UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 78

Sortiert nach

Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features

The Journal of clinical investigation, 2013-07, Vol.123 (7), p.3037-3041

2013

Volltextzugriff (PDF)

Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity

The Journal of clinical investigation, 2000-07, Vol.106 (2), p.253-262

2000

Volltextzugriff (PDF)

Novel LEPR mutations in obese Pakistani children identified by PCR‐based enrichment and next generation sequencing

Obesity (Silver Spring, Md.), 2014-04, Vol.22 (4), p.1112-1117

2014

Volltextzugriff (PDF)

Combined effects of MC4R and FTO common genetic variants on obesity in European general populations

Journal of molecular medicine (Berlin, Germany), 2009-05, Vol.87 (5), p.537-546

2009

Volltextzugriff (PDF)

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

American journal of human genetics, 2000-12, Vol.67 (6), p.1470-1480

2000

Volltextzugriff (PDF)

KAT2B Is Required for Pancreatic Beta Cell Adaptation to Metabolic Stress by Controlling the Unfolded Protein Response

Cell reports (Cambridge), 2016-05, Vol.15 (5), p.1051-1061

2016

Volltextzugriff (PDF)

Defective mutations in the insulin promoter factor-1 (IPF-1) gene in late-onset type 2 diabetes mellitus

The Journal of clinical investigation, 1999-11, Vol.104 (9), p.R41-R48

1999

Volltextzugriff (PDF)

Polymorphisms in the Amino Acid Transporter Solute Carrier Family 6 (Neurotransmitter Transporter) Member 14 Gene Contribute to Polygenic Obesity in French Caucasians

Diabetes (New York, N.Y.), 2004-09, Vol.53 (9), p.2483-2486

2004

Volltextzugriff (PDF)

Genetic variants in LEP, LEPR, and MC4R explain 30% of severe obesity in children from a consanguineous population

Obesity (Silver Spring, Md.), 2015-08, Vol.23 (8), p.1687-1695

2015

Volltextzugriff (PDF)

Temporal Prediction in lieu of Periodic Stimulation

The Journal of neuroscience, 2016-02, Vol.36 (8), p.2342-2347

2016

Volltextzugriff (PDF)

Variation in FTO contributes to childhood obesity and severe adult obesity

Nature genetics, 2007-06, Vol.39 (6), p.724-726

2007

Volltextzugriff (PDF)

Glutamatergic synapse in autism: a complex story for a complex disorder

Molecular psychiatry, 2023-02, Vol.28 (2), p.801-809

2023

Volltextzugriff (PDF)

Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of Pakistan

Diabetes (New York, N.Y.), 2020-07, Vol.69 (7), p.1424-1438

2020

Volltextzugriff (PDF)

Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia

Nature genetics, 2009-10, Vol.41 (10), p.1110-1115

2009

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population

BMC medical genetics, 2007-06, Vol.8 (1), p.37-37, Article 37

2007

Volltextzugriff (PDF)

Brief Report: Early VEPs to Pattern-Reversal in Adolescents and Adults with Autism

Journal of autism and developmental disorders, 2016-10, Vol.46 (10), p.3377-3386

2016

Volltextzugriff (PDF)

Monogenic diabetes characteristics in a transnational multicenter study from Mediterranean countries

Diabetes research and clinical practice, 2021-01, Vol.171, p.108553-108553, Article 108553

2021

Volltextzugriff (PDF)

Common Variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population

Obesity (Silver Spring, Md.), 2012-02, Vol.20 (2), p.389-395

2012

Volltextzugriff (PDF)

Adaptation of cognitive remediation to adults with ASD: Feasibility and interest from two pilot groups

La Presse médicale (1983), 2019-10, Vol.48 (10), p.1019-1025

2019

Volltextzugriff (PDF)

Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

Human molecular genetics, 2008-07, Vol.17 (13), p.1916-1921

2008

Volltextzugriff (PDF)

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

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

2003

Volltextzugriff (PDF)

Influence of environmental factors on disease activity in spondyloarthritis: a prospective cohort study

Journal of rheumatology, 2013-04, Vol.40 (4), p.469

2013

Volltextzugriff (PDF)

1 – 25 von 78

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(78)
Mit Volltextzugriff
(71)

Publikationsform

Artikel
(78)

Sprache

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features

Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity

Novel LEPR mutations in obese Pakistani children identified by PCR‐based enrichment and next generation sequencing

Combined effects of MC4R and FTO common genetic variants on obesity in European general populations

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

KAT2B Is Required for Pancreatic Beta Cell Adaptation to Metabolic Stress by Controlling the Unfolded Protein Response

Defective mutations in the insulin promoter factor-1 (IPF-1) gene in late-onset type 2 diabetes mellitus

Polymorphisms in the Amino Acid Transporter Solute Carrier Family 6 (Neurotransmitter Transporter) Member 14 Gene Contribute to Polygenic Obesity in French Caucasians

Genetic variants in LEP, LEPR, and MC4R explain 30% of severe obesity in children from a consanguineous population

Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension

Temporal Prediction in lieu of Periodic Stimulation

Variation in FTO contributes to childhood obesity and severe adult obesity

Glutamatergic synapse in autism: a complex story for a complex disorder

Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of Pakistan

Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia

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

TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population

Brief Report: Early VEPs to Pattern-Reversal in Adolescents and Adults with Autism

Monogenic diabetes characteristics in a transnational multicenter study from Mediterranean countries

Common Variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population

Pathogenic variants in actionable MODY genes are associated with type 2 diabetes

Adaptation of cognitive remediation to adults with ASD: Feasibility and interest from two pilot groups

Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

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

Influence of environmental factors on disease activity in spondyloarthritis: a prospective cohort study

Aktive Filter

Suchergebnisse filtern