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Timothy E. Richardson

Researcher at University of Texas Health Science Center at San Antonio

Publications -  89
Citations -  1159

Timothy E. Richardson is an academic researcher from University of Texas Health Science Center at San Antonio. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 17, co-authored 61 publications receiving 727 citations. Previous affiliations of Timothy E. Richardson include State University of New York Upstate Medical University & University of Texas Southwestern Medical Center.

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Sohlh2 Knockout Mice Are Male-Sterile Because of Degeneration of Differentiating Type A Spermatogonia

TL;DR: One conclusion originating from these studies would be that testicular factors normally regulate the viability of differentiating spermatogonia by signaling through Sohlh2, which would provide a crucial checkpoint to optimize the numbers of sperMatocytes entering meiosis during each cycle of sPermatogenesis.
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Spermatogonial Culture Medium: An Effective and Efficient Nutrient Mixture for Culturing Rat Spermatogonial Stem Cells

TL;DR: Spermatogonial lines derived and propagated using SG medium were characterized as homogeneous populations of ZBTB16+ DAZL+ cells endowed with sperMatogonial stem cell potential, which transmitted the donor cell haplotype to more than 75% of progeny by natural breeding.
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An N-heterocyclic amine chelate capable of antioxidant capacity and amyloid disaggregation.

TL;DR: Spectroscopic, transmission electron microscopy, and scanning electron microscope imaging studies show that 1 (pyclen) is capable of both preventing and disrupting Cu(2+) induced AB(1-40) aggregation and the pyridine backbone is responsible for the antioxidant capacity observed.
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Estrogen Prevents Oxidative Damage to the Mitochondria in Friedreich's Ataxia Skin Fibroblasts

TL;DR: It is demonstrated that phenolic estrogens, independent of any known ER, are able to prevent lipid peroxidation and mitochondrial membrane potential (ΔΨm) collapse, maintain ATP at near control levels, increase oxidative phosphorylation and maintain activity of aconitase.