نتایج جستجو برای: insig2

تعداد نتایج: 96  

Journal: :Human molecular genetics 2008
Yong-Jun Liu Xiao-Gang Liu Liang Wang Christian Dina Han Yan Jian-Feng Liu Shawn Levy Christopher J Papasian Betty M Drees James J Hamilton David Meyre Jerome Delplanque Yu-Fang Pei Lei Zhang Robert R Recker Philippe Froguel Hong-Wen Deng

Obesity is a major public health problem with strong genetic determination; however, the genetic factors underlying obesity are largely unknown. In this study, we performed a genome-wide association scan for obesity by examining approximately 500 000 single-nucleotide polymorphisms (SNPs) in a sample of 1000 unrelated US Caucasians. We identified a novel gene, CTNNBL1, which has multiple SNPs a...

Journal: :Journal of oleo science 2012
Natthanan Nukitrangsan Takafumi Okabe Takayoshi Toda Masashi Inafuku Hironori Iwasaki Hirosuke Oku

Supplementation of the diet with Peucedanum japonicum Thunb (PJT) powder inhibits high-fat diet-induced obesity in mice. Either the fiber component or other bioactive components in the PJT powder may inhibit obesity. This study, therefore, was an attempt to identify the components, fiber or other phytochemicals of PJT that were responsible for the anti-obesity activity, and also studied the mod...

Journal: :Diabetes 2008
Marina Ciullo Teresa Nutile Cyril Dalmasso Rossella Sorice Céline Bellenguez Vincenza Colonna Maria Graziella Persico Catherine Bourgain

OBJECTIVE Obesity is a complex trait with a variety of genetic susceptibility variants. Several loci linked to obesity and/or obesity-related traits have been identified, and relatively few regions have been replicated. Studying isolated populations can be a useful approach to identify rare variants that will not be detected with whole-genome association studies in large populations. RESEARCH...

Journal: :Diabetes 2009
Steven C. Elbein Swapan K. Das D. Michael Hallman Craig L. Hanis Sandra J. Hasstedt

OBJECTIVE We used a single nucleotide polymorphism (SNP) map in a large cohort of 580 African American families to identify regions linked to type 2 diabetes, age of type 2 diabetes diagnosis, and BMI. RESEARCH DESIGN AND METHODS After removing outliers and problematic samples, we conducted linkage analysis using 5,914 SNPs in 1,344 individuals from 530 families. Linkage analysis was conducte...

2014
Marta Futema Vincent Plagnol KaWah Li Ros A Whittall H Andrew W Neil Mary Seed Stefano Bertolini Sebastiano Calandra Olivier S Descamps Colin A Graham Robert A Hegele Fredrik Karpe Ronen Durst Eran Leitersdorf Nicholas Lench Devaki R Nair Handrean Soran Frank M Van Bockxmeer Steve E Humphries

BACKGROUND Familial hypercholesterolaemia (FH) is an autosomal dominant disease of lipid metabolism, which leads to early coronary heart disease. Mutations in LDLR, APOB and PCSK9 can be detected in 80% of definite FH (DFH) patients. This study aimed to identify novel FH-causing genetic variants in patients with no detectable mutation. METHODS AND RESULTS Exomes of 125 unrelated DFH patients ...

Journal: :Genetics 2012
Scott A Kelly Derrick L Nehrenberg Kunjie Hua Theodore Garland Daniel Pomp

The biological basis of voluntary exercise is complex and simultaneously controlled by peripheral (ability) and central (motivation) mechanisms. The accompanying natural reward, potential addiction, and the motivation associated with exercise are hypothesized to be regulated by multiple brain regions, neurotransmitters, peptides, and hormones. We generated a large (n = 815) advanced intercross ...

2009
Gwendal Le Martelot Thierry Claudel David Gatfield Olivier Schaad Benoît Kornmann Giuseppe Lo Sasso Antonio Moschetta Ueli Schibler

In mammals, many aspects of behavior and physiology, and in particular cellular metabolism, are coordinated by the circadian timing system. Molecular clocks are thought to rely on negative feedback loops in clock gene expression that engender oscillations in the accumulation of transcriptional regulatory proteins, such as the orphan receptor REV-ERBalpha. Circadian transcription factors then dr...

Journal: :Journal of nutrigenetics and nutrigenomics 2014
J Alfredo Martínez

Obesity can result from the disequilibrium between energy intake and expenditure associated with alterations of many metabolic pathways [1] . As many cellular functions related to energy homeostasis are regulated by gene expression and gene-environment interactions, individual variation in body weight/composition and adipose metabolism could be influenced by genetic makeup and nutrient intake. ...

2015
Juan M. Decara Francisco Javier Pavón Juan Suárez Miguel Romero-Cuevas Elena Baixeras Mariam Vázquez Patricia Rivera Ana L. Gavito Bruno Almeida Jesús Joglar Rafael de la Torre Fernando Rodrıǵuez de Fonseca Antonia Serrano

Fatty liver disease is one of the main hepatic complications associated with obesity. To date, there are no effective treatments for this pathology apart from the use of classical fibrates. In this study, we have characterized the in vivo effects of a novel conjugation of oleic acid with an amphetamine derivative (OLHHA) in an animal model of genetic obesity. Lean and obese Zucker rats received...

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