Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Select your species
LRP4 c.2552C>G (p.(T851R) variant was identified in the family with Chiari malformation type 1.
A novel splice variant in LRP4 (c.316+1G > A) segregated with Cenani-Lenz syndactyly phenotype in a five generations family.
LRP4 mutations alter Wnt (zeige WNT2 ELISA Kits)/beta catenin (zeige CTNNB1 ELISA Kits) signaling and cause limb and kidney malformations in Cenani-Lenz syndrome.
the first evidence suggesting that LRP4 is responsible for the retention of sclerostin (zeige SOST ELISA Kits) in the bone environment in humans.
study presents 2 sibling fetuses with a prenatal lethal presentation of mesomelic limb reductions, oligosyndactyly, genitourinary malformation and compound heterozygosity for 2 novel truncating mutations in LRP4
MuSK (zeige MUSK ELISA Kits) myasthenia gravis IgG4 disrupts the interaction of LRP4 with MuSK (zeige MUSK ELISA Kits) but both IgG4 and IgG1-3 can disperse preformed agrin (zeige AGRN ELISA Kits)-independent AChR clusters
LRP4 is essential for maintaining the structural and functional activity of the neuromuscular junction.
LRP4 is a new CMS (zeige Cd2ap ELISA Kits) disease gene and the 3rd beta propeller domain of LRP4 mediates two signaling pathways in a position-specific manner.
[review] Autoantibodies against LRP4 differentially alter neuromuscular transmission, demonstrating how myasthenia gravis can be classified according to the profile of the antibodies; management of myasthenia gravis patients can be adapted accordingly.
pathogenic IgG4 antibodies to MuSK (zeige MUSK ELISA Kits) bind to a structural epitope in the first Ig-like domain of MuSK (zeige MUSK ELISA Kits), prevent binding between MuSK (zeige MUSK ELISA Kits) and Lrp4, and inhibit Agrin (zeige AGRN ELISA Kits)-stimulated MuSK (zeige MUSK ELISA Kits) phosphorylation.
LRP4 (zeige CORIN ELISA Kits) is expressed by embryonic cortical and hippocampal neurons, and downregulation of LRP4 (zeige CORIN ELISA Kits) in these neurons causes a reduction in density of synapses and number of primary dendrites. Collectively, the results demonstrate an essential and novel role of neuronal LRP4 (zeige CORIN ELISA Kits) in dendritic development and synaptogenesis in the central nervous system.
data suggest a model whereby Lrp4 (zeige CORIN ELISA Kits) modulates Wnt (zeige WNT2 ELISA Kits)/beta-catenin (zeige CTNNB1 ELISA Kits) signaling via interaction with Wnt (zeige WNT2 ELISA Kits) ligands and antagonists in a context-dependent manner.
a critical role for Lrp4 (zeige CORIN ELISA Kits), in response to agrin (zeige AGRN ELISA Kits), in modulating astrocytic ATP release and synaptic transmission
We show that prepatterning in mice requires Lrp4 (zeige CORIN ELISA Kits) but not the MuSK (zeige MUSK ELISA Kits) Fz-like domain
The loss of low density lipoprotein receptor-related protein 4 (zeige CORIN ELISA Kits) compromised foetal swallowing and breathing-like movements and downregulated the expression of aquaporin-9 (zeige AQP9 ELISA Kits) in the foetal membrane and aquaporin-1 (zeige AQP1 ELISA Kits) in the placenta, which possibly affected the amniotic fluid clearance.
Reveal novel roles for APP (zeige APP ELISA Kits) in regulating neuromuscular synapse formation through hetero-oligomeric interaction with LRP4 (zeige CORIN ELISA Kits) and agrin (zeige AGRN ELISA Kits) and thereby provide new insights into the molecular mechanisms that govern NMJ formation and maintenance.
Results suggest that mdig may contribute to silica-induced lung fibrosis by altering the balance between Th17 and Treg cells.
These studies demonstrate a role for Lrp4 (zeige CORIN ELISA Kits) in hippocampal function.
Lrp4 (zeige CORIN ELISA Kits) is a critical player in bone-mass homeostasis.
Data indicate that LRP4 (low-density lipoprotein receptor-related protein 4 (zeige CORIN ELISA Kits)) deficiency in bone dramatically elevated serum sclerostin (zeige SOST ELISA Kits) levels whereas bone expression of Sost (zeige SOST ELISA Kits) encoding for sclerostin (zeige SOST ELISA Kits) was unaltered.
identification of a doublet mutation in complete linkage disequilibrium with syndactyly in one gene of the critical interval: LRP4
autosomal recessive loss-of-function mutations in Megf7/Lrp4 result in a form of syndactyly, mulefoot disease
4 new LRP4 non-synonymous missense point mutations co-segregating in Holstein, German Simmental & Simmental-Charolais families represent independent mutations affecting different conserved protein domains.
This gene encodes a member of the low-density lipoprotein receptor-related protein family. The encoded protein may be a regulator of Wnt signaling. Mutations in this gene are associated with Cenani-Lenz syndrome.
low-density lipoprotein receptor-related protein 4
, multiple epidermal growth factor-like domains 7
, LDLR dan
, low density lipoprotein receptor-related protein 4
, low density lipoprotein receptor-related protein 4-like
, low-density lipoprotein receptor-related protein 4-like