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Acta Neuropathologica|April 28, 2012
Neuronal sensitivity to TDP-43 overexpression is dependent on timing of inductionAshley Cannon, Baoli Yang, Joshua Knight, et al.Acta Neuropathologica|May 14, 2013
Robust cytoplasmic accumulation of phosphorylated TDP-43 in transgenic models of tauopathyAmy K Clippinger, Simon D'Alton, Wen-Lang Lin, et al.Journal of Genetic Counseling|March 29, 2020
Recruiting diversity where it exists: The Alabama Genomic Health InitiativeThomas May, Ashley Cannon, Irene P Moss, et al.The British Journal of Dermatology|October 25, 2023
A core outcome domain set to assess cutaneous neurofibromas related to neurofibromatosis type 1 in clinical trialsLaura Fertitta, Christina Bergqvist, Kavita Y Sarin, et al.Research Square|July 1, 2024
The UTHealth Houston Adult Cardiovascular Genomics Certificate Program: Efficacy and Impact on Healthcare ProfessionalsMelyssa Garner, Bansari Rajani, Priyanka Vaidya, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 19, 2019
Subsequent Neoplasms After a Primary Tumor in Individuals With Neurofibromatosis Type 1Smita Bhatia, Yanjun Chen, F Lennie Wong, et al.Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 27, 2020
A state-based approach to genomics for rare disease and population screeningKelly M East, Whitley V Kelley, Ashley Cannon, et al.Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.Pageof 5