| Published Application/Species/Sample/Dilution | Reference |
|---|
- western blot; human; 1:100; fig 3d
| Castillo P, Aisagbonhi O, Saenz C, ElShamy W. Novel insights linking BRCA1-IRIS role in mammary gland development to formation of aggressive PABCs: the case for longer breastfeeding. Am J Cancer Res. 2022;12:396-426 pubmed |
- immunocytochemistry; human; 1:100; loading ...; fig s1c
| Elhussieny A, Nogami K, Sakai Takemura F, Maruyama Y, Takemura N, Soliman W, et al. Mesenchymal stem cells derived from human induced pluripotent stem cells improve the engraftment of myogenic cells by secreting urokinase-type plasminogen activator receptor (uPAR). Stem Cell Res Ther. 2021;12:532 pubmed publisher |
- immunocytochemistry; human; 1:50; loading ...; fig s1c
| Yoo J, Lee D, Park S, Shin H, Lee K, Kim D, et al. Trophoblast glycoprotein is a marker for efficient sorting of ventral mesencephalic dopaminergic precursors derived from human pluripotent stem cells. NPJ Parkinsons Dis. 2021;7:61 pubmed publisher |
- immunocytochemistry; human; 1:500; loading ...; fig s13b
| Truong D, Phlairaharn T, Eßwein B, Gruber C, Tümen D, Baligács E, et al. Non-invasive and high-throughput interrogation of exon-specific isoform expression. Nat Cell Biol. 2021;23:652-663 pubmed publisher |
- immunocytochemistry; human; 1:100; fig s2a
| Low B, Lim C, Ding S, Tan Y, Ng N, Krishnan V, et al. Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells. Nat Commun. 2021;12:3133 pubmed publisher |
- immunocytochemistry; human; 1:40; loading ...; fig 1c
| Seol B, Kim Y, Cho Y. Modeling Sialidosis with Neural Precursor Cells Derived from Patient-Derived Induced Pluripotent Stem Cells. Int J Mol Sci. 2021;22: pubmed publisher |
- immunohistochemistry; mouse; 1:1000; loading ...
| Hanna R, Flamier A, Barabino A, Bernier G. G-quadruplexes originating from evolutionary conserved L1 elements interfere with neuronal gene expression in Alzheimer's disease. Nat Commun. 2021;12:1828 pubmed publisher |
| Huang C, Qiu L, Zhou W, Shao C, Wang X, Zhang Q, et al. A human-induced pluripotent stem cell (iPSC) line (SMUSHi006-A) from an ALS patient carrying a mutation c.1126C > T in the FUS gene. Stem Cell Res. 2025;82:103604 pubmed publisher |
| Ma X, Dai L, Tan C, Li J, He X, Wang Y, et al. β-catenin mediates endodermal commitment of human ES cells via distinct transactivation functions. Cell Biosci. 2024;14:96 pubmed publisher |
| Dattani A, Corujo Simon E, Radley A, Heydari T, Taheriabkenar Y, Carlisle F, et al. Naive pluripotent stem cell-based models capture FGF-dependent human hypoblast lineage specification. Cell Stem Cell. 2024;31:1058-1071.e5 pubmed publisher |
| Tonin R, Feo F, Falliano S, Giunti L, Calamai M, Procopio E, et al. Generation of a human induced pluripotent stem cell line from a patient with GM3 synthase deficiency using self-replicating RNA vector. Stem Cell Res. 2024;77:103431 pubmed publisher |
| Villegas L, Chandrasekaran A, Andersen S, N xf8 rrem xf8 lle A, Schmid B, Pouladi M, et al. Generation of three isogenic gene-edited Huntington's disease human embryonic stem cell lines with DOX-inducible NGN2 expression cassette in the AAVS1 safe locus. Stem Cell Res. 2024;77:103408 pubmed publisher |
| Weatherbee B, Weberling A, Gantner C, Iwamoto Stohl L, Barnikel Z, Barrie A, et al. Distinct pathways drive anterior hypoblast specification in the implanting human embryo. Nat Cell Biol. 2024;26:353-365 pubmed publisher |
