Sentences with phrase «cell fate during»

We are studying the mechanisms that maintain multipotent cell fate during quiescence (reversible cell cycle arrest) using C. elegans as a model for aging stem cells.

Differentially activated macrophages orchestrate myogenic precursor cell fate during human skeletal muscle regeneration

With our unique robotic microscope technology, can we identify the major determinants of cell fate during normal development of stem cells and in neurodegenerative disease?

Martin Kragl (Tanaka, MPG)-- «Studying the patterning mechanisms and cell fates during limb regeneration in Ambystoma mexicanum» (2007)

Not exact matches

The search for answers might shed light on how cells» fates become fixed during development, and how plants manage to retain such flexibility.

In a similar way to how they work in other cells, epigenetic markers push PGCs to their fate during embryonic development, but PGCs are unique because when they develop into sperm and eggs, the epigenetic markers are erased.

It involves the way an egg cell is built and how information positioned during that construction affects the fate of the embryo.

Another provocative observation from the new study was that transient gene expression events during brain development set up broad distinctions in neural fate between cells in different areas in the cerebral cortex.

Abstract During muscle regeneration, the conversion of muscle stem cells to terminally differentiated myofibers requires multiple cell fate transitions.

Asymmetric Localization of < i > Cdx2 mRNA during the First Cell - Fate Decision in Early Mouse Development.

The project will focus on answering the question, how an embryonic stem cell computes cues from its environment to elicit a regulated, exact cell fate choice during a process called «differentiation».

While TSCs give rise to the placenta, these stem cells establish their identity long before the placenta develops; their fate is determined during the early embryo.

The regulation of transcription during the transitions from fertilization to genome activation to cell fate specification is a critical developmental process, yet it is poorly understood.

The sorting out of cells with different identities and fates during animal development is an important process to organize functional tissues and organs.

First, we find that microRNA activity is modulated during dauer in order to regulate cell fate.

The single - cell perspective has helped to better understand gene regulation and regulatory networks during exit from pluripotency, cell - fate determination as well as molecular mechanisms driving cellular reprogramming of somatic cells to induced pluripotent stage.