RalA and PLD1 promote lipid droplet growth in response to nutrient withdrawal.

Autor: Hussain SS; Department of Microbiology, Immunology and Cancer Biology, University of Virginia Health System, Charlottesville, VA 22908, USA., Tran TM; Department of Microbiology, Immunology and Cancer Biology, University of Virginia Health System, Charlottesville, VA 22908, USA., Ware TB; Department of Chemistry, University of Virginia, Charlottesville, VA 22904, USA., Luse MA; Department of Microbiology, Immunology and Cancer Biology, University of Virginia Health System, Charlottesville, VA 22908, USA., Prevost CT; Department of Microbiology, Immunology and Cancer Biology, University of Virginia Health System, Charlottesville, VA 22908, USA., Ferguson AN; Department of Microbiology, Immunology and Cancer Biology, University of Virginia Health System, Charlottesville, VA 22908, USA., Kashatus JA; Department of Microbiology, Immunology and Cancer Biology, University of Virginia Health System, Charlottesville, VA 22908, USA., Hsu KL; Department of Chemistry, University of Virginia, Charlottesville, VA 22904, USA; University of Virginia Cancer Center, University of Virginia Health System, Charlottesville, VA 22903, USA., Kashatus DF; Department of Microbiology, Immunology and Cancer Biology, University of Virginia Health System, Charlottesville, VA 22908, USA; University of Virginia Cancer Center, University of Virginia Health System, Charlottesville, VA 22903, USA. Electronic address: kashatus@virginia.edu.

Publikováno v: Cell reports [Cell Rep] 2021 Jul 27; Vol. 36 (4), pp. 109451.

Biallelic variants in CTU2 cause DREAM-PL syndrome and impair thiolation of tRNA wobble U34.

Autor: Shaheen R; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Mark P; Spectrum Health Division of Medical Genetics, Grand Rapids, Michigan., Prevost CT; Department of Biology, Center for RNA Biology, University of Rochester, Rochester, New York., AlKindi A; Genetics Department, Sultan Qaboos University Hospital, Muscat, Oman., Alhag A; Department of Pediatrics, Specialized Medical Center Hospital, Riyadh, Saudi Arabia., Estwani F; Department of Pediatrics, Specialized Medical Center Hospital, Riyadh, Saudi Arabia., Al-Sheddi T; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Alobeid E; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Alenazi MM; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Ewida N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Ibrahim N; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Hashem M; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Abdulwahab F; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia., Bryant EM; Epilepsy Center and Division of Neurology, Ann & Robert H Lurie Children's Hospital of Chicago, Chicago, Illinois.; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois., Spinelli E; Epilepsy Center and Division of Neurology, Ann & Robert H Lurie Children's Hospital of Chicago, Chicago, Illinois., Millichap J; Epilepsy Center and Division of Neurology, Ann & Robert H Lurie Children's Hospital of Chicago, Chicago, Illinois.; Department of Pediatrics and Neurology, Northwestern University Feinberg School of Medicine, Chicago, Illinois., Barnett SS; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota., Kearney HM; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota., Accogli A; Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Istituto Giannina Gaslini, University of Genoa, Genoa, Italy., Scala M; Department of Neurosurgery, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Istituto Giannina Gaslini, University of Genoa, Genoa, Italy., Capra V; Department of Neurosurgery, IRCCS Istituto Giannina Gaslini, Genoa, Italy., Nigro V; Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy.; Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy., Fu D; Department of Biology, Center for RNA Biology, University of Rochester, Rochester, New York., Alkuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Saudi Arabia.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

Publikováno v: Human mutation [Hum Mutat] 2019 Nov; Vol. 40 (11), pp. 2108-2120. Date of Electronic Publication: 2019 Jul 29.

Roles for the Rad27 Flap Endonuclease in Mitochondrial Mutagenesis and Double-Strand Break Repair in Saccharomyces cerevisiae .

Autor: Nagarajan P; Department of Biology, University of Rochester, New York 14627., Prevost CT; Department of Biology, University of Rochester, New York 14627., Stein A; Department of Biology, University of Rochester, New York 14627., Kasimer R; Department of Biology, University of Rochester, New York 14627., Kalifa L; Department of Biology, University of Rochester, New York 14627., Sia EA; Department of Biology, University of Rochester, New York 14627 elaine.sia@rochester.edu.

Publikováno v: Genetics [Genetics] 2017 Jun; Vol. 206 (2), pp. 843-857. Date of Electronic Publication: 2017 Apr 26.

[Postpartum pituitary infarction; Sheehan's syndrome; report of three cases].

Autor: PREVOST CT

Publikováno v: Journal of the South Carolina Medical Association [J S C Med Assoc] 1956 Feb; Vol. 52 (2), pp. 48-52.