Functional polymorphisms in the P2X7 receptor gene are associated with osteoporosis

Osteoporosis International

Volumn 24, Issue 3, 2013, Pages 949-959

  Husted, L B ^a   Harslof T ^a   Stenkjaer L ^a   Carstens, M ^a   Jorgensen N R ^b   Langdahl, B L ^a  

^a AARHUS UNIVERSITY HOSPITAL   (Denmark)

^b GLOSTRUP UNIVERSITY HOSPITAL   (Denmark)

Author keywords

Genetics; Osteoporosis; P2X7 receptor; Polymorphisms; Vertebral fracture

Indexed keywords

ALANINE; ARGININE; GLUTAMIC ACID; GLUTAMINE; HISTIDINE; PURINERGIC P2X7 RECEPTOR; THREONINE; TYROSINE;

ADULT; AGED; ALLELE; AMINO ACID SUBSTITUTION; ANIMAL EXPERIMENT; ARTICLE; BONE DENSITY; CONTROLLED STUDY; DUAL ENERGY X RAY ABSORPTIOMETRY; FEMALE; GAIN OF FUNCTION MUTATION; GENE EXPRESSION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HIP; HIP FRACTURE; HISTOPATHOLOGY; HUMAN; LOSS OF FUNCTION MUTATION; LUMBAR SPINE; MAJOR CLINICAL STUDY; MALE; MONOCYTE; MOUSE; NONHUMAN; OSTEOPOROSIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; SPINE FRACTURE; SPINE RADIOGRAPHY; CASE CONTROL STUDY; FRAGILITY FRACTURE; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; PATHOPHYSIOLOGY; POSTMENOPAUSE OSTEOPOROSIS; RISK ASSESSMENT;

AGED; BONE DENSITY; CASE-CONTROL STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; OSTEOPOROSIS; OSTEOPOROSIS, POSTMENOPAUSAL; OSTEOPOROTIC FRACTURES; POLYMORPHISM, GENETIC; RECEPTORS, PURINERGIC P2X7; RISK ASSESSMENT; SPINAL FRACTURES;

MLCS; MLOWN;

EID: 84878819756     PISSN: 0937941X     EISSN: 14332965     Source Type: Journal    
DOI: 10.1007/s00198-012-2035-5     Document Type: Article

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