Published Application/Species/Sample/Dilution | Reference |
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- flow cytometry; human; loading ...; fig 1e
| Ruiz Gutierrez M, Bölükbaşı Ö, Alexe G, Kotini A, Ballotti K, Joyce C, et al. Therapeutic discovery for marrow failure with MDS predisposition using pluripotent stem cells. JCI Insight. 2019;5: pubmed publisher
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- flow cytometry; human; loading ...; fig 3a
| Hayashi R, Ishikawa Y, Katayama T, Quantock A, Nishida K. CD200 facilitates the isolation of corneal epithelial cells derived from human pluripotent stem cells. Sci Rep. 2018;8:16550 pubmed publisher
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| Suila H, Pitkänen V, Hirvonen T, Heiskanen A, Anderson H, Laitinen A, et al. Are globoseries glycosphingolipids SSEA-3 and -4 markers for stem cells derived from human umbilical cord blood?. J Mol Cell Biol. 2011;3:99-107 pubmed publisher
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| Mitchell M, Grandizio C, Turan N, Requesens D. An induced pluripotent stem cell line (CIMRi001-A) from a Vici syndrome donor with a homozygous recessive c.1007A>G (p.Q336R) mutation in the EPG5 gene. Stem Cell Res. 2022;63:102833 pubmed publisher
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| Bi Y, Tu Z, Zhou J, Zhu X, Wang H, Gao S, et al. Cell fate roadmap of human primed-to-naive transition reveals preimplantation cell lineage signatures. Nat Commun. 2022;13:3147 pubmed publisher
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| Gill D, Parry A, Santos F, Okkenhaug H, Todd C, Hernando Herraez I, et al. Multi-omic rejuvenation of human cells by maturation phase transient reprogramming. elife. 2022;11: pubmed publisher
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| Houweling P, Coles C, Tiong C, Nielsen B, Graham A, McDonald P, et al. Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patient. Stem Cell Res. 2021;54:102429 pubmed publisher
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| Ababneh N, Barham R, Al Kurdi B, Ali D, Sharar N, Al Hadidi S, et al. Generation of an induced pluripotent stem cell (iPSC) line (JUCTCi017-A) from a patient with limb-girdle muscular dystrophy (LGMD) due to a homozygous p.Lue287Ser fs14* mutation in the SGCB gene. Stem Cell Res. 2021;54:102358 pubmed publisher
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| Hohmann M, Habiel D, Espíndola M, Huang G, Jones I, Narayanan R, et al. Antibody-mediated depletion of CCR10+EphA3+ cells ameliorates fibrosis in IPF. JCI Insight. 2021;6: pubmed publisher
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| Leavens K, Liao C, Gagne A, Kishore S, Cardenas Diaz F, French D, et al. Generation of a double insulin and somatostatin reporter line, SCSe001-A-3, for the advancement of stem cell-derived pancreatic islets. Stem Cell Res. 2020;50:102112 pubmed publisher
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| Ababneh N, Al Kurdi B, Barham R, Ali D, Sharar N, Abuarqoub D, et al. Derivation of three human induced pluripotent stem cell lines (JUCTCi014-A, JUCTCi015-A, JUCTCi016-A) from mesenchymal stem cells (MSCs) derived from bone marrow, adipose tissue and Wharton's jelly samples. Stem Cell Res. 2020;49:102000 pubmed publisher
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| Ababneh N, Ali D, Barham R, Al Kurdi B, Sharar N, Al Hadidi S, et al. Establishment of a human induced pluripotent stem cell line, JUCTCi012-A, from multiple symmetric lipomatosis (MSL) patient carrying a homozygous Arg707Trp (c.2119C > T) mutation in the MFN2 gene. Stem Cell Res. 2020;48:101967 pubmed publisher
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| Ababneh N, Al Kurdi B, Ali D, Abuarqoub D, Barham R, Alzibdeh A, et al. Generation and characterization of induced pluripotent stem cell (iPSC) line (JUCTCi002-A) from a patient with ataxia with oculomotor apraxia type 1 (AOA1) harboring a homozygous mutation in the APTX gene. Stem Cell Res. 2020;48:101925 pubmed publisher
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| Döpper H, Horstmann M, Menges J, Bozet M, Kanber D, Steenpass L. Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines. Stem Cell Res. 2020;45:101779 pubmed publisher
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| Bi Y, Tu Z, Zhang Y, Yang P, Guo M, Zhu X, et al. Identification of ALPPL2 as a Naive Pluripotent State-Specific Surface Protein Essential for Human Naive Pluripotency Regulation. Cell Rep. 2020;30:3917-3931.e5 pubmed publisher
