Results 1 to 10 of about 11,468 (139)

Brain Organoids to Evaluate Cellular Therapies

open access: yesAnimals, 2022
Animal models currently used to test the efficacy and safety of cell therapies, mainly murine models, have limitations as molecular, cellular, and physiological mechanisms are often inherently different between species, especially in the brain. Therefore,
Ana Belén García-Delgado   +8 more
doaj   +1 more source

Bioengineered tissue and cell therapy products are efficiently cryopreserved with pathogen-inactivated human platelet lysate-based solutions

open access: yesStem Cell Research & Therapy, 2023
Background There remains much interest in improving cryopreservation techniques for advanced therapy medicinal products (ATMPs). Recently, human platelet lysate (hPL) has emerged as a promising candidate to replace fetal bovine serum (FBS) as a xeno-free
María Martín-López   +8 more
doaj   +1 more source

Retrieval of germinal zone neural stem cells from the cerebrospinal fluid of premature infants with intraventricular hemorrhage

open access: yesStem Cells Translational Medicine, 2020
Intraventricular hemorrhage is a common cause of morbidity and mortality in premature infants. The rupture of the germinal zone into the ventricles entails loss of neural stem cells and disturbs the normal cytoarchitecture of the region, compromising ...
Beatriz Fernández‐Muñoz   +14 more
doaj   +1 more source

A Clonal NG2-Glia Cell Response in a Mouse Model of Multiple Sclerosis

open access: yesCells, 2020
NG2-glia, also known as oligodendrocyte precursor cells (OPCs), have the potential to generate new mature oligodendrocytes and thus, to contribute to tissue repair in demyelinating diseases like multiple sclerosis (MS).
Sonsoles Barriola   +4 more
doaj   +1 more source

Plaque-Associated Oligomeric Amyloid-Beta Drives Early Synaptotoxicity in APP/PS1 Mice Hippocampus: Ultrastructural Pathology Analysis

open access: yesFrontiers in Neuroscience, 2021
Alzheimer’s disease (AD) is a devastating neurodegenerative disorder characterized by initial memory impairments that progress to dementia. In this sense, synaptic dysfunction and loss have been established as the pathological features that best ...
Raquel Sanchez-Varo   +34 more
doaj   +1 more source

Both CD133 Cells and Monocytes Provide Significant Improvement for Hindlimb Ischemia, Although They do not Transdifferentiate Into Endothelial Cells

open access: yesCell Transplantation, 2010
To address a number of questions regarding the experimental use of bone marrow (BM) stem cells in hindlimb ischemia, including which is the best cell type (e.g., purified hematopoietic stem cell or monocytes), the best route of delivery [intramuscular ...
Fermin M. Sanchez-Guijo M.D., PhD.   +11 more
doaj   +1 more source

Effects of MSC Coadministration and Route of Delivery on Cord Blood Hematopoietic Stem Cell Engraftment

open access: yesCell Transplantation, 2013
Hematopoietic stem cell transplantation (HSCT) using umbilical cord blood (UCB) progenitors is increasingly being used. One of the problems that may arise after UCB transplantation is an impaired engraftment.
S. Carrancio   +10 more
doaj   +1 more source

Assessment of Olfactory Behavior in Mice: Odorant Detection and Habituation-Dishabituation Tests

open access: yesBio-Protocol, 2015
Olfaction has adaptive value for rodents as it is essential for feeding and mating, the establishment of social and territorial relationships, or the detection of potential predators, among others (Apfelbach et al., 2005).
Ana Perez-Villalba   +3 more
doaj   +1 more source

Mercury intoxication and ophthalmic involvement: An update review

open access: yesFrontiers in Toxicology, 2023
Human intoxication after mercury exposure is a rare condition that can cause severe damage to the central nervous, respiratory, cardiovascular, renal, gastrointestinal, skin, and visual systems and represents a major public health concern.
Cristian de los Santos   +5 more
doaj   +1 more source

Generation of an induced pluripotent stem cell line from a compound heterozygous patient in TK2 gene

open access: yesStem Cell Research, 2022
Autosomal recessive mutations in Thymidine kinase 2 (TK2) gene cause depletion and multiple deletions in mtDNA which normally lead to fatal and progressive neuromyopathy in infants and children.
Carmen Hernández-Ainsa   +6 more
doaj   +1 more source

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