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Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and backscattered electron imaging

Journal of bone and mineral research, 2012-04, Vol.27 (4), p.876-890

2012

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Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function

EMBO molecular medicine, 2019-09, Vol.11 (9), p.e10288-n/a

2019

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International Mouse Phenotyping Consortium: past and future perspectives on mouse phenotyping

Mammalian genome, 2012-10, Vol.23 (9-10), p.632-640

2012

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Novel Mouse Model of Autosomal Semidominant Adult Hypophosphatasia Has a Splice Site Mutation in the Tissue Nonspecific Alkaline Phosphatase Gene Akp2

Journal of bone and mineral research, 2007-09, Vol.22 (9), p.1397-1407

2007

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IGF-1 receptor antagonism inhibits autophagy

Human molecular genetics, 2013-11, Vol.22 (22), p.4528-4544

2013

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Cellular content plays a crucial role in Non‐typeable Haemophilus influenzae infection of preinflamed Junbo mouse middle ear

Cellular microbiology, 2019-01, Vol.21 (1), p.e12960-n/a

2019

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Otitis media in the Tgif knockout mouse implicates TGF[beta] signalling in chronic middle ear inflammatory disease

Human molecular genetics, 2013-07, Vol.22 (13), p.2553-2565

2013

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Quiet as a mouse: dissecting the molecular and genetic basis of hearing

Nature reviews. Genetics, 2008-04, Vol.9 (4), p.277-290

2008

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ENU mutagenesis, a way forward to understand gene function

Annual review of genomics and human genetics, 2008-01, Vol.9 (1), p.49-69

2008

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Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway

PloS one, 2016-12, Vol.11 (12), p.e0167916

2016

Volltextzugriff (PDF)

Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity

The Journal of biological chemistry, 2011-01, Vol.286 (1), p.192-198

2011

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The functional annotation of mammalian genomes: the challenge of phenotyping

Annual review of genetics, 2009-12, Vol.43 (1), p.305-333

2009

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HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants

PLoS genetics, 2011-10, Vol.7 (10), p.e1002336-e1002336

2011

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Unraveling the genetics of otitis media: from mouse to human and back again

Mammalian genome, 2011-02, Vol.22 (1-2), p.66-82

2011

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Gelsolin plays a role in the actin polymerization complex of hair cell stereocilia

PloS one, 2010-07, Vol.5 (7), p.e11627-e11627

2010

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Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations

PLoS genetics, 2013-01, Vol.9 (1), p.e1003219

2013

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Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition

Nature communications, 2013-11, Vol.4 (1), p.2816, Article 2816

2013

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EVI1 acts as an inducible negative-feedback regulator of NF-κB by inhibiting p65 acetylation

The Journal of immunology (1950), 2012-06, Vol.188 (12), p.6371-6380

2012

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Understanding mammalian genetic systems: the challenge of phenotyping in the mouse

PLoS genetics, 2006-08, Vol.2 (8), p.e118

2006

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Ikzf2/helios is a key transcriptional regulator of outer hair cell maturation

Nature (London), 2018-11, Vol.563 (7733), p.696-700

2018

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Whirlin Complexes with p55 at the Stereocilia Tip during Hair Cell Development

Proceedings of the National Academy of Sciences - PNAS, 2006-07, Vol.103 (29), p.10973-10978

2006

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A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse

Human molecular genetics, 2006-11, Vol.15 (22), p.3273-3279

2006

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Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media

PLoS genetics, 2006-10, Vol.2 (10), p.e149-e149

2006

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Genetic analysis of the mouse brain proteome

Nature genetics, 2002-04, Vol.30 (4), p.385-393

2002

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Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and backscattered electron imaging

Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function

International Mouse Phenotyping Consortium: past and future perspectives on mouse phenotyping

Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing

Novel Mouse Model of Autosomal Semidominant Adult Hypophosphatasia Has a Splice Site Mutation in the Tissue Nonspecific Alkaline Phosphatase Gene Akp2

IGF-1 receptor antagonism inhibits autophagy

Cellular content plays a crucial role in Non‐typeable Haemophilus influenzae infection of preinflamed Junbo mouse middle ear

Otitis media in the Tgif knockout mouse implicates TGF[beta] signalling in chronic middle ear inflammatory disease

Quiet as a mouse: dissecting the molecular and genetic basis of hearing

ENU mutagenesis, a way forward to understand gene function

Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway

Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity

The functional annotation of mammalian genomes: the challenge of phenotyping

HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants

Unraveling the genetics of otitis media: from mouse to human and back again

Gelsolin plays a role in the actin polymerization complex of hair cell stereocilia

Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations

Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition

EVI1 acts as an inducible negative-feedback regulator of NF-κB by inhibiting p65 acetylation

Understanding mammalian genetic systems: the challenge of phenotyping in the mouse

Ikzf2/helios is a key transcriptional regulator of outer hair cell maturation

Whirlin Complexes with p55 at the Stereocilia Tip during Hair Cell Development

A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse

Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media

Genetic analysis of the mouse brain proteome

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