Citations for
1ARSB, BMP4, CHST11, WNT9A
Regulation of chondroitin-4-sulfotransferase (CHST11) expression by opposing effects of arylsulfatase B on BMP4 and Wnt9A.
Bhattacharyya S, Feferman L, Tobacman JK.
Biochim Biophys Acta 1849(3):342-52. doi: 10.1016/j.bbagrm.2014.12.009. Epub 2014 Dec 12. 2015
2ARSB, MPS6
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) with a predominantly cardiac phenotype.
Jurecka A, Golda A, Opoka-Winiarska V, Piotrowska E, Tylki-Szymańska A.
Mol Genet Metab 104(4):695-9. doi: 10.1016/j.ymgme.2011.08.024. Epub 2011 Aug 27. 2011
3ARSB
Arylsulfatase B regulates colonic epithelial cell migration by effects on MMP9 expression and RhoA activation.
Bhattacharyya S, Tobacman JK.
Clin Exp Metastasis 26(6):535-45. Epub 2009 Mar 22. 2009
4ARSB, CAND1, MAGI2, PRUNE2
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.
Potkin SG, Guffanti G, Lakatos A, Turner JA, Kruggel F, Fallon JH, Saykin AJ, Orro A, Lupoli S, Salvi E, Weiner M, Macciardi F; Alzheimer's Disease Neuroimaging Initiative.
PLoS One 4(8):e6501. doi: 10.1371/journal.pone.0006501. 2009
5ARSB, MPS6
Maroteaux-Lamy syndrome: functional characterization of pathogenic mutations and polymorphisms in the arylsulfatase B gene.
Garrido E, Cormand B, Hopwood JJ, Chab‡s A, Grinberg D, Vilageliu L.
Mol Genet Metab 94(3):305-12. Epub 2008 Apr 10. 2008
6ARSB, MPS6
Identification of the molecular defects in Spanish and Argentinian mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) patients, including 9 novel mutations.
Garrido E, Chabás A, Coll MJ, Blanco M, Domínguez C, Grinberg D, Vilageliu L, Cormand B.
Mol Genet Metab 92(1-2):122-30. Epub 2007 Jul 20. 2007
7ARSB, MPS6
Mutational analysis of 105 mucopolysaccharidosis type VI patients.
Karageorgos L, Brooks DA, Pollard A, Melville EL, Hein LK, Clements PR, Ketteridge D, Swiedler SJ, Beck M, Giugliani R, Harmatz P, Wraith JE, Guffon N, Leão Teles E, Sá Miranda MC, Hopwood JJ.
Hum Mutat 28(9):897-903. 2007
8ARSA, ARSB, ARSC2, ARSD, ARSE, ARSF, ARSG, ARSH, ARSJ, ARSK, ARSI, SUMF1, GALNS, SULF1, SULF2, SGSH, GNS, IDS
Sulfatases and sulfatase modifying factors: an exclusive and promiscuous relationship.
Sardiello M, Annunziata I, Roma G, Ballabio A.
Hum Mol Genet 14(21):3203-17. Epub 2005 Sep 20. 2005
9ARSB, MPS6
Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene in South American patients.
Petry MF, Nonemacher K, Sebben JC, Schwartz IV, Azevedo AC, Burin MG, de Rezende AR, Kim CA, Giugliani R, Leistner-Segal S.
J Inherit Metab Dis 28(6):1027-34. 2005
10ARSB, MPS6
Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VI.
Azevedo AC, Schwartz IV, Kalakun L, Brustolin S, Burin MG, Beheregaray AP, Leistner S, Giugliani C, Rosa M, Barrios P, Marinho D, Esteves P, Valadares E, Boy R, Horovitz D, Mabe P, da Silva LC, de Souza IC, Ribeiro M, Martins AM, Palhares D, Kim CA, Giugliani R.
Clin Genet 66(3):208-13. 2004
11MPS6, ARSB
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): a Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network.
Bradford TM, Litjens T, Parkinson EJ, Hopwood JJ, Brooks DA.
Biochemistry 41(15):4962-71. 2002
12ARSB, MPS6
Mucopolysaccharidosis type VI: Structural and clinical implications of mutations in N-acetylgalactosamine-4-sulfatase.
Litjens T, Hopwood JJ.
Hum Mutat 18(4):282-95. 2001
13MPS6, ARSB
Maroteaux-lamy syndrome: five novel mutations and their structural localization.
Villani GR, et al.
Biochim Biophys Acta 1453(2):185-92. 1999
14MPS4A, ARSB
Identification, expression, and biochemical characterization of N-acetylgalactosamine-4- sulfatase mutations and relationship with clinical phenotype in MPS-VI patients.
Litjens T, et al.
Am J Hum Genet 58 : 1127-1134. 1996
15ARSB, MPS6
Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Matoreaux-Lamy syndrome.
Isbrandt D, et al.
Hum Mutat 7 : 361-363. 1996
16ARSB, MPS6
N-acetylgalactosamine-4-sulfatase : identification of four new mutations within the conserved sulfatase region causing mucopolysaccharidosis type VI.
Simonaro CM, et al.
Biochim Biophys Acta 1272 : 129-132. 1995
17MPS6, ARSB
Four novel mutant alleles of the arylsulfatase B gene in two patients with intermediate form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome).
Voskoboeva E, et al.
Hum Genet 93 : 259-264. 1994
18MPS6, ARSB
Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) : six unique arylsulfatase B gene alleles causing variable disease phenotypes.
Isbrandt D, et al.
Am J Hum Genet 54 : 454-463. 1994
19MPS6, ARSB
Juvenile form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome).
Arlt G, et al.
J Biol Chem 269 : 9638-9643. 1994
20ARSB, MPS6
Mucopolysaccharidosis type VI : identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneity.
Jin WD, et al.
Am J Hum Genet 50 : 795-800. 1992
21ARSB
A common polymorphism in the human arylsulfatase B (ARSB) gene at 5q13-q14.
Jin WD, et al.
Nucleic Acids Res 19 : 4305. 1991
22ARSB, MPS6
Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). An intermediate clinical phenotype caused by substitution of valine for glycine at position 137 of arylsulfatase B.
Wicker G, et al.
J Biol Chem 266 : 21386-21391. 1991
23ARSB
Chromosomal localization of ARSB, the gene for humanN-acetylgalactosamine-4-sulfatase.
Litjens T, et al.
Hum Genet 82 : 67-68. 1989
24ARSB, HEXB
Interstitial deletion of band q12 of chromosome 5.
Dudin G, et al.
Clin Genet 25 : 455