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| Nur Patria Y, Lilianty J, Elefanty A, Stanley E, Labonne T, Bateman J, et al. Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editing. Stem Cell Res. 2019;42:101689 pubmed publisher
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| Menges J, Cremanns M, Steenpass L. Generation of two H1 hESC sublines carrying deletions of RB1 exon 1/promoter in heterozygous or compound heterozygous state. Stem Cell Res. 2019;39:101517 pubmed publisher
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| Simic M, Moehle E, Schinzel R, Lorbeer F, Halloran J, Heydari K, et al. Transient activation of the UPRER is an essential step in the acquisition of pluripotency during reprogramming. Sci Adv. 2019;5:eaaw0025 pubmed publisher
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| Li X, Dong T, Li Y, Wu F, Lan F. Generation of a human iPSC line from a patient with Marfan syndrome caused by mutation in FBN1. Stem Cell Res. 2019;36:101414 pubmed publisher
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| Maguire J, Gagne A, Gonzalez Alegre P, Davidson B, Shakkottai V, Gadue P, et al. Generation of Spinocerebellar Ataxia Type 2 induced pluripotent stem cell lines, CHOPi002-A and CHOPi003-A, from patients with abnormal CAG repeats in the coding region of the ATXN2 gene. Stem Cell Res. 2019;34:101361 pubmed publisher
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| Schipper L, Kanber D, Steenpass L. Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1. Stem Cell Res. 2018;33:41-45 pubmed publisher
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| Neureiter A, Brändl B, Hiber M, Tandon R, Muller F, Steenpass L. Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect. Stem Cell Res. 2018;33:20-24 pubmed publisher
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| Gagne A, Maguire J, Gandre Babbe S, Chou S, Tasian S, Loh M, et al. Generation of a human Juvenile myelomonocytic leukemia iPSC line, CHOPi001-A, with a mutation in CBL. Stem Cell Res. 2018;31:157-160 pubmed publisher
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| Marrone L, Bus C, Schöndorf D, Fitzgerald J, Kübler M, Schmid B, et al. Generation of iPSCs carrying a common LRRK2 risk allele for in vitro modeling of idiopathic Parkinson's disease. PLoS ONE. 2018;13:e0192497 pubmed publisher
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| Gao Y, Wilson G, Bozaoglu K, Elefanty A, Stanley E, Dottori M, et al. Generation of RAB39B knockout isogenic human embryonic stem cell lines to model RAB39B-mediated Parkinson's disease. Stem Cell Res. 2018;28:161-164 pubmed publisher
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| Steenpass L. Generation of two H1 hESC sublines carrying a heterozygous and homozygous knock-out of RB1. Stem Cell Res. 2017;25:270-273 pubmed publisher
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| Slamecka J, McClellan S, Wilk A, Laurini J, Manci E, Hoerstrup S, et al. Induced pluripotent stem cells derived from human amnion in chemically defined conditions. Cell Cycle. 2018;17:330-347 pubmed publisher
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| Xia H, Gilbertsen A, Herrera J, Racila E, Smith K, Peterson M, et al. Calcium-binding protein S100A4 confers mesenchymal progenitor cell fibrogenicity in idiopathic pulmonary fibrosis. J Clin Invest. 2017;127:2586-2597 pubmed publisher
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| Pashos E, Park Y, Wang X, Raghavan A, Yang W, Abbey D, et al. Large, Diverse Population Cohorts of hiPSCs and Derived Hepatocyte-like Cells Reveal Functional Genetic Variation at Blood Lipid-Associated Loci. Cell Stem Cell. 2017;20:558-570.e10 pubmed publisher
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| Bi X, Pashos E, Cuchel M, Lyssenko N, Hernandez M, Picataggi A, et al. ATP-Binding Cassette Transporter A1 Deficiency in Human Induced Pluripotent Stem Cell-Derived Hepatocytes Abrogates HDL Biogenesis and Enhances Triglyceride Secretion. EBioMedicine. 2017;18:139-145 pubmed publisher
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| Yang W, Liu Y, Slovik K, Wu J, Duncan S, Rader D, et al. Generation of iPSCs as a Pooled Culture Using Magnetic Activated Cell Sorting of Newly Reprogrammed Cells. PLoS ONE. 2015;10:e0134995 pubmed publisher
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| Chou S, Byrska Bishop M, Tober J, Yao Y, Vandorn D, Opalinska J, et al. Trisomy 21-associated defects in human primitive hematopoiesis revealed through induced pluripotent stem cells. Proc Natl Acad Sci U S A. 2012;109:17573-8 pubmed publisher
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