A missense mutation in LRR8 of RXFP2 is associated with cryptorchidism

Mammalian Genome

Volumn 21, Issue 9-10, 2010, Pages 442-449

  Harris, Rebecca M ^a   Finlayson, Courtney ^a   Weiss, Jeffrey ^a   Fisher, Lisa ^a   Hurley, Lisa ^a   Barrett, Tim ^a   Emge, Donna ^a   Bathgate, Ross A D ^b   Agoulnik, Alexander I ^c   Jameson, J Larry ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c FLORIDA INTERNATIONAL UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASPARTIC ACID; CELL PROTEIN; CYCLIC AMP; ETHYLNITROSOUREA; HORMONE RECEPTOR; LEUCINE RICH REPEAT 7 PROTEIN; LEUCINE RICH REPEAT 8 PROTEIN; LEUCINE RICH REPEAT 9 PROTEIN; RELAXIN FAMILY PEPTIDE RECEPTOR 2; UNCLASSIFIED DRUG;

ALLELE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BETA SHEET; CELL LOSS; CELL STRAIN HEK293; CELL SURFACE; COMPUTER MODEL; CONTROLLED STUDY; CRYPTORCHISM; EXON; FEMALE; GENE LOCATION; GENE MAPPING; GENETIC ASSOCIATION; GENETIC COMPLEMENTATION; GENETIC TRANSFECTION; GENOME ANALYSIS; GERM CELL; HISTOPATHOLOGY; HUMAN; HUMAN CELL; LOSS OF FUNCTION ALLELE; MALE; MISSENSE MUTATION; MOUSE; MUTAGENESIS; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN TRANSPORT; SERTOLI CELL; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SPERMATOGENESIS; TESTIS WEIGHT; WILD TYPE;

ANIMALS; CHROMOSOME MAPPING; CRYPTORCHIDISM; DISEASE MODELS, ANIMAL; DNA MUTATIONAL ANALYSIS; ETHYLNITROSOUREA; GENE KNOCKOUT TECHNIQUES; GENETIC COMPLEMENTATION TEST; MALE; MICE; MICE, INBRED C57BL; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTAGENESIS; MUTATION, MISSENSE; POLYMERASE CHAIN REACTION; PROTEIN CONFORMATION; PROTEIN FOLDING; RECEPTORS, G-PROTEIN-COUPLED; SIGNAL TRANSDUCTION; TESTIS;

MUS;

EID: 78249260914     PISSN: 09388990     EISSN: 14321777     Source Type: Journal    
DOI: 10.1007/s00335-010-9291-5     Document Type: Article

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