「Disrupted Cav1.2 Selectivity Causes Overlapping Long QT and Brugada Syndrome Phenotypes in CACNA1C-E1115K iPS Cell Model」の関連論文
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Incontinentia pigmenti in a female infant with somatic mosaicism due to the IKBKG variant
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Single-cell transcriptomics of human cholesteatoma identifies an activin A-producing osteoclastogenic fibroblast subset inducing bone destruction
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Identification of T cell receptors targeting a neoantigen derived from recurrently mutated FGFR3
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Clinical and serological features of dermatomyositis and systemic lupus erythematosus patients with autoantibodies to ADAR1
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Three-dimensional human placenta-like bud synthesized from induced pluripotent stem cells
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Calcium-Binding Protein S100A4 Is Upregulated in Carotid Atherosclerotic Plaques and Contributes to Expansive Remodeling
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One-step induction of photoreceptor-like cells from human iPSCs by delivering transcription factors
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MYCL promotes iPSC-like colony formation via MYC Box 0 and 2 domains
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Generation of two human induced pluripotent stem cell lines derived from two X-linked adrenoleukodystrophy patients with ABCD1 mutations
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Combination of tumor necrosis factor-α and epidermal growth factor induces the adrenergic-to-mesenchymal transdifferentiation in SH-SY5Y neuroblastoma cells
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Prophylactic treatment of rapamycin ameliorates naturally developing and episode -induced heterotopic ossification in mice expressing human mutant ACVR1
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Local application of Usag-1 siRNA can promote tooth regeneration in Runx2-deficient mice
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MafB is important for pancreatic β-cell maintenance under a MafA deficient condition
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Systemic recombination in a novel Cre transgenic line, CAG-Cre C57BL/6N mouse
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Gradient-based parameter optimization method to determine membrane ionic current composition in human induced pluripotent stem cell-derived cardiomyocytes
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Pathogenic mutation of TDP-43 impairs RNA processing in a cell type-specific manner : implications for the pathogenesis of ALS/FTLD (本文)
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Setd1a plays pivotal roles for the survival and proliferation of retinal progenitors via histone modifications of Uhrf1
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St8sia1-deficiency in mice alters tumor environments of gliomas, leading to reduced disease severity
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TEAD1 trapping by the Q353R–Lamin A/C causes dilated cardiomyopathy
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Transplantation of rat cranial bone-derived mesenchymal stem cells promotes functional recovery in rats with spinal cord injury
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Transplantation of rat cranial bone-derived mesenchymal stem cells promotes functional recovery in rats with spinal cord injury
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Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes
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Differentiation of Human Induced Pluripotent Stem Cells Into Testosterone-Producing Leydig-like Cells
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Ferroptosis resistance determines high susceptibility of murine A/J strain to iron-induced renal carcinogenesis
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β-Cell senescence in the pathogenesis of type 2 diabetes.
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A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease
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Non-Genetic Cell-Surface Modification with a Self-Assembling Molecular Glue
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Human induced pluripotent stem cells generated from a patient with idiopathic basal ganglia calcification
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Expression dynamics of HAND1/2 in in vitro human cardiomyocyte differentiation
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Improvement of mouse genome editing protocol and the application:investigation of the physiological roles of glycine receptor alpha 4 subunit.
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Neural Isoforms of Agrin Are Generated by Reduced PTBP1−RNA Interaction Network Spanning the Neuron−Specific Splicing Regions in AGRN
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ILF2 enhances the DNA cytosine deaminase activity of tumor mutator APOBEC3B in multiple myeloma cells
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Trp53 Mutation in Keratin 5 (Krt5)-Expressing Basal Cells Facilitates the Development of Basal Squamous-Like Invasive Bladder Cancer in the Chemical Carcinogenesis of Mouse Bladder
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Lineage tracing analysis defines erythropoietin-producing cells as a distinct subpopulation of resident fibroblasts with unique behaviors
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In vitro methods to ensure absence of residual undifferentiated human induced pluripotent stem cells intermingled in induced nephron progenitor cells
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CDK5/p35-dependent microtubule reorganization contributes to homeostatic shortening of the axon initial segment
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Carbonic anhydrase 9 confers resistance to ferroptosis/apoptosis in malignant mesothelioma under hypoxia
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Studies on multifunctional genome elements functioning in mouse spermatogenesis [an abstract of entire text]
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Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease
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Tsga8 is required for spermatid morphogenesis and male fertility in mice
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Osteocrin ameliorates adriamycin nephropathy via p38 mitogen-activated protein kinase inhibition
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Comprehensive analysis of TCR function using a novel system reveals the multiple unconventional tumor-reactive T cells in breast cancer-infiltrating lymphocytes
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Orthogonal Protein-Responsive mRNA Switches for Mammalian Synthetic Biology
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Network-guided analysis of hippocampal proteome identifies novel proteins that colocalize with Aβ in a mice model of early-stage Alzheimer’s disease
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高純度間葉系幹細胞は機能的ミトコンドリア投入に優れている
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Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency
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A motor neuron disease-associated mutation produces non-glycosylated Seipin that induces ER stress and apoptosis by inactivating SERCA2b
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TDO2 Overexpression Is Associated with Cancer Stem Cells and Poor Prognosis in Esophageal Squamous Cell Carcinoma
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TDO2 Overexpression Is Associated with Cancer Stem Cells and Poor Prognosis in Esophageal Squamous Cell Carcinoma
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A clinically applicable and scalable method to regenerate T-cells from iPSCs for off-the-shelf T-cell immunotherapy