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Site-Specific Genome Engineering in Human Pluripotent Stem Cells

International Journal of Molecular Sciences, 2016-07, Vol.17 (7), p.1000-1000

2016

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Generation of Induced Pluripotent Stem Cells from Human Cord Blood

Cell stem cell, 2009-10, Vol.5 (4), p.434-441

2009

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Targeted genome engineering using designer nucleases: State of the art and practical guidance for application in human pluripotent stem cells

Stem cell research, 2016-03, Vol.16 (2), p.377-386

2016

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Reprogramming triggers endogenous L1 and Alu retrotransposition in human induced pluripotent stem cells

Nature communications, 2016-01, Vol.7 (1), p.10286-14, Article 10286

2016

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Congenital deficiency reveals critical role of ISG15 in skin homeostasis

The Journal of clinical investigation, 2022-02, Vol.132 (3), p.1-19

2022

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Generation of two human NRF2 knockout iPSC clones using CRISPR/Cas9 editing

Stem cell research, 2023-06, Vol.69, p.103090-103090, Article 103090

2023

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A 3D iPSC-differentiation model identifies interleukin-3 as a regulator of early human hematopoietic specification

Haematologica (Roma), 2021-05, Vol.106 (5), p.1354-1367

2021

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Gene correction of human induced pluripotent stem cells repairs the cellular phenotype in pulmonary alveolar proteinosis

American journal of respiratory and critical care medicine, 2014-01, Vol.189 (2), p.167-182

2014

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Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC line

Stem cell research, 2022-10, Vol.64, p.102918-102918, Article 102918

2022

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Continuous WNT Control Enables Advanced hPSC Cardiac Processing and Prognostic Surface Marker Identification in Chemically Defined Suspension Culture

Stem cell reports, 2019-08, Vol.13 (2), p.366-379

2019

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Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN

Stem cell research, 2017-08, Vol.23 (C), p.95-97

2017

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High-Throughput Screening for Modulators of CFTR Activity Based on Genetically Engineered Cystic Fibrosis Disease-Specific iPSCs

Stem cell reports, 2019-06, Vol.12 (6), p.1389-1403

2019

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Generation of pulmonary arterial hypertension patient-specific induced pluripotent stem cell lines from three unrelated patients with a heterozygous missense mutation in exon 12, a heterozygous in-frame deletion in exon 3 and a missense mutation in exon 11 of the BMPR2 gene

Stem cell research, 2021-08, Vol.55, p.102488-102488, Article 102488

2021

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Generation of a NKX2.1 knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-2)

Stem cell research, 2019-08, Vol.39, p.101492-101492, Article 101492

2019

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Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis

Stem cell research, 2020-03, Vol.43, p.101713-101713, Article 101713

2020

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Generation of an induced pluripotent stem cell line (MHHi018-A) from a patient with Cystic Fibrosis carrying p.Asn1303Lys (N1303K) mutation

Stem cell research, 2020-04, Vol.44, p.101744-101744, Article 101744

2020

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Generation of human induced pluripotent stem cell lines encoding for genetically encoded calcium indicators RCaMP1h and GCaMP6f

Stem cell research, 2022-04, Vol.60, p.102697-102697, Article 102697

2022

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Generation of a NKX2.1 – p63 double transgenic knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-4)

Stem cell research, 2020-01, Vol.42, p.101659-101659, Article 101659

2020

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Long term expansion of undifferentiated human iPS and ES cells in suspension culture using a defined medium

Stem cell research, 2010-07, Vol.5 (1), p.51-64

2010

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ISG15 deficiency features a complex cellular phenotype that responds to treatment with itaconate and derivatives

Clinical and translational medicine, 2022-07, Vol.12 (7), p.e931-n/a

2022

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An Improved Protocol for Targeted Differentiation of Primed Human Induced Pluripotent Stem Cells into HLA-G-Expressing Trophoblasts to Enable the Modeling of Placenta-Related Disorders

Cells (Basel, Switzerland), 2023-08, Vol.12 (16), p.2070

2023

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Generation of three induced pluripotent stem cell lines (MHHi012-A, MHHi013-A, MHHi014-A) from a family with Loeys-Dietz syndrome carrying a heterozygous p.M253I (c.759G>A) mutation in the TGFBR1 gene

Stem cell research, 2020-03, Vol.43, p.101707-101707, Article 101707

2020

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Author Correction: Reprogramming triggers endogenous L1 and Alu retrotransposition in human induced pluripotent stem cells

Nature communications, 2018-12, Vol.9 (1), p.5398-1, Article 5398

2018

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Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages

Stem cell reports, 2018-01, Vol.10 (1), p.7-16

2018

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Generation of a human CDX2 knock-in reporter iPSC line (MHHi007-A-1) to model human trophoblast differentiation

Stem cell research, 2018-07, Vol.30, p.117-121

2018

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Site-Specific Genome Engineering in Human Pluripotent Stem Cells

Generation of Induced Pluripotent Stem Cells from Human Cord Blood

Targeted genome engineering using designer nucleases: State of the art and practical guidance for application in human pluripotent stem cells

Reprogramming triggers endogenous L1 and Alu retrotransposition in human induced pluripotent stem cells

Congenital deficiency reveals critical role of ISG15 in skin homeostasis

Generation of two human NRF2 knockout iPSC clones using CRISPR/Cas9 editing

A 3D iPSC-differentiation model identifies interleukin-3 as a regulator of early human hematopoietic specification

Gene correction of human induced pluripotent stem cells repairs the cellular phenotype in pulmonary alveolar proteinosis

Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC line

Continuous WNT Control Enables Advanced hPSC Cardiac Processing and Prognostic Surface Marker Identification in Chemically Defined Suspension Culture

Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN

High-Throughput Screening for Modulators of CFTR Activity Based on Genetically Engineered Cystic Fibrosis Disease-Specific iPSCs

Generation of pulmonary arterial hypertension patient-specific induced pluripotent stem cell lines from three unrelated patients with a heterozygous missense mutation in exon 12, a heterozygous in-frame deletion in exon 3 and a missense mutation in exon 11 of the BMPR2 gene

Generation of a NKX2.1 knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-2)

Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis

Generation of an induced pluripotent stem cell line (MHHi018-A) from a patient with Cystic Fibrosis carrying p.Asn1303Lys (N1303K) mutation

Generation of human induced pluripotent stem cell lines encoding for genetically encoded calcium indicators RCaMP1h and GCaMP6f

Generation of a NKX2.1 – p63 double transgenic knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-4)

Long term expansion of undifferentiated human iPS and ES cells in suspension culture using a defined medium

ISG15 deficiency features a complex cellular phenotype that responds to treatment with itaconate and derivatives

An Improved Protocol for Targeted Differentiation of Primed Human Induced Pluripotent Stem Cells into HLA-G-Expressing Trophoblasts to Enable the Modeling of Placenta-Related Disorders

Generation of three induced pluripotent stem cell lines (MHHi012-A, MHHi013-A, MHHi014-A) from a family with Loeys-Dietz syndrome carrying a heterozygous p.M253I (c.759G>A) mutation in the TGFBR1 gene

Author Correction: Reprogramming triggers endogenous L1 and Alu retrotransposition in human induced pluripotent stem cells

Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages

Generation of a human CDX2 knock-in reporter iPSC line (MHHi007-A-1) to model human trophoblast differentiation

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