In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts - Wikidata - awgldk - TriplyDB

In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

http://www.wikidata.org/entity/Q36279958

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Reprogramming of various cell types to a beta-like state by Pdx1, Ngn3 and MafA Report from IPITA-TTS Opinion Leaders Meeting on the Future of β-Cell Replacement Animal models of diabetes mellitus for islet transplantation Transcription factor regulation of pancreatic organogenesis, differentiation and maturation Concise review: carbon nanotechnology: perspectives in stem cell research Adult tissue sources for new β cells.β-Cell Replacement Strategies: The Increasing Need for a "β-Cell Dogma".The novel tool of cell reprogramming for applications in molecular medicine.Revealing transcription factors during human pancreatic β cell development.Loss of Fbw7 reprograms adult pancreatic ductal cells into α, δ, and β cells.BMP-7 Induces Adult Human Pancreatic Exocrine-to-Endocrine Conversion.Colony-forming progenitor cells in the postnatal mouse liver and pancreas give rise to morphologically distinct insulin-expressing colonies in 3D cultures Sox9: a master regulator of the pancreatic program.The versatile functions of Sox9 in development, stem cells, and human diseases Generation of insulin-producing cells from the mouse liver using β cell-related gene transfer including Mafa and Mafb.The ACE2/Ang-(1-7)/Mas Axis Regulates the Development of Pancreatic Endocrine Cells in Mouse Embryos.Adult Human Biliary Tree Stem Cells Differentiate to β-Pancreatic Islet Cells by Treatment with a Recombinant Human Pdx1 Peptide.Identification of miRNAs Involved in Reprogramming Acinar Cells into Insulin Producing Cells.Minireview: Directed Differentiation and Encapsulation of Islet β-Cells-Recent Advances and Future Considerations.Characterization of an apparently novel β-cell line-enriched 80-88 kDa transcriptional activator of the MafA and Pdx1 genes The FOXP1, FOXP2 and FOXP4 transcription factors are required for islet alpha cell proliferation and function in mice.Mechanistic basis of immunotherapies for type 1 diabetes mellitus Direct Reprogramming for Pancreatic Beta-Cells Using Key Developmental Genes Brief demethylation step allows the conversion of adult human skin fibroblasts into insulin-secreting cells Stage specific reprogramming of mouse embryo liver cells to a beta cell-like phenotype.Stepwise reprogramming of liver cells to a pancreas progenitor state by the transcriptional regulator Tgif2.Concise review: a population shift view of cellular reprogramming.Concise review: pluripotent stem cell-based regenerative applications for failing β-cell function In vivo reprogramming for tissue repair.Regeneration through reprogramming adult cell identity in vivo.Engineering Cell Fate for Tissue Regeneration by In Vivo Transdifferentiation.Chemical transdifferentiation: closer to regenerative medicine.Regeneration of pancreatic insulin-producing cells by in situ adaptive cell conversion.Molecular mechanisms of Sox transcription factors during the development of liver, bile duct, and pancreas.Reprogramming of Pancreatic Exocrine Cells AR42J Into Insulin-producing Cells Using mRNAs for Pdx1, Ngn3, and MafA Transcription Factors.Lineage conversion of mouse fibroblasts to pancreatic α-cells.Neuroregeneration using in vivo cellular reprogramming.Reprogramming human gallbladder cells into insulin-producing β-like cells.Stable insulin-secreting ducts formed by reprogramming of cells in the liver using a three-gene cocktail and a PPAR agonist.Regenerative medicine: transdifferentiation in vivo.

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In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

http://www.wikidata.org/entity/Q36279958

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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name

In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

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In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

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type

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In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

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In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

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In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

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In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

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PNAS.1201701109

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Proceedings of the National Academy of Sciences of the United States of America

P1476

In vivo reprogramming of Sox9+ cells in the liver to insulin-secreting ducts

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Anannya Banga

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Ersin Akinci

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James R Dutton

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Jonathan M W Slack

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Lucas V Greder

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P2860

Direct conversion of fibroblasts to functional neurons by defined factors

Skipping the co-expression problem: the new 2A "CHYSEL" technology

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

Generation of germline-competent induced pluripotent stem cells

In vivo reprogramming of adult pancreatic exocrine cells to beta-cells

Pancreatic and duodenal homeobox gene 1 induces expression of insulin genes in liver and ameliorates streptozotocin-induced hyperglycemia

Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors.

Intrahepatic bile ducts develop according to a new mode of tubulogenesis regulated by the transcription factor SOX9

A global double-fluorescent Cre reporter mouse

Glycemic control promotes pancreatic beta-cell regeneration in streptozotocin-induced diabetic mice.

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