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Biorxiv : the Preprint Server for Biology|December 9, 2024
Mitochondrial respiratory capacity in kidney podocytes is high, age-dependent, and sexually dimorphicMatthew D Campbell, Monica Sanchez-Contreras, Britta D Sibley, et al.
Experimental Physiology|April 1, 2025
Phylogenetic allometric scaling of near basal breathing frequency in terrestrial, semi-aquatic and aquatic mammalsAndreas Fahlman, Elliot Stielstra, Ethan Wilstermann, et al.
Journal of Neuropathology and Experimental Neurology|October 2, 2015
A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick DiseasePawel Tacik, Michael DeTure, Kelly M Hinkle, et al.
American Journal of Human Genetics|August 18, 2015
A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen SyndromeJennifer J Johnston, Monica Y Sanchez-Contreras, Kim M Keppler-Noreuil, et al.
Animals : an Open Access Journal From MDPI|May 14, 2025
Assessing Bottlenose Dolphins' (<i>Tursiops truncatus</i>) Health Status Through Functional Muscle Analysis, and Oxidative and Metabolic Stress Evaluation: A Preliminary StudyClaudia Gatta, Eugenio Luigi Iorio, Carla Genovese, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 24, 2016
Distribution and characteristics of transactive response DNA binding protein 43 kDa pathology in progressive supranuclear palsyShunsuke Koga, Monica Sanchez-Contreras, Keith A Josephs, et al.
JMIR Research Protocols|September 10, 2025
Strong Families Start at Home/Familias Fuertes Comienzan en Casa-Improving Child Diet Quality and Parental Feeding Practices: Protocol for a Randomized Controlled TrialAlison Tovar, Kelly Lynn Bouchard, Amy M Moore, et al.
NAR Molecular Medicine|May 23, 2024
Frequencies and spectra of aflatoxin B<sub>1</sub>-induced mutations in liver genomes of NEIL1-deficient mice as revealed by duplex sequencingIrina G Minko, Michael M Luzadder, Vladimir L Vartanian, et al.
Neuropathology and Applied Neurobiology|November 19, 2016
Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathyP Tacik, M Sanchez-Contreras, M DeTure, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 8, 2008
Rapid Virulence Annotation (RVA): identification of virulence factors using a bacterial genome library and multiple invertebrate hostsNicholas R Waterfield, Maria Sanchez-Contreras, Ioannis Eleftherianos, et al.
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