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Michael H. Donovan

Researcher at University of Texas Southwestern Medical Center

Publications -  6
Citations -  1259

Michael H. Donovan is an academic researcher from University of Texas Southwestern Medical Center. The author has contributed to research in topics: Neurogenesis & Dentate gyrus. The author has an hindex of 5, co-authored 5 publications receiving 1152 citations. Previous affiliations of Michael H. Donovan include University of Texas at Dallas.

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Decreased adult hippocampal neurogenesis in the PDAPP mouse model of Alzheimer's disease.

TL;DR: An age‐dependent decrease in SGZ proliferation in homozygous PDAPP mice is reported, suggesting altered neurogenesis in the PDAPP mouse may contribute to the age‐related cognitive deficits reported in this model of AD and may be a useful adjunct target for assessing the impact of AD therapies.
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Adult hippocampal neurogenesis is functionally important for stress-induced social avoidance

TL;DR: Supporting a functional role for adult-generated dentate gyrus neurons, ablation of neurogenesis via cranial ray irradiation robustly inhibited social avoidance and shows that the time window after cessation of stress is a critical period for the establishment of persistent cellular and behavioral responses to stress.
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Dynamic expression of TrkB receptor protein on proliferating and maturing cells in the adult mouse dentate gyrus.

TL;DR: Evidence is provided that maturing, but not proliferating, cells in the adult mouse SGZ have the molecular machinery necessary to respond directly to BDNF, and lays critical groundwork for further exploration of the role of BDNF‐TrkB signaling in regulation of adult hippocampal neurogenesis.
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Stress-Induced Anxiety- and Depressive-Like Phenotype Associated with Transient Reduction in Neurogenesis in Adult Nestin-CreERT2/Diphtheria Toxin Fragment A Transgenic Mice

TL;DR: A functional association between adult neurogenesis and stress induced anxiety- and depressive-like behaviors is suggested, where induced reduction in DCX+ cells at the time of behavioral testing is coupled with stress-induced anxiety and a depressive phenotype, and recovery ofDCX+ cell number corresponds to normalization of these behaviors.