Citations for
1ADSL, ADSLD
Pathway-specific effects of ADSL deficiency on neurodevelopment.
Dutto I, Gerhards J, Herrera A, Souckova O, Škopová V, Smak JA, Junza A, Yanes O, Boeckx C, Burkhalter MD, Zikánová M, Pons S, Philipp M, Lüders J, Stracker TH.
Elife. Feb 8;11:e70518. doi: 10.7554/eLife.70518 2022
2ADSL
Carcinogenic effect of adenylosuccinate lyase (ADSL) in prostate cancer development and progression through the cell cycle pathway.
Liao J, Song Q, Li J, Du K, Chen Y, Zou C, Mo Z.
Cancer Cell Int. Sep 6;21(1):467. doi: 10.1186/s12935-021-02174-6. 2021
3ADSL, ADSLD
Clinical and molecular characterization of patients with adenylosuccinate lyase deficiency.
Mastrogiorgio G, Macchiaiolo M, Buonuomo PS, Bellacchio E, Bordi M, Vecchio D, Brown KP, Watson NK, Contardi B, Cecconi F, Tartaglia M, Bartuli A.
Orphanet J Rare Dis. Mar 1;16(1):112. doi: 10.1186/s13023-021-01731-6 2021
4ADSL
Targeting the De Novo Purine Synthesis Pathway Through Adenylosuccinate Lyase Depletion Impairs Liver Cancer Growth by Perturbing Mitochondrial Function
Jiang T, Sánchez-Rivera FJ, Soto-Feliciano YM, Yang Q, Song CQ, Bhuatkar A, Haynes CM, Hemann MT, Xue W.
Hepatology. Jul;74(1):233-247. doi: 10.1002/hep.31685. Epub 2021 Jul 12. 2021
5ADSL, ADSLD
Very mild isolated intellectual disability caused by adenylosuccinate lyase deficiency: a new phenotype.
Macchiaiolo M, Buonuomo PS, Mastrogiorgio G, Bordi M, Testa B, Weber G, Bellacchio E, Tartaglia M, Cecconi F, Bartuli A.
Mol Genet Metab Rep. May 6;23:100592. doi: 10.1016/j.ymgmr.2020.100592. 2020
6ADSL, ATIC
Mutations of ATIC and ADSL affect purinosome assembly in cultured skin fibroblasts from patients with AICA-ribosiduria and ADSL deficiency.
Baresova V, Skopova V, Sikora J, Patterson D, Sovova J, Zikanova M, Kmoch S.
Hum Mol Genet 21(7):1534-43. doi: 10.1093/hmg/ddr591. Epub 2011 Dec 16. 2012
7ADSL, ADSLD
Biochemical and structural analysis of 14 mutant adsl enzyme complexes and correlation to phenotypic heterogeneity of adenylosuccinate lyase deficiency.
Zikanova M, Skopova V, Hnizda A, Krijt J, Kmoch S.
Hum Mutat. Apr;31(4):445-55. doi: 10.1002/humu.21212. 2010
8ADSL, ADSLD, AS
Misleading behavioural phenotype with adenylosuccinate lyase deficiency.
Gitiaux C, Ceballos-Picot I, Marie S, Valayannopoulos V, Rio M, Verrieres S, Benoist JF, Vincent MF, Desguerre I, Bahi-Buisson N.
Eur J Hum Genet 17(1):133-6. Epub 2008 Oct 1. 2009
9ADSL, ADSLD
Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the equivalent mutant Bacillus subtilis ASL.
Sivendran S, Patterson D, Spiegel E, McGown I, Cowley D, Colman RF.
J Biol Chem 279(51):53789-97. Epub 2004 Oct 7. 2004
10ADSL, ADSLD
Adenylosuccinate lyase deficiency--first British case.
Marinaki AM, Champion M, Kurian MA, Simmonds HA, Marie S, Vincent MF, van den Berghe G, Duley JA, Fairbanks LD.
Nucleosides Nucleotides Nucleic Acids 23(8-9):1231-3. 2004
11ADSL, ADSLD
Mutation of a nuclear respiratory factor 2 binding site in the 5' untranslated region of the ADSL gene in three patients with adenylosuccinate lyase deficiency.
Marie S, Race V, Nassogne MC, Vincent MF, Van den Berghe G.
Am J Hum Genet 71(1):14-21. 2002
12ADSL, ADSLD
Human adenylosuccinate lyase (ADSL), cloning and characterization of full-length cDNA and its isoform, gene structure and molecular basis for ADSL deficiency in six patients.
Kmoch S, Hartmannova H, Stiburkova B, Krijt J, Zikanova M, Sebesta I.
Hum Mol Genet 9(10):1501-13. 2000
13ADSL, ADSLD
Clinical, biochemical and molecular genetic correlations in adenylosuccinate lyase deficiency.
Race V, Marie S, Vincent MF, Van Den Berghe G.
Hum Mol Genet 9(14):2159-65. 2000
14ADSL
Mutation analysis in adenylosuccinate lyase deficiency: eight novel mutations in the re-evaluated full ADSL coding sequence.
Marie S, et al.
Hum Mutat 13(3):197-202. 1999
15ADSL
Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1-q13.2.
Fon EA, et al.
Cytogenet Cell Genet 64 : 201-203. 1993
16ADSL, ADSLD
A mutation in adenylosuccinate lyase associated with mental retardation and autistic features.
Stone RL, et al.
Nat Genet 1 : 59-63. 1992
17ADSL
Isolation and regional localization of the human adenylosuccine lyase gene.
Budarf ML, et al.
(HGM11) Cytogenet Cell Genet 58 : 2046. 1991
18ADSL, ADSLD
Adenylosuccinase deficiency : an inborn error of purine nucleotide synthesis.
Jaeken J, et al.
Eur J Pediatr 148 : 126-131. 1988
19ADSL
Chimpanzee chromosome 23 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity.
Jones C, et al.
(HGM9) Cytogenet Cell Genet 46 : 635. 1987
20ADSL
A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity.
Van Keuren ML, et al.
Cytogenet Cell Genet 44 : 142-147. 1987
21ADSL, ADSLD
An infantile autistic syndrome characterised by the presence of succinylpurines in body fluids.
Jaeken J, et al.
Lancet II : 1058-1061. 1984