LGR4/GPR48 Inactivation Leads to Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome Defects
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference66 articles.
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4. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism;Xu;Cytogenet. Genome Res.,2008
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1. LGR4 and LGR5 form distinct homodimers that only LGR4 complexes with RNF43/ZNRF3 to provide high affinity binding of R-spondin ligands;Scientific Reports;2023-07-04
2. LGR4: A New Receptor Member in Endocrine and Metabolic Diseases;Endocrine Reviews;2023-02-15
3. Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation;Journal of Clinical Investigation;2023-02-15
4. LGR4, a G Protein-Coupled Receptor With a Systemic Role: From Development to Metabolic Regulation;Frontiers in Endocrinology;2022-05-30
5. Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review;Molecular Syndromology;2022-02-11
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