LRP4, LDL receptor related protein 4, 4038

N. diseases: 151; N. variants: 23
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE In total, 16 (0.8%) patients with LRP4-MG were found amongst 2172 total patients, including three patients with AChR/LRP4-MG. Additionally, 13 (2.9%) patients with LRP4-MG were found amongst 455 patients with double seronegative MG. 31050101 2019
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Results from experimental autoimmune MG animal models indicate that anti-LRP4 antibodies are causal to MG. Clinical studies have begun to reveal the significance of the new biomarkers. 29377176 2018
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Patients with dSNMG cortactin<sup>+</sup> MG were negative for anti-striated muscle and anti-LRP4 antibodies. 29068555 2018
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Anti-AChR, MuSK, and LRP4 antibodies coexistence: A rare and distinct subtype of myasthenia gravis from Indian subcontinent. 30006288 2018
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Neonatal MG with temporary muscle weakness occurs in 10% of newborn babies where the mother has MG, due to transplacental transfer of antibodies against acetylcholine receptor (AChR), muscle-specific kinase (MuSK) or lipoprotein receptor-related protein 4 (LRP4). 30133097 2018
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE The features of LRP4-EAMG are more similar to those of AChR-EAMG, indicating a similar clinical treatment for LRP4- and AChR-positive MG patients, compared to MuSK-positive MG patients. 29421431 2018
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Low-Density Lipoprotein Receptor-Related Protein 4-Positive Myasthenia Gravis in a Double-Seronegative, Electromyography-Negative Patient. 28350570 2017
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Double-seropositive myasthenia gravis with acetylcholine receptor and low-density lipoprotein receptor-related protein 4 antibodies associated with invasive thymoma. 28694075 2017
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Agrin-LRP4-MuSK signaling as a therapeutic target for myasthenia gravis and other neuromuscular disorders. 28825343 2017
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Focusing on neural agrin, Wnts, muscle-specific tyrosine kinase (a mediator of agrin and Wnts signalings and regulator of trans-synaptic communication), low-density lipoprotein receptor-related protein 4 (the receptor of agrin and Wnts and participant in retrograde signaling), laminin-network (including muscle-derived agrin), extracellular matrix proteins (participating in the synaptic stabilization) and presynaptic receptors (including muscarinic and adenosine receptors), we review the functional structures of the synapse by making reference to immunological pathogenecities in postsynaptic disease, myasthenia gravis. 28441759 2017
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE This study shows that LRP4-Ab is a pathogenic antibody in MG. LRP4-MG seems to be characterized by mild disease severity and favorable therapeutic effect in contrast with other types of MG.Muscle Nerve 56: 938-942, 2017. 28120340 2017
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE LRP4-MG presented late-onset age, mild symptoms, good therapeutic response, and no thymic changes. 28516329 2017
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Our results clearly demonstrate that active immunization of mice with LRP4 proteins causes myasthenia similar to the MG induced by anti-MuSK Abs. 28823823 2017
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE Mutations in MuSK and in genes that function in the MuSK signaling pathway, including Dok-7, cause congenital myasthenia, and autoantibodies to MuSK, Lrp4, and acetylcholine receptors are responsible for myasthenia gravis. 23637281 2013
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE In the present study we tested if autoantibodies against LRP4 are detectable in patients with myasthenia gravis. 21814823 2012
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 Biomarker disease BEFREE A third type of autoantibodies (Lrp4) has been detected to cause myasthenia gravis. 21825986 2011