1N 3JH, UK., Martinez C; Department of Pediatrics and Psychiatry, The Mount Sinai Hospital, New York, NY 1468, USA., Bueno C; Department of Neurology, Clinical Hospital of the Faculty of Medicine, University of São Paulo, São Paulo 05403-010, Brazil., Machado I; Neuropediatric Department, Hospital Universitario Clínico San Cecilio, Granada 18016, Spain., Rodríguez-Pombo P; Centro de Diagnóstico de Enfermedades Moleculares, Centro de Biología Molecular Severo Ochoa, CBM-CSIC, Departamento de Biología Molecular, Institute for Molecular Biology-IUBM, Universidad Autónoma Madrid, CIBERER, IDIPAZ, 28049 Madrid, Spain., Al-Sannaa N; Pediatric Services Division, Johns Hopkins Aramco Healthcare, Dhahran 34465, Saudi Arabia., De Los Santos M; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid 28029, Spain.; Neurometabolic Unit, Department of Gastroenterology and Nutrition, Sant Joan de Déu Hospital, Barcelona 08950, Spain., López JM; Institut de Recerca Sant Joan de Déu, Pediatric Radiology Department Esplugues de Llobregat, Hospital Sant Joan de Déu, 08950 Barcelona, Spain., Ozturkmen-Akay H; Department of Radiology, Baskent University School of Medicine, Ankara 06790, Turkey., Karaca M; Department of Pediatric Metabolic Diseases, University of Harran, Sanliurfa 63000, Turkey., Tekin M; Dr. John T. Macdonald Foundation Department of Human Genetics and John P.Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33136, USA., Pajares S; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid 28029, Spain.; Section of Inborn Errors of Metabolism-IBC, Department of Biochemistry and Molecular Genetics, Hospital Clínic, Barcelona 08036, Spain., Ormazabal A; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid 28029, Spain.; Department of Clinical Biochemistry, Sant Joan de Déu Hospital, Barcelona 08950, Spain., Stoway SD; Norwegian National Unit for Newborn Screening, Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo 0424, Norway.; Biochemical Genetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, NY 55905, USA., Artuch R; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid 28029, Spain.; Department of Clinical Biochemistry, Sant Joan de Déu Hospital, Barcelona 08950, Spain., Dixon M; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Dietetics, Great Ormond Street Hospital for Children, NHS Foundation Trust, London WC1N, 3JH, UK., Mørkrid L; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Department of Medical Biochemistry, Oslo University Hospital-Rikshospitalet, PO Box 4950 Nydalen, OUS HF Rikshospitalet, 0424 Oslo, Norway.; Institute of Clinical Medicine, University of Oslo, Nydalen, Oslo 0424, Norway., García-Cazorla A; European Reference Network for Hereditary Metabolic Diseases (MetabERN).; Neurometabolic Unit and Synaptic Metabolism Laboratory, Department of Neurology, Sant Joan de Déu Hospital, IPR, Barcelona 08950, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid 28029, Spain.

Publikováno v: Brain : a journal of neurology [Brain] 2023 Jul 03; Vol. 146 (7), pp. 3003-3013.

UK Dietary Practices for Tyrosinaemias: Time for Change.

Autor: Daly A; Birmingham Women's and Children's Hospital, NHS Foundation Trust, Steelhouse Lane, Birmingham B4 6NH, UK., Adam S; Royal Hospital for Children, Glasgow G51 4TF, UK., Allen H; Sheffield Children's NHS Foundation Trust, Sheffield S10 2TH, UK., Ash J; University Hospital of Wales, Cardiff CF4 4XW, UK., Dale C; University Hospitals Birmingham NHS Foundation Trust, Birmingham B15 2TH, UK., Dixon M; Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3JH, UK., Dunlop C; Royal Hospital for Sick Children, Edinburgh EH9 1LF, UK., Ellerton C; University College London Hospitals NHS Foundation Trust, London WC1N 3BG, UK., Evans S; Birmingham Women's and Children's Hospital, NHS Foundation Trust, Steelhouse Lane, Birmingham B4 6NH, UK., Firman S; Guy's and St Thomas' NHS Foundation Trust, London SE1 7EU, UK., Ford S; Southmead Hospital North Bristol Trust, Bristol BS10 5NB, UK., Freedman F; University College London Hospitals NHS Foundation Trust, London WC1N 3BG, UK., Gribben J; Evelina London Children's Healthcare, London SE1 7EH, UK., Howe S; University Hospitals Birmingham NHS Foundation Trust, Birmingham B15 2TH, UK., Khan F; Bradford Teaching Hospitals, NHS Foundation Trust, Bradford BD5 0NA, UK., McDonald J; Belfast Health and Social Care Trust, Belfast BT9 7AB, UK., McStravick N; Belfast Health and Social Care Trust, Belfast BT9 7AB, UK., Nguyen P; University College London Hospitals NHS Foundation Trust, London WC1N 3BG, UK., Oxley N; Bradford Teaching Hospitals, NHS Foundation Trust, Bradford BD5 0NA, UK., Skeath R; Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3JH, UK., Simpson E; Royal Manchester Children's Hospital, Manchester M13 9WL, UK., Terry A; Alder Hey Children's NHS Foundation Trust, Liverpool L12 2AP, UK., Woodall A; Salford Royal NHS Foundation Trust, Manchester M6 8HD, UK., White L; Sheffield Children's NHS Foundation Trust, Sheffield S10 2TH, UK., MacDonald A; Birmingham Women's and Children's Hospital, NHS Foundation Trust, Steelhouse Lane, Birmingham B4 6NH, UK.

Publikováno v: Nutrients [Nutrients] 2022 Dec 07; Vol. 14 (24). Date of Electronic Publication: 2022 Dec 07.

Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiency.

Autor: Keshavan N; Department of Paediatric Metabolic Medicine Great Ormond Street Hospital NHS Trust London UK.; UCL Great Ormond Street Hospital Institute of Child Health London UK., Wood M; Department of Physiotherapy Great Ormond Street Hospital NHS Trust London UK., Alderson LM; UCL Great Ormond Street Hospital Institute of Child Health London UK.; Department of Physiotherapy Great Ormond Street Hospital NHS Trust London UK., Cortina-Borja M; Population, Policy and Practice Research and Teaching Department UCL Great Ormond Street Hospital Institute of Child Health London UK., Skeath R; Department of Dietetics Great Ormond Street Hospital NHS Trust London UK., McSweeney M; Department of Paediatric Metabolic Medicine Great Ormond Street Hospital NHS Trust London UK., Dixon M; Department of Dietetics Great Ormond Street Hospital NHS Trust London UK., Cleary MA; Department of Paediatric Metabolic Medicine Great Ormond Street Hospital NHS Trust London UK., Footitt E; Department of Paediatric Metabolic Medicine Great Ormond Street Hospital NHS Trust London UK., Batzios S; Department of Paediatric Metabolic Medicine Great Ormond Street Hospital NHS Trust London UK.

Publikováno v: JIMD reports [JIMD Rep] 2021 Dec 30; Vol. 63 (2), pp. 123-130. Date of Electronic Publication: 2021 Dec 30 (Print Publication: 2022).