A Golgi study of neuronal architecture in a genetic mouse model for Lesch–Nyhan disease
Neurobiology of Disease, 2005 Lesch–Nyhan disease (LND) is an inherited disorder associated with deficiency of hypoxanthine-guanine phosphoribosyltransferase (HPRT), an enzyme essential for purine recycling.
Ivan Mikolaenko +4 more
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Characterization of the Dopamine Defect in Primary Cultures of Dopaminergic Neurons from Hypoxanthine Phosphoribosyltransferase Knockout Mice [PDF]
, 2000 Doug W. Smith, Theodore Friedmann
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Differential regulation of the von Willebrand factor and Flt-1 promoters in the endothelium of hypoxanthine phosphoribosyltransferase–targeted mice [PDF]
, 2002 Takashi Minami +4 more
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Kelley–Seegmiller syndrome due to a new variant of the hypoxanthine–guanine phosphoribosyltransferase (I136T) encoding gene (HPRT Marseille) [PDF]
, 2004 B. Dussol +5 more
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Plasmodium falciparum hypoxanthine guanine phosphoribosyltransferase [PDF]
, 2005 Jayalakshmi Raman +5 more
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A case of partial deficiency of hypoxanthine-guanine phosphoribosyltransferase.
, 1988 Kazutaka FUJITA +3 more
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Hypoxanthine phosphoribosyltransferase (HPRT)‐deficiency is associated with impaired fertility in the female rat [PDF]
, 2020 Stephen Meek +6 more
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Transient change in GABA receptor subunit mRNA expression in cerebellar nuclei during Purkinje cell degeneration [PDF]
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