Professor Morley Sewell M.A., Vet. M.B., Ph.D., M.R.C.V.S., 1932–2022

Autor: Leslie JS Harrison

Publikováno v: Tropical Animal Health and Production. 54

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0db30edf2573d1ce94e96368f64129ef
https://doi.org/10.1007/s11250-022-03163-1

Characterization of the Taenia spp HDP2 sequence and development of a novel PCR-based assay for discrimination of Taenia saginata from Taenia asiatica

Autor: McManus Donald P, Parkhouse Michael RE, Harrison Leslie JS, García Maria, Ferrer Elizabeth, Bailo Begoña, González Luis M, Gárate Teresa

Publikováno v: Parasites & Vectors, Vol 3, Iss 1, p 51 (2010)

Abstract A previously described Taenia saginata HDP2 DNA sequence, a 4-kb polymorphic fragment, was previously used as the basis for developing PCR diagnostic protocols for the species-specific discrimination of T. saginata from T. solium and for the

Externí odkaz: https://doaj.org/article/929fcb6560ee484c9178f60c0c7490a3

Characterization of the Taenia spp HDP2 sequence and development of a novel PCR-based assay for discrimination of Taenia saginata from Taenia asiatica

Autor: Leslie Js Harrison, Maria D Fernandez García, Teresa Gárate, Elizabeth Ferrer, Michael Parkhouse, Begoña Bailo, Luis Miguel González, Donald P. McManus

Publikováno v: Parasites & Vectors, Vol 3, Iss 1, p 51 (2010)
Parasites & Vectors
Repisalud
Instituto de Salud Carlos III (ISCIII)

A previously described Taenia saginata HDP2 DNA sequence, a 4-kb polymorphic fragment, was previously used as the basis for developing PCR diagnostic protocols for the species-specific discrimination of T. saginata from T. solium and for the differen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c493a7403beb8896bcf70cf3a0d8aaf
https://hdl.handle.net/20.500.12105/7042

Elucidating the clinical and genetic spectrum of inositol polyphosphate phosphatase INPP4A-related neurodevelopmental disorder.

