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Derivation of Airway Basal Stem Cells from Human Pluripotent Stem Cells

Cell stem cell, 2021-01, Vol.28 (1), p.79-95.e8

2021

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Proximity ligation assay to detect DUX4 protein in FSHD1 muscle: a pilot study

BMC research notes, 2022-05, Vol.15 (1), p.163-163, Article 163

2022

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A multimodal iPSC platform for cystic fibrosis drug testing

Nature communications, 2022-07, Vol.13 (1), p.4270-4270, Article 4270

2022

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Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Human molecular genetics, 2012-10, Vol.21 (20), p.4419-4430

2012

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Myogenic Enhancers Regulate Expression of the Facioscapulohumeral Muscular Dystrophy-Associated DUX4 Gene

Molecular and cellular biology, 2014-06, Vol.34 (11), p.1942-1955

2014

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Pathology is alleviated by doxycycline in a laminin-α2-null model of congenital muscular dystrophy

Annals of neurology, 2009-01, Vol.65 (1), p.47-56

2009

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Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy

Human molecular genetics, 2011-07, Vol.20 (13), p.2662-2672

2011

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Expression of FSHD‐related DUX4‐FL alters proteostasis and induces TDP‐43 aggregation

Annals of clinical and translational neurology, 2015-02, Vol.2 (2), p.151-166

2015

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Differentiation of human pluripotent stem cells into functional airway basal stem cells

STAR protocols, 2021-09, Vol.2 (3), p.100683-100683, Article 100683

2021

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Functional domains of the FSHD-associated DUX4 protein

Biology open, 2018, Vol.7 (4), p.bio033977-bio033977

2018

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Prdm1 (Blimp-1) and the expression of fast and slow myosin heavy chain isoforms during avian myogenesis in vitro

PloS one, 2010-04, Vol.5 (4), p.e9951-e9951

2010

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Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4

Skeletal muscle, 2016-12, Vol.6 (1), p.42-42, Article 42

2016

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Airway Disease Modeling with Gene-edited Human Basal Cell Transplantation

American journal of respiratory and critical care medicine, 2024-11

2024

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Airway stem cell reconstitution by the transplantation of primary or pluripotent stem cell-derived basal cells

Cell stem cell, 2023-09, Vol.30 (9), p.1199-1216.e7

2023

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De Novo Generation of Pulmonary Ionocytes from Normal and Cystic Fibrosis Human Induced Pluripotent Stem Cells

American journal of respiratory and critical care medicine, 2023-05, Vol.207 (9), p.1249-1253

2023

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Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Human molecular genetics, 2012-10, Vol.21 (20), p.4419-4430

2012

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Human airway lineages derived from pluripotent stem cells reveal the epithelial responses to SARS-CoV-2 infection

American journal of physiology. Lung cellular and molecular physiology, 2022-03, Vol.322 (3), p.L462-L478

2022

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Generation of Airway Epithelial Cell Air-Liquid Interface Cultures from Human Pluripotent Stem Cells

Journal of visualized experiments, 2022-06 (184)

2022

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Generation of Airway Epithelial Cell Air-Liquid Interface Cultures from Human Pluripotent Stem Cells

Journal of visualized experiments, 2022-06 (184)

2022

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Pathology is alleviated by doxycycline in a laminin- alpha 2-null model of congenital muscular dystrophy

Annals of neurology, 2009-01, Vol.65 (1), p.47-56

2009

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Efficient system for upstream mRNA trans-splicing to generate covalent, head-to-tail, protein multimers

Scientific reports, 2019-02, Vol.9 (1), p.2274-2274, Article 2274

2019

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Transcriptional analysis of primary ciliary dyskinesia airway cells reveals a dedicated cilia glutathione pathway

JCI insight, 2024-07, Vol.9 (17)

2024

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Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

Clinical epigenetics, 2015-03, Vol.7 (1), p.37-37, Article 37

2015

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A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function

European journal of human genetics : EJHG, 2012-04, Vol.20 (4), p.404-410

2012

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SARS-CoV-2 Infection of Pluripotent Stem Cell-Derived Human Lung Alveolar Type 2 Cells Elicits a Rapid Epithelial-Intrinsic Inflammatory Response

Derivation of Airway Basal Stem Cells from Human Pluripotent Stem Cells

Proximity ligation assay to detect DUX4 protein in FSHD1 muscle: a pilot study

A multimodal iPSC platform for cystic fibrosis drug testing

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Myogenic Enhancers Regulate Expression of the Facioscapulohumeral Muscular Dystrophy-Associated DUX4 Gene

Pathology is alleviated by doxycycline in a laminin-α2-null model of congenital muscular dystrophy

Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy

Expression of FSHD‐related DUX4‐FL alters proteostasis and induces TDP‐43 aggregation

Differentiation of human pluripotent stem cells into functional airway basal stem cells

Functional domains of the FSHD-associated DUX4 protein

Prdm1 (Blimp-1) and the expression of fast and slow myosin heavy chain isoforms during avian myogenesis in vitro

Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4

Airway Disease Modeling with Gene-edited Human Basal Cell Transplantation

Airway stem cell reconstitution by the transplantation of primary or pluripotent stem cell-derived basal cells

De Novo Generation of Pulmonary Ionocytes from Normal and Cystic Fibrosis Human Induced Pluripotent Stem Cells

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Human airway lineages derived from pluripotent stem cells reveal the epithelial responses to SARS-CoV-2 infection

Generation of Airway Epithelial Cell Air-Liquid Interface Cultures from Human Pluripotent Stem Cells

Generation of Airway Epithelial Cell Air-Liquid Interface Cultures from Human Pluripotent Stem Cells

Pathology is alleviated by doxycycline in a laminin- alpha 2-null model of congenital muscular dystrophy

Efficient system for upstream mRNA trans-splicing to generate covalent, head-to-tail, protein multimers

Transcriptional analysis of primary ciliary dyskinesia airway cells reveals a dedicated cilia glutathione pathway

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function

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