Related references
Note: Only part of the references are listed.Variants in the fat mass- and obesity-associated (FTO) gene are not associated with obesity in a Chinese Han population
Huaixing Li et al.
DIABETES (2008)
Genome Wide Association (GWA) Study for Early Onset Extreme Obesity Supports the Role of Fat Mass and Obesity Associated Gene (FTO) Variants
Anke Hinney et al.
PLOS ONE (2007)
FTO polymorphisms in oceanic populations
Jun Ohashi et al.
JOURNAL OF HUMAN GENETICS (2007)
Contribution of CDP/Cux, a transcription factor, to cell cycle progression
Xifeng Fei et al.
ACTA BIOCHIMICA ET BIOPHYSICA SINICA (2007)
Disruption of intraflagellar in adult mice leads to transport obesity and slow-onset cystic kidney disease
James R. Davenport et al.
CURRENT BIOLOGY (2007)
Ftm is a novel basal body protein of cilia involved in Shh signalling
Jeanette Vierkotten et al.
DEVELOPMENT (2007)
Bardet-Biedl syndrome: beyond the cilium
Jonathan L. Tobin et al.
PEDIATRIC NEPHROLOGY (2007)
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
Angelo Scuteri et al.
PLOS GENETICS (2007)
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
Laura J. Scott et al.
SCIENCE (2007)
Variation in FTO contributes to childhood obesity and severe adult obesity
Christian Dina et al.
NATURE GENETICS (2007)
Defects in brain patterning and head morphogenesis in the mouse mutant Fused toes
Isabelle Anselme et al.
DEVELOPMENTAL BIOLOGY (2007)
No evidence of association of ENPP1 variants with type 2 diabetes or obesity in a study of 8,089 UK caucasians
Michael N. Weedon et al.
DIABETES (2006)
Common variants in the ENPP1 gene are not reproducibly associated with diabetes or obesity
Helen N. Lyon et al.
DIABETES (2006)
A common genetic variant is associated with adult and childhood obesity
A Herbert et al.
SCIENCE (2006)
The p110 isoform of the CDP/Cux transcription factor accelerates entry into S phase
L Sansregret et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Association of K121Q polymorphism in ENPP1 (PC-1) with BMI in Caucasian and African-American adults
N Matsuoka et al.
INTERNATIONAL JOURNAL OF OBESITY (2006)
Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP
BS Pawlyk et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2005)
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes
D Meyre et al.
NATURE GENETICS (2005)
Homozygous Ft embryos are affected in floor plate maintenance and ventral neural tube patterning
K Götz et al.
DEVELOPMENTAL DYNAMICS (2005)
Expression of ADP-ribosylation factor (ARF)-like protein 6 during mouse embryonic development
T Takada et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY (2005)
Trophic action of leptin on hypothalamic neurons that regulate feeding
SG Bouret et al.
SCIENCE (2004)
Establishing a connection between cilia and Bardet-Biedl Syndrome
K Mykytyn et al.
TRENDS IN MOLECULAR MEDICINE (2004)
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin
DY Nishimura et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
CDP/Cux stimulates transcription from the DNA polymerase α gene promoter
M Truscott et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
The Fused toes (Ft) mouse mutation causes anteroposterior and dorsoventral polydactyly
L Grotewold et al.
DEVELOPMENTAL BIOLOGY (2002)
Assembly of centrosomal proteins and microtubule organization depends on PCM-1
A Dammermann et al.
JOURNAL OF CELL BIOLOGY (2002)
Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species
TA Mavlyutov et al.
HUMAN MOLECULAR GENETICS (2002)
Deregulated expression of the homeobox gene Cux-1 in transgenic mice results in downregulation of p27kip1 expression during nephrogenesis, glomerular abnormalities, and multiorgan hyperplasia
AW Ledford et al.
DEVELOPMENTAL BIOLOGY (2002)
Obesity and health risks
RP Raman
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION (2002)
The mouse Fused toes (Ft) mutation is the result of a 1.6-Mb deletion including the entire Iroquois B gene cluster
T Peters et al.
MAMMALIAN GENOME (2002)
Interleukin-13 induces a hypersecretory ion transport phenotype in human bronchial epithelial cells
H Danahay et al.
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY (2002)
Genetic ablation of the CDP/Cux protein C terminus results in hair cycle defects and reduced male fertility
MX Luong et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)
Lymphoid apoptosis and myeloid hyperplasia in CCAAT displacement protein mutant mice
AM Sinclair et al.
BLOOD (2001)
Role of the multifunctional CDP/Cut/Cux homeodomain transcription factor in regulating differentiation, cell growth and development
A Nepveu
GENE (2001)
Retinitis pigmentosa GTPase regulator (RPGR)-interacting protein is stably associated with the photoreceptor ciliary axoneme and anchors RPGR to the connecting cilium
DH Hong et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)