Under in vitro culture conditions, oxidative modifications of cell components via increased reactive oxygen species (ROS) represent a major culture induced stress. Anti-oxidant systems such as glutathione (GSH) can attenuate the deleterious effects of oxidative stress by scavenging ROS. It has been suggested that GSH content in oocytes may serve as a reservoir protecting the zygote and the early embryos from oxidative damage before genomic activation and de novo GSH synthesis occur. Addition of low molecular weight compounds to culture media, such as cysteamine, can increase GSH levels by increasing cysteine uptake. Quite naturally, effects of supplementation of in vitro maturation (IVM) media with low molecular weight thiols have been stu...
The purpose of this investigation was to determine the effect of P-mercaptoethanol (P-ME) and cystea...
An improved developmental competence of oocytes matured in presence of cysteamine was recorded in bu...
Sheep oocytes were collected either by vacuum aspiration with a 20-gauge needle or by slicing ovarie...
Under in vitro culture conditions, oxidative modifications of cell components via increased reactive...
In in vitro embryo production (IVP), oxidative modifications via increased reactive oxygen species (...
Low nuclear maturation and fertilization rate is one obstacle in the in vitro embryo production whic...
Cysteamine and beta-mercaptoethanol supplementation of in vitro maturation (IVM) medium has been fou...
Background: Preparation of oocytes is one of the critical factors that determine the developmental c...
Cysteamine and beta-mercaptoethanol supplementation of in vitro maturation (IVM) medium has been fou...
Rate of in vitro maturation of oocytes is one of the challenges of assisted reproductive techniques....
Oxidative stress during in vitro culture leads to defects in development of gametes and embryos. Sev...
The purpose of this study was to evaluate whether enriching the oocyte in vitro maturation medium wi...
The purpose of this study was to evaluate whether enriching the oocyte in vitro maturation medium wi...
It was demonstrated that cysteamine supplementation during in vitro maturation (IVM) improves embryo...
It was demonstrated that cysteamine supplementation during in vitro maturation (IVM) improves embryo...
The purpose of this investigation was to determine the effect of P-mercaptoethanol (P-ME) and cystea...
An improved developmental competence of oocytes matured in presence of cysteamine was recorded in bu...
Sheep oocytes were collected either by vacuum aspiration with a 20-gauge needle or by slicing ovarie...
Under in vitro culture conditions, oxidative modifications of cell components via increased reactive...
In in vitro embryo production (IVP), oxidative modifications via increased reactive oxygen species (...
Low nuclear maturation and fertilization rate is one obstacle in the in vitro embryo production whic...
Cysteamine and beta-mercaptoethanol supplementation of in vitro maturation (IVM) medium has been fou...
Background: Preparation of oocytes is one of the critical factors that determine the developmental c...
Cysteamine and beta-mercaptoethanol supplementation of in vitro maturation (IVM) medium has been fou...
Rate of in vitro maturation of oocytes is one of the challenges of assisted reproductive techniques....
Oxidative stress during in vitro culture leads to defects in development of gametes and embryos. Sev...
The purpose of this study was to evaluate whether enriching the oocyte in vitro maturation medium wi...
The purpose of this study was to evaluate whether enriching the oocyte in vitro maturation medium wi...
It was demonstrated that cysteamine supplementation during in vitro maturation (IVM) improves embryo...
It was demonstrated that cysteamine supplementation during in vitro maturation (IVM) improves embryo...
The purpose of this investigation was to determine the effect of P-mercaptoethanol (P-ME) and cystea...
An improved developmental competence of oocytes matured in presence of cysteamine was recorded in bu...
Sheep oocytes were collected either by vacuum aspiration with a 20-gauge needle or by slicing ovarie...