A missense mutation in LRR8 of RXFP2 is associated with cryptorchidism

INIS

• receptors 100%
• peptides 66%
• insulin 66%
• mutations 58%
• mice 50%
• testes 50%
• comparative evaluations 33%
• mutants 33%
• proteins 25%
• surfaces 16%
• losses 16%
• accumulation 16%
• weight 16%
• nitrosoureas 16%
• genetics 8%
• histology 8%
• mutagenesis 8%
• modeling 8%
• failures 8%
• defects 8%
• mapping 8%
• causality 8%
• sheets 8%
• tubules 8%
• exons 8%
• aspartic acid 8%
• germ cells 8%
• leucine 8%

Medicine and Dentistry

• Peptide Receptor 66%
• Insulin 66%
• Relaxin 66%
• Family 66%
• Cyclic Adenosine Monophosphate 50%
• Receptor 33%
• Mutant 33%
• Testes 25%
• Protein 16%
• Missense Mutation 16%
• Cell Surface 16%
• Cryptorchism 16%
• Nitrosourea 16%
• Gene Map 8%
• Histology 8%
• Causality 8%
• Leucine 8%
• Aspartic Acid 8%
• In Silico 8%
• Exon 8%
• Germ Cell 8%
• Protein Misfolding 8%
• Sertoli Cell 8%
• Mutagenesis 8%
• Cell Loss 8%
• Genetic Complementation 8%
• Analysis 8%
• Cells 8%

Biochemistry, Genetics and Molecular Biology

• Relaxin/Insulin-Like Family Peptide Receptor 2 66%
• Mutation 41%
• Mouse 41%
• Wild Type 25%
• Mutant 25%
• Missense Mutation 16%
• Allele 16%
• Surface Property 16%
• Testis Weight 16%
• Testis Descent 16%
• Protein 16%
• Mutagenesis 8%
• Mouse Mutant 8%
• Computer Model 8%
• EC50 8%
• Germ Cell 8%
• Aspartic Acid 8%
• Cell Loss 8%
• Gene Mapping 8%
• Sertoli Cell 8%
• Protein Misfolding 8%
• Leucine-Rich Repeat 8%
• Genetic Complementation 8%
• INSL3 8%
• Sequencing 8%