Reprogramming stem cells using the measles virus vector
A method has been developed to reprogram stem cells using the measles virus vector, cutting a four-step process to only one stage...
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Stem cells are undifferentiated biological cells that can differentiate into specialised cells and can divide to produce more stem cells.
A method has been developed to reprogram stem cells using the measles virus vector, cutting a four-step process to only one stage...
Sartorius Stedim Biotech (SSB), a leading international supplier for the biopharmaceutical industry announced the launch of the BIOSTAT® RM TX single-use bioreactor, a new wave mixed system developed specifically for closed, automated expansion of consistent quality cell products such as ex vivo cellular immunotherapies...
14 February 2019 | By Sartorius
The BIOSTAT® RM TX system consists of an automated control unit and a rocking platform, for gently agitating a single-use Flexsafe® RM bag...
Stem cells generated from mice have shown to be functional when transplanted, leading to the possibility of future therapies...
The development of a brain stem cell into a neuron often occurs without problems, but there are times when it can transform into cancer...
Researchers have transformed stem cells into cells that are able to produce insulin - the hormone that produces blood sugar...
Researchers have been able to grow perfect human blood vessels in the lab, and are now looking to conduct disease research for vascular diseases...
Strathmin2 could be used as a biomarker for amyotrophic lateral sclerosis (ALS), a debilitating condition with no proper diagnostic tests or treatments...
A stem cell therapy rectifying the FoxP3 gene has been developed to treat IPEX, and has virtually cleared symptoms of the condition in mice...
Learn everything you need to know about the most widely-used mouse in biomedical research with this free whitepaper.
A study has shown how stem cells that are transplanted act in a different way to those ordinarily present, without a transplant...
Learn how the continued development of CRISPR gene editing technologies opens fresh possibilities for in vivo model design.
Rapid drug response screening for leukaemia stem cells offers clues to relapse and to improving patient-specific therapies...
Researchers are always looking more effective and efficient ways of making their work more successful. In this supplement, some of our commercial partners share their data, detailing the application of their technology.
There is substantial interest in the scientific community in using human induced pluripotent stem cell (hiPSC)-derived neural cells to study basic mechanisms of brain development, neuronal function, and drug-induced effects. In vitro-generated brain organoids are promising models, because they show a remarkable degree of maturation and can be kept in…