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Stem Cell Research

IF0.7
Papers138
Citations
Journal Papers 138
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Generation of hiPSCs (JUCGRMi008-A) from a β-propeller protein-associated neurodegeneration patient with WDR45 mutation
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deleteKamikura, Rino; Liu, Xing; Ishikawa, Kei-ichi; Yoshino, Hiroyo; Hattori, Nobutaka; Akamatsu, Wado
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Generation of iPSC lines from myotonic dystrophy type 1 patients with varying CTG repeat lengths
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deleteHoekman, Thomas D.; Rahm, Lisa; Albert, Silvia; Wansink, Derick G.; van Bokhoven, Hans; Raaijmakers, Renee H. L.
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Generation of an iPSC line IUFi004-A-13 with homozygous NDUFS1 mutation for the study of Leigh syndrome
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deleteJerred, Caleb; Ramachandran, Haribaskar; Hildebrandt, Barbara; Zink, Annika; Ventura, Natascia; Rossi, Andrea; Prigione, Alessandro
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Three donor-matched iPSC lines derived from human postmortem dura mater for modeling neurodegenerative diseases
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deleteShim, Yu-mi; Yoo, Sooyeon; Kwon, Hyung-jin; Lee, Kwanghoon; Park, Sung-Hye; Won, Jae-Kyung
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Generation of six hiPSC lines from patients with WDR45-related neurodegenerative disease (Beta-propeller Protein-Associated Neurodegeneration, BPAN)
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deleteTournois, Johana; Chatrousse, Laure; Giraud-Triboult, Karine; Rousselot, Justine; El Kassar, Lina; Lesueur, Lea; Mahiou, Hamel; Bouquier, Margot; Walter, Ludivine; Mollereau, Bertrand; Beaumont, Anais; des Portes, Vincent; Poulat, Anne-Lise; Lesca, Gaetan; Benchoua, Alexandra
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Generation of four human induced pluripotent stem cell lines derived from patients with corticosteroid-associated central serous chorioretinopathy
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deleteGaluh, Sekar; Raymond, Karine; Brinks, Joost; van Dijk, Elon H. C.; Freund, Christian; Meijer, Onno C.; Boon, Camiel J. F.
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Derivation of an induced pluripotent stem cell line from a long QT syndrome type 1 patient with a pathogenic KCNQ1 c.1552C > T (p.Arg518Ter) variant
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deleteDing, Dingqian; Choi, Jonathan; Gollatz, Elisa Marie; Harbuzariu, Adriana; Itzhaki, Ilanit
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Generation of an induced pluripotent stem cell line from an Alstro¨m syndrome patient with biallelic ALMS1 pathogenic variants
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deleteSecula, Samira; Erkilic, Nejla; Obringer, Cathy; Jaeger, Catherine; Leuvrey, Anne Sophie; Muller, Jean; Kalatzis, Vasiliki; Dollfus, Helene
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Generation and characterization of SOX17-specific EGFP expressing human induced pluripotent stem cell line, KSCBi017-A-4, using CRISPR/Cas9
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deleteYoo, Dae Hoon; Bayarsaikhan, Delger; Lee, Jaewon; Im, Young Sam; Bayarsaikhan, Govigerel; Kang, Hyun-A; Lee, Bonghee; Kim, Yong-Ou
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Characterization of an induced pluripotent stem cell line from a long QT syndrome type 1 patient possessing the KCNQ1 c.691C > T (p.Arg231Cys) variant
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deleteChoi, Jonathan; Ding, Dingqian; Gollatz, Elisa Marie; Harbuzariu, Adriana; Itzhaki, Ilanit
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Derivation and characterization of the iPSC line IITGi001-B from primary human adult dermal fibroblasts
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deleteSundaravadivelu, Pradeep Kumar; Raina, Khyati; Borthakur, Atreyee; Mahto, Priya; Shetty, Dhanlaxmi; Dhamne, Chetan; Kaveeshwar, Vishwas; Martin, Catherine Ann; Radhakrishnan, Subathra; Rela, Mohamed; Thummer, Rajkumar P.
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Derivation of an iPSC line using the Sendai virus from a newborn boy with Alagille Syndrome
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deleteZhou, Rui; Liu, Pan; Peng, Xiaokang; Tang, Li; Zhang, Yanmin; Liu, Xiaoguai
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CRISPR-Cas9 genome editing in the parental iPSC line PCIi033-A to introduce the homozygous mutation p.F508del (c.1521_1523del) in the CFTR gene
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deleteSimonneau, Benjamin; Baghdoyan, Sandrine; Cailleret, Michel; Simon, Stephanie; Ruckebusch, Odile; Vrablikova, Barbora; Giraud-Triboult, Karine; El Kassar, Lina; Fanen, Pascale; Duriez, Benedicte
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Generation of two isogenic control iPSC lines (LCSBi001-A-2 and LCSBi001-A-3) from a Parkinson's disease patient line (LCSBi001-A) carrying the pathogenic VPS35 p.D620N mutation
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deleteBoumpoureka, Ioanna; Gorgogietas, Vyron; Petkovski, Elizabet; Massart, Francois; Mellick, George D.; Kruger, Rejko
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Establishment and characterization of induced pluripotent stem cell lines from individuals with Down syndrome and age-matched euploid donors
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deleteAgostinho, Rafaela R.; Calado, Sofia M.; Braganca, Jose E.; Nzwalo, Hipolito; Marques, Vera Mascarenhas; Bota, Monica; Medeiros, Raquel Melo; Mendonca, Carla; Martinez-Ruiz, Antonio; Simao, Sonia; Araujo, Ines M.
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Generation of human induced pluripotent stem cell lines carrying a heterozygous and homozygous PRKD1 c.1774G > A genetic variant causing syndromic congenital defects
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deleteWitthoff, Fabian; Pietsch, Niels; Henning, Philipp; Meier, Leah S.; Fuchs, Sigrid; Augustin, Christa; Orth, Julia; Stathopoulou, Konstantina; Orthey, Ellen; Kraemer, Elisabeth; Carrier, Lucie; Herberg, Friedrich W.; Spielmann, Nadine; Hitz, Marc-Philip; Brook, J. David; Loughna, Siobhan; Cuello, Friederike
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