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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Bibliografiske detaljer
Hovedforfatter:	Bhutta, M
Andre forfattere:	Burton, M
Format:	Thesis
Sprog:	English
Udgivet:	2012
Fag:	Otolaryngology Genetics (life sciences) Genetics (medical sciences) Infectious diseases

Lignende værker

Characterisation of pitch: an early onset model of sensorineural deafness
af: Carrott, L
Udgivet: (2014)

edison - a novel model of otitis media
af: Crompton, M
Udgivet: (2014)

Human genetic resistance to malaria.
af: Williams, T
Udgivet: (2009)

Genetic analyses of MAP kinase signalling in mouse gonad development
af: Brixey, R
Udgivet: (2011)

Genetics determinants of vaccine responses
af: O'Connor, D
Udgivet: (2014)

Genetic susceptibility to common mycobacterial diseases
af: Wong, H
Udgivet: (2010)

Homozygosity and risk of childhood death due to invasive bacterial disease
af: Lyons, E, et al.
Udgivet: (2009)

On the origin of the Treponematoses: a phylogenetic approach
af: Harper, K, et al.
Udgivet: (2008)

Functional genomics of severe sepsis and septic shock
af: Radhakrishnan, J
Udgivet: (2013)

Human population structure and demographic history using genetic markers
af: Wilson, J, et al.
Udgivet: (2002)

Staphylococcus aureus: the host-organism relationship
af: Miller, R, et al.
Udgivet: (2011)

Sialic acid mediated transcriptional modulation of a highly conserved sialometabolism gene cluster in Haemophilus influenzae and its effect on virulence
af: Jenkins, G, et al.
Udgivet: (2010)

The molecular epidemiology of dengue virus serotype 4 in Bangkok, Thailand
af: Klungthong, C, et al.
Udgivet: (2004)

Assessment of Mycobacterium tuberculosis transmission in Oxfordshire, UK, 2007-12, with whole pathogen genome sequences: an observational study.
af: Walker, T, et al.
Udgivet: (2014)

Genetic recombination in bacteriophage lambda
af: Hillyar, C
Udgivet: (2012)

Genetic recombination in bacteriophage lambda
af: Hillyar, C
Udgivet: (2012)

Genetic mapping of variation in spatial learning in the mouse
af: Steinberger, D, et al.
Udgivet: (2003)

Control of expression of human snRNA genes
af: Zaborowska, J, et al.
Udgivet: (2013)

Applications of whole genome sequencing to understanding the mechanisms, evolution and transmission of antibiotic resistance in Escherichia coli and Klebsiella pneumonia
af: Stoesser, N, et al.
Udgivet: (2014)

Examining the relationship between genetic variation at G6PD and severe malaria
af: Shah, SS
Udgivet: (2011)

The genetics of amyotrophic lateral sclerosis
af: Schymick, J
Udgivet: (2009)

A high-resolution single nucleotide polymorphism genetic map of the mouse genome
af: Shifman, S, et al.
Udgivet: (2006)

Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection
af: Gupta, P
Udgivet: (2014)

Inflammatory and myeloid-associated gene expression before and one day after infant vaccination with MVA85A correlates with induction of a T cell response.
af: Matsumiya, M, et al.
Udgivet: (2014)

The genetics of handedness and dyslexia
af: Brandler, W
Udgivet: (2014)

The nicotinic acid receptor in human adipose tissue
af: Chamas, L, et al.
Udgivet: (2013)

Functional characterisation of a multiple sclerosis-associated genetic variant
af: Gregory, A
Udgivet: (2012)

B cell response to pneumococcal vaccines
af: Trück, J
Udgivet: (2014)

Identification of novel genes involved in brain abnormality syndromes using next generation sequencing
af: Howard, M, et al.
Udgivet: (2014)

Identifying causative elements within structural variants associated with developmental disorders
af: Boulding, H
Udgivet: (2013)

On genetic variants underlying common disease
af: Hechter, E
Udgivet: (2011)

Preimplantation genetic diagnosis - new methods for the detection of genetic abnormalities in human preimplantation embryos
af: Konstantinidis, M
Udgivet: (2013)

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

The Lipopolysaccharide of Haemophilus parainfluenzae
af: Young, R
Udgivet: (2011)

Prevalence of Staphylococcus aureus protein A (spa) mutants in the community and hospitals in Oxfordshire.
af: Votintseva, A, et al.
Udgivet: (2014)

Accessing complex genomic variation in Plasmodium falciparum natural infections
af: Wendler, J
Udgivet: (2015)

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

Epigenetic regulation of the myeloid cell lineage
af: Pliuskys, L
Udgivet: (2014)

Genetic susceptibility to endometrial cancer
af: Cheng, T
Udgivet: (2015)

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