Autor: Rawlins LE; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK; Peninsula Clinical Genetics Service, Royal Devon University Healthcare NHS Foundation Trust (Heavitree), Gladstone Road, Exeter, UK. Electronic address: L.Rawlins@exeter.ac.uk., Maroofian R; Department of Neuromuscular Diseases, Queen Square, Institute of Neurology, University College London, London, UK., Cannon SJ; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK., Daana M; Child Development Center, Clalit health care services, Jerusalem., Zamani M; Department of Neuromuscular Diseases, Queen Square, Institute of Neurology, University College London, London, UK; Department of Biology, Faculty of Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz, Iran., Ghani S; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK; Department of Biological Sciences, International Islamic University Islamabad, H-10, Islamabad, 44000, Pakistan., Leslie JS; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK., Ubeyratna N; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK., Khan N; Interdisciplinary Nanoscience Center, Gustav Wieds Vej 14, Aarhus University, Aarhus 8000, Denmark., Khan H; Department of Biological Sciences, International Islamic University Islamabad, H-10, Islamabad, 44000, Pakistan., Scardamaglia A; Department of Neuromuscular Diseases, Queen Square, Institute of Neurology, University College London, London, UK., Cloarec R; Centre de Référence Déficiences Intellectuelles et Polyhandicaps de causes rares, APHM, Hôpital de la Timone-Enfants, Marseille., Khan SA; Department of Biological Sciences, International Islamic University Islamabad, H-10, Islamabad, 44000, Pakistan., Umair M; Department of Life Sciences, School of Science, University of Management and Technology, Lahore, Pakistan; Medical Genomics Research Department, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia., Sadeghian S; Department of Pediatric Neurology, Golestan Medical, Educational, and Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran., Galehdari H; Department of Biology, Faculty of Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran., Al-Maawali A; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman; Genetic and Developmental Medicine Clinic, Department of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University, Muscat, Oman., Al-Kindi A; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman; Genetic and Developmental Medicine Clinic, Department of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University, Muscat, Oman., Azizimalamiri R; Department of Pediatric Neurology, Golestan Medical, Educational, and Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran., Shariati G; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz, Iran; Department of Medical Genetics, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran., Ahmad F; Department of Child Health, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman., Al-Futaisi A; Department of Child Health, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman., Rodriguez Cruz PM; Department of Neuromuscular Diseases, Queen Square, Institute of Neurology, University College London, London, UK; Centro Nacional de Análisis Genómico, Barcelona, Spain; Department of Neurology, Centre Hospitalier National Universitaire de Fann, Dakar, Senegal., Salazar-Villacorta A; Department of Neuromuscular Diseases, Queen Square, Institute of Neurology, University College London, London, UK., Ndiaye M; Department of Neurology, Centre Hospitalier National Universitaire de Fann, Dakar, Senegal., Diop AG; Department of Neurology, Centre Hospitalier National Universitaire de Fann, Dakar, Senegal., Sedaghat A; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz, Iran; Diabetes Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran., Saberi A; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Kianpars, Ahvaz, Iran; Department of Medical Genetics, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran., Hamid M; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran., Zaki MS; Department of Clinical Genetics, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., Vona B; Institute of Human Genetics, University Medical Center Göttingen, Heinrich-Düker-Weg 12, 37073, Göttingen, Germany; Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Robert-Koch-Str. 40, 37075, Göttingen, Germany., Owrang D; Institute of Human Genetics, University Medical Center Göttingen, Heinrich-Düker-Weg 12, 37073, Göttingen, Germany; Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Robert-Koch-Str. 40, 37075, Göttingen, Germany., Alhashem AM; Department of Radiology, Prince Sultan Medical Military City, Riyadh, Saudi Arabia., Obeid M; The American University of Beirut, Beirut, Lebanon., Khan A; Faculty of Biological Sciences, Department of Zoology, University of Lakki Marwat, Lakki, Khyber Pakhtunkhwa, Pakistan; Institute for Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany., Beydoun A; The American University of Beirut, Beirut, Lebanon., Najjar M; The American University of Beirut, Beirut, Lebanon., Tajsharghi H; School of Health Sciences, Division Biomedicine, University of Skovde, Skovde, Sweden., Zifarelli G; Centogene GmbH, Am Strande 7, 18055 Rostock, Germany., Bauer P; Centogene GmbH, Am Strande 7, 18055 Rostock, Germany., Hakami WS; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia., Hashem AMA; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia., Boustany RN; The American University of Beirut, Beirut, Lebanon., Burglen L; Developmental Brain Disorders Laboratory, Imagine Institute, INSERM UMR 1163, Paris, France; Centre de Référence des Malformations et Maladies congénitales du cervelet et Département de génétique, Hôpital Trousseau, APHP, Sorbonne Université, 26 avenue du Dr A Netter 75012 Paris, France., Alavi S; Department of Neuromuscular Diseases, Queen Square, Institute of Neurology, University College London, London, UK; Palindrome, Isfahan, Iran., Gunning AC; Exeter Genomics Laboratory (NHS South West Genomic Laboratory Hub), Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK., Owens M; Exeter Genomics Laboratory (NHS South West Genomic Laboratory Hub), Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK., Karimiani EG; Molecular and Clinical Sciences Institute, St. George's, University of London, Cranmer Terrace, London, UK; Department of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran., Gleeson JG; Department of Neurosciences, University of California San Diego, La Jolla, CA, USA; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA., Milh M; Centre de Référence Déficiences Intellectuelles et Polyhandicaps de causes rares, APHM, Hôpital de la Timone-Enfants, Marseille; Aix-Marseille Université, APHM, service de neurologie pédiatrique, Hôpital de la Timone-Enfants, Marseille., Salah S; Department of Genetics, Hebrew University Medical Center, Hadassah, Jerusalem., Khan J; Department of Biological Sciences, International Islamic University Islamabad, H-10, Islamabad, 44000, Pakistan., Haucke V; Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Robert-Roessle-Str. 10, Berlin, Germany; Department of Biology, Chemistry, Pharmacy, Freie Universita¨t Berlin, 14195 Berlin, Germany., Wright CF; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK., McGavin L; University Hospitals Plymouth NHS Trust, Plymouth, UK; University of Plymouth, Plymouth, UK., Elpeleg O; Department of Genetics, Hebrew University Medical Center, Hadassah, Jerusalem., Shabbir MI; Department of Biological Sciences, International Islamic University Islamabad, H-10, Islamabad, 44000, Pakistan., Houlden H; Department of Neuromuscular Diseases, Queen Square, Institute of Neurology, University College London, London, UK., Ebner M; Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Robert-Roessle-Str. 10, Berlin, Germany., Baple EL; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK; Peninsula Clinical Genetics Service, Royal Devon University Healthcare NHS Foundation Trust (Heavitree), Gladstone Road, Exeter, UK. Electronic address: E.Baple@exeter.ac.uk., Crosby AH; Department of Clinical and Biomedical Sciences (Medical School), Faculty of Health and Life Sciences, University of Exeter, Research, Innovation, Learning and Development Building, Royal Devon and Exeter Hospital, Barrack Road, Exeter, UK. Electronic address: A.H.Crosby@exeter.ac.uk.

Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2024 Sep 20, pp. 101278. Date of Electronic Publication: 2024 Sep 20.

Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach.

Autor: Best S; Division of Molecular Medicine, Leeds Institute of Medical Research, University of Leeds, Leeds, UK.; Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, UK., Yu J; Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, UK., Lord J; University Hospital Southampton NHS Foundation Trust, Southampton, UK.; Faculty of Medicine, Human Development and Health, University of Southampton, Southampton, UK., Roche M; Windsor House Group Practice, Mid Yorkshire Hospitals NHS Trust, Leeds, UK., Watson CM; Division of Molecular Medicine, Leeds Institute of Medical Research, University of Leeds, Leeds, UK.; North East and Yorkshire Genomic Laboratory Hub, Central Lab, Leeds Teaching Hospitals NHS Trust, Leeds, UK., Bevers RPJ; Genomics England, Queen Mary University of London, London, UK., Stuckey A; Genomics England, Queen Mary University of London, London, UK., Madhusudhan S; St. Paul's Eye Unit, Royal Liverpool University Hospital, Liverpool, UK., Jewell R; Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, UK., Sisodiya SM; University College London (UCL) Queen Square Institute of Neurology, London, UK.; Chalfont Centre for Epilepsy, Chalfont, UK., Lin S; Department of Ophthalmology, Torbay and South Devon NHS Foundation Trust, Torquay, UK.; Exeter Genomics Laboratory, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK., Turner S; Department of Ophthalmology, Torbay and South Devon NHS Foundation Trust, Torquay, UK., Robinson H; Exeter Genomics Laboratory, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK., Leslie JS; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, UK., Baple E; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Exeter, UK.; Peninsula Clinical Genetics Service, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK., Toomes C; Division of Molecular Medicine, Leeds Institute of Medical Research, University of Leeds, Leeds, UK., Inglehearn C; Division of Molecular Medicine, Leeds Institute of Medical Research, University of Leeds, Leeds, UK., Wheway G; University Hospital Southampton NHS Foundation Trust, Southampton, UK.; Faculty of Medicine, Human Development and Health, University of Southampton, Southampton, UK., Johnson CA; Division of Molecular Medicine, Leeds Institute of Medical Research, University of Leeds, Leeds, UK c.johnson@leeds.ac.uk.

Publikováno v: Journal of medical genetics [J Med Genet] 2022 Dec; Vol. 59 (12), pp. 1151-1164. Date of Electronic Publication: 2022 Jun 28.