| Tang M, Xiong M, Zhou W, Lei J, Huang M, Huang C, et al. Generation of a human induced pluripotent stem cell line (SMUSHi002-A) from an ALS patient carrying a heterozygous mutation c.1562G > A in the FUS gene. Stem Cell Res. 2024;74:103286 pubmed publisher |
| Isaac E, Berg D, Pfeffer P. Using extended growth of cattle embryos in culture to gain insights into bovine developmental events on embryonic days 8 to 10. Theriogenology. 2024;214:10-20 pubmed publisher |
| Militi S, Nibhani R, Jalali M, Pauklin S. RBL2-E2F-GCN5 guide cell fate decisions during tissue specification by regulating cell-cycle-dependent fluctuations of non-cell-autonomous signaling. Cell Rep. 2023;42:113146 pubmed publisher |
| Montero Calle P, Flandes Iparraguirre M, Kuebler B, Ar xe1 n B, Larequi E, Anaut I, et al. Generation of an induced pluripotent stem cell line (ESi107-A) from a transthyretin amyloid cardiomyopathy (ATTR-CM) patient carrying a p.Ser43Asn mutation in the TTR gene. Stem Cell Res. 2023;71:103189 pubmed publisher |
| Hsu F, Wu Q, Fabyanic E, Wei A, Wu H, Clark A. TET1 facilitates specification of early human lineages including germ cells. iScience. 2023;26:107191 pubmed publisher |
| Chohra I, Giri S, Malgrange B. Generation of a Well-Characterized Homozygous Chromodomain-Helicase-DNA-Binding Protein 4G1003D Mutant hESC Line Using CRISPR/eCas9 (ULIEGEe001-A-1). Int J Mol Sci. 2023;24: pubmed publisher |
| Valtonen J, Prajapati C, Cherian R, Vanninen S, Ojala M, Leivo K, et al. The Junctophilin-2 Mutation p.(Thr161Lys) Is Associated with Hypertrophic Cardiomyopathy Using Patient-Specific iPS Cardiomyocytes and Demonstrates Prolonged Action Potential and Increased Arrhythmogenicity. Biomedicines. 2023;11: pubmed publisher |
| Cooke J, Voigt A, Collingwood M, Stone N, Whitmore S, DeLuca A, et al. Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell Replacement. Stem Cells Transl Med. 2023;12:365-378 pubmed publisher |
| Teague S, Primavera G, Chen B, Freeburne E, Khan H, Jo K, et al. The time integral of BMP signaling determines fate in a stem cell model for early human development. bioRxiv. 2023;: pubmed publisher |
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| Mou Y, Nandi G, Mukte S, Chai E, Chen Z, Nielsen J, et al. Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patients. Orphanet J Rare Dis. 2023;18:72 pubmed publisher |
| Sharma S, Reddy B, Pal R, Ritakari T, Cooper J, Selvaraj B, et al. Astrocytes mediate cell non-autonomous correction of aberrant firing in human FXS neurons. Cell Rep. 2023;42:112344 pubmed publisher |
| Shigyo M, Kobayashi Y, Platoshyn O, Marsala S, Kato T, Takamura N, et al. Derivation of Sendai-Virus-Reprogrammed Human iPSCs-Neuronal Precursors: In Vitro and In Vivo Post-grafting Safety Characterization. Cell Transplant. 2023;32:9636897231163232 pubmed publisher |
| Son N, Son Y, Jung C, Son M. Generation of a human fibroblast-derived induced pluripotent stem cell line KRIBBi009-A from a patient with breast cancer. Stem Cell Res. 2023;68:103060 pubmed publisher |
| Zuo Q, Yang Y, Lyu Y, Yang C, Chen C, Salman S, et al. Plexin-B3 expression stimulates MET signaling, breast cancer stem cell specification, and lung metastasis. Cell Rep. 2023;42:112164 pubmed publisher |
| Seita Y, Cheng K, McCarrey J, Yadu N, Cheeseman I, Bagwell A, et al. Efficient generation of marmoset primordial germ cell-like cells using induced pluripotent stem cells. elife. 2023;12: pubmed publisher |
