Abstract:
:Human iPSC line N44SV.5 was generated from primary normal human dermal fibroblasts belonging to the European mitochondrial haplogroup U. For this purpose, reprogramming factors Oct3/4, Sox2, Klf4, and cMyc were delivered using a non-integrative methodology that involves the use of Sendai virus.
journal_name
Stem Cell Resjournal_title
Stem cell researchauthors
Galera T,Zurita F,González-Páramos C,Moreno-Izquierdo A,Fraga MF,Fernández AF,Garesse R,Gallardo MEdoi
10.1016/j.scr.2015.12.010subject
Has Abstractpub_date
2016-01-01 00:00:00pages
88-91issue
1eissn
1873-5061issn
1876-7753pii
S1873-5061(15)00190-7journal_volume
16pub_type
杂志文章abstract::X-linked Alport syndrome (XLAS) is a rare form of hereditary nephritis caused by mutations in the COL4A5 gene encoding the type IV collagen α5 chain. A skin biopsy was performed on one female patient with XLAS who carried a heterozygous p.G409S (c. 1225 G > A) mutation in the COL4A5 gene. A human-induced pluripotent s...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101833
更新日期:2020-05-01 00:00:00
abstract::Interactions between acute myeloid leukemia (AML) blasts and neighboring stromal cells are important for disease development and chemosensitivity. However, the molecular mechanisms involved in the cytokine-mediated crosstalk between mesenchymal stem cells (MSCs) and AML cells are largely unknown. Leukemic cells derive...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.09.008
更新日期:2015-11-01 00:00:00
abstract::We have established the patient-specific induced pluripotent stem (iPS) cell line CSUASOi004-A by using peripheral blood mononuclear cells (PBMCs) of a retinitis pigmentosa (RP) patient with a PRPF6 gene mutation (c.G2699A:p.R900H). CSUASOi004-A was established by a non-integrative method with four episomal plasmids c...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101793
更新日期:2020-05-01 00:00:00
abstract::Gene therapy mediated by bone marrow-derived hematopoietic stem cells (BM-HSC) has been widely used in treating genetic deficiencies in both pre-clinical and clinical settings. Using mitotically inactive cell-targeting lentivirus with separate promoters for our gene of interest (the murine MHC class II (MHCII) chapero...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2013.10.010
更新日期:2014-01-01 00:00:00
abstract::Cell-mediated gene therapy is a possible means to treat muscular dystrophies like Duchenne muscular dystrophy. Autologous patient stem cells can be genetically-corrected and transplanted back into the patient, without causing immunorejection problems. Regenerated muscle fibres derived from these cells will express the...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.05.004
更新日期:2018-07-01 00:00:00
abstract::Human embryonic stem cells (hESCs) can undergo unlimited self-renewal and differentiate into hepatic cells, including expandable hepato-blasts (HBs) and hepatocyte-like cells (HLCs) in vitro. Therefore, hESC-derived HBs have the potential to become a renewable cell source for cell therapy of serious liver damage. Howe...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102010
更新日期:2020-12-01 00:00:00
abstract::Autism is a heterogeneous neurodevelopmental disorder defined by deficits in socialization, communication, and patterns of behavior. Using stem cells to model brain disordersmay yield new understanding about the underlying neuropathological processes and could prove essential for drug development. We present here a ne...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102038
更新日期:2020-12-01 00:00:00
abstract::Thrombocytopenia 2 (THC2) is a major type of inherited thrombocytopenia caused by the persistent ANKRD26 expression during the late stage of megakaryocytopoiesis. For the first time, we generated a human induced pluripotent stem cell (hiPSC) line SHAMUi001-A from the bone marrow hematopoietic progenitor cells of a THC...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102002
更新日期:2020-10-01 00:00:00
abstract::Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disease caused by a CAG repeat expansion in the region of the ATXN3 gene. The main feature of SCA3 is progressive ataxia, which affects balance, gait, and speech. Urine cells (UCs) of a SCA3 patient were successfully translated to induced...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.01.027
更新日期:2018-04-01 00:00:00
abstract::The European Bank for induced Pluripotent Stem Cells (EBiSC), a non-profit repository for storage, banking, Quality Control (QC) and subsequent distribution of research-grade human induced Pluripotent Stem Cell (iPSC) lines, has centralised iPSC lines generated internationally across >35 disease areas and made them av...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102034
更新日期:2020-12-01 00:00:00
abstract::Expanded human T cells from a Japanese female with recessive dystrophic epidermolysis bullosa (RDBE) were used to generate integration-free induced pluripotent stem cells (iPSCs) by exogenous expression of four reprogramming factors, OCT3/4, SOX2, cMYC, KLF4, using Sendai virus vector (SeVdp). The authenticity of esta...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.05.003
更新日期:2016-07-01 00:00:00
abstract::Two distinct types of embryonic pluripotent stem cells can be established from either the inner cell mass (ICM) of preimplantation blastocyst (leukemia inhibitory factor (LIF)-dependent embryonic stem cell, ESC, called naive state) or the epiblast of postimplantation fetuses (fibroblast growth factor 2 (FGF2)-dependen...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2014.04.012
更新日期:2014-07-01 00:00:00
abstract::Urine resource cells were collected from a 23-year-old male with multiple endocrine neoplasia type 1 syndrome (MEN1) for generating iPS cells with episomal plasmids. Two stable iPSC lines with free of episomal plasmid were established. The patient has a heterozygous G>T mutation on the exon 9 of Men1 gene that was con...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.12.002
更新日期:2017-01-01 00:00:00
abstract::Both BMP and Wnt signaling control stem cells in bulge/dermal papilla, intestinal crypt, and bone marrow. To explore their roles in the limbal niche, which govern corneal epithelial homeostasis, we established an in vitro model of sphere growth by reunion between single limbal epithelial progenitor cells (LEPCs) and a...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2014.01.003
更新日期:2014-03-01 00:00:00
abstract::Umbilical cord blood (UCB) transplantation has emerged as a promising therapy, but it is challenged by scarcity of stem cells. Eltrombopag is a non-peptide, thrombopoietin (TPO) receptor agonist, which selectively activates c-Mpl in humans and chimpanzees. We investigated eltrombopag's effects on human UCB hematopoiet...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2012.05.001
更新日期:2012-09-01 00:00:00
abstract::SLC26A4 is the second most frequent gene implicated in congenital hearing loss after GJB2 mutations. Here, we report the generation of induced pluripotent stem cells (iPSCs), from a patient who was carrying a homozygous c.919-2A>G variant in the SLC26A4 gene. This is the most common variant of SLC26A4 gene in the Chin...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101524
更新日期:2019-10-01 00:00:00
abstract::Heredity is the major factor contributing to the susceptibility to ankylosing spondylitis(AS). Janus kinase 2 (JAK2) has been associated with AS. Urine-derived cells from an AS patient with JAK2 mutation were used to generate induced pluripotent stem cells (iPSCs) with five episomal iPSC reprogramming vectors (pCXLE-h...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101788
更新日期:2020-05-01 00:00:00
abstract::Salisphere-derived adult epithelial cells have been used to improve saliva production of irradiated mouse salivary glands. Importantly, optimization of the cellular composition of salispheres could improve their regenerative capabilities. The Rho Kinase (ROCK) inhibitor, Y27632, has been used to increase the prolifera...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101608
更新日期:2019-12-01 00:00:00
abstract::Crumbs homologue 1 (CRB1) mutations have been found in retinitis pigmentosa (RP) patients lead to severe retinal dystrophies. The human induced pluripotent stem (iPS) cell line CSUASOi003-A derived from peripheral blood mononuclear cells (PBMCs) of a patient carrying two heterozygous mutations (2249G>A p.G750D and c.2...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101742
更新日期:2020-04-01 00:00:00
abstract:BACKGROUND:Non-random segregation of DNA strands during stem cell replication has been proposed as a mechanism to minimize accumulated genetic errors in stem cells of rapidly dividing tissues. According to this hypothesis, an "immortal" DNA strand is passed to the stem cell daughter and not the more differentiated cell...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.01.005
更新日期:2015-03-01 00:00:00
abstract::Liver cirrhosis accompanied with hepatic encephalopathy commonly causes cognitive impairment in patients. To model this disease, two independent patient specific induced pluripotent stem cell-line (iPSC) clones, NCCSi011-A and NCCSi011-B were generated by reprogramming the CD4+ T cells of an Indian male patient suffer...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101992
更新日期:2020-10-01 00:00:00
abstract::The Genea016 human embryonic stem cell line was derived from a donated, fully commercially consented ART blastocyst, through ICM outgrowth on inactivated human feeders. The line showed pluripotent cell morphology and genomic analysis verified a 46, XX karyotype and female Allele pattern through traditional karyotyping...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.11.009
更新日期:2016-01-01 00:00:00
abstract::Tumor protein p63 (p63) encodes for a transcription factor of the p53 family and is a marker for respiratory basal cells. Based on a NKX2.1 knock-in reporter cell line from human induced pluripotent stem cells (hiPSCs) (MHHi06-A-2) we established a NKX2.1/p63 double transgenic knock-in reporter cell line using TALEN t...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101659
更新日期:2020-01-01 00:00:00
abstract::Mesenchymal stromal cells (MSCs) suppress T cell responses through mechanisms not completely understood. Adenosine is a strong immunosuppressant that acts mainly through its receptor A(2a) (ADORA2A). Extracellular adenosine levels are a net result of its production (mediated by CD39 and CD73), and of its conversion in...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2011.04.001
更新日期:2011-07-01 00:00:00
abstract::Human iPSC line was generated from patient-specific adipose tissue-derived mesenchymal multipotent stromal cells carrying two mutations in plakophilin-2 (PKP2) gene using non-integrative reprogramming method. Reprogramming factors OCT4, KLF4, SOX2, CMYC were delivered using Sendai viruses. Pluripotency was confirmed i...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2017.08.014
更新日期:2017-10-01 00:00:00
abstract::A DAND5-control human iPSC line was generated from the urinary cells of a phenotypically normal donor. Exfoliated renal epithelial (RE) cells were collected and reprogrammed into iPSCs using Sendai virus reprogramming system. The pluripotency, in vitro differentiation potential, karyotype stability, and the transgene-...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.04.015
更新日期:2018-05-01 00:00:00
abstract::The KCL035 human embryonic stem cell line was derived from an embryo donated for research that carried a mutation in the HBB gene, which is linked to the β-thalassemia syndrome. The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propag...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.01.007
更新日期:2016-03-01 00:00:00
abstract::Friedreich's ataxia is caused by large homozygous, intronic expansions of GAA repeats in the frataxin (FXN) gene, resulting in severe downregulation of its expression. Pathogenic repeats are located in intron one, hence patients express unaffected FXN protein, albeit in low quantities. Although FRDA symptoms typically...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101529
更新日期:2019-10-01 00:00:00
abstract::The KCL018 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the DMPK gene encoding the dystrophia myotonica protein kinase (2200 trinucleotide repeats; 14 for the normal allele). The ICM was isolated using laser microsurg...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.01.004
更新日期:2016-03-01 00:00:00
abstract::Human epicardium-derived cells (EPDC) were reprogrammed to generate two iPSC lines, MCDU1i-EPDC and MCDU2i-EPDC, by nucleofection of episomal-based plasmids expressing the reprogramming factors OCT4, SOX2, KLF4, c-MYC, NANOG and LIN28. Pluripotency was confirmed in vitro by immunofluorescence analysis and embryoid bod...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2017.02.007
更新日期:2017-04-01 00:00:00