Novel Pannexin 1 isoform is increased in cancer.

Autor: O'Donnell BL, Stefan D, Chiu YH, Zeitz MJ, Tang J, Johnston D, Leighton SE, Kessel CV, Barr K, Gyenis L, Freeman TJ, Kelly JJ, Sayedyahossein S, Litchfield DW, Roth K, Smyth JW, Hebb M, Ronald J, Bayliss DA, Penuela S

Publikováno v: BioRxiv : the preprint server for biology [bioRxiv] 2024 Sep 11. Date of Electronic Publication: 2024 Sep 11.

Cx31.1 can selectively intermix with co-expressed connexins to facilitate its assembly into gap junctions.

Autor: Leighton SE; Department of Anatomy and Cell Biology, University of Western Ontario, London, ON N6A 5C1, Canada., Wong RS; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada., Lucaciu SA; Department of Anatomy and Cell Biology, University of Western Ontario, London, ON N6A 5C1, Canada.; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada., Hauser A; Department of Anatomy and Cell Biology, University of Western Ontario, London, ON N6A 5C1, Canada., Johnston D; Department of Anatomy and Cell Biology, University of Western Ontario, London, ON N6A 5C1, Canada., Stathopulos PB; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada., Bai D; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada., Penuela S; Department of Anatomy and Cell Biology, University of Western Ontario, London, ON N6A 5C1, Canada.; Western's Bone and Joint Institute, The Dr. Sandy Kirkley Centre for Musculoskeletal Research, University Hospital, London, ON N6A 5B9, Canada.; Division of Experimental Oncology, Department of Oncology, University of Western Ontario, London, ON N6A 5W9, Canada., Laird DW; Department of Anatomy and Cell Biology, University of Western Ontario, London, ON N6A 5C1, Canada.; Department of Physiology and Pharmacology, University of Western Ontario, London, ON N6A 5C1, Canada.

Publikováno v: Journal of cell science [J Cell Sci] 2024 Apr 01; Vol. 137 (7). Date of Electronic Publication: 2024 Apr 17.

Diversity in connexin biology.

Autor: Lucaciu SA; Department of Anatomy and Cell Biology, University of Western Ontario, London, Ontario, Canada; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada., Leighton SE; Department of Anatomy and Cell Biology, University of Western Ontario, London, Ontario, Canada., Hauser A; Department of Anatomy and Cell Biology, University of Western Ontario, London, Ontario, Canada., Yee R; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada., Laird DW; Department of Anatomy and Cell Biology, University of Western Ontario, London, Ontario, Canada; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada. Electronic address: dale.laird@schulich.uwo.ca.

Publikováno v: The Journal of biological chemistry [J Biol Chem] 2023 Nov; Vol. 299 (11), pp. 105263. Date of Electronic Publication: 2023 Sep 20.

Genome sequencing in congenital cataracts improves diagnostic yield.

Autor: Ma A; Eye Genetics Research Unit, The Children's Hospital at Westmead, Save Sight Institute, Children's Medical Research Institute, University of Sydney, Sydney, New South Wales, Australia.; Department of Clinical Genetics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Specialties of Genomic Medicine & Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia., Grigg JR; Eye Genetics Research Unit, The Children's Hospital at Westmead, Save Sight Institute, Children's Medical Research Institute, University of Sydney, Sydney, New South Wales, Australia.; Department of Ophthalmology, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Specialty of Ophthalmology, University of Sydney, Sydney, New South Wales, Australia.; Save Sight Institute, Sydney Eye Hospital, Sydney, New South Wales, Australia., Flaherty M; Department of Ophthalmology, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Specialty of Ophthalmology, University of Sydney, Sydney, New South Wales, Australia., Smith J; Department of Ophthalmology, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Specialty of Ophthalmology, University of Sydney, Sydney, New South Wales, Australia., Minoche AE; Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia., Cowley MJ; Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.; Children's Cancer Institute, Lowy Cancer Research Centre, University of New South Wales, Randwick, New South Wales, Australia.; St Vincent's Clinical School, Faculty of Medicine, UNSW Australia, Sydney, New South Wales, Australia., Nash BM; Eye Genetics Research Unit, The Children's Hospital at Westmead, Save Sight Institute, Children's Medical Research Institute, University of Sydney, Sydney, New South Wales, Australia.; Specialties of Genomic Medicine & Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Ho G; Specialties of Genomic Medicine & Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Gayagay T; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Lai T; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Farnsworth E; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Hackett EL; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Slater K; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Wong K; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Holman KJ; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Jenkins G; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Cheng A; Eye Genetics Research Unit, The Children's Hospital at Westmead, Save Sight Institute, Children's Medical Research Institute, University of Sydney, Sydney, New South Wales, Australia., Martin F; Department of Ophthalmology, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Specialty of Ophthalmology, University of Sydney, Sydney, New South Wales, Australia., Brown NJ; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia., Leighton SE; Tasmanian Clinical Genetics Service, Hobart, Australia., Amor DJ; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia., Goel H; Hunter Genetics, Newcastle, New South Wales, Australia., Dinger ME; Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.; School of Biotechnology and Biomolecular Sciences, Faculty of Science, UNSW, Sydney, New South Wales, Australia., Bennetts B; Specialties of Genomic Medicine & Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.; Sydney Genome Diagnostics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia., Jamieson RV; Eye Genetics Research Unit, The Children's Hospital at Westmead, Save Sight Institute, Children's Medical Research Institute, University of Sydney, Sydney, New South Wales, Australia.; Department of Clinical Genetics, Western Sydney Genetics Program, The Children's Hospital at Westmead, Sydney, New South Wales, Australia.; Specialties of Genomic Medicine & Child and Adolescent Health, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.

Publikováno v: Human mutation [Hum Mutat] 2021 Sep; Vol. 42 (9), pp. 1173-1183. Date of Electronic Publication: 2021 Jun 15.

Utilization and Findings of Flexible Naso-Pharyngo-Laryngoscopy in Upper Airway Disorders: A Clinic Audit.

Autor: Abdullahi, Idris¹ idrisabdullahi70@gmail.com, Shofoluwe, Nurudden Adebola¹, Shuaibu, Iliyasu Yunusa¹, Usman, Mohammed Aminu¹, Chitumu, Dotiro¹, Mohammed, Ibrahim Babatunde¹, Omodele, Abdurrahman¹, Zubairu, Saleem Shehu¹

Publikováno v: Nigerian Medical Journal. 2024, Vol. 65 Issue 2, p206-212. 7p.