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Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia

PloS one, 2012-04, Vol.7 (4), p.e36074-e36074

2012

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Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

Nature, 2006-09, Vol.443 (7107), p.50-55

2006

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The harlequin mouse mutation downregulates apoptosis-inducing factor

Nature (London), 2002-09, Vol.419 (6905), p.367-374

2002

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The Chloride Intracellular Channel Protein CLIC5 Is Expressed at High Levels in Hair Cell Stereocilia and Is Essential for Normal Inner Ear Function

The Journal of neuroscience, 2006-10, Vol.26 (40), p.10188-10198

2006

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A Missense Mutation in the Previously Undescribed Gene Tmhs Underlies Deafness in Hurry-Scurry (hscy) Mice

Proceedings of the National Academy of Sciences - PNAS, 2005-05, Vol.102 (22), p.7894-7899

2005

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Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice

Hearing research, 2012-01, Vol.283 (1-2), p.80-88

2012

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Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation

Mammalian genome, 2007-09, Vol.18 (9), p.646-656

2007

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Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice

Genetics (Austin), 2018-03, Vol.208 (3), p.1165-1179

2018

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The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice

The Journal of neuroscience, 2010-07, Vol.30 (29), p.9683-9694

2010

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A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice

Mammalian genome, 2015-08, Vol.26 (7-8), p.338-347

2015

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Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice

The Journal of clinical investigation, 2008-03, Vol.118 (3), p.1176-1185

2008

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Hearing Impairment in Hypothyroid Dwarf Mice Caused by Mutations of the Thyroid Peroxidase Gene

Journal of the Association for Research in Otolaryngology, 2014-02, Vol.15 (1), p.45-55

2014

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Deletion in Catna2 , encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Nature genetics, 2002-07, Vol.31 (3), p.279-284

2002

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Genetic and Physical Mapping of the Cerebellar Deficient Folia (cdf) Locus on Mouse Chromosome 6

Genomics (San Diego, Calif.), 2000-10, Vol.69 (1), p.135-138

2000

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The harlequin mouse mutation down-regulates apoptosis-inducing factor

Nature (London), 2002-09, Vol.419 (6905), p.367-374

2002

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Mutations of the Mouse ELMO Domain Containing 1 Gene

PloS one, 2012-04, Vol.7 (4), p.e36074

2012

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Mutation of the Cyba gene encoding p22^sup phox^ causes vestibular and immune defects in mice

The Journal of clinical investigation, 2008-03, Vol.118 (3), p.1176

2008

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Mutation of the Cyba gene encoding [p22.sup.phox] causes vestibular and immune defects in mice

The Journal of clinical investigation, 2008-03, Vol.118 (3), p.1176

2008

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Deletion in Catna2, encoding aN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Nature genetics, 2002-07, Vol.31 (3), p.279-284

2002

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Deletion in Catna2, encoding [alpha]N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Nature genetics, 2002-07, Vol.31 (3), p.279

2002

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Performance of glomerular filtration rate estimation equations in Congolese healthy adults: The inopportunity of the ethnic correction

PloS one, 2018-03, Vol.13 (3), p.e0193384-e0193384

2018

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Early-life antibiotic use and risk of asthma and eczema: results of a discordant twin study

The European respiratory journal, 2020-04, Vol.55 (4), p.1902021

2020

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NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

Human molecular genetics, 2011-02, Vol.20 (3), p.482-496

2011

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Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts

Human molecular genetics, 2017-10, Vol.26 (19), p.3722-3735

2017

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Albuminuria, serum antioxidant enzyme levels and markers of hemolysis and inflammation in steady state children with sickle cell anemia

BMC nephrology, 2016-11, Vol.17 (1), p.178-178, Article 178

2016

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Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia

Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

The harlequin mouse mutation downregulates apoptosis-inducing factor

The Chloride Intracellular Channel Protein CLIC5 Is Expressed at High Levels in Hair Cell Stereocilia and Is Essential for Normal Inner Ear Function

A Missense Mutation in the Previously Undescribed Gene Tmhs Underlies Deafness in Hurry-Scurry (hscy) Mice

Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice

Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation

Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice

The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice

A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice

Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice

Hearing Impairment in Hypothyroid Dwarf Mice Caused by Mutations of the Thyroid Peroxidase Gene

Deletion in Catna2 , encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Genetic and Physical Mapping of the Cerebellar Deficient Folia (cdf) Locus on Mouse Chromosome 6

The harlequin mouse mutation down-regulates apoptosis-inducing factor

Mutations of the Mouse ELMO Domain Containing 1 Gene

Mutation of the Cyba gene encoding p22^sup phox^ causes vestibular and immune defects in mice

Mutation of the Cyba gene encoding [p22.sup.phox] causes vestibular and immune defects in mice

Deletion in Catna2, encoding aN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Deletion in Catna2, encoding [alpha]N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Performance of glomerular filtration rate estimation equations in Congolese healthy adults: The inopportunity of the ethnic correction

Early-life antibiotic use and risk of asthma and eczema: results of a discordant twin study

NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts

Albuminuria, serum antioxidant enzyme levels and markers of hemolysis and inflammation in steady state children with sickle cell anemia

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