Literature DB >> 14627688

Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defects.

R Zannolli, V Micheli, M A Mazzei, P Sacco, P Piomboni, E Bruni, C Miracco, M M de Santi, P Terrosi Vagnoli, L Volterrani, L Pellegrini, W Livi, B Lucani, S Gonnelli, A B Burlina, G Jacomelli, F Macucci, L Pucci, M Fimiani, J A Swift, M Zappella, G Morgese.   

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Year:  2003        PMID: 14627688      PMCID: PMC1735325          DOI: 10.1136/jmg.40.11.e121

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  4 in total

1.  An effort toward molecular neuroeconomics of food deprivation induced food hoarding in mice: focus on xanthine oxidoreductase gene expression and xanthine oxidase activity.

Authors:  Isaac Karimi; Shima Motamedi; Lora A Becker
Journal:  Metab Brain Dis       Date:  2017-12-19       Impact factor: 3.584

2.  Classical xanthinuria: a rare cause of pediatric urolithiasis.

Authors:  Nurver Akıncı; Adviye Çakıl; Ayşe Öner
Journal:  Turk J Urol       Date:  2013-12

3.  Allopurinol and oxypurinol promote osteoblast differentiation and increase bone formation.

Authors:  Isabel R Orriss; Timothy R Arnett; Jacob George; Miles D Witham
Journal:  Exp Cell Res       Date:  2016-03-08       Impact factor: 3.905

Review 4.  Physiology, Development, and Disease Modeling in the Drosophila Excretory System.

Authors:  Erez Cohen; Jessica K Sawyer; Nora G Peterson; Julian A T Dow; Donald T Fox
Journal:  Genetics       Date:  2020-02       Impact factor: 4.562

  4 in total

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