scispace - formally typeset
A

Andrea B. Zepeda

Researcher at University of La Frontera

Publications -  20
Citations -  842

Andrea B. Zepeda is an academic researcher from University of La Frontera. The author has contributed to research in topics: Oxidative stress & Pichia pastoris. The author has an hindex of 12, co-authored 20 publications receiving 674 citations. Previous affiliations of Andrea B. Zepeda include Arturo Prat University.

Papers
More filters
Journal ArticleDOI

The hypoxic testicle: physiology and pathophysiology.

TL;DR: It is suggested that conditions such as germ cell apoptosis and DNA damage are common features in hypoxia and varicocele and testicular torsion and oxidative damage seems to be present in these conditions during the initiation stages of germ cell damage and apoptosis.
Journal ArticleDOI

Antioxidant Therapeutic Strategies for Cardiovascular Conditions Associated with Oxidative Stress

TL;DR: The participation of OS in the pathophysiology of cardiovascular conditions such as myocardial infarction, anthracycline cardiotoxicity and congenital heart disease is described, giving support for novel pharmacological therapies such as omega 3 fatty acids, non-selective betablockers and microRNAs.
Journal ArticleDOI

Cellular and molecular mechanisms in the hypoxic tissue: role of HIF-1 and ROS.

TL;DR: New developments in HIF‐mediated O2 sensing mechanisms and their interactions with reactive oxygen species–generating pathways in normal and abnormal physiology are summarized.
Journal ArticleDOI

Applications of recombinant Pichia pastoris in the healthcare industry

TL;DR: The attempt of this review is to embrace several research lines that have adopted Pichia pastoris as their expression system to produce a protein on an industrial scale in the health care industry.
Journal ArticleDOI

Oxidative stress in rat testis and epididymis under intermittent hypobaric hypoxia: protective role of ascorbate supplementation.

TL;DR: In conclusion, AA was capable of decreasing oxidative stress in testis and epididymis under IHH, and this protection by AA of the IHH-induced lipid peroxidation can be explained in part by the preservation of glutathione reductase activity in these organs.