Latest papers

Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels.

Gbetagamma activates GSK3 to promote LRP6-mediated beta-catenin transcriptional activity.

Macrophage response to apoptotic cells varies with the apoptotic trigger and is not altered by a deficiency in LRP expression.

Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: identification of a 7.2-kb microdeletion using oligonucleotide tiling microarray.

Apolipoprotein E controls ATP-binding cassette transporters in the ischemic brain.

Patterns of Wnt/Fzd/LRP gene expression during embryonic hematopoiesis.

[Intestinal serotonin and regulation of bone mass].

Cholesteryl ester transfer protein (CETP) increases postprandial triglyceridaemia and delays triacylglycerol plasma clearance in transgenic mice

The role of the Ser/Thr cluster in the phosphorylation of PPPSP motifs in Wnt coreceptors.

Association between the A1330V polymorphism of the low-density lipoprotein receptor-related protein 5 gene and bone mineral density: a meta-analysis.

LRP5 Polymorphisms and response to risedronate treatment in osteoporotic men.

N-cadherin interacts with axin and LRP5 to negatively regulate Wnt/beta-catenin signaling, osteoblast function, and bone formation.

Midkine translocated to nucleoli and involved in carcinogenesis.

A gust of WNT: analysis of the canonical WNT pathway.

[Familial hypercholesterolemia in Russia: genetic and phenotypic characteristics].

Mechanical signaling for bone modeling and remodeling.

A1330V polymorphism of low-density lipoprotein receptor-related protein 5 gene and self-reported incident fractures in Japanese female patients with rheumatoid arthritis.

Functional characterization of genetic variation in the Frizzled 1 (FZD1) promoter and association with bone phenotypes: more to the LRP5 story?

N-cadherin negatively regulates osteoblast proliferation and survival by antagonizing Wnt, ERK and PI3K/Akt signalling.

Ocular coloboma and dorsoventral neuroretinal patterning defects in Lrp6 mutant eyes.