Unlike other fetal - derived
stem cell origin, the amniotic fluid contains cells that arise from the developing fetus, at ratios and from origins that vary throughout pregnancy.
Not exact matches
In fact, the latest research in epigenetics,
stem cells, and the developmental
origins of health and disease is unlocking a whole new line of understanding of what breastmilk contains and its role in development.
The fourth theme addresses the ethical, legal, social, and policy issues related to the
origins and use of
stem cells.
«Genetic
origins of myelodysplastic syndrome discovered using
stem cells.»
Blood formation was the first process for which scientists formulated and proved the theory that
stem cells are the common
origin that gives rise to various types of mature
cells.
Further dissecting the MDS
stem cells at the molecular level could provide insights into the
origins and development of MDS and other blood cancers.
Last May in Nature Neuroscience, his lab and a team at Columbia University reported that embryonic
stem cells could be used to shed light on the
origins of amyotrophic lateral sclerosis (ALS), the progressive neurodegenerative disease in which motor neurons in the brain die.
Because biologists like Daley are convinced that embryonic
stem cells — the most generic, versatile type — may not only lead to dramatically different new treatments but can also uniquely illuminate the
origins of disease in a way adult
stem cells never will.
Conventional wisdom has long held that adult
stem cells are only capable of forming their tissue of
origin.
The MDS
stem cells were rare, sat at the top of a hierarchy of MDS
cells, could sustain themselves, replenish the other MDS
cells, and were the
origin of all stable DNA changes and mutations that drove the progression of the disease.
«New tools to study the
origin of embryonic
stem cells.»
The study had its
origins in Anguera's postdoctoral research, which focused on X inactivation in pluripotent
stem cells.
Recent studies highlighted significant differences between these two types of
stem cells, although only a limited number of
cell lines of different
origins were analyzed.
Potential scientific questions from this research relate to the
origin and function of
stem cell clones and to whether they could be used to predict future outcomes.
Experiments conducted by lead author Fatima Syed - Picard, Ph.D., also of Pitt's Department of Ophthalmology, and the team showed that
stem cells of the dental pulp, obtained from routine human third molar, or wisdom tooth, extractions performed at Pitt's School of Dental Medicine, could be turned into corneal stromal
cells called keratocytes, which have the same embryonic
origin.
Harvard
Stem Cell Institute scientists at Brigham and Women's Hospital have found the cellular
origin of the tissue scarring caused by organ damage associated with diabetes, lung disease, high blood pressure, kidney disease, and other conditions.
Derivation of pluripotent
stem cells, either of embryonic
origin or following genetic reprogramming, has opened the path for an alternative source for epidermal
cell therapy as these
cells are both immortal and pluripotent, theoretically capable of providing any requested number of
cells of any desired phenotype.
We will have major players give state of the art talks in sessions including Avian Behavior, Avian Physiology, Avian
Stem Cell & Transgenesis - related Techniques, Developmental Biology, Genetic / Genomic Analysis and the
Origin and Evolution of Birds, etc..
Showing that
stem cells or transient amplifying
cells may exist in the periphery might explain the
origin of HCECs and indicate a source for these
cells in wound repair.
Researchers using ethically uncontroversial induced pluripotent
stem cells (iPSCs) have achieved what appears to be a major breakthrough in understanding the
origin and development of Down syndrome, according to a new study recently published in Nature Communications.
Matson JP, Dumitru R, Coryell P, et al., Rapid DNA replication
origin licensing protects
stem cell pluripotency.
Disease - specific human pluripotent
stem cells, from embryonic
origin or derived from reprogramming somatic
cells, offer the unique opportunity to have access to a large spectrum of disease - specific
cell models.
The actual
cell of
origin is different in each type of tumor, and does not have to be atumor
stem cell.
Review of «Rapid DNA replication
origin licensing protects
stem cell pluripotency» from eLife by Stuart P. Atkinson
iPS
cells are virtually identical to human embryonic
stem cells (also called hESCs), which this column has discussed previously, except for their
origins.
Unlike embryonic
stem cells, which are developmental blank slates that can generate virtually all types of
cells found in adult humans, adult
stem cells are thought to possess limited potential to transform into
cells found in their tissues of
origin.
We developed and implemented such a nomenclature for the European human pluripotent
stem cell registry (hPSCreg), which needs to: 1) unambiguously identify a registered
cell line; 2) allow tracing of subclones of a particular line; and 3) enable the assignment of different lines to a specific donor
origin.
Virtually identical to human embryonic
stem cells (hESCs) except for their
origin of isolation, the recently created induced pluripotent
stem cells (iPSCs)(Yu et al., 2007; Takahashi et al., 2007) hold much potential for use in regenerative therapies.
The specific vocation of I -
Stem is to explore all the therapeutic potential of human pluripotent stem cells for applications in patients affected by rare diseases of genetic ori
Stem is to explore all the therapeutic potential of human pluripotent
stem cells for applications in patients affected by rare diseases of genetic ori
stem cells for applications in patients affected by rare diseases of genetic
origin.
Applying these paradigms on various neural differentiation schemes of human pluripotent
stem cells allows us to identify and isolate new types of neural
stem and progenitor
cells, to characterize their cellular properties and molecular foundations, to expose their progenitor
origin and track their imminent potential, to reveal their in vivo counterparts and learn about their regenerative potential.
New research from the University of North Carolina establishes a link between rapid
origin licensing and the maintenance of
stem cell pluripotency
Dr. Péault, a professor in the Department of Pediatrics,
Cell Biology and Physiology at the University of Pittsburgh School of Medicine, recognized the importance of determining the
origin of these muscle - derived
stem cells.
25) Barker N., Ridgway R.A., van Es J.H., van de Wetering M., Begthel H., van den Born M., Danenberg E., Clarke A.R., Sansom O.J., Clevers H. Crypt
Stem Cells as the
Cells - of -
Origin of Intestinal Cancer Nature 457:608 - 611 (2009)
51) Drost, J., van Boxtel, R., Blokzijl, F., Mizutani, T., Sasaki, N., Sasselli, V., de Ligt, J., Behjati, S., Grolleman, J.E., van Wezel, T., Nik - Zainal, S., Kuiper, R.P., Cuppen, E., and Clevers, H. Use of CRISPR - modified human
stem cell organoids to study the
origin of mutational signatures in cancer.
Dr. Péault is internationally recognized principally for his work on the prospective identification and characterization of human hematopoietic (blood)
stem cells, of which his laboratory has also deciphered the ultimate
origin during embryonic life.
«Use of CRISPR - modified
stem cell organoids to study the
origin of mutational signatures in cancer»
Created in 2005 through a collaboration between Inserm — National Institute of Health and Medical Research — and AFM - Telethon — French Association against Myopathies — I -
Stem is the largest French laboratory for research and development dedicated to human pluripotent stem cells, of embryonic origin or obtained by reprogramming g
Stem is the largest French laboratory for research and development dedicated to human pluripotent
stem cells, of embryonic origin or obtained by reprogramming g
stem cells, of embryonic
origin or obtained by reprogramming gene.
This abnormality helps drive malignancy at the point of
origin, and facilitates cancer
stem cells to renew over the long term.
Hence, the FLI focuses on the
origin of the aging - induced increases in molecular damage aiming to elucidate how it contributes to impairments in
stem cell function and the evolution of organ dysfunction and diseases in aging.