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A Pesticide Decision Support Tool to guide the selection of less environmentally harmful pesticides for the sugar cane industry.

Autor: St John Warne M; Reef Catchments Science Partnership, School of the Environment, University of Queensland, Brisbane, QLD, 4108, Australia. michael.warne@uq.edu.au.; Water Quality and Investigations, Environmental Monitoring and Assessment Science, Science Delivery, Department of Environment and Science, Brisbane, Queensland, 4102, Australia. michael.warne@uq.edu.au.; Centre for Agroecology, Water and Resilience, Coventry University, Coventry, UK. michael.warne@uq.edu.au., Neale PA; Reef Catchments Science Partnership, School of the Environment, University of Queensland, Brisbane, QLD, 4108, Australia., Macpherson MJ; Farmacist Pty Ltd, Mackay, Queensland, Australia.

Publikováno v: Environmental science and pollution research international [Environ Sci Pollut Res Int] 2023 Oct; Vol. 30 (49), pp. 108036-108050. Date of Electronic Publication: 2023 Sep 25.

Prenatal Genetic Testing in the Era of Next Generation Sequencing: A One-Center Canadian Experience.

Autor: Almubarak A; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada., Zhang D; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada., Kosak M; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada., Rathwell S; Women's and Children's Health Research Institute, University of Alberta, Edmonton, AB T6G 1C9, Canada., Doonanco J; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada., Eaton AJ; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada.; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada., Kannu P; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada.; Women's and Children's Health Research Institute, University of Alberta, Edmonton, AB T6G 1C9, Canada.; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada., Lazier J; Regional Genetics Program, Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada., Lui M; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada., Niederhoffer KY; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada.; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada., MacPherson MJ; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada.; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada., Sorsdahl M; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada., Caluseriu O; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada.; Women's and Children's Health Research Institute, University of Alberta, Edmonton, AB T6G 1C9, Canada.; Maternal Fetal Medicine Clinic, Royal Alexandra Hospital, Edmonton, AB T5H 3V9, Canada.

Publikováno v: Genes [Genes (Basel)] 2022 Nov 03; Vol. 13 (11). Date of Electronic Publication: 2022 Nov 03.

Nucleocytoplasmic transport of the RNA-binding protein CELF2 regulates neural stem cell fates.

Autor: MacPherson MJ; Department of Medial Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada; Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada., Erickson SL; Department of Medial Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada., Kopp D; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada., Wen P; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada., Aghanoori MR; Department of Medial Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada., Kedia S; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada., Burns KML; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada., Vitobello A; UFR Des Sciences de Santé, INSERM-Université de Bourgogne UMR1231 GAD Génétique des Anomalies du Développement, FHU-TRANSLAD, Dijon, France; Unité Fonctionnelle d'Innovation diagnostique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France., Tran Mau-Them F; UFR Des Sciences de Santé, INSERM-Université de Bourgogne UMR1231 GAD Génétique des Anomalies du Développement, FHU-TRANSLAD, Dijon, France; Unité Fonctionnelle d'Innovation diagnostique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France., Thomas Q; UFR Des Sciences de Santé, INSERM-Université de Bourgogne UMR1231 GAD Génétique des Anomalies du Développement, FHU-TRANSLAD, Dijon, France; Centre de Génétique, Hôpital d'Enfants, CHU, 14 rue Paul Gaffarel, BP 77908, 21079 Dijon Cedex, France., Gold NB; Division of Medical Genetics and Metabolism, Massachusetts General Hospital, Boston, MA 02115, USA; Harvard Medical School, Department of Pediatrics, Boston, MA, USA., Brucker W; Division of Genetics and Genomics 300 Longwood Avenue, Boston Children's Hospital, Boston, MA 02115, USA., Amlie-Wolf L; Nemours/Alfred I. duPont Hospital for Children, 1600 Rockland Road, Wilmington, DE 19803, USA., Gripp KW; Nemours/Alfred I. duPont Hospital for Children, 1600 Rockland Road, Wilmington, DE 19803, USA., Bodamer O; Division of Genetics and Genomics 300 Longwood Avenue, Boston Children's Hospital, Boston, MA 02115, USA., Faivre L; UFR Des Sciences de Santé, INSERM-Université de Bourgogne UMR1231 GAD Génétique des Anomalies du Développement, FHU-TRANSLAD, Dijon, France; Centre de Génétique, Hôpital d'Enfants, CHU, 14 rue Paul Gaffarel, BP 77908, 21079 Dijon Cedex, France., Muona M; Blueprint Genetics, Espoo, Finland; Folkhälsan Research Center, Helsinki, Finland., Menzies L; Department of Clinical Genetics, Great Ormond Street Hospital, London, UK., Baptista J; Exeter Genomics Laboratory, Royal Devon and Exeter NHS Hospital, Exeter, UK; College of Medicine and Health, University of Exeter, Exeter, UK., Guegan K; Exeter Genomics Laboratory, Royal Devon and Exeter NHS Hospital, Exeter, UK., Male A; Department of Clinical Genetics, Great Ormond Street Hospital, London, UK., Wei XC; Diagnostic Imaging, Alberta Children's Hospital, 28 Oki Drive NW, Calgary, AB T3B 6A8, Canada., He G; Institute of Neuroscience, Chongqing Medical University, Chongqing 400016, China., Long Q; Department of Medial Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada., Innes AM; Department of Medial Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada. Electronic address: micheil.innes@albertahealthservices.ca., Yang G; Department of Medial Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada; Alberta Children's Hospital Research Institute, Calgary, AB T2N 4N1, Canada; Department of Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada. Electronic address: guang.yang2@ucalgary.ca.

Publikováno v: Cell reports [Cell Rep] 2021 Jun 08; Vol. 35 (10), pp. 109226.

The CTCF insulator protein forms an unusual DNA structure.

Autor: MacPherson MJ; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada., Sadowski PD

Publikováno v: BMC molecular biology [BMC Mol Biol] 2010 Dec 21; Vol. 11, pp. 101. Date of Electronic Publication: 2010 Dec 21.