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Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice

Nature medicine, 2023-02, Vol.29 (2), p.412-421

2023

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Impaired lymphatic contraction associated with immunosuppression

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.18784-18789

2011

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Regulation of tendon differentiation by scleraxis distinguishes force-transmitting tendons from muscle-anchoring tendons

Development (Cambridge), 2007-07, Vol.134 (14), p.2697-2708

2007

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Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome-associated PTPN11 mutation

The Journal of clinical investigation, 2011-03, Vol.121 (3), p.1026-1043

2011

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Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model

Proceedings of the National Academy of Sciences - PNAS, 2022-07, Vol.119 (28), p.e2204174119-e2204174119

2022

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Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia

The Journal of clinical investigation, 2007-07, Vol.117 (7), p.1814-1823

2007

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Wnt9a signaling is required for joint integrity and regulation of Ihh during chondrogenesis

Development (Cambridge), 2006-08, Vol.133 (15), p.3039-3049

2006

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Surfactant protein-C chromatin-bound green fluorescence protein reporter mice reveal heterogeneity of surfactant protein C-expressing lung cells

American journal of respiratory cell and molecular biology, 2013-03, Vol.48 (3), p.288-298

2013

Volltextzugriff (PDF)

β-Arrestin 1 and 2 Differentially Regulate Heptahelical Receptor Signaling and Trafficking

Proceedings of the National Academy of Sciences - PNAS, 2001-02, Vol.98 (4), p.1601-1606

2001

Volltextzugriff (PDF)

LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart

Journal of the American Heart Association, 2021-09, Vol.10 (17), p.e018829-e018829

2021

Volltextzugriff (PDF)

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease

Journal of molecular and cellular cardiology, 2008-02, Vol.44 (2), p.293-303

2008

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5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy

The Journal of clinical investigation, 2014-03, Vol.124 (3), p.1364-1370

2014

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Increased NMDA current and spine density in mice lacking the NMDA receptor subunit NR3A

Nature (London), 1998-05, Vol.393 (6683), p.377-381

1998

Volltextzugriff (PDF)

Select G-Protein-Coupled Receptors Modulate Agonist-Induced Signaling via a ROCK, LIMK, and β-Arrestin 1 Pathway

Cell reports (Cambridge), 2013-11, Vol.5 (4), p.1010-1021

2013

Volltextzugriff (PDF)

The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy

PloS one, 2008-07, Vol.3 (7), p.e2642-e2642

2008

Volltextzugriff (PDF)

Cardiac Myosin Missense Mutations Cause Dilated Cardiomyopathy in Mouse Models and Depress Molecular Motor Function

Proceedings of the National Academy of Sciences - PNAS, 2006-09, Vol.103 (39), p.14525-14530

2006

Volltextzugriff (PDF)

Eya4-deficient mice are a model for heritable otitis media

The Journal of clinical investigation, 2008-02, Vol.118 (2), p.651-658

2008

Volltextzugriff (PDF)

A Mouse Model of Familial Hypertrophic Cardiomyopathy

Science (American Association for the Advancement of Science), 1996-05, Vol.272 (5262), p.731-734

1996

Volltextzugriff (PDF)

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Nature genetics, 1995-12, Vol.11 (4), p.389-394

1995

Volltextzugriff (PDF)

Glucose Transporter-1-Deficient Mice Exhibit Impaired Development and Deformities That Are Similar to Diabetic Embryopathy

Proceedings of the National Academy of Sciences - PNAS, 2003-12, Vol.100 (26), p.15613-15618

2003

Volltextzugriff (PDF)

beta-Arrestin1 Knockout Mice Appear Normal but Demonstrate Altered Cardiac Responses to beta-Adrenergic Stimulation

Circulation research, 1997-12, Vol.81 (6), p.1021-1026

1997

Volltextzugriff (PDF)

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice

The Journal of clinical investigation, 1999-11, Vol.104 (9), p.1235-1244

1999

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Comparison of Two Murine Models of Familial Hypertrophic Cardiomyopathy

Circulation research, 2001-03, Vol.88 (4), p.383-389

2001

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Cardiomyopathy in Irx4-Deficient Mice Is Preceded by Abnormal Ventricular Gene Expression

Molecular and Cellular Biology, 2001-03, Vol.21 (5), p.1730-1736

2001

Volltextzugriff (PDF)

Targeted Ablation of the Murine alpha-Tropomyosin Gene

Circulation research, 1997-12, Vol.81 (6), p.1005-1010

1997

Volltextzugriff (PDF)

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Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice

Impaired lymphatic contraction associated with immunosuppression

Regulation of tendon differentiation by scleraxis distinguishes force-transmitting tendons from muscle-anchoring tendons

Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome-associated PTPN11 mutation

Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model

Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia

Wnt9a signaling is required for joint integrity and regulation of Ihh during chondrogenesis

Surfactant protein-C chromatin-bound green fluorescence protein reporter mice reveal heterogeneity of surfactant protein C-expressing lung cells

β-Arrestin 1 and 2 Differentially Regulate Heptahelical Receptor Signaling and Trafficking

LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease

5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy

Increased NMDA current and spine density in mice lacking the NMDA receptor subunit NR3A

Select G-Protein-Coupled Receptors Modulate Agonist-Induced Signaling via a ROCK, LIMK, and β-Arrestin 1 Pathway

The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy

Cardiac Myosin Missense Mutations Cause Dilated Cardiomyopathy in Mouse Models and Depress Molecular Motor Function

Eya4-deficient mice are a model for heritable otitis media

A Mouse Model of Familial Hypertrophic Cardiomyopathy

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Glucose Transporter-1-Deficient Mice Exhibit Impaired Development and Deformities That Are Similar to Diabetic Embryopathy

beta-Arrestin1 Knockout Mice Appear Normal but Demonstrate Altered Cardiac Responses to beta-Adrenergic Stimulation

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice

Comparison of Two Murine Models of Familial Hypertrophic Cardiomyopathy

Cardiomyopathy in Irx4-Deficient Mice Is Preceded by Abnormal Ventricular Gene Expression

Targeted Ablation of the Murine alpha-Tropomyosin Gene

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