Genetics of chronic otitis media: a mouse to man approach

Genetics of chronic otitis media: a mouse to man approach

<p>Chronic otitis media (OM) is an archetypal complex disease, which is particularly prevalent in childhood. Epidemiological data suggest high heritability for disease susceptibility, but previous genetic association studies have had methodological flaws, and none have specifically focused on...

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Manylion Llyfryddiaeth
Prif Awdur:	Bhutta, M
Awduron Eraill:	Burton, M
Fformat:	Traethawd Ymchwil
Iaith:	English
Cyhoeddwyd:	2012
Pynciau:	Otolaryngology Genetics (life sciences) Genetics (medical sciences) Infectious diseases

Eitemau Tebyg

Characterisation of pitch: an early onset model of sensorineural deafness
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Cyhoeddwyd: (2014)

edison - a novel model of otitis media
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Cyhoeddwyd: (2014)

Human genetic resistance to malaria.
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Cyhoeddwyd: (2009)

Genetic analyses of MAP kinase signalling in mouse gonad development
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Cyhoeddwyd: (2011)

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Cyhoeddwyd: (2014)

Genetic susceptibility to common mycobacterial diseases
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Cyhoeddwyd: (2010)

Homozygosity and risk of childhood death due to invasive bacterial disease
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Cyhoeddwyd: (2009)

On the origin of the Treponematoses: a phylogenetic approach
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Functional genomics of severe sepsis and septic shock
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Cyhoeddwyd: (2013)

Human population structure and demographic history using genetic markers
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Cyhoeddwyd: (2002)

Staphylococcus aureus: the host-organism relationship
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Cyhoeddwyd: (2011)

Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
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Cyhoeddwyd: (2010)

The molecular epidemiology of dengue virus serotype 4 in Bangkok, Thailand
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Cyhoeddwyd: (2004)

Assessment of Mycobacterium tuberculosis transmission in Oxfordshire, UK, 2007-12, with whole pathogen genome sequences: an observational study.
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Cyhoeddwyd: (2012)

Genetic recombination in bacteriophage lambda
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Genetic mapping of variation in spatial learning in the mouse
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Cyhoeddwyd: (2014)

Examining the relationship between genetic variation at G6PD and severe malaria
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Cyhoeddwyd: (2011)

The genetics of amyotrophic lateral sclerosis
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A high-resolution single nucleotide polymorphism genetic map of the mouse genome
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Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection
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Cyhoeddwyd: (2014)

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Cyhoeddwyd: (2014)

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Cyhoeddwyd: (2013)

Functional characterisation of a multiple sclerosis-associated genetic variant
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Cyhoeddwyd: (2012)

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Identification of novel genes involved in brain abnormality syndromes using next generation sequencing
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Cyhoeddwyd: (2014)

Identifying causative elements within structural variants associated with developmental disorders
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Cyhoeddwyd: (2013)

On genetic variants underlying common disease
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Cyhoeddwyd: (2011)

Preimplantation genetic diagnosis - new methods for the detection of genetic abnormalities in human preimplantation embryos
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Cyhoeddwyd: (2013)

Genetics and pathophysiology of coronal craniosynostosis revealed by next-generation DNA sequencing
gan: Sharma, V
Cyhoeddwyd: (2015)

The Lipopolysaccharide of Haemophilus parainfluenzae
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Cyhoeddwyd: (2011)

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Accessing complex genomic variation in Plasmodium falciparum natural infections
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Cyhoeddwyd: (2015)

Reproducing speech intervals in the sub-hundred millisecond (ms) range with a translocation in 7q31
gan: Garcia-Bellido, P
Cyhoeddwyd: (2013)

Epigenetic regulation of the myeloid cell lineage
gan: Pliuskys, L
Cyhoeddwyd: (2014)

Genetic susceptibility to endometrial cancer
gan: Cheng, T
Cyhoeddwyd: (2015)

The role of DOCK8 in the maintenance of CD8+ T cell memory and invariant NKT cells
gan: Crawford, G
Cyhoeddwyd: (2012)