UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 617

Sortiert nach

Estimating sleep parameters using an accelerometer without sleep diary

Scientific reports, 2018-08, Vol.8 (1), p.12975-11, Article 12975

2018

Volltextzugriff (PDF)

C-reactive protein levels and body mass index: elucidating direction of causation through reciprocal Mendelian randomization

International Journal of Obesity, 2011-02, Vol.35 (2), p.300-308

2011

Volltextzugriff (PDF)

Genome-wide association studies: the good, the bad and the ugly

Clinical medicine (London, England), 2014-08, Vol.14 (4), p.428-431

Frayling, TM

2014

Volltextzugriff (PDF)

Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population

Diabetologia, 2007-01, Vol.50 (1), p.63-67

2007

Volltextzugriff (PDF)

Is the thrifty genotype hypothesis supported by evidence based on confirmed type 2 diabetes- and obesity-susceptibility variants

Diabetologia, 2009-09, Vol.52 (9), p.1846-1851

2009

Volltextzugriff (PDF)

genetic link between type 2 diabetes and prostate cancer

Diabetologia, 2008-10, Vol.51 (10), p.1757-1760

2008

Volltextzugriff (PDF)

A common variant of the interleukin 6 receptor ( ) gene increases IL-6r and IL-6 levels, without other inflammatory effects

Genes and immunity, 2007-10, Vol.8 (7), p.552-559

2007

Volltextzugriff (PDF)

Common genetic variation in the melatonin receptor 1B gene (MTNR1B) is associated with decreased early-phase insulin response

Diabetologia, 2009-08, Vol.52 (8), p.1537-1542

2009

Volltextzugriff (PDF)

An FTO variant is associated with Type 2 diabetes in South Asian populations after accounting for body mass index and waist circumference

Diabetic medicine, 2011-06, Vol.28 (6), p.673-680

2011

Volltextzugriff (PDF)

Beta cell glucose sensitivity is decreased by 39% in non-diabetic individuals carrying multiple diabetes-risk alleles compared with those with no risk alleles

Diabetologia, 2008-11, Vol.51 (11), p.1989-1992

2008

Volltextzugriff (PDF)

Genetic studies of diabetes following the advent of the genome-wide association study: where do we go from here

Diabetologia, 2007-11, Vol.50 (11), p.2229-2233

2007

Volltextzugriff (PDF)

Mutations in the human Delta homologue, DLL3 , cause axial skeletal defects in spondylocostal dysostosis

Nature genetics, 2000-04, Vol.24 (4), p.438-441

2000

Volltextzugriff (PDF)

Multiple genetic variants explain measurable variance in type 2 diabetes-related traits in Pakistanis

Diabetologia, 2012-08, Vol.55 (8), p.2193-2204

2012

Volltextzugriff (PDF)

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

Diabetes (New York, N.Y.), 2001-02, Vol.50 (suppl 1), p.S94-S100

2001

Volltextzugriff (PDF)

Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes

Diabetologia, 2008-12, Vol.51 (12), p.2205-2213

2008

Volltextzugriff (PDF)

Large-scale studies of the association between variation at the TNF/LTA locus and susceptibility to type 2 diabetes

Diabetologia, 2005-10, Vol.48 (10), p.2013-2017

2005

Volltextzugriff (PDF)

Assessing association of common variation in the C1Q gene cluster with systemic lupus erythematosus

Clinical and experimental immunology, 2010-08, Vol.161 (2), p.284-289

2010

Volltextzugriff (PDF)

role for coding functional variants in HNF4A in type 2 diabetes susceptibility

Diabetologia, 2011-01, Vol.54 (1), p.111-119

2011

Volltextzugriff (PDF)

association of common genetic variants in the APOA5, LPL and GCK genes with longitudinal changes in metabolic and cardiovascular traits

Diabetologia, 2009, Vol.52 (1), p.106-114

2009

Volltextzugriff (PDF)

Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes

Diabetic medicine, 2011-06, Vol.28 (6), p.681-684

2011

Volltextzugriff (PDF)

Circulating β-carotene levels and type 2 diabetes--cause or effect

Diabetologia, 2009-10, Vol.52 (10), p.2117-2121

2009

Volltextzugriff (PDF)