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| Li L, Si X, Yang J, Lei M, Liu H, Ruan J, et al. Generation of a human iPSC line (CIBi014-A) from a patient with Parkinson's disease carrying a novel heterozygotic PARK8 (LRRK2) mutation. Stem Cell Res. 2023;66:102995 pubmed publisher |
| Yang L, Lu S, Yang Z, Yao J, Zhou P, Zhao M. Generation of an induced pluripotent stem cell line (IPCASi001-A) from an autism spectrum disorder individual without intellectual disability. Stem Cell Res. 2023;66:102994 pubmed publisher |
| Akda x15f E, Turan S, Guhathakurta D, Ekici A, Salar S, Chichung Lie D, et al. CRISPR/Cas9-mediated generation of hESC lines with homozygote and heterozygote p.R331W mutation in CTBP1 to model HADDTS syndrome. Stem Cell Res. 2022;67:103012 pubmed publisher |
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| Re xe9 D, F xf3 thi x, Varga N, Kolacsek O, Orb xe1 n T, Ap xe1 ti x. Partial Disturbance of Microprocessor Function in Human Stem Cells Carrying a Heterozygous Mutation in the DGCR8 Gene. Genes (Basel). 2022;13: pubmed publisher |
| Tongbaen M, Matsumura Y, Okita K, Leecharoenkiat K. Generation of human induced pluripotent stem cells (CHULAi001-A) from peripheral blood mononuclear cells of a glucose-6-phosphate dehydrogenase (G6PD) deficient subject carrying the Viangchan mutation. Stem Cell Res. 2022;65:102953 pubmed publisher |
| Han Y, Tan L, Zhou T, Yang L, Carrau L, Lacko L, et al. A human iPSC-array-based GWAS identifies a virus susceptibility locus in the NDUFA4 gene and functional variants. Cell Stem Cell. 2022;29:1475-1490.e6 pubmed publisher |
| Chimienti R, Baccega T, Torchio S, Manenti F, Pellegrini S, Cospito A, et al. Engineering of immune checkpoints B7-H3 and CD155 enhances immune compatibility of MHC-I-/- iPSCs for β cell replacement. Cell Rep. 2022;40:111423 pubmed publisher |
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| Steiner T, Zink A, Henke M, Cecchetto G, Buenning M, Rossi A, et al. RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother. Stem Cell Res. 2022;64:102920 pubmed publisher |
| Rust R, Weber R, Generali M, Kehl D, Bodenmann C, Uhr D, et al. Xeno-free induced pluripotent stem cell-derived neural progenitor cells for in vivo applications. J Transl Med. 2022;20:421 pubmed publisher |
| Zheng Y, Yan R, Sun S, Kobayashi M, Xiang L, Yang R, et al. Single-cell analysis of embryoids reveals lineage diversification roadmaps of early human development. Cell Stem Cell. 2022;29:1402-1419.e8 pubmed publisher |
| Ai Z, Xiang X, Xiang Y, Szczerbinska I, Qian Y, Xu X, et al. Krüppel-like factor 5 rewires NANOG regulatory network to activate human naive pluripotency specific LTR7Ys and promote naive pluripotency. Cell Rep. 2022;40:111240 pubmed publisher |
| Schmidt S, Luecken M, Tr xfc mbach D, Hembach S, Niedermeier K, Wenck N, et al. Primary cilia and SHH signaling impairments in human and mouse models of Parkinson's disease. Nat Commun. 2022;13:4819 pubmed publisher |
| L xe1 szl xf3 L, Maczelka H, Tak xe1 cs T, Kurilla A, Tilajka x, Buday L, et al. A Novel Cell-Based Model for a Rare Disease: The Tks4-KO Human Embryonic Stem Cell Line as a Frank-Ter Haar Syndrome Model System. Int J Mol Sci. 2022;23: pubmed publisher |
| Jiang Z, Gu X, Su W, Duan Q, Lin J, Cao B, et al. Production of a human iPSC line from an early-onset Parkinson's disease patient with a novel CHCHD2 gene truncated mutation. Stem Cell Res. 2022;64:102881 pubmed publisher |
