scholarly journals Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion

2022 ◽  
pp. 102634
Author(s):  
Xinna Ji ◽  
Yanyan Gao ◽  
Pingping Zhang ◽  
ZiQi Jin ◽  
Yan Zhang ◽  
...  
Keyword(s):  
Epilepsy Patient ◽  
Ipsc Line ◽  
Infantile Epilepsy ◽  
Human Ipsc

scholarly journals Establishment of MHHi001-A-5, a GCaMP6f and RedStar dual reporter human iPSC line for in vitro and in vivo characterization and in situ tracing of iPSC derivatives

2021 ◽  
Vol 52 ◽  
pp. 102206
Author(s):  
Alexandra Haase ◽  
Tim Kohrn ◽  
Veronika Fricke ◽  
Maria Elena Ricci Signorini ◽  
Merlin Witte ◽  
...  
Keyword(s):  
Ipsc Line ◽  
Dual Reporter ◽  
In Vivo Characterization ◽  
Human Ipsc

scholarly journals Generation and characterization of a human iPSC line SANi006-A from a Gray Platelet Syndrome patient

2021 ◽  
pp. 102443
Author(s):  
Cathelijn E.M. Aarts ◽  
Eszter Varga ◽  
Steven Webbers ◽  
Judy Geissler ◽  
Marieke von Lindern ◽  
...  
Keyword(s):  
Syndrome Patient ◽  
Ipsc Line ◽  
Gray Platelet Syndrome ◽  
Human Ipsc

scholarly journals Generation of integration free human iPSC line SORMi002-A from neonatal foreskin fibroblasts

2019 ◽  
Vol 40 ◽  
pp. 101534
Author(s):  
Akshatha Shivaraj ◽  
Shagufta Parveen
Keyword(s):  
Ipsc Line ◽  
Human Ipsc

scholarly journals Generation of a human iPSC line ZZUNEUi015-A from a patient with hypertrophic cardiomyopathy caused by mutation in ALPK3

2021 ◽  
Vol 52 ◽  
pp. 102247
Author(s):  
Xiaoxu Tian ◽  
Wanrong Fu ◽  
Guangli Guo ◽  
Shujian Huang ◽  
Yiming Dong ◽  
...  
Keyword(s):  
Hypertrophic Cardiomyopathy ◽  
Ipsc Line ◽  
Human Ipsc

scholarly journals Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2

2018 ◽  
Vol 33 ◽  
pp. 247-250 ◽  
Author(s):  
Carla Sanjurjo-Soriano ◽  
Nejla Erkilic ◽  
Gaël Manes ◽  
Gregor Dubois ◽  
Christian P. Hamel ◽  
...  
Keyword(s):  
Usher Syndrome ◽  
Syndrome Type ◽  
Ipsc Line ◽  
Human Ipsc ◽  
Usher Syndrome Type

scholarly journals Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutation

2018 ◽  
Vol 33 ◽  
pp. 146-150 ◽  
Author(s):  
Daniele Pollini ◽  
Rosa Loffredo ◽  
Marina Cardano ◽  
Luciano Conti ◽  
Serena Lattante ◽  
...  
Keyword(s):  
Ipsc Line ◽  
Human Ipsc

scholarly journals Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy

2020 ◽  
Vol 48 ◽  
pp. 101993
Author(s):  
Kee-Pyo Kim ◽  
Juyong Yoon ◽  
Johnny Kim ◽  
Albrecht Röpke ◽  
Borami Shin ◽  
...  
Keyword(s):  
Metachromatic Leukodystrophy ◽  
Ipsc Line ◽  
Human Ipsc

scholarly journals Establishment of human iPSC line from patient of Indian ethnicity carrying homozygous CD8/9 (+G) beta thalassemia mutation

2020 ◽  
Vol 44 ◽  
pp. 101772
Author(s):  
Shruti Tembe ◽  
Sophia Fernandes ◽  
Nikhat Khan ◽  
Sameer Melinkeri ◽  
Vaijayanti Kale ◽  
...  
Keyword(s):  
Beta Thalassemia ◽  
Ipsc Line ◽  
Human Ipsc ◽  
Thalassemia Mutation
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