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4. Human argininosuccinate lyase: a structural basis for intragenic complementation. Turner MA; Simpson A; McInnes RR; Howell PL Proc Natl Acad Sci U S A; 1997 Aug; 94(17):9063-8. PubMed ID: 9256435 [TBL] [Abstract][Full Text] [Related]
5. Mechanisms for intragenic complementation at the human argininosuccinate lyase locus. Yu B; Thompson GD; Yip P; Howell PL; Davidson AR Biochemistry; 2001 Dec; 40(51):15581-90. PubMed ID: 11747433 [TBL] [Abstract][Full Text] [Related]
6. Functional complementation in yeast allows molecular characterization of missense argininosuccinate lyase mutations. Trevisson E; Burlina A; Doimo M; Pertegato V; Casarin A; Cesaro L; Navas P; Basso G; Sartori G; Salviati L J Biol Chem; 2009 Oct; 284(42):28926-34. PubMed ID: 19703900 [TBL] [Abstract][Full Text] [Related]
7. Intragenic complementation and the structure and function of argininosuccinate lyase. Yu B; Howell PL Cell Mol Life Sci; 2000 Oct; 57(11):1637-51. PubMed ID: 11092456 [TBL] [Abstract][Full Text] [Related]
8. Interallelic complementation in an inborn error of metabolism: genetic heterogeneity in argininosuccinate lyase deficiency. McInnes RR; Shih V; Chilton S Proc Natl Acad Sci U S A; 1984 Jul; 81(14):4480-4. PubMed ID: 6589607 [TBL] [Abstract][Full Text] [Related]
9. Understanding the role of argininosuccinate lyase transcript variants in the clinical and biochemical variability of the urea cycle disorder argininosuccinic aciduria. Hu L; Pandey AV; Eggimann S; Rüfenacht V; Möslinger D; Nuoffer JM; Häberle J J Biol Chem; 2013 Nov; 288(48):34599-611. PubMed ID: 24136197 [TBL] [Abstract][Full Text] [Related]
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11. Bacterial expression of mutant argininosuccinate lyase reveals imperfect correlation of in-vitro enzyme activity with clinical phenotype in argininosuccinic aciduria. Engel K; Vuissoz JM; Eggimann S; Groux M; Berning C; Hu L; Klaus V; Moeslinger D; Mercimek-Mahmutoglu S; Stöckler S; Wermuth B; Häberle J; Nuoffer JM J Inherit Metab Dis; 2012 Jan; 35(1):133-40. PubMed ID: 21667091 [TBL] [Abstract][Full Text] [Related]
12. Argininosuccinate lyase (ASL) deficiency: mutation analysis in 27 patients and a completed structure of the human ASL gene. Linnebank M; Tschiedel E; Häberle J; Linnebank A; Willenbring H; Kleijer WJ; Koch HG Hum Genet; 2002 Oct; 111(4-5):350-9. PubMed ID: 12384776 [TBL] [Abstract][Full Text] [Related]
13. Molecular analysis of human argininosuccinate lyase: mutant characterization and alternative splicing of the coding region. Walker DC; McCloskey DA; Simard LR; McInnes RR Proc Natl Acad Sci U S A; 1990 Dec; 87(24):9625-9. PubMed ID: 2263616 [TBL] [Abstract][Full Text] [Related]
14. Arg-7 mutant X wild-type crosses in Chlamydomonas reinhardi: study of the enzyme produced in diploid strains. Matagne RF Mol Gen Genet; 1976 Jul; 146(2):209-14. PubMed ID: 958202 [TBL] [Abstract][Full Text] [Related]
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16. Argininosuccinic aciduria: assignment of the argininosuccinate lyase gene to the pter to q22 region of human chromosome 7 by bioautography. Naylor SL; Klebe RJ; Shows TB Proc Natl Acad Sci U S A; 1978 Dec; 75(12):6159-62. PubMed ID: 282632 [TBL] [Abstract][Full Text] [Related]
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19. A novel stop codon mutation (X465Y) in the argininosuccinate lyase gene in a patient with argininosuccinic aciduria. Tanaka T; Nagao M; Mori T; Tsutsumi H Tohoku J Exp Med; 2002 Oct; 198(2):119-24. PubMed ID: 12512996 [TBL] [Abstract][Full Text] [Related]
20. The argininosuccinate lyase gene of Chlamydomonas reinhardtii: an important tool for nuclear transformation and for correlating the genetic and molecular maps of the ARG7 locus. Debuchy R; Purton S; Rochaix JD EMBO J; 1989 Oct; 8(10):2803-9. PubMed ID: 2583083 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]