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Generation of hepatic cell from placental stem cell for congenital metabolic disorders

  • Post author:
  • Post published:June 30, 2026
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Approximately 1 in 1,500 children has a congenital metabolic disorder. These inborn errors of metabolism are caused by deficiencies of different enzymes and result in accumulation of various substances inside…

Continue ReadingGeneration of hepatic cell from placental stem cell for congenital metabolic disorders

Generation of safe and therapeutically effective human induced hepatocyte-like cells

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  • Post published:June 30, 2026
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Although the liver can regenerate itself, chronic or overwhelming damage can cause life-threatening liver failure. Currently, the only therapy for liver failure is liver transplantation. Because the supply of cadaveric…

Continue ReadingGeneration of safe and therapeutically effective human induced hepatocyte-like cells

Biological relevance of microRNAs in hESC differentiation to endocrine pancreas

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  • Post published:June 30, 2026
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There remains an urgent and critical need for a cell-based cure of diabetes, one of the most costly diseases in California. Islet transplantation with persistent immune suppression has shown promise…

Continue ReadingBiological relevance of microRNAs in hESC differentiation to endocrine pancreas

Antibody tools to deplete or isolate teratogenic, cardiac, and blood stem cells from hESCs

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  • Post published:June 30, 2026
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Purity is as important for cell-based therapies as it is for treatments based on small-molecule drugs or biologics. Pluripotent stem cells possess two properties: they are capable of self regeneration…

Continue ReadingAntibody tools to deplete or isolate teratogenic, cardiac, and blood stem cells from hESCs

Pluripotent and Somatic Stem Cell Models to Study Inherited Diarrheal Disorders

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  • Post published:June 30, 2026
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Our research group at [REDACTED] has had a long-standing interest in understanding the cause of several disorders that result in severe, and often times fatal forms of diarrhea in children.…

Continue ReadingPluripotent and Somatic Stem Cell Models to Study Inherited Diarrheal Disorders

Liver Cell Transplantation

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  • Post published:June 30, 2026
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Because there is still considerable morbidity and mortality associated with the process of whole liver transplantation, and because more than a thousand people die each year while on the liver…

Continue ReadingLiver Cell Transplantation

Bone Marrow Mesenchymal Stem Cells to Heal Chronic Diabetic Wounds

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  • Post published:June 30, 2026
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Diabetic foot ulcers (DFU), chronic, non-healing wounds on the feet of diabetic patients, present a serious challenge to global health. These ulcers affect between 15-25% of the 18-21 million Americans…

Continue ReadingBone Marrow Mesenchymal Stem Cells to Heal Chronic Diabetic Wounds

Methods for detection and elimination of residual human embryonic stem cells in a differentiated cell product

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  • Post published:June 30, 2026
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Human embryonic stem cells (hESC), and other related pluripotent stem cells, have great potential as starting material for the manufacture of curative cell therapies. This is primarily for two reasons.…

Continue ReadingMethods for detection and elimination of residual human embryonic stem cells in a differentiated cell product

Developing induced pluripotent stem cells into human therapeutics and disease models

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  • Post published:June 30, 2026
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Human embryonic stem cells (hESCs) can undergo unlimited self-renewal and differentiate into all the cell types in the human body, and thus hold great promise for cell replacement therapy. However,…

Continue ReadingDeveloping induced pluripotent stem cells into human therapeutics and disease models

Stem cell tolerance through the use of engineered antigen-specific regulatory T cells

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  • Post published:June 30, 2026
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Type 1 Diabetes (T1D) occurs as a consequence of uncontrolled immune activation, culminating in the destruction of insulin-producing beta-cells. Efforts to prevent or reverse diabetes have been limited by the…

Continue ReadingStem cell tolerance through the use of engineered antigen-specific regulatory T cells
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