142 related articles for article (PubMed ID: 3752080)
21. Cloning, characterization, and nucleotide sequence analysis of the argH gene from Campylobacter jejuni TGH9011 encoding argininosuccinate lyase.
Hani EK; Chan VL
J Bacteriol; 1994 Apr; 176(7):1865-71. PubMed ID: 8144452
[TBL] [Abstract][Full Text] [Related]
22. Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated families.
Kleijer WJ; Garritsen VH; Linnebank M; Mooyer P; Huijmans JG; Mustonen A; Simola KO; Arslan-Kirchner M; Battini R; Briones P; Cardo E; Mandel H; Tschiedel E; Wanders RJ; Koch HG
J Inherit Metab Dis; 2002 Sep; 25(5):399-410. PubMed ID: 12408190
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Arginine auxotrophs of Candida albicans deficient in argininosuccinate lyase.
Gibbons GF; Howard DH
J Gen Microbiol; 1986 Feb; 132(2):263-8. PubMed ID: 3519855
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. [Molecular basis of urea cycle disorders].
Matsuda I; Matsuura T; Hoshide R; Uchino T; Matsubasa T
Nihon Rinsho; 1993 Feb; 51(2):520-4. PubMed ID: 8464164
[TBL] [Abstract][Full Text] [Related]
29. Gene symbol: ASL. Disease: Argininosuccinate lyase deficiency.
Trevisson E; Salviati L; Baldoin MC; Casarin A; Basso G; Burlina A
Hum Genet; 2008 Oct; 124(3):303. PubMed ID: 18846632
[No Abstract] [Full Text] [Related]
30. Gene symbol: ASL. Disease: Argininosuccinate lyase deficiency.
Trevisson E; Salviati L; Baldoin MC; Casarin A; Basso G; Burlina A
Hum Genet; 2008 Oct; 124(3):303. PubMed ID: 18846631
[No Abstract] [Full Text] [Related]
31. Purification and subunit structure of argininosuccinate lyase from Chlamydomonas reinhardi.
Matagne RF; Schlösser JP
Biochem J; 1977 Oct; 167(1):71-5. PubMed ID: 588268
[TBL] [Abstract][Full Text] [Related]
32. [Argininosuccinate lyase deficiency].
Matsubasa T
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):179-81. PubMed ID: 9590021
[No Abstract] [Full Text] [Related]
33. 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]
34. 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]
35. Molecular evolution from argininosuccinate lyase to delta-crystallin.
Mori M; Matsubasa T; Amaya Y; Takiguchi M
Prog Clin Biol Res; 1990; 344():683-99. PubMed ID: 2203059
[TBL] [Abstract][Full Text] [Related]
36. Argininosuccinate Lyase Deficiency Causes an Endothelial-Dependent Form of Hypertension.
Kho J; Tian X; Wong WT; Bertin T; Jiang MM; Chen S; Jin Z; Shchelochkov OA; Burrage LC; Reddy AK; Jiang H; Abo-Zahrah R; Ma S; Zhang P; Bissig KD; Kim JJ; Devaraj S; Rodney GG; Erez A; Bryan NS; Nagamani SCS; Lee BH
Am J Hum Genet; 2018 Aug; 103(2):276-287. PubMed ID: 30075114
[TBL] [Abstract][Full Text] [Related]
37. Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry.
Stadler S; Gempel K; Bieger I; Pontz BF; Gerbitz KD; Bauer MF; Hofmann S
J Inherit Metab Dis; 2001 Jun; 24(3):370-8. PubMed ID: 11486903
[TBL] [Abstract][Full Text] [Related]
38. Generation of induced pluripotent stem cells (UCLi024-A) from a patient with argininosuccinate lyase deficiency carrying a homozygous c.437G > A (p.Arg146Gln) mutation.
Duff C; Islam M; Gagliano O; Pramod H; Rashidi H; Kurian MA; Gissen P; Baruteau J
Stem Cell Res; 2024 Apr; 76():103365. PubMed ID: 38422816
[TBL] [Abstract][Full Text] [Related]
39. Prolidase deficiency: biochemical classification of alleles.
Boright AP; Scriver CR; Lancaster GA; Choy F
Am J Hum Genet; 1989 May; 44(5):731-40. PubMed ID: 2705457
[TBL] [Abstract][Full Text] [Related]
40. Lethal neonatal argininosuccinate lyase deficiency in four children from one sibship.
van der Heiden C; Gerards LJ; van Biervliet JP; Desplanque J; de Bree PK; van Sprang FJ; Wadman SK
Helv Paediatr Acta; 1976 Dec; 31(4-5):407-17. PubMed ID: 1017984
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
