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Article title matches
- Category:Lesch-nyhan (42 bytes)
1: List of pages with the keyword Lesch-nyhan - Category:Lesch, C (39 bytes)
- Category:Lesch C (38 bytes)
Page text matches
- 2jbh (5,589 bytes)
24: ...s a result of genetic mutations is linked to both Lesch-Nyhan disease and gout. In the present study, we have c... - 8tpv (4,783 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 8tpy (4,758 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 1bzy (5,675 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 1d6n (4,286 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 1hmp (4,184 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 1z7g (6,101 bytes)
10: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 2ow9 (6,132 bytes)
- 2ozr (4,536 bytes)
- 4ijq (3,262 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 1qk5 (5,461 bytes)
24: ...id that directly contacts the Mg(2+) ions, causes Lesch-Nyhan syndrome (HGPRT(Kinston), D193N). The Leu78-Lys79... - Category:Lesch-nyhan (42 bytes)
1: List of pages with the keyword Lesch-nyhan - 2vfa (6,463 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 3gep (5,440 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 3ggc (5,399 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - 3ggj (5,401 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032... - Sandbox Reserved 317 (4,030 bytes)
9: ... divalent magnesium cation. HGPRT is deficient in Lesch-Nyhan syndrome, a severe neurological disorder characte... - 1tc2 (4,741 bytes)
24: ... inherited mutations in the human HPRT leading to Lesch-Nyhan syndrome (D193N) or gout (S103R or S109L), as the... - Phosphoribosyltransferase (2,816 bytes)
15: Mutations in HPRT are involved in Lesch-Nyhan syndrome and hereditary gout<ref>PMID:8112742</re... - 4kn6 (3,279 bytes)
11: ...MAN HPRT_HUMAN] Defects in HPRT1 are the cause of Lesch-Nyhan syndrome (LNS) [MIM:[https://omim.org/entry/30032...
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