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Stem Cell Research|May 14, 2020
Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 geneBei Liu, Lang Chen, Jian Sun, et al.
Stem Cell Research|June 17, 2015
Novel surface markers directed against adult human gallbladderFeorillo H Galivo, Craig Dorrell, Maria T Grompe, et al.
Stem Cell Research|May 23, 2015
Impact of preconditioning with retinoic acid during early development on morphological and functional characteristics of human induced pluripotent stem cell-derived neuronsSandra Horschitz, Friederike Matthäus, Anja Groß, et al.
Stem Cell Research|June 24, 2015
Pancreatic duct glands (PDGs) are a progenitor compartment responsible for pancreatic ductal epithelial repairJunpei Yamaguchi, Andrew S Liss, Alexandra Sontheimer, et al.
Stem Cell Research|April 30, 2023
Generation of a genetically-modified induced pluripotent stem cell line harboring an oncogenic gene variant KRAS p.G12VAlexandra Viktoria Busley, Mandy Kleinsorge, Lukas Cyganek
Stem Cell Research|June 5, 2015
The effect of low-frequency electromagnetic field on human bone marrow stem/progenitor cell differentiationChristina L Ross, Mevan Siriwardane, Graça Almeida-Porada, et al.
Stem Cell Research|May 4, 2020
Generation of an INSULIN-H2B-Cherry reporter human iPSC lineAnna Karolina Blöchinger, Johanna Siehler, Katharina Wißmiller, et al.
Stem Cell Research|April 10, 2020
An integration-free iPSC line SDQLCHi025-A from a girl with multiminicore disease carrying compound heterozygote mutations in RYR1 geneHaiyan Zhang, Yanyan Ma, Yuqiang Lv, et al.
Stem Cell Research|April 11, 2020
Hypoxia/Hif1α prevents premature neuronal differentiation of neural stem cells through the activation of Hes1Josef Večeřa, Jiřina Procházková, Veronika Šumberová, et al.
Stem Cell Research|April 12, 2020
Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutationsVijay Bhaskar Reddy Konala, Swapna Nandakumar, Rajani Battu, et al.
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