| Spermatogonial stem cells and spermatogenesis in mice, monkeys and men |
42 |
| Oxidative stress and altered mitochondrial protein expression in the absence of amyloid-beta and tau pathology in iPSC-derived neurons from sporadic Alzheimer's disease patients |
19 |
| Optimized procedures for generating an enhanced, near physiological 2D culture system from porcine intestinal organoids |
16 |
| Culture and transplantation of spermatogonial stem cells |
13 |
| Effect of prolonged differentiation on functional maturation of human pluripotent stem cell-derived neuronal cultures |
12 |
| LncRNA TINCR/miR-31-5p/C/EBP-alpha feedback loop modulates the adipogenic differentiation process in human adipose tissue-derived mesenchymal stem cells |
12 |
| Volumetric muscle loss injury repair using in situ fibrin gel cast seeded with muscle-derived stem cells (MDSCs) |
11 |
| NEK1 loss-of-function mutation induces DNA damage accumulation in ALS patient-derived motoneurons |
11 |
| Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury |
11 |
| Potential therapeutic roles of stem cells in ischemia-reperfusion injury |
10 |
| Bone-forming peptide-3 induces osteogenic differentiation of bone marrow stromal cells via regulation of the ERK1/2 and Smad1/5/8 pathways |
9 |
| Accelerated photoreceptor differentiation of hiPSC-derived retinal organoids by contact co-culture with retinal pigment epithelium |
9 |
| Efficient and high yield isolation of myoblasts from skeletal muscle |
9 |
| Improving single-cell cloning workflow for gene editing in human pluripotent stem cells |
8 |
| Characterization of the lncRNA transcriptome in mESC-derived motor neurons: Implications for FUS-ALS |
8 |
| Enhanced chondrogenesis from human embryonic stem cells |
8 |
| Long-term organoid culture reveals enrichment of organoid-forming epithelial cells in the fimbrial portion of mouse fallopian tube |
8 |
| Rapid and efficient differentiation of functional motor neurons from human iPSC for neural injury modelling |
8 |
| Actin depolymerization enhances adipogenic differentiation in human stromal stem cells |
8 |
| Production of live fish derived from frozen germ cells via germ cell transplantation |
8 |
| NKX6.1 induced pluripotent stem cell reporter lines for isolation and analysis of functionally relevant neuronal and pancreas populations |
7 |
| Cymerus (TM) iPSC-MSCs significantly prolong survival in a pre-clinical, humanized mouse model of Graft-vs-host disease |
7 |
| The role of nuclear receptors in the differentiation of oligodendrocyte precursor cells derived from fetal and adult neural stem cells |
7 |
| Permeability analyses and three dimensional imaging of interferon gamma-induced barrier disintegration in intestinal organoids |
7 |
| Electron transport chain complex II sustains high mitochondrial membrane potential in hematopoietic stem and progenitor cells |
7 |
| A single cell transcriptional portrait of embryoid body differentiation and comparison to progenitors of the developing embryo |
7 |
| A2E-associated cell death and inflammation in retinal pigmented epithelial cells from human induced pluripotent stem cells |
7 |
| Colorectal cancer liver metastases organoids retain characteristics of original tumor and acquire chemotherapy resistance |
7 |
| Dendritic cells and M2 macrophage play an important role in suppression of Th2-mediated inflammation by adipose stem cells-derived extracellular vesicles |
7 |
| Patterning factors during neural progenitor induction determine regional identity and differentiation potential in vitro |
7 |
| A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres |
7 |
| Motor neuron differentiation of iPSCs obtained from peripheral blood of a mutant TARDBP ALS patient |
7 |
| NOSTRIN: A novel modulator of trophoblast giant cell differentiation |
7 |
| Robust generation of erythroid and multilineage hematopoietic progenitors from human iPSCs using a scalable monolayer culture system |
6 |
| Cell surface markers for the identification and study of human naive pluripotent stem cells |
6 |
| PRDM14 is expressed in germ cell tumors with constitutive overexpression altering human germline differentiation and proliferation |
6 |
| Reproducible and efficient generation of functionally active neurons from human hiPSCs for preclinical disease modeling |
6 |
| Mitochondrial ROS direct the differentiation of murine pluripotent P19 cells |
6 |
| Alterations in genetic and protein content of swine adipose tissue-derived mesenchymal stem cells in the metabolic syndrome |
6 |
| High fat diet activates adult mouse lung stem cells and accelerates several aging-induced effects |
6 |
| Epidermal YAP activity drives canonical WNT16/beta-catenin signaling to promote keratinocyte proliferation in vitro and in the murine skin |
5 |
| Skeletal-muscle-derived mesenchymal stem/stromal cells from patients with osteoarthritis show superior biological properties compared to bone-derived cells |
5 |
| GDNF enhances the anti-inflammatory effect of human adipose-derived mesenchymal stem cell-based therapy in renal interstitial fibrosis |
5 |
| Three lines of induced pluripotent stem cells derived from a 15q11.2-q13.1 duplication syndrome patient |
5 |
| Use of induced pluripotent stem cell models to probe the pathogenesis of Choroideremia and to develop a potential treatment |
5 |
| Establishment of human induced pluripotent stem cell line from a patient with Angelman syndrome carrying the deletion of maternal chromosome 15q11.2-q13 |
5 |
| Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease |
5 |
| Genomic functions of developmental pluripotency associated factor 4 (Dppa4) in pluripotent stem cells and cancer |
5 |
| Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome |
5 |
| CD133+cells derived from skeletal muscles of Duchenne muscular dystrophy patients have a compromised myogenic and muscle regenerative capability |
4 |
