Inherited LRP2 dysfunction in human disease and animal models
Inherited LRP2 dysfunction in human disease and animal models
Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes | Nature Genetics
Megalin/LRP2 Expression Is Induced by Peroxisome Proliferator-Activated Receptor -Alpha and -Gamma: Implications for PPARs' Roles in Renal Function | PLOS ONE
Endocytic receptor LRP2/megalin—of holoprosencephaly and renal Fanconi syndrome | SpringerLink
LRP2 is structurally similar to LRP1. The ECD of LRP2 contains four... | Download Scientific Diagram
MicroRNA‐146a represses LRP2 translation and leads to cell apoptosis in Alzheimer's disease - Zhang - 2016 - FEBS Letters - Wiley Online Library
LRP2, an auxiliary receptor that controls sonic hedgehog signaling in development and disease - Christ - 2016 - Developmental Dynamics - Wiley Online Library
LRP2/megalin-mediated endocytosis controls SHH trafficking and... | Download Scientific Diagram
The role of megalin (LRP-2/Gp330) during development - ScienceDirect
BioRender | Life Science Icons
LRP2/megalin-mediated endocytosis in epithelial cells of the renal... | Download Scientific Diagram
LRP2, an auxiliary receptor that controls sonic hedgehog signaling in development and disease - Christ - 2016 - Developmental Dynamics - Wiley Online Library
LRP2 - Wikipedia
Proteolytic processing of LRP2 on RPE cells regulates BMP activity to control eye size and refractive error | bioRxiv
Figures and data in Patient-specific genomics and cross-species functional analysis implicate LRP2 in hypoplastic left heart syndrome | eLife
Megalin/LRP2 Protein Overview: Sequence, Structure, Function and Protein Interaction | Sino Biological
Frontiers | LRP-1 and LRP-2 receptors function in the membrane neuron. Trafficking mechanisms and proteolytic processing in Alzheimer's disease
New Insights into the Roles of Megalin/LRP2 and the Regulation of its Functional Expression
Anti-Lrp2 / Megalin antibody (ab76969) | Abcam
Expanding the phenotypic spectrum of mutations in LRP2: a novel candidate gene of non-syndromic familial comitant strabismus | Journal of Translational Medicine | Full Text
