Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity

M Pigeyre, FT Yazdi, Y Kaur, D Meyre - Clinical science, 2016 - portlandpress.com
In high-, middle-and low-income countries, the rising prevalence of obesity is the underlying
cause of numerous health complications and increased mortality. Being a complex and …

[HTML][HTML] Obesity genetics in mouse and human: back and forth, and back again

FT Yazdi, SM Clee, D Meyre - PeerJ, 2015 - peerj.com
Obesity is a major public health concern. This condition results from a constant and complex
interplay between predisposing genes and environmental stimuli. Current attempts to …

NPP-type ectophosphodiesterases: unity in diversity

C Stefan, S Jansen, M Bollen - Trends in biochemical sciences, 2005 - cell.com
Nucleotide pyrophosphatase/phosphodiesterase (NPP)-type ectophosphodiesterases are
found at the cell surface as type-I or type-II transmembrane proteins, but are also found …

Autotaxin—an LPA producing enzyme with diverse functions

K Nakanaga, K Hama, J Aoki - The journal of biochemistry, 2010 - academic.oup.com
Autotaxin (ATX) is an ecto-enzyme responsible for lysophosphatidic acid (LPA) production in
blood. ATX is present in various biological fluids such as cerebrospinal and seminal fluids …

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes

D Meyre, N Bouatia-Naji, A Tounian, C Samson… - Nature …, 2005 - nature.com
We identified a locus on chromosome 6q16. 3–q24. 2 (ref.) associated with childhood
obesity that includes 2.4 Mb common to eight genome scans for type 2 diabetes (T2D) or …

ENPP1 in the regulation of mineralization and beyond

F Roberts, D Zhu, C Farquharson, VE Macrae - Trends in biochemical …, 2019 - cell.com
ENPP1 is well known for its role in regulating skeletal and soft tissue mineralization. It
primarily exerts its function through the generation of pyrophosphate, a key inhibitor of …

Pathomechanisms of type 2 diabetes genes

H Staiger, F Machicao, A Fritsche… - Endocrine …, 2009 - academic.oup.com
Type 2 diabetes mellitus is a complex metabolic disease that is caused by insulin resistance
and β-cell dysfunction. Furthermore, type 2 diabetes has an evident genetic component and …

[HTML][HTML] Altered Bone Development and an Increase in FGF-23 Expression in Enpp1−/− Mice

NCW Mackenzie, D Zhu, EM Milne, R van't Hof… - PloS one, 2012 - journals.plos.org
Nucleotide pyrophosphatase phosphodiesterase 1 (NPP1) is required for the conversion of
extracellular ATP into inorganic pyrophosphate (PPi), a recognised inhibitor of …

Crystal structure of Enpp1, an extracellular glycoprotein involved in bone mineralization and insulin signaling

K Kato, H Nishimasu, S Okudaira… - Proceedings of the …, 2012 - National Acad Sciences
Enpp1 is a membrane-bound glycoprotein that regulates bone mineralization by hydrolyzing
extracellular nucleotide triphosphates to produce pyrophosphate. Enpp1 dysfunction causes …

Current studies on molecular mechanisms of insulin resistance

J Pei, B Wang, D Wang - Journal of Diabetes Research, 2022 - Wiley Online Library
Diabetes is a metabolic disease that raises the risk of microvascular and neurological
disorders. Insensitivity to insulin is a characteristic of type II diabetes, which accounts for 85 …