Examining the relationships between the Pro12Ala variant in PPARG and Type 2 diabetes-related traits in UK samples

Diabetic medicine, 2005-12, Vol.22 (12), p.1696-1700

2005

Volltextzugriff (PDF)

Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles

Diabetes (New York, N.Y.), 2000-01, Vol.49 (1), p.126-130

2000

Volltextzugriff (PDF)

Common variations in the ALMS1 gene do not contribute to susceptibility to type 2 diabetes in a large white UK population

Diabetologia, 2006-06, Vol.49 (6), p.1209-1213

2006

Volltextzugriff (PDF)

The transcription factor 7-like 2 (TCF7L2) gene is associated with Type 2 diabetes in UK community-based cases, but the risk allele frequency is reduced compared with UK cases selected for genetic studies

Diabetic medicine, 2007-10, Vol.24 (10), p.1067-1072

2007

Volltextzugriff (PDF)

1 – 25 von 617

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(598)
Mit Volltextzugriff
(535)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(457)
Humans
(433)
Life Sciences & Biomedicine
(392)
Female
(233)
Male
(218)
Genetics & Heredity
(169)
Adult
(167)
Biological And Medical Sciences
(165)
Diabetes Mellitus, Type 2 - Genetics
(153)
Genomes
(146)
Diabetes
(142)
Polymorphism, Single Nucleotide
(140)
Middle Aged
(138)
Medical Sciences
(134)
Genome-Wide Association Study
(130)
Genetic Aspects
(125)
Genetics
(118)
Genetic Predisposition To Disease
(109)
Endocrinology & Metabolism
(107)
Genotype
(105)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Diabetes
(88)
Nature Genetics
(53)
Plos Genetics
(39)
Diabetologia
(33)
Human Molecular Genetics
(27)
American Journal Of Human Genetics
(24)
Nature Communications
(20)
Nature
(15)
International Journal Of Epidemiology
(14)
Gut
(11)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Estimating sleep parameters using an accelerometer without sleep diary

C-reactive protein levels and body mass index: elucidating direction of causation through reciprocal Mendelian randomization

Genome-wide association studies: the good, the bad and the ugly

Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population

Is the thrifty genotype hypothesis supported by evidence based on confirmed type 2 diabetes- and obesity-susceptibility variants

genetic link between type 2 diabetes and prostate cancer

A common variant of the interleukin 6 receptor ( ) gene increases IL-6r and IL-6 levels, without other inflammatory effects

Common genetic variation in the melatonin receptor 1B gene (MTNR1B) is associated with decreased early-phase insulin response

An FTO variant is associated with Type 2 diabetes in South Asian populations after accounting for body mass index and waist circumference

Beta cell glucose sensitivity is decreased by 39% in non-diabetic individuals carrying multiple diabetes-risk alleles compared with those with no risk alleles

Genetic studies of diabetes following the advent of the genome-wide association study: where do we go from here

Mutations in the human Delta homologue, DLL3 , cause axial skeletal defects in spondylocostal dysostosis

Multiple genetic variants explain measurable variance in type 2 diabetes-related traits in Pakistanis

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes

Large-scale studies of the association between variation at the TNF/LTA locus and susceptibility to type 2 diabetes

Assessing association of common variation in the C1Q gene cluster with systemic lupus erythematosus

role for coding functional variants in HNF4A in type 2 diabetes susceptibility

association of common genetic variants in the APOA5, LPL and GCK genes with longitudinal changes in metabolic and cardiovascular traits

Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetes

Circulating β-carotene levels and type 2 diabetes--cause or effect

Examining the relationships between the Pro12Ala variant in PPARG and Type 2 diabetes-related traits in UK samples

Analysis of parent-offspring trios provides evidence for linkage and association between the insulin gene and type 2 diabetes mediated exclusively through paternally transmitted class III variable number tandem repeat alleles

Common variations in the ALMS1 gene do not contribute to susceptibility to type 2 diabetes in a large white UK population

The transcription factor 7-like 2 (TCF7L2) gene is associated with Type 2 diabetes in UK community-based cases, but the risk allele frequency is reduced compared with UK cases selected for genetic studies

Suchergebnisse filtern