Current perspectives on “Off-The-Shelf” allogeneic NK and CAR-NK cell therapies

EL Heipertz, ER Zynda, TE Stav-Noraas… - Frontiers in …, 2021 - frontiersin.org
Natural killer cells (NK cells) are the first line of the innate immune defense system, primarily
located in peripheral circulation and lymphoid tissues. They kill virally infected and …

Induced pluripotent stem cell technology: a decade of progress

Y Shi, H Inoue, JC Wu, S Yamanaka - Nature reviews Drug discovery, 2017 - nature.com
Since the advent of induced pluripotent stem cell (iPSC) technology a decade ago,
enormous progress has been made in stem cell biology and regenerative medicine. Human …

[HTML][HTML] Derivation of human midbrain-specific organoids from neuroepithelial stem cells

AS Monzel, LM Smits, K Hemmer, S Hachi, EL Moreno… - Stem cell reports, 2017 - cell.com
Research on human brain development and neurological diseases is limited by the lack of
advanced experimental in vitro models that truly recapitulate the complexity of the human …

The reciprocal interactions between microglia and T cells in Parkinson's disease: a double-edged sword

Y Xu, Y Li, C Wang, T Han, H Liu, L Sun, J Hong… - Journal of …, 2023 - Springer
In Parkinson's disease (PD), neurotoxic microglia, Th1 cells, and Th17 cells are
overactivated. Overactivation of these immune cells exacerbates the disease process and …

ER stress and autophagic perturbations lead to elevated extracellular α-synuclein in GBA-N370S Parkinson's iPSC-derived dopamine neurons

HJR Fernandes, EM Hartfield, HC Christian… - Stem cell reports, 2016 - cell.com
Heterozygous mutations in the glucocerebrosidase gene (GBA) represent the strongest
common genetic risk factor for Parkinson's disease (PD), the second most common …

C9orf72 Hexanucleotide Expansions Are Associated with Altered Endoplasmic Reticulum Calcium Homeostasis and Stress Granule Formation in Induced Pluripotent …

R Dafinca, J Scaber, N Ababneh, T Lalic, G Weir… - Stem …, 2016 - academic.oup.com
An expanded hexanucleotide repeat in a noncoding region of the C9orf72 gene is a major
cause of amyotrophic lateral sclerosis (ALS), accounting for up to 40% of familial cases and …

A new glucocerebrosidase chaperone reduces α-synuclein and glycolipid levels in iPSC-derived dopaminergic neurons from patients with Gaucher disease and …

E Aflaki, DK Borger, N Moaven… - Journal of …, 2016 - jneurosci.org
Among the known genetic risk factors for Parkinson disease, mutations in GBA1, the gene
responsible for the lysosomal disorder Gaucher disease, are the most common. This genetic …

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

E Meyer, KJ Carss, J Rankin, JME Nichols, D Grozeva… - Nature …, 2017 - nature.com
Histone lysine methylation, mediated by mixed-lineage leukemia (MLL) proteins, is now
known to be critical in the regulation of gene expression, genomic stability, cell cycle and …

Cellular α-synuclein pathology is associated with bioenergetic dysfunction in Parkinson's iPSC-derived dopamine neurons

F Zambon, M Cherubini, HJR Fernandes… - Human Molecular …, 2019 - academic.oup.com
Parkinson's disease (PD) is the second most common neurodegenerative disorder and a
central role for α-synuclein (αSyn; SNCA) in disease aetiology has been proposed based on …

Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson's disease in midbrain dopaminergic neurons

GS Virdi, ML Choi, JR Evans, Z Yao, D Athauda… - npj Parkinson's …, 2022 - nature.com
Mutations in the SNCA gene cause autosomal dominant Parkinson's disease (PD), with loss
of dopaminergic neurons in the substantia nigra, and aggregation of α-synuclein. The …