Primary rat LSECs preserve their characteristic phenotype after cryopreservation

The aim of this present study was to improve the longevity of AWD spermatozoa after thawing by testing two sperm freezing protocols which routinely yield high quality

The aim of this present study was to improve the longevity of AWD spermatozoa after thawing by testing two sperm freezing protocols which routinely yield high quality

Here, we studied the uptake and degradation of T4-phages in primary cultures of freshly isolated rat LSECs, demonstrating the transport of the particles to the lysosomes in

The uptake of 125 I-RAP was not inhibited by ligands to known endocytosis receptors in LSECs, while uptake of 125 I- 2 M* was significantly inhibited by RAP, suggesting

Furthermore, rat LSECs showed high mRNA and protein expression of Clec4g (LSECtin) and Clec4m (DC-SIGNR) (Fig. 6a, b), as was also reported in a study of human LSECs [61], where

For this project emphasis was placed upon high-resolution methods enabling the study of liver sinusoidal endothelial cells (LSECs) below the diffraction limit of

For this project emphasis was placed upon high-resolution methods enabling the study of liver sinusoidal endothelial cells (LSECs) below the diffraction limit of

Trial 4: Assessment of sperm viability on cryopreserved sperm To assess if the cryopreserved sperm maintains its viability after the freezing and thawing process sperm was