Genetic Modulation of Human Pluripotent Stem Cells

Submission deadline: 31 October 2024
Special Issue Editor
  • Balázs Sarkadi, MD, PhD
    Hungarian Academy of Sciences, Research Centre for Natural Sciences, Semmelweis University, Budapest, Hungary
    Interests: induced pluripotent stem cells; gene expression; membrane transporters; drug metabolism
Special Issue Information

Dear Colleagues,

Human pluripotent stem cells, with a major potential in advanced medical applications, became the center of current cell and molecular biology studies. The fantasy of both scientists and lay people has been captured by culturing immortal human cell lines with a full potential of generating any kind of tissues or organs, including non-regenerating neuronal or heart muscle tissues. The ethical concerns regarding research on human embryonic stem cells disappeared when it was discovered that human induced pluripotent stem cells (iPSCs) can be generated from a range of differentiated cell types, and these iPSCs fully mimic the regenerative and differentiation properties of the embryonic stem cells.

The major current challenges of working with human pluripotent stem cells are to establish proper methods for targeted genetic modulation together with directed tissue differentiation, to devise human cell-based disease models for applications in drug screening, and to develop safe and efficient medical use of pluripotent cell-derived tissues or organs. For all these aims, the specific use and further development of the tools of genetic engineering are essential and remain a challenge. In addition, any stem cell derived preparations for advanced drug screening or therapeutic applications have to comply with the strict regulatory requirements of GLP and GMP environments.

The aim of this Special Issue is to publish original research as well as comprehensive reviews on the recent advances in the field of targeted genetic modifications in human pluripotent stem cells and their derivatives. A special emphasis is placed on the most advanced site-directed gene knock-out, modification and insertion technologies, especially with relevance for the application of human tissues in drug development, advanced diagnostics and cellular therapies.

Balázs Sarkadi
Guest Editor

Keywords
human pluripotent stem cells
induced pluripotent stem cells
gene expression
genetic modification
stem cell differentiation
organoids
membrane transporters
disease models
Manuscript Submission Information

Manuscripts should be submitted via our online editorial system at https://imr.propub.com by registering and logging in to this website. Once you are registered, click here to start your submission. Manuscripts can be submitted now or up until the deadline. All papers will go through peer-review process. Accepted papers will be published in the journal (as soon as accepted) and meanwhile listed together on the special issue website. Research articles, reviews as well as short communications are preferred. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office to announce on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts will be thoroughly refereed through a double-blind peer-review process. Please visit the Instruction for Authors page before submitting a manuscript. The Article Processing Charge (APC) in this open access journal is 2500 USD. Submitted manuscripts should be well formatted in good English.

Planned Paper (1 Paper)
The below list represents only planned manuscripts. Some of these manuscripts have not been received by the Editorial Office yet. Papers submitted to IMR Press journals will subject to peer-review before acceptance

A Review of the Notch Signaling Pathway in the Differentiation of Human Umbilical Cord Mesenchymal Stem Cells

Wanhong Xing

Published Paper (1 Paper)
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