(Q37812277)

23 August 2017

title

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

1 reference

23 August 2017

1

0 references

David Burgner

4

0 references

Jenefer Blackwell

5

object named as

Jenefer M Blackwell

1 reference

23 August 2017

Mahmood F Bhutta

2

1 reference

23 August 2017

Michael T Cheeseman

3

1 reference

23 August 2017

Steve D M Brown

6

1 reference

23 August 2017

Sarra E Jamieson

7

1 reference

23 August 2017

publication date

25 November 2010

1 reference

23 August 2017

number of pages

17

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

23 August 2017

volume

22

1 reference

23 August 2017

issue

1-2

1 reference

23 August 2017

page(s)

66-82

1 reference

ENU mutagenesis, a way forward to understand gene function

23 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Toll-like receptor signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Evaluation of the polymorphism in the Toll-like receptor 4 (TLR4) genes of tympanosclerosis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Towards better mouse models: enhanced genotypes, systemic phenotyping and envirotype modelling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Epidemiology and pathogenesis of chronic suppurative otitis media: implications for prevention and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

EYA4, a novel vertebrate gene related to Drosophila eyes absent

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Systematic approaches to mouse mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

The functional annotation of mammalian genomes: the challenge of phenotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Chronic and recurrent otitis media: a genome scan for susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

E2f4 is required for normal development of the airway epithelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Identification of direct p73 target genes combining DNA microarray and chromatin immunoprecipitation analyses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Cytokine gene polymorphisms moderate illness severity in infants with respiratory syncytial virus infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Trends in large-scale mouse mutagenesis: from genetics to functional genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Otitis media in a mouse model for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Development of sensory, motor and behavioral deficits in the murine model of Sanfilippo syndrome type B

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Myeloid differentiation primary response gene 88 is required for the resolution of otitis media

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

E2F4 is essential for normal erythrocyte maturation and neonatal viability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Systematic analysis and nomenclature of mammalian F-box proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Transforming growth factor-beta -Smad signaling pathway cooperates with NF-kappa B to mediate nontypeable Haemophilus influenzae-induced MUC2 mucin transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Transforming Growth Factor-β-Smad Signaling Pathway Negatively Regulates Nontypeable Haemophilus influenzae-induced MUC5AC Mucin Transcription via Mitogen-activated Protein Kinase (MAPK) Phosphatase-1-dependent Inhibition of p38 MAPK

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

21 January 2018

Mouse ENU mutagenesis

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

HLA Frequency in Patients With Recurrent Acute Otitis Media

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Bacteriology of acute otitis media in a cohort of Finnish children followed for the first two years of life.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Overview on mouse mutagenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

The oncoprotein Evi-1 represses TGF-beta signalling by inhibiting Smad3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Distribution and heritability of recurrent ear infections.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

TLR4-mediated induction of TLR2 signaling is critical in the pathogenesis and resolution of otitis media.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

C3H/HeJ mouse model for spontaneous chronic otitis media

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Recognition of pneumolysin by Toll-like receptor 4 confers resistance to pneumococcal infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

A mouse model with postnatal endolymphatic hydrops and hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Molecular mechanisms of leukemogenesis by AML1/EVI-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Initial sequencing and comparative analysis of the mouse genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Role of mannose-binding lectin (MBL2) genotyping in predicting the risk of recurrent otitis media (rOM).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Role of respiratory syncytial virus in acute otitis media: implications for vaccine development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Hush puppy: a new mouse mutant with pinna, ossicle, and inner ear defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Association of surfactant protein A polymorphisms with otitis media in infants at risk for asthma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Effects of Disruption of The Plasminogen Gene on Thrombosis, Growth, and Health in Mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Association between cytokine gene polymorphisms and risk for upper respiratory tract infection and acute otitis media

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

The role of Fas-mediated apoptosis in otitis media: observations in the lpr/lpr mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Heritability of symptom domains in otitis media: a longitudinal study of 1,373 twin pairs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

