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Elusive Liver Stem Cell Identified in Mice by Researchers
Friday, August 07, 2015
Researchers have found a previously unknown population of cells in mice that function as liver stem cells. The finding could aid drug testing and increase understanding of liver biology and disease.

ZKT gGmbH Awarded AMG Manufacturing Licence for Platelet Lysate
Thursday, August 06, 2015
Turbo-drive for stem cell cultivation.

From Pluripotency to Totipotency
Thursday, August 06, 2015
Studies results provide new elements for the understanding of pluripotency and could increase the efficiency of reprogramming somatic cells to be used for applications in regenerative medicine.

Cancer Treatment Models get Real
Thursday, August 06, 2015
Researchers at Rice Univ. and Univ. of Texas MD Anderson Cancer Center have developed a way to mimic the conditions under which cancer tumors grow in bones.

Potential Treatment for Muscular Dystrophy
Wednesday, August 05, 2015
A new method for producing muscle cells could offer a better model for studying muscle diseases, such as muscular dystrophy, and for testing potential treatment options.

Shire Acquires Foresight Biotherapeutics
Tuesday, August 04, 2015
With the acquisition, Shire acquires the global rights to FST-100 a therapy in late-stage development for the treatment of infectious conjunctivitis, an ocular surface condition commonly referred to as pink eye.

Crucial for Stem Cell Survival Protein Identified Using Editing Tool CRISPR
Monday, August 03, 2015
A team of University of Wisconsin-Madison engineers has identified a protein that is integral to the survival and self-renewal processes of human pluripotent stem cells (hPSC).

Malvern Instruments Establishes New Biopharmaceutical Applications Laboratory
Friday, July 31, 2015
Malvern Instruments has established a new biopharmaceutical applications laboratory in the heart of San Diego’s biotechnology cluster.

A Gene-Sequence Swap Using CRISPR to Cure Haemophilia
Thursday, July 30, 2015
For the first time chromosomal defects responsible for hemophilia have been corrected in patient-specific iPSCs using CRISPR-Cas9 nucleases

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