A new era for Type 2 diabetes genetics

A new era for Type 2 diabetes genetics

Bibliographic Details
Main Author:	Zeggini, E
Other Authors:	Diabetes UK
Format:	Journal article
Language:	English
Published:	Blackwell Publishing 2007
Subjects:	Diabetes Medical Sciences Genetics (medical sciences)

Similar Items

TCF7L2: the biggest story in diabetes genetics since HLA?
by: Zeggini, E, et al.
Published: (2007)

Mechanisms of Type 2 diabetes susceptibility
by: Travers, M, et al.
Published: (2013)

Low frequency variants in the exons only encoding isoform A of HNF1A do not contribute to susceptibility to Type 2 diabetes
by: Jafar-Mohammadi, B, et al.
Published: (2009)

The clinical and genetic characterisation of young-onset diabetes
by: Mughal, S
Published: (2014)

Combining information from common type 2 diabetes risk polymorphisms improves disease prediction
by: Weedon, M, et al.
Published: (2006)

Understanding the role of islet development in type 2 diabetes susceptibility
by: Pérez Alcántara, MC
Published: (2019)

The evaluation of the contribution of low frequency, intermediate penetrance sequence variants to the pathogenesis of Type 2 Diabetes
by: Jafar-Mohammadi, B
Published: (2012)

The role of genetic variation in glucokinase and glucokinase regulatory protein in diabetes and related traits
by: Beer, N, et al.
Published: (2011)

The molecular genetics of insulin secretion and signalling
by: McCulloch, L, et al.
Published: (2011)

Mechanisms of genome regulation in human islets and their role in the pathogenesis of type 2 diabetes
by: van de Bunt, G, et al.
Published: (2014)

Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetes.
by: Männikkö, R, et al.
Published: (2011)

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

Type 1 diabetes mellitus and multiple sclerosis: common etiological features
by: Handel, A, et al.
Published: (2009)

Genetic susceptibility to endometrial cancer
by: Cheng, T
Published: (2015)

Characterisation of the genomic architecture of human chromosome 17q and evaluation of different methods for haplotype block definition
by: Zeggini, E, et al.
Published: (2005)

The peoples of Britain: population genetics, archaeology and linguistics
by: Royrvik, E
Published: (2012)

Molecular Genetics of Language Impairment
by: Nudel, R
Published: (2015)

Investigation of expression quantitative trait loci and regulatory genetic variants in primary human immune cells
by: Makino, S
Published: (2013)

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

Multidisciplinary Intention: Revealing The Consequence of Psychosocial Factors on the Adherence to Treatment of the Patients with Type 2 Diabetes Mellitus
by: Anna Kohut, et al.
Published: (2019-10-01)

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

Comparison of different therapies for neonatal diabetes – glibenclamide vs insulin
by: Iberl, M
Published: (2012)

Genetic susceptibility to common mycobacterial diseases
by: Wong, H
Published: (2010)

Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences.
by: Czyz, W, et al.
Published: (2012)

The genetics of amyotrophic lateral sclerosis
by: Schymick, J
Published: (2009)

Impact of genetic variation on gene regulatory effects of vitamin D in immunity and inflammation
by: Berlanga-Taylor, A
Published: (2013)

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
by: Broadbent, H, et al.
Published: (2008)

Human genetic resistance to malaria.
by: Williams, T
Published: (2009)

Interferon lambdas: the next cytokine storm
by: Kelly, C, et al.
Published: (2011)

Genetic recombination in bacteriophage lambda
by: Hillyar, C
Published: (2012)

Genetic recombination in bacteriophage lambda
by: Hillyar, C
Published: (2012)

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

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

SGCE missense mutations that cause myoclonus-dystonia syndrome impair ε-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA
by: Esapa, C, et al.
Published: (2007)

Haplotype homozygosity and derived alleles in the human genome
by: Fry, A, et al.
Published: (2006)

Exploring the developmental overnutrition hypothesis using parental-offspring associations and FTO as an instrumental variable
by: Lawlor, D, et al.
Published: (2008)

Gene modifiers and novel therapies for multiple endocrine neoplasia type 1
by: Javid, M
Published: (2012)

The genetic relationship between handedness and neurodevelopmental disorders
by: Brandler, W, et al.
Published: (2014)

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

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