The multifaceted role of Fas signaling in immune cell homeostasis and autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Differential roles of TLR2 and TLR4 in recognition of gram-negative and gram-positive bacterial cell wall components

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Regulation of TGF-beta signalling by Fbxo11, the gene mutated in the Jeff otitis media mouse mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Epidemiology of otitis media during the first seven years of life in children in greater Boston: a prospective, cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Removal of an intra-parotid foreign body without parotidectomy and dissection of the facial nerve

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

A meta-analytic review of the risk factors for acute otitis media

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

The Sequence of the Human Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

A novel model of murine mucopolysaccharidosis type VII due to an intracisternal a particle element transposition into the beta-glucuronidase gene: clinical and pathologic findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Pyogenic bacterial infections in humans with MyD88 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Inactivation of Chibby affects function of motile airway cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

A Sall4 mutant mouse model useful for studying the role of Sall4 in early embryonic development and organogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Association of CD14 promoter polymorphism with otitis media and pneumococcal vaccine responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

p73-deficient mice have neurological, pheromonal and inflammatory defects but lack spontaneous tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Gram-negative pathogen Klebsiella oxytoca is associated with spontaneous chronic otitis media in Toll-like receptor 4-deficient C3H/HeJ mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-010-9295-1

Effects of frequent ultrasound during pregnancy: a randomised controlled trial

21 January 2018

1 reference

12 December 2020

Recurrent otitis media: genetic immunoglobulin markers in children and their parents

1 reference

12 December 2020

Conditional biallelic Nf2 mutation in the mouse promotes manifestations of human neurofibromatosis type 2.

1 reference

12 December 2020

Regulation of the innate immune response by threonine-phosphatase of Eyes absent

1 reference

12 December 2020

Role of Toll-like receptor 4 in innate immune responses in a mouse model of acute otitis media

1 reference

12 December 2020

The 4G/4G plasminogen activator inhibitor-1 genotype is associated with frequent recurrence of acute otitis media

1 reference

12 December 2020

Otitis media: viruses, bacteria, biofilms and vaccines.

1 reference

12 December 2020

Spontaneous development of otitis media in plasminogen-deficient mice

1 reference

12 December 2020

Genetic polymorphisms in immunoresponse genes TNFA, IL6, IL10, and TLR4 are associated with recurrent acute otitis media

1 reference

12 December 2020

Surfactant protein-A gene locus associated with recurrent otitis media

1 reference

12 December 2020

Cytokine polymorphisms predict the frequency of otitis media as a complication of rhinovirus and RSV infections in children

1 reference

12 December 2020

A pooling-based genome-wide association study implicates the p73 gene in chronic rhinosinusitis

1 reference

12 December 2020

HLA frequency in patients with chronic secretory otitis media

1 reference

12 December 2020

Immunological status in the aetiology of recurrent otitis media with effusion: serum immunoglobulin levels, functional mannose-binding lectin and Fc receptor polymorphisms for IgG

1 reference

12 December 2020

Association of proinflammatory cytokine gene polymorphisms with susceptibility to otitis media

1 reference

12 December 2020

The heritability of otitis media: a twin and triplet study

1 reference

12 December 2020

A new partner for the international knockout mouse consortium

1 reference

12 December 2020

Functional polymorphisms in the mannan-binding lectin 2 gene: effect on MBL levels and otitis media

1 reference

12 December 2020

FBXO11, a regulator of the TGFβ pathway, is associated with severe otitis media in Western Australian children.

1 reference

12 December 2020

p63 and p73: roles in development and tumor formation

1 reference

12 December 2020

Mucin gene polymorphisms in otitis media patients.

1 reference

12 December 2020

Requirement of NF-kappaB/Rel for the development of hair follicles and other epidermal appendices

1 reference

12 December 2020

Cytokine gene polymorphism in recurrent acute otitis media

1 reference

12 December 2020

Eya4-deficient mice are a model for heritable otitis media

1 reference

12 December 2020

10.1007/S00335-010-9295-1

Identifiers

DOI

1 reference

23 August 2017

1 reference