UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 44

Sortiert nach

Monogenic Diabetes in the Young, Pharmacogenetics and Relevance to Multifactorial Forms of Type 2 Diabetes

Endocrine reviews, 2008-05, Vol.29 (3), p.254-264

2008

Link zum Volltext

Verfügbarkeit prüfen

Genetics of obesity and the prediction of risk for health

Human molecular genetics, 2006-10, Vol.15 (suppl-2), p.R124-R130

2006

Link zum Volltext

Verfügbarkeit prüfen

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity

Human molecular genetics, 2008-06, Vol.17 (12), p.1803-1813

2008

Link zum Volltext

Verfügbarkeit prüfen

A Variation in the Ghrelin Gene Increases Weight and Decreases Insulin Secretion in Tall, Obese Children

The journal of clinical endocrinology and metabolism, 2002-08, Vol.87 (8), p.4005-4008

2002

Link zum Volltext

Verfügbarkeit prüfen

Childhood Obesity Is Associated with Shorter Leukocyte Telomere Length

The journal of clinical endocrinology and metabolism, 2011-05, Vol.96 (5), p.1500-1505

2011

Link zum Volltext

Verfügbarkeit prüfen

What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations

International journal of epidemiology, 2012-02, Vol.41 (1), p.273-286

2012

Link zum Volltext

Verfügbarkeit prüfen

NACHO: an R package for quality control of NanoString nCounter data

Bioinformatics, 2020-02, Vol.36 (3), p.970-971

2020

Link zum Volltext

Verfügbarkeit prüfen

Postnatal weight and height growth velocities at different ages between birth and 5 y and body composition in adolescent boys and girls

The American journal of clinical nutrition, 2008-06, Vol.87 (6), p.1760-1768

2008

Link zum Volltext

Verfügbarkeit prüfen

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

Human molecular genetics, 2009-09, Vol.18 (17), p.3257-3265

2009

Link zum Volltext

Verfügbarkeit prüfen

Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02)

The Journal of infectious diseases, 2009-02, Vol.199 (3), p.419-426

2009

Link zum Volltext

Verfügbarkeit prüfen

TCF7L2 splice variants have distinct effects on β-cell turnover and function

Human molecular genetics, 2011-05, Vol.20 (10), p.1906-1915

2011

Link zum Volltext

Verfügbarkeit prüfen

High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children

The journal of clinical endocrinology and metabolism, 2018-02, Vol.103 (2), p.539-545

2018

Link zum Volltext

Verfügbarkeit prüfen

Direct estimates of natural selection in Iberia indicate calcium absorption was not the only driver of lactase persistence in Europe

Molecular biology and evolution, 2014-04, Vol.31 (4), p.975-983

2014

Link zum Volltext

Verfügbarkeit prüfen

Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians

Human molecular genetics, 2002-10, Vol.11 (21), p.2607-2614

2002

Link zum Volltext

Verfügbarkeit prüfen

Monogenic Diabetes in the Young, Pharmacogenetics and Relevance to Multifactorial Forms of Type 2 Diabetes: Novel Nonimmunological Forms of β-Cell Dysfunction: Diabetic Syndromes and Pathogenic Mechanisms

Endocrine reviews, 2008, Vol.29 (3), p.254-264

2008

Link zum Volltext

Verfügbarkeit prüfen

Is Obesity Our Genetic Legacy?

The journal of clinical endocrinology and metabolism, 2008-11, Vol.93 (11_supplement_1), p.s51-s56

2008

Link zum Volltext

Verfügbarkeit prüfen

High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children

The journal of clinical endocrinology and metabolism, 2018-02, Vol.103 (2), p.539-545

2018

Link zum Volltext

Verfügbarkeit prüfen

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Human molecular genetics, 2002-08, Vol.11 (17), p.1997-2004

2002

Link zum Volltext

Verfügbarkeit prüfen

Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations

Human molecular genetics, 2003-01, Vol.12 (2), p.145-153

2003

Link zum Volltext

Verfügbarkeit prüfen

Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03)

The Journal of infectious diseases, 2009-10, Vol.200 (8), p.1194-1201

2009

Link zum Volltext

Verfügbarkeit prüfen

A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27

Human molecular genetics, 2001-11, Vol.10 (24), p.2751-2765

2001

Link zum Volltext

Verfügbarkeit prüfen

Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians

Human molecular genetics, 2002, Vol.21, p.2607-2614

Froguel, Philippe

2002

Link zum Volltext

Verfügbarkeit prüfen

Is Obesity Our Genetic Legacy?: Obesity: Epidemiology, Etiology, Morbidity, and Management

The journal of clinical endocrinology and metabolism, 2008, Vol.93

2008

Link zum Volltext

Verfügbarkeit prüfen

Leptin Receptor Genotype at Gln223Arg is Associated With Body Composition, BMD, and Vertebral Fracture in Postmenopausal Danish Women

Journal of bone and mineral research, 2007-04, Vol.22 (4), p.544-550

2007

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 44

Suche als RSS-Feed

Aktive Filter

ThemaAdult

KollektionOxford Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(44)
Mit Volltextzugriff
(44)

Publikationsform

Artikel
(44)

Sprache

Englisch
(44)
Japanisch
(10)

Erscheinungsjahr

n.n

Thema

Humans
(31)
Life Sciences & Biomedicine
(30)
Science & Technology
(30)
Biological And Medical Sciences
(27)
Life Sciences
(20)
Medical Sciences
(20)
Fundamental And Applied Biological Sciences. Psychology
(19)
Genetics
(16)
Biochemistry & Molecular Biology
(15)
Human Genetics
(15)
Male
(14)
Female
(13)
Genetics & Heredity
(13)
Polymorphism, Single Nucleotide
(12)
Endocrinopathies
(10)
Obesity
(10)
Endocrinology & Metabolism
(9)
Obesity - Genetics
(9)
Cohort Studies
(8)
Genotype
(8)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

4 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Monogenic Diabetes in the Young, Pharmacogenetics and Relevance to Multifactorial Forms of Type 2 Diabetes

Genetics of obesity and the prediction of risk for health

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity

A Variation in the Ghrelin Gene Increases Weight and Decreases Insulin Secretion in Tall, Obese Children

Childhood Obesity Is Associated with Shorter Leukocyte Telomere Length

What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations

NACHO: an R package for quality control of NanoString nCounter data

Postnatal weight and height growth velocities at different ages between birth and 5 y and body composition in adolescent boys and girls

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism

Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02)

TCF7L2 splice variants have distinct effects on β-cell turnover and function

High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children

Direct estimates of natural selection in Iberia indicate calcium absorption was not the only driver of lactase persistence in Europe

Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians

Monogenic Diabetes in the Young, Pharmacogenetics and Relevance to Multifactorial Forms of Type 2 Diabetes: Novel Nonimmunological Forms of β-Cell Dysfunction: Diabetic Syndromes and Pathogenic Mechanisms

Is Obesity Our Genetic Legacy?

High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutations

Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03)

A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27

Multiple-cohort genetic association study reveals CXCR6 as a new chemokine receptor involved in long-term nonprogression to AIDS

Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians

Is Obesity Our Genetic Legacy?: Obesity: Epidemiology, Etiology, Morbidity, and Management

Leptin Receptor Genotype at Gln223Arg is Associated With Body Composition, BMD, and Vertebral Fracture in Postmenopausal Danish Women

Aktive Filter

Suchergebnisse filtern