Searching journal content for articles similar to McGuire et al. 26 (9): 1165.

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  1. Research: Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young
    • D. Nicole R. Methner,
    • Steven E. Scherer,
    • Katherine Welch,
    • Magdalena Walkiewicz,
    • Christine M. Eng,
    • John W. Belmont,
    • Mark C. Powell,
    • Viktoriya Korchina,
    • Harsha Vardhan Doddapaneni,
    • Donna M. Muzny,
    • Richard A. Gibbs,
    • Dwayne A. Wolf,
    • Luis A. Sanchez,
    • and Roger Kahn
    Genome Res. September 2016 26: 1170-1177; Published in Advance July 19, 2016, doi:10.1101/gr.195800.115
    ...an undetermined cause of death after postmortem investigation and autopsy. Heritable genetic variants have been suggested as the cause of up to a third of sudden death (SD) cases. Elucidation of the genetic variants involved in SD cases is important to not only help establish cause and manner of death...
  2. Research: Human-specific features of spatial gene expression and regulation in eight brain regions
    • Chuan Xu,
    • Qian Li,
    • Olga Efimova,
    • Liu He,
    • Shoji Tatsumoto,
    • Vita Stepanova,
    • Takao Oishi,
    • Toshifumi Udono,
    • Katsushi Yamaguchi,
    • Shuji Shigenobu,
    • Akiyoshi Kakita,
    • Hiroyuki Nawa,
    • Philipp Khaitovich,
    • and Yasuhiro Go
    Genome Res. August 2018 28: 1097-1110; Published in Advance June 13, 2018, doi:10.1101/gr.231357.117
    ...), the National Institutes of Natural Sciences Bioethics Committee (No. 24-02, 25-03, 25-04), and the Kyoto University Medical Ethics Committee (No. G421). All ape brain samples were obtained from institutes or zoos after their natural deaths under the collaborative research project of the Great Ape Information...
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  3. Research: Transcriptional alterations in glioma result primarily from DNA methylation–independent mechanisms
    • Franck Court,
    • Elisa Le Boiteux,
    • Anne Fogli,
    • Mélanie Müller-Barthélémy,
    • Catherine Vaurs-Barrière,
    • Emmanuel Chautard,
    • Bruno Pereira,
    • Julian Biau,
    • Jean-Louis Kemeny,
    • Toufic Khalil,
    • Lucie Karayan-Tapon,
    • Pierre Verrelle,
    • and Philippe Arnaud
    Genome Res. October 2019 29: 1605-1621; Published in Advance September 18, 2019, doi:10.1101/gr.249219.119
  4. LETTER: Uterine Dysfunction and Genetic Modifiers in Centromere Protein B-deficient Mice
    • Kerry J. Fowler,
    • Damien F. Hudson,
    • Lois A. Salamonsen,
    • Stephanie R. Edmondson,
    • Elizabeth Earle,
    • Mandy C. Sibson,
    • and K.H. Andy Choo
    Genome Res. January 1, 2000 10: 30-41; doi:10.1101/gr.10.1.30
    ...overdue (by up to 10 days) or difficulty with delivery. Autopsy of these sickened mice revealed dead fetuses in all cases. Where discernible, fetal development appeared normal (Fig. 4 B,D). Causes of fetal death in utero included placental necrosis (Fig. 4 B), fetal growth arrest or resorption (Fig. 4 B...
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