{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,19]],"date-time":"2026-09-19T20:19:16Z","timestamp":1789849156322,"version":"4.0.1"},"reference-count":37,"publisher":"The Company of Biologists","issue":"3-4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2009,2,25]]},"abstract":"<jats:p>Lesch-Nyhan disease (LND) is a rare inherited disorder caused by mutations in the gene encoding hypoxanthine-guanine phosphoribosyltransferase (HPRT). LND is characterized by overproduction of uric acid, leading to gouty arthritis and nephrolithiasis. Affected patients also have characteristic neurological and behavioral anomalies. Multiple cell models have been developed to study the molecular and metabolic aspects of LND, and several animal models have been developed to elucidate the basis for the neurobehavioral syndrome. The models have different strengths and weaknesses rendering them suitable for studying different aspects of the disease. The extensive modeling efforts in LND have questioned the concept that an \u2018ideal\u2019 disease model is one that replicates all of its features because the pathogenesis of different elements of the disease involves different mechanisms. Instead, the modeling efforts have suggested a more fruitful approach that involves developing specific models, each tailored for addressing specific experimental questions.<\/jats:p>","DOI":"10.1242\/dmm.002543","type":"journal-article","created":{"date-parts":[[2009,2,26]],"date-time":"2009-02-26T19:48:30Z","timestamp":1235677710000},"page":"116-121","source":"Crossref","is-referenced-by-count":63,"title":["Lesch-Nyhan disease: from mechanism to model and back again"],"prefix":"10.1242","volume":"2","author":[{"given":"H. 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