Generation of an induced pluripotent stem cell line from chorionic villi of a Turner syndrome spontaneous abortion
Author:
Funder
CSIR
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes;Li;Hum. Mol. Genet.,2012
2. Uniparental disomy of the entire X chromosome in Turner syndrome patient-speci fi c induced pluripotent stem cells;Luo;Nat. Publ. Group,2015
3. Characterization of pluripotent stem cells;Martí;Nat. Protoc.,2013
4. A method to identify and isolate pluripotent human stem cells and mouse epiblast stem cells using lipid body-associated retinyl ester fluorescence;Muthusamy;Stem Cell Rep.,2014
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1. Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs;Stem Cell Research & Therapy;2023-12-20
2. Comparative cytogenetics of anembryonic pregnancies and missed abortions in human;Vavilov Journal of Genetics and Breeding;2023-03-06
3. Establishment of a non‐integrated induced pluripotent stem cell line derived from human chorionic villi cells;Journal of Clinical Laboratory Analysis;2022-05-09
4. Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome;Journal of Visualized Experiments;2021-12-04
5. Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells;Frontiers in Cellular Neuroscience;2020-08-13
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