scispace - formally typeset
N

Nicholas R.F. Hannan

Researcher at University of Nottingham

Publications -  42
Citations -  4409

Nicholas R.F. Hannan is an academic researcher from University of Nottingham. The author has contributed to research in topics: Induced pluripotent stem cell & Stem cell. The author has an hindex of 21, co-authored 37 publications receiving 3865 citations. Previous affiliations of Nicholas R.F. Hannan include Wellcome Trust & University of Cambridge.

Papers
More filters
Journal ArticleDOI

Modeling inherited metabolic disorders of the liver using human induced pluripotent stem cells

TL;DR: These patient-derived hepatocytes demonstrate that it is possible to model diseases whose phenotypes are caused by pathological dysregulation of key processes within adult cells, and a simple and effective platform for hepatocyte generation from patient-specific human iPS cells.
Journal ArticleDOI

Generation of functional hepatocytes from human embryonic stem cells under chemically defined conditions that recapitulate liver development

TL;DR: A robust and efficient method to differentiate pluripotent stem cells into hepatic cells, which exhibit characteristics of human hepatocytes are reported, which should facilitate the development of clinical grade hepatocytes for transplantation and for research on drug discovery.
Journal ArticleDOI

Transplantation of Expanded Fetal Intestinal Progenitors Contributes to Colon Regeneration after Injury

TL;DR: It is shown that human and mouse fetal intestine contains proliferative, immature progenitors, which can be expanded in vitro as Fetal Enterospheres (FEnS), which contribute to regeneration of colonic epithelium by forming epithelial crypt-like structures expressing region-specific differentiation markers.
Journal ArticleDOI

Production of hepatocyte-like cells from human pluripotent stem cells

TL;DR: A 25-d protocol to direct the differentiation of human pluripotent stem cells into a near-homogenous population of hepatocyte-like cells and expresses genes in a chronological manner similar to that described during in vivo hepatic development is described.