| Sun Y, Fu J, Yang J, Zhao J, Rong J. Generation of a RRAGA knockout human iPSC line GIBHi002-A-5 using CRISPR/Cas9 technology. Stem Cell Res. 2022;63:102859 pubmed publisher |
| D Ignazio L, Jacomini R, Qamar B, Benjamin K, Arora R, Sawada T, et al. Variation in TAF1 expression in female carrier induced pluripotent stem cells and human brain ontogeny has implications for adult neostriatum vulnerability in X-linked Dystonia Parkinsonism. Eneuro. 2022;9: pubmed publisher |
| Lotila J, Hyv xe4 rinen T, Skottman H, Airas L, Narkilahti S, Hagman S. Establishment of a human induced pluripotent stem cell line (TAUi008-A) derived from a multiple sclerosis patient. Stem Cell Res. 2022;63:102865 pubmed publisher |
| Ohgushi M, Taniyama N, Vandenbon A, Eiraku M. Delamination of trophoblast-like syncytia from the amniotic ectodermal analogue in human primed embryonic stem cell-based differentiation model. Cell Rep. 2022;39:110973 pubmed publisher |
| Chen Y, Huang P, Wen M, Pan M, Lee D, Chen T. Generation of a homozygous knock-in human embryonic stem cell line expressing mEos4b-tagged CTR1. Stem Cell Res. 2022;63:102845 pubmed publisher |
| Francescangeli F, De Angelis M, Rossi R, Sette G, Eramo A, Boe A, et al. CRIPTO Is a Marker of Chemotherapy-Induced Stem Cell Expansion in Non-Small Cell Lung Cancer. Front Oncol. 2022;12:830873 pubmed publisher |
| Närvä E, Taskinen M, Lilla S, Isomursu A, Pietila M, Weltner J, et al. MASTL is enriched in cancerous and pluripotent stem cells and influences OCT1/OCT4 levels. iScience. 2022;25:104459 pubmed publisher |
| Simunovic M, Siggia E, Brivanlou A. In vitro attachment and symmetry breaking of a human embryo model assembled from primed embryonic stem cells. Cell Stem Cell. 2022;29:962-972.e4 pubmed publisher |
| Jiao H, Lee M, Sivapatham A, Leiferman E, Li W. Epigenetic regulation of BAF60A determines efficiency of miniature swine iPSC generation. Sci Rep. 2022;12:9039 pubmed publisher |
| Shi Y, Wu S, Yang B, Yu B, Yan Y, Yang J, et al. Generation of a human iPSC line CIBi011-A from amniocytes of a healthy fetus. Stem Cell Res. 2022;62:102801 pubmed publisher |
| Koide T, Koyanagi Aoi M, Uehara K, Kakeji Y, Aoi T. CDX2-induced intestinal metaplasia in human gastric organoids derived from induced pluripotent stem cells. iScience. 2022;25:104314 pubmed publisher |
| Molugu K, Battistini G, Heaster T, Rouw J, Guzman E, Skala M, et al. Label-Free Imaging to Track Reprogramming of Human Somatic Cells. GEN Biotechnol. 2022;1:176-191 pubmed publisher |
| Sesé B, Íñiguez Muñoz S, Ensenyat Mendez M, Llinàs Arias P, Ramis G, Orozco J, et al. Glioblastoma Embryonic-like Stem Cells Exhibit Immune-Evasive Phenotype. Cancers (Basel). 2022;14: pubmed publisher |
| Fu J, Jiang L, Yu B, Liu Y, Wei R, Hu Y, et al. Generation of a human iPSC line CIBi010-A with a reporter for ASGR1 using CRISPR/Cas9. Stem Cell Res. 2022;62:102800 pubmed publisher |
| Takahashi K, Okubo C, Nakamura M, Iwasaki M, Kawahara Y, Tabata T, et al. A stress-reduced passaging technique improves the viability of human pluripotent cells. Cell Rep Methods. 2022;2:100155 pubmed publisher |
| Hu X, Xiong S, Zhou X, Sun L. Generation of a human induced pluripotent stem cell line FMUPDCi001-A from a patient with mental retardation, autosomal recessive 36 (MRT36) carrying the variants c.219dupA and c.587C > T in ADAT3. Stem Cell Res. 2022;61:102777 pubmed publisher |
| Jo K, Teague S, Chen B, Khan H, Freeburne E, Li H, et al. Efficient differentiation of human primordial germ cells through geometric control reveals a key role for Nodal signaling. elife. 2022;11: pubmed publisher |
| Collier A, Bendall A, Fabian C, Malcolm A, Tilgner K, Semprich C, et al. Genome-wide screening identifies Polycomb repressive complex 1.3 as an essential regulator of human naïve pluripotent cell reprogramming. Sci Adv. 2022;8:eabk0013 pubmed publisher |
| Breyer M, Klein T, Klug K, Klopocki E, Uceyler N. Generation of the induced pluripotent stem cell line UKWNLi005-A derived from a patient with the GLA mutation c.376A > G of unknown pathogenicity in Fabry disease. Stem Cell Res. 2022;61:102747 pubmed publisher |
| Lorenz C, Zink A, Henke M, Staege S, Mlody B, Bünning M, et al. Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6. Stem Cell Res. 2022;61:102742 pubmed publisher |
| Lu V, Roy I, Torres A, Joly J, Ahsan F, Graham N, et al. Glutamine-dependent signaling controls pluripotent stem cell fate. Dev Cell. 2022;57:610-623.e8 pubmed publisher |
| Xiang X, Tao Y, DiRusso J, Hsu F, Zhang J, Xue Z, et al. Human reproduction is regulated by retrotransposons derived from ancient Hominidae-specific viral infections. Nat Commun. 2022;13:463 pubmed publisher |
| Fagerlund I, Dougalis A, Shakirzyanova A, G xf3 mez Budia M, Pelkonen A, Konttinen H, et al. Microglia-like Cells Promote Neuronal Functions in Cerebral Organoids. Cells. 2021;11: pubmed publisher |
| van den Brink L, Brand xe3 o K, Yiangou L, Blanch Asensio A, Mol M, Mummery C, et al. The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2. Front Physiol. 2021;12:755642 pubmed publisher |
| Jewell B, Xu A, Zhu D, Huang M, Lu L, Liu M, et al. Patient-derived iPSCs link elevated mitochondrial respiratory complex I function to osteosarcoma in Rothmund-Thomson syndrome. PLoS Genet. 2021;17:e1009971 pubmed publisher |
| Ozgencil M, Barwell J, Tischkowitz M, Izatt L, Kesterton I, Simpson M, et al. Assessing BRCA1 activity in DNA damage repair using human induced pluripotent stem cells as an approach to assist classification of BRCA1 variants of uncertain significance. PLoS ONE. 2021;16:e0260852 pubmed publisher |
| Sabatier P, Beusch C, Saei A, Aoun M, Moruzzi N, Coelho A, et al. An integrative proteomics method identifies a regulator of translation during stem cell maintenance and differentiation. Nat Commun. 2021;12:6558 pubmed publisher |
| Valcourt J, Huang R, Kundu S, Venkatasubramanian D, Kingston R, Ramanathan S. Modulating mesendoderm competence during human germ layer differentiation. Cell Rep. 2021;37:109990 pubmed publisher |
| Pagliaroli L, Porazzi P, Curtis A, Scopa C, Mikkers H, Freund C, et al. Inability to switch from ARID1A-BAF to ARID1B-BAF impairs exit from pluripotency and commitment towards neural crest formation in ARID1B-related neurodevelopmental disorders. Nat Commun. 2021;12:6469 pubmed publisher |
| Shin Y, Mun S, Lee J, Chung K, Kim M, Kun Cheon C, et al. Generation of human induced pluripotent stem cell line, KRIBBi003-A, from urinary cells of a patient with glycogen storage disease type IXa. Stem Cell Res. 2021;57:102584 pubmed publisher |
| Ting H, Yang H, Harn H, Chiu I, Su H, Li X, et al. Coactivation of GSK3β and IGF-1 Attenuates Amyotrophic Lateral Sclerosis Nerve Fiber Cytopathies in SOD1 Mutant Patient-Derived Motor Neurons. Cells. 2021;10: pubmed publisher |
| Krumm L, Pozner T, Kaindl J, Regensburger M, Günther C, Turan S, et al. Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in. Stem Cell Res. 2021;56:102520 pubmed publisher |
| Huang X, Park K, Gontarz P, Zhang B, Pan J, McKenzie Z, et al. OCT4 cooperates with distinct ATP-dependent chromatin remodelers in naïve and primed pluripotent states in human. Nat Commun. 2021;12:5123 pubmed publisher |
| Kang Y, Zhou Y, Li Y, Han Y, Xu J, Niu W, et al. A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies. Nat Neurosci. 2021;24:1377-1391 pubmed publisher |
| Mackinlay K, Weatherbee B, Souza Rosa V, Handford C, Hudson G, Coorens T, et al. An in vitro stem cell model of human epiblast and yolk sac interaction. elife. 2021;10: pubmed publisher |
| Lee J, Liu Z, Tusing Y, Li C, Westin E, Li W, et al. Generation of inducible pluripotent stem cell lines from Alzheimer's disease patients with APOE e3/e3 genotype. Stem Cell Res. 2021;55:102498 pubmed publisher |
| Hogrebe N, Maxwell K, Augsornworawat P, Millman J. Generation of insulin-producing pancreatic β cells from multiple human stem cell lines. Nat Protoc. 2021;16:4109-4143 pubmed publisher |
| Aarts C, Varga E, Webbers S, Geissler J, von Lindern M, Kuijpers T, et al. Generation and characterization of a human iPSC line SANi006-A from a Gray Platelet Syndrome patient. Stem Cell Res. 2021;55:102443 pubmed publisher |
| Pandolfi E, Hunt T, Goldsmith S, Hurlbut K, Silber S, Clark A. Generation of three human induced pluripotent stem cell sublines (UCLAi004-A, UCLAi004-B, and UCLAi004-C) for reproductive science research. Stem Cell Res. 2021;54:102446 pubmed publisher |
| Ma L, Schmidt M, Morrow E. Human iPSC lines from a Christianson syndrome patient with NHE6 W523X mutation, a biologically-related control, and CRISPR/Cas9 gene-corrected isogenic controls. Stem Cell Res. 2021;54:102435 pubmed publisher |
| Lee M, Stebbins M, Jiao H, Huang H, Leiferman E, Walczak B, et al. Comparative evaluation of isogenic mesodermal and ectomesodermal chondrocytes from human iPSCs for cartilage regeneration. Sci Adv. 2021;7: pubmed publisher |
| Pandolfi E, Hunt T, Goldsmith S, Hurlbut K, Silber S, Clark A. Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research. Stem Cell Res. 2021;54:102409 pubmed publisher |
| Huang P, Wen M, Xie X, Xu A, Lee D, Chen T. Generation of a homozygous knock-in human embryonic stem cell line expressing SNAP-tagged SOD1. Stem Cell Res. 2021;54:102415 pubmed publisher |
| Yan R, Wu S, Wang W, Chu M, Liu P. Generation of a human induced pluripotent stem cell line (SMUSHi001-A) from a patient with 46, XX male sex reversal syndrome carrying the SRY gene. Stem Cell Res. 2021;54:102397 pubmed publisher |
| Zhou Z, Ma L, Zhang X. Protocol for genome-scale CRISPR screening in engineered lineage reporter hPSCs to study cell fate determination. STAR Protoc. 2021;2:100548 pubmed publisher |
| Wu S, Zhang Z, Wang L, Yu J. Generation of a human iPSC line QDMHi001-A from a patient with Marfan syndrome carrying a heterozygous c.6772 T > C variant in FBN1. Stem Cell Res. 2021;54:102390 pubmed publisher |
| Borsoi J, Morato Marques M, de Araújo Tofoli F, Assis Pereira L, Farinha Arcieri L, Delgado Sarafian R, et al. Generation of two human induced pluripotent stem cell (hiPSC) lines derived from unrelated Marfan Syndrome patients. Stem Cell Res. 2021;54:102407 pubmed publisher |
| Meistermann D, Bruneau A, Loubersac S, Reignier A, Firmin J, François Campion V, et al. Integrated pseudotime analysis of human pre-implantation embryo single-cell transcriptomes reveals the dynamics of lineage specification. Cell Stem Cell. 2021;28:1625-1640.e6 pubmed publisher |
| Yanagida A, Spindlow D, Nichols J, Dattani A, Smith A, Guo G. Naive stem cell blastocyst model captures human embryo lineage segregation. Cell Stem Cell. 2021;28:1016-1022.e4 pubmed publisher |
| Bayerl J, Ayyash M, Shani T, Manor Y, Gafni O, Massarwa R, et al. Principles of signaling pathway modulation for enhancing human naive pluripotency induction. Cell Stem Cell. 2021;: pubmed publisher |
| Mertens J, Herdy J, Traxler L, Schäfer S, Schlachetzki J, Böhnke L, et al. Age-dependent instability of mature neuronal fate in induced neurons from Alzheimer's patients. Cell Stem Cell. 2021;: pubmed publisher |
| Ge W, Song Y, Chu M, Liu Y, Yang B, Wang K, et al. Generation of a human iPSC line CIBi009-A from a patient with familial hypercholesterolemia carrying variants of LDLR c.T1241G and APOB c.G1618T. Stem Cell Res. 2021;53:102347 pubmed publisher |
| Sutcliffe D, Dinasarapu A, Visser J, Hoed J, Seifar F, Joshi P, et al. Induced pluripotent stem cells from subjects with Lesch-Nyhan disease. Sci Rep. 2021;11:8523 pubmed publisher |
| Raj N, McEachin Z, Harousseau W, Zhou Y, Zhang F, Merritt Garza M, et al. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis. Cell Rep. 2021;35:108991 pubmed publisher |
| Guo G, Stirparo G, Strawbridge S, Spindlow D, Yang J, Clarke J, et al. Human naive epiblast cells possess unrestricted lineage potential. Cell Stem Cell. 2021;28:1040-1056.e6 pubmed publisher |
| Devito L, Healy L, Mohammed S, Guillemot F, Dias C. Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder. Stem Cell Res. 2021;53:102304 pubmed publisher |
| Inak G, Rybak Wolf A, Lisowski P, Pentimalli T, Jüttner R, Glažar P, et al. Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome. Nat Commun. 2021;12:1929 pubmed publisher |
| Kim S, Wong Y, Gao F, Krainc D. Dysregulation of mitochondria-lysosome contacts by GBA1 dysfunction in dopaminergic neuronal models of Parkinson's disease. Nat Commun. 2021;12:1807 pubmed publisher |
| Sahni G, Chang S, Meng J, Tan J, Fatien J, Bonnard C, et al. A Micropatterned Human-Specific Neuroepithelial Tissue for Modeling Gene and Drug-Induced Neurodevelopmental Defects. Adv Sci (Weinh). 2021;8:2001100 pubmed publisher |
| Tang C, Han J, Dalvi S, Manian K, Winschel L, Volland S, et al. A human model of Batten disease shows role of CLN3 in phagocytosis at the photoreceptor-RPE interface. Commun Biol. 2021;4:161 pubmed publisher |
| Simkin D, Marshall K, Vanoye C, Desai R, Bustos B, Piyevsky B, et al. Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy. elife. 2021;10: pubmed publisher |
| Hathy E, Szabó E, Vincze K, Haltrich I, Kiss E, Varga N, et al. Generation of multiple iPSC clones from a male schizophrenia patient carrying de novo mutations in genes KHSRP, LRRC7, and KIR2DL1, and his parents. Stem Cell Res. 2021;51:102140 pubmed publisher |
| Guénantin A, Jebeniani I, Leschik J, Watrin E, Bonne G, Vignier N, et al. Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy. J Clin Invest. 2021;131: pubmed publisher |
| Medina D, Boehringer A, Dominick M, Lorenzini I, Saez Atienzar S, Pioro E, et al. Generation of two induced pluripotent stem cell (iPSC) lines from an ALS patient with simultaneous mutations in KIF5A and MATR3 genes. Stem Cell Res. 2020;50:102141 pubmed publisher |
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