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Stem Cell Research|November 25, 2015
Characterization of neurons from immortalized dental pulp stem cells for the study of neurogenetic disordersNora Urraca, Rawaha Memon, Ikbale El-Iyachi, et al.Stem Cell Research|October 22, 2017
Generation and characterization of human iPSC lines SANi001-A and SANi002-A from mobilized peripheral blood derived megakaryoblastsMarten Hansen, Eszter Varga, Tatjana Wüst, et al.Stem Cell Research|July 25, 2022
Mesenchymal stem cells and prostate cancer: A concise review of therapeutic potentials and biological aspectsMaryam Rahimi Tesiye, Zahra Abrishami Kia, Hassan Rajabi-MahamStem Cell Research|April 30, 2022
Generation of an induced pluripotent stem cell line from a patient with Angelman syndrome carrying UBE3A mutationShasha Li, Qunyan Zhu, Yaoyao Cai, et al.Stem Cell Research|July 22, 2022
Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP geneChih-Hsin Ou-Yang, Han-I Lin, Chin-Hsien LinStem Cell Research|July 23, 2022
Generation of a RRAGA knockout human iPSC line GIBHi002-A-5 using CRISPR/Cas9 technologyYilu Sun, Jian Fu, Jiayin Yang, et al.Stem Cell Research|July 25, 2022
A critical review on induced totipotent stem cells: Types and methodsMohammad H Ghazimoradi, Ali Khalafizadeh, Sadegh BabashahStem Cell Research|July 16, 2022
Establishment of a human induced pluripotent stem cell line (CSUASOi010-A) by reprogramming peripheral blood mononuclear cells of a type 2 diabetic mellitus patientChengcheng Ding, Feng Tan, Yalan Zhou, et al.Stem Cell Research|July 14, 2022
Establishment of a human induced pluripotent stem cell line, KMUGMCi002-A, from a patient bearing a heterozygous c.6362_6364del mutation in the NIPBL gene leading Cornelia de Lange syndrome (CdLS)Hiroki Ura, Sumihito Togi, Yumiko Iwata, et al.Stem Cell Research|July 17, 2022
Generation of induced pluripotent stem cell line (RCMGi008-A) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/CFTRdele2.3 mutations in CFTR geneEkaterina Kondrateva, Irina Panchuk, Anna Demchenko, et al.Pageof 392