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Chemically defined generation of human cardiomyocytes

Nature methods, 2014-08, Vol.11 (8), p.855

2014

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E-cadherin is crucial for embryonic stem cell pluripotency and can replace OCT4 during somatic cell reprogramming

EMBO reports, 2011-07, Vol.12 (7), p.720-726

2011

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Drug Screening Using a Library of Human Induced Pluripotent Stem Cell―Derived Cardiomyocytes Reveals Disease-Specific Patterns of Cardiotoxicity

Circulation (New York, N.Y.), 2013-04, Vol.127 (16), p.1677-1691

2013

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Activation of PDGF pathway links LMNA mutation to dilated cardiomyopathy

Nature (London), 2019-08, Vol.572 (7769), p.335-340

2019

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Mutations in Disordered Regions Can Cause Disease by Creating Dileucine Motifs

Cell, 2018-09, Vol.175 (1), p.239-253.e17

2018

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Embryos and embryonic stem cells from the white rhinoceros

Nature communications, 2018-07, Vol.9 (1), p.2589-9, Article 2589

2018

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A Comprehensive TALEN-Based Knockout Library for Generating Human-Induced Pluripotent Stem Cell–Based Models for Cardiovascular Diseases

Circulation research, 2017-05, Vol.120 (10), p.1561-1571

2017

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The centrosomal protein 83 (CEP83) regulates human pluripotent stem cell differentiation toward the kidney lineage

eLife, 2022-10, Vol.11

2022

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FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells

Developmental cell, 2018-09, Vol.46 (5), p.611-626.e12

2018

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iPSC-derived reactive astrocytes from patients with multiple sclerosis protect cocultured neurons in inflammatory conditions

The Journal of clinical investigation, 2023-07, Vol.133 (13), p.1-16

2023

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The Role of SIRT6 Protein in Aging and Reprogramming of Human Induced Pluripotent Stem Cells

The Journal of biological chemistry, 2013-06, Vol.288 (25), p.18439-18447

2013

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Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes as an In Vitro Model for Coxsackievirus B3–Induced Myocarditis and Antiviral Drug Screening Platform

Circulation research, 2014-08, Vol.115 (6), p.556-566

2014

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Naïve-like pluripotency to pave the way for saving the northern white rhinoceros from extinction

Scientific reports, 2022-03, Vol.12 (1), p.3100-3100, Article 3100

2022

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Microfluidic Single-Cell Analysis of Transplanted Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes After Acute Myocardial Infarction

Circulation (New York, N.Y.), 2015-08, Vol.132 (8), p.762-771

2015

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Generation of two mother–child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations

Stem cell research, 2023-03, Vol.67, p.103030-103030, Article 103030

2023

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The ART of bringing extinction to a freeze – History and future of species conservation, exemplified by rhinos

Theriogenology, 2021-07, Vol.169, p.76-88

2021

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Transplanted terminally differentiated induced pluripotent stem cells are accepted by immune mechanisms similar to self-tolerance

Nature communications, 2014-05, Vol.5 (1), p.3903-3903, Article 3903

2014

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Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome

Kidney international, 2020-07, Vol.98 (1), p.159-167

2020

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Cores laboratories: Organization for stem cell technology advancement

Stem cell research, 2021-05, Vol.53, p.102266-102266, Article 102266

2021

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Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor

Stem cell research, 2020-10, Vol.48, p.101998-101998, Article 101998

2020

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Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells

Nature communications, 2023-12, Vol.14 (1), p.8043-8043, Article 8043

2023

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Generation of three age and gender matched pairs of human induced pluripotent stem cells derived from myoblasts (MDCi011-A, MDCi012-A, MDCi013-A) and from peripheral blood mononuclear cells (MDCi011-B, MDCi012-B, MDCi013-B) from the same donor

Stem cell research, 2020-10, Vol.48, p.101987-101987, Article 101987

2020

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Generation of an induced pluripotent stem cell line from a Huntington’s disease patient with a long HTT-PolyQ sequence

Stem cell research, 2023-04, Vol.68, p.103056-103056, Article 103056

2023

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ASSURED-optimized CRISPR protocol for knockout/SNP knockin in hiPSCs

STAR protocols, 2023-09, Vol.4 (3), p.102406-102406, Article 102406

2023

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Generation of an NCS1 gene knockout human induced pluripotent stem cell line using CRISPR/Cas9

Stem cell research, 2023-12, Vol.73, p.103253-103253, Article 103253

2023

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Chemically defined generation of human cardiomyocytes

E-cadherin is crucial for embryonic stem cell pluripotency and can replace OCT4 during somatic cell reprogramming

Drug Screening Using a Library of Human Induced Pluripotent Stem Cell―Derived Cardiomyocytes Reveals Disease-Specific Patterns of Cardiotoxicity

Activation of PDGF pathway links LMNA mutation to dilated cardiomyopathy

Mutations in Disordered Regions Can Cause Disease by Creating Dileucine Motifs

Embryos and embryonic stem cells from the white rhinoceros

A Comprehensive TALEN-Based Knockout Library for Generating Human-Induced Pluripotent Stem Cell–Based Models for Cardiovascular Diseases

The centrosomal protein 83 (CEP83) regulates human pluripotent stem cell differentiation toward the kidney lineage

FACT Sets a Barrier for Cell Fate Reprogramming in Caenorhabditis elegans and Human Cells

iPSC-derived reactive astrocytes from patients with multiple sclerosis protect cocultured neurons in inflammatory conditions

The Role of SIRT6 Protein in Aging and Reprogramming of Human Induced Pluripotent Stem Cells

Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes as an In Vitro Model for Coxsackievirus B3–Induced Myocarditis and Antiviral Drug Screening Platform

Naïve-like pluripotency to pave the way for saving the northern white rhinoceros from extinction

Microfluidic Single-Cell Analysis of Transplanted Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes After Acute Myocardial Infarction

Generation of two mother–child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations

The ART of bringing extinction to a freeze – History and future of species conservation, exemplified by rhinos

Transplanted terminally differentiated induced pluripotent stem cells are accepted by immune mechanisms similar to self-tolerance

Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome

Cores laboratories: Organization for stem cell technology advancement

Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor

Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells

Generation of three age and gender matched pairs of human induced pluripotent stem cells derived from myoblasts (MDCi011-A, MDCi012-A, MDCi013-A) and from peripheral blood mononuclear cells (MDCi011-B, MDCi012-B, MDCi013-B) from the same donor

Generation of an induced pluripotent stem cell line from a Huntington’s disease patient with a long HTT-PolyQ sequence

ASSURED-optimized CRISPR protocol for knockout/SNP knockin in hiPSCs

Generation of an NCS1 gene knockout human induced pluripotent stem cell line using CRISPR/Cas9

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