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مرکز نوآوری سلول‌های بنیادی و پزشکی بازساختی

دانشگاه علوم پزشکی تهران

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Organoid model systems are taking research to the next dimension

Organoid model systems are taking research to the next dimension

The term organoid first gained use in the mid-1960?s to describe cell aggregates observed during dissociation and re-aggregation experiments in classic developmental biology. Today, the term organoid refers to three-dimensional structures containing multiple organotypic cell types, recapitulating some of

Induced pluripotent stem (iPS) cells from a donor cell bank may open a new paradigm shift in stem cell treatment

Induced pluripotent stem (iPS) cells from a donor cell bank may open a new paradigm shift in stem cell treatment

Researchers from the Japanese RIKEN Centre have reportedly delivered induced pluripotent stem (iPS) cells from an anonymous donor to a 60 year old male patient. The milestone is understood to represent a world first in the development of stem cell technology, in addition to changing the medical approach to how such treatments may become more widely available than first anticipated. Previous protocols have focused on the delivery of a patient?s own cells using a very different clinical procedure to that which may be envisioned from using a ?democratized? cell bank.

Stem cell treatment could be a proven therapy for diabetes, autism

Stem cell treatment could be a proven therapy for diabetes, autism

Stem cell therapy has turned out to be a ray of hope for most patients who are trying to find a cure for incurable diseases. Researchers and experts believe India has been at the top in the development of stem cell treatment followed by several other countries like China and Japan. However, due to lack of awareness, most people don't think of stem cell therapy as an option for treating most of the incurable diseases.

CRISPR gene editing takes on rare immunodeficiency disorder

CRISPR gene editing takes on rare immunodeficiency disorder

Researchers have harnessed the CRISPR-Cas9 technology to correct mutations in the blood stem cells of patients with a rare immunodeficiency disorder; the engineered cells successfully engrafted in mice for up to five months.

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