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Abbreviation: hiPSC
Appearance Frequency: 735 time(s)
Long forms: 16

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
human induced pluripotent stem cell
(686 times)
Cell Biology
(182 times)
hESC (47 times)
RPE (23 times)
CMs (22 times)
2009 Natural and synthetic regulators of embryonic stem cell cardiogenesis.
human iPSC
(17 times)
Cell Biology
(6 times)
iPSC (11 times)
iPSCs (4 times)
hESC (2 times)
2010 Human induced pluripotent stem cell lines show stress defense mechanisms and mitochondrial regulation similar to those of human embryonic stem cells.
human pluripotent stem cell
(10 times)
Stem Cells
(4 times)
hESC (2 times)
PBMCs (2 times)
BMI (1 time)
2016 Influence of field potential duration on spontaneous beating rate of human induced pluripotent stem cell-derived cardiomyocytes: Implications for data analysis and test system selection.
human induced Pluripotent Stem Cells
(7 times)
Molecular Biology
(2 times)
BBB (2 times)
EC (2 times)
hiPSC-ECs (2 times)
2017 Temporally coordinated spiking activity of human induced pluripotent stem cell-derived neurons co-cultured with astrocytes.
human induced PSC
(3 times)
Cell Biology
(2 times)
CMs (1 time)
EpiSCs (1 time)
hESC (1 time)
2014 A simple, cost-effective but highly efficient system for deriving ventricular cardiomyocytes from human pluripotent stem cells.
human iPS cell
(2 times)
Genetics, Medical
(1 time)
BD (1 time)
BEST1 (1 time)
hfRPE (1 time)
2012 iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration.
HD patient-derived induced pluripotent stem cell
(1 time)
Molecular Biology
(1 time)
HD (1 time)
HTT (1 time)
MAO (1 time)
2014 Inhibition of Excessive Monoamine Oxidase A/B Activity Protects Against Stress-induced Neuronal Death in Huntington Disease.
Here, we describe an induced pluripotent stem cell
(1 time)
Cell Biology
(1 time)
LVNC (1 time)
2021 Generation and cardiac differentiation of a human induced pluripotent stem cell line UALGi002-A from a female patient with Left-Ventricular Noncompaction Cardiomyopathy.
heteroplasmic induced pluripotent stem cell
(1 time)
Natural Science Disciplines
(1 time)
--- 2017 Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation.
10  homeostasis-human induced pluripotent stem cell
(1 time)
Cardiology
(1 time)
DFP (1 time)
EC (1 time)
FRDA (1 time)
2015 Efficient attenuation of Friedreich's ataxia (FRDA) cardiomyopathy by modulation of iron homeostasis-human induced pluripotent stem cell (hiPSC) as a drug screening platform for FRDA.
11  human cardiac tissue, induced pluripotent stem cell
(1 time)
Cardiology
(1 time)
--- 2021 ESC working group on cardiac cellular electrophysiology position paper: relevance, opportunities, and limitations of experimental models for cardiac electrophysiology research.
12  human embryonic stem cells and induced pluripotent stem cells
(1 time)
Natural Science Disciplines
(1 time)
EHT (1 time)
2016 Anisotropic engineered heart tissue made from laser-cut decellularized myocardium.
13  human in vitro models, such as induced pluripotent stem cell
(1 time)
Environmental Health
(1 time)
AOPs (1 time)
BDNF (1 time)
CKEs (1 time)
2020 Assessment of developmental neurotoxicity induced by chemical mixtures using an adverse outcome pathway concept.
14  human iPSC-derived
(1 time)
NMDs (1 time)
NMJ (1 time)
2021 Neuromuscular Development and Disease: Learning From in vitro and in vivo Models.
15  human neuronal cultures cannot be expanded.Human-induced pluripotent stem cell
(1 time)
Neurology
(1 time)
ANS (1 time)
2019 Induced pluripotent stem cells for disease modeling, cell therapy and drug discovery in genetic autonomic disorders: a review.
16  UNIPDi002-A-human induced pluripotent stem cell
(1 time)
Cell Biology
(1 time)
EEC (1 time)
hOMESCs (1 time)
2018 Generation of a transgene-free induced pluripotent stem cells line (UNIPDi002-A) from oral mucosa epithelial stem cells carrying the R304Q mutation in TP63 gene.