140 related articles for article (PubMed ID: 11092456)
1. 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]
2. Three-dimensional structure of the argininosuccinate lyase frequently complementing allele Q286R.
Sampaleanu LM; Vallée F; Thompson GD; Howell PL
Biochemistry; 2001 Dec; 40(51):15570-80. PubMed ID: 11747432
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyond.
Erez A; Nagamani SC; Lee B
Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):45-53. PubMed ID: 21312326
[TBL] [Abstract][Full Text] [Related]
5. A mouse model of argininosuccinic aciduria: biochemical characterization.
Reid Sutton V; Pan Y; Davis EC; Craigen WJ
Mol Genet Metab; 2003 Jan; 78(1):11-6. PubMed ID: 12559843
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. Argininosuccinic acid synthetase deficiency in a hamster cell line and its complementation of argininosuccinic aciduria human fibroblasts.
González-Noriega A; Verduzco J; Prieto E; Velázquez A
J Inherit Metab Dis; 1980; 3(2):45-8. PubMed ID: 6777600
[TBL] [Abstract][Full Text] [Related]
11. Intragenic complementation at the argininosuccinate lyase locus: reconstruction of the active site.
Howell PL; Turner MA; Christodoulou J; Walker DC; Craig HJ; Simard LR; Ploder L; McInnes RR
J Inherit Metab Dis; 1998; 21 Suppl 1():72-85. PubMed ID: 9686346
[TBL] [Abstract][Full Text] [Related]
12. Mutational analysis of duck delta 2 crystallin and the structure of an inactive mutant with bound substrate provide insight into the enzymatic mechanism of argininosuccinate lyase.
Sampaleanu LM; Yu B; Howell PL
J Biol Chem; 2002 Feb; 277(6):4166-75. PubMed ID: 11698398
[TBL] [Abstract][Full Text] [Related]
13. Intragenic complementation at the human argininosuccinate lyase locus. Identification of the major complementing alleles.
Walker DC; Christodoulou J; Craig HJ; Simard LR; Ploder L; Howell PL; McInnes RR
J Biol Chem; 1997 Mar; 272(10):6777-83. PubMed ID: 9045711
[TBL] [Abstract][Full Text] [Related]
14. Studies on complementation in argininosuccinate synthetase and argininosuccinate lyase deficiencies in human fibroblasts.
Cathelineau L; Pham Dinh D; Briand P; Kamoun P
Hum Genet; 1981; 57(3):282-4. PubMed ID: 7250970
[TBL] [Abstract][Full Text] [Related]
15. Structural studies of duck delta 1 and delta 2 crystallin suggest conformational changes occur during catalysis.
Sampaleanu LM; Vallée F; Slingsby C; Howell PL
Biochemistry; 2001 Mar; 40(9):2732-42. PubMed ID: 11258884
[TBL] [Abstract][Full Text] [Related]
16. [Argininosuccinic aciduria].
Kobayashi K; Tatsuno M; Matuo S; Saheki T
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):510-3. PubMed ID: 3270856
[No Abstract] [Full Text] [Related]
17. 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]
18. Argininosuccinate lyase deficiency.
Nagamani SC; Erez A; Lee B
Genet Med; 2012 May; 14(5):501-7. PubMed ID: 22241104
[TBL] [Abstract][Full Text] [Related]
19. Neonatal argininosuccinic aciduria with normal brain and kidney but absent liver argininosuccinate lyase activity.
Glick NR; Snodgrass PJ; Schafer IA
Am J Hum Genet; 1976 Jan; 28(1):22-30. PubMed ID: 174426
[TBL] [Abstract][Full Text] [Related]
20. Biochemical characterization of argininosuccinate lyase from M. tuberculosis: significance of a c-terminal cysteine in catalysis and thermal stability.
Mishra A; Surolia A
IUBMB Life; 2017 Nov; 69(11):896-907. PubMed ID: 29044950
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]