4.5 Article

Deconstructing Pancreas Developmental Biology

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COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/cshperspect.a012401

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资金

  1. NIH [5 T32 GM007790-29]
  2. National Science Foundation
  3. Medical Scientist Training Program (NIH/NIGMS)
  4. American Diabetes Association
  5. Snyder Foundation
  6. Mead Foundation
  7. Juvenile Diabetes Research Foundation
  8. California Institute of Regenerative Medicine
  9. Helmsley Charitable Trust
  10. U.S. NIH
  11. Howard Hughes Medical Institute (HHMI)

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The relentless nature and increasing prevalence of human pancreatic diseases, in particular, diabetes mellitus and adenocarcinoma, has motivated further understanding of pancreas organogenesis. The pancreas is a multifunctional organ whose epithelial cells govern a diversity of physiologically vital endocrine and exocrine functions. The mechanisms governing the birth, differentiation, morphogenesis, growth, maturation, and maintenance of the endocrine and exocrine components in the pancreas have been discovered recently with increasing tempo. This includes recent studies unveiling mechanisms permitting unexpected flexibility in the developmental potential of immature and mature pancreatic cell subsets, including the ability to interconvert fates. In this article, we describe how classical cell biology, genetic analysis, lineage tracing, and embryological investigations are being complemented by powerful modern methods including epigenetic analysis, time-lapse imaging, and flow cytometry-based cell purification to dissect fundamental processes of pancreas development.

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