2022
Sex differences in developmental patterns of neocortical astroglia: A mouse translatome database
Rurak GM, Simard S, Freitas-Andrade M, Lacoste B, Charih F, Van Geel A, Stead J, Woodside B, Green JR, Coppola G, Salmaso N. Sex differences in developmental patterns of neocortical astroglia: A mouse translatome database. Cell Reports 2022, 38: 110310. PMID: 35108542, DOI: 10.1016/j.celrep.2022.110310.Peer-Reviewed Original ResearchConceptsGene expression patternsRibosome affinity purificationDevelopmental time pointsAstroglial phenotypeMaintenance of neuronsRNA sequencingAffinity purificationExpression patternsTelencephalic developmentAstroglial cellsSteroid hormone receptorsSex differencesKey playersNeuronal networksHormone receptorsDevelopmental patternsImportant sex differencesPhenotypeDevelopmental sex differencesWindow of vulnerabilityFemale miceHormonal manipulationPostnatal developmentAstrogliaTranslatome
2020
Genetic pathways disrupted by ENPP1 deficiency provide insight into mechanisms of osteoporosis, osteomalacia, and paradoxical mineralization
Maulding ND, Kavanagh D, Zimmerman K, Coppola G, Carpenter TO, Jue NK, Braddock DT. Genetic pathways disrupted by ENPP1 deficiency provide insight into mechanisms of osteoporosis, osteomalacia, and paradoxical mineralization. Bone 2020, 142: 115656. PMID: 32980560, PMCID: PMC7744330, DOI: 10.1016/j.bone.2020.115656.Peer-Reviewed Original ResearchConceptsGenetic pathwaysSkeletal phenotypeGene expressionHuman disease phenotypesAsj/Suppression of WntTranscript countsGene transcriptionENPP1-deficient miceGene pathwaysEnzyme functionENPP1 deficiencyWnt ligandsSoluble Wnt inhibitorsWnt activityReduced gene transcriptionBiomechanical phenotypeTranscriptionWnt inhibitorsBone findingsUnbiased analysisDisease phenotypePhenotypeOld miceStrong signature