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Nesprin-1 mutations in human and murine cardiomyopathy

Journal of molecular and cellular cardiology, 2010-04, Vol.48 (4), p.600-608

2010

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Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates

eLife, 2016-12, Vol.5

2016

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Lunatic fringe-mediated Notch signaling regulates adult hippocampal neural stem cell maintenance

eLife, 2017-07, Vol.6

2017

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Eya4-deficient mice are a model for heritable otitis media

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

2008

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Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide

Human molecular genetics, 2017-09, Vol.26 (18), p.3482-3494

2017

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Hearing differences in Hartley guinea pig stocks from two breeders

Hearing research, 2019-08, Vol.379, p.69-78

2019

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Antisense oligonucleotides delivered to the amniotic cavity in utero modulate gene expression in the postnatal mouse

Nucleic acids research, 2016-11, Vol.44 (20), p.9519

2016

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Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss

Nature genetics, 2005-04, Vol.37 (4), p.418-422

2005

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Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment

Journal of the Association for Research in Otolaryngology, 2018-02, Vol.19 (1), p.1-16

2018

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Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations

Human molecular genetics, 2015-08, Vol.24 (15), p.4284-4295

2015

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Antisense oligonucleotide therapy rescues disruptions in organization of exploratory movements associated with Usher syndrome type 1C in mice

Behavioural brain research, 2018-02, Vol.338, p.76-87

2018

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Gene expression, chromosome position and lamin A/C mutations

Nucleus (Austin, Tex.), 2011-05, Vol.2 (3), p.162-167

2011

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Sex Genotyping of Archival Fixed and Immunolabeled Guinea Pig Cochleas

Scientific reports, 2018-03, Vol.8 (1), p.5156-7, Article 5156

2018

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Ca²⁺ dysregulation in Ryr1I⁴⁸⁹⁵T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (51), p.21813-21818

2009

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Statins protect mice from high-decibel noise-induced hearing loss

Biomedicine & pharmacotherapy, 2023-07, Vol.163, p.114674-114674, Article 114674

2023

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Ryr1I⁴⁸⁹⁵T mutation abolishes Ca²⁺ release channel function and delays development in homozygous offspring of a mutant mouse line

Proceedings of the National Academy of Sciences - PNAS, 2007-11, Vol.104 (47), p.18537-18542

2007

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Ca²⁺ dysregulation in$Ryr1^{14895T/wt} $Mice Causes Congenital Myopathy with Progressive Formation of Minicores, Cores, and Nemaline Rods

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (51), p.21813-21818

2009

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An$Ryr1^{I4895T}$Mutation Abolishes Ca²⁺ Release Channel Function and Delays Development in Homozygous Offspring of a Mutant Mouse Line

Proceedings of the National Academy of Sciences - PNAS, 2007-11, Vol.104 (47), p.18537-18542

2007

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Ca^sup 2+^ dysregulation in Ryr1^sup I4895T/wt^ mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (51), p.21813

2009

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Ca 2+ dysregulation in Ryr1 I4895T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Proceedings of the National Academy of Sciences - PNAS, 2009-12, Vol.106 (51), p.21813-21818

2009

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Ca super(2+) dysregulation in Ryr1 super(I)4895T/wtmice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Proceedings of the National Academy of Sciences - PNAS, 2009-01, Vol.106 (51), p.21813-21818

2009

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Gene expression, chromosome position and lamin A/C mutations

Nucleus (Austin, Tex.), 2011-05, Vol.2 (3), p.162-167

2011

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An Ryr1^sup I4895T^ mutation abolishes Ca^sup 2+^ release channel function and delays development in homozygous offspring of a mutant mouse line

Proceedings of the National Academy of Sciences - PNAS, 2007-11, Vol.104 (47), p.18537

2007

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An Ryr1 I4895T mutation abolishes Ca 2+ release channel function and delays development in homozygous offspring of a mutant mouse line

Proceedings of the National Academy of Sciences - PNAS, 2007-11, Vol.104 (47), p.18537-18542

2007

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An Ryr1 super(I4895T) mutation abolishes Ca super(2+) release channel function and delays development in homozygous offspring of a mutant mouse line

Proceedings of the National Academy of Sciences - PNAS, 2007-11, Vol.104 (47), p.18537-18542

2007

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Nesprin-1 mutations in human and murine cardiomyopathy

Fine-tuning of Notch signaling sets the boundary of the organ of Corti and establishes sensory cell fates

Lunatic fringe-mediated Notch signaling regulates adult hippocampal neural stem cell maintenance

Eya4-deficient mice are a model for heritable otitis media

Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide

Hearing differences in Hartley guinea pig stocks from two breeders

Antisense oligonucleotides delivered to the amniotic cavity in utero modulate gene expression in the postnatal mouse

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss

Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment

Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations

Antisense oligonucleotide therapy rescues disruptions in organization of exploratory movements associated with Usher syndrome type 1C in mice

Gene expression, chromosome position and lamin A/C mutations

Sex Genotyping of Archival Fixed and Immunolabeled Guinea Pig Cochleas

Ca²⁺ dysregulation in Ryr1I⁴⁸⁹⁵T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Statins protect mice from high-decibel noise-induced hearing loss

Ryr1I⁴⁸⁹⁵T mutation abolishes Ca²⁺ release channel function and delays development in homozygous offspring of a mutant mouse line

Ca²⁺ dysregulation in$Ryr1^{14895T/wt} $Mice Causes Congenital Myopathy with Progressive Formation of Minicores, Cores, and Nemaline Rods

An$Ryr1^{I4895T}$Mutation Abolishes Ca²⁺ Release Channel Function and Delays Development in Homozygous Offspring of a Mutant Mouse Line

Ca^sup 2+^ dysregulation in Ryr1^sup I4895T/wt^ mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Ca 2+ dysregulation in Ryr1 I4895T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Ca super(2+) dysregulation in Ryr1 super(I)4895T/wtmice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Gene expression, chromosome position and lamin A/C mutations

An Ryr1^sup I4895T^ mutation abolishes Ca^sup 2+^ release channel function and delays development in homozygous offspring of a mutant mouse line

An Ryr1 I4895T mutation abolishes Ca 2+ release channel function and delays development in homozygous offspring of a mutant mouse line

An Ryr1 super(I4895T) mutation abolishes Ca super(2+) release channel function and delays development in homozygous offspring of a mutant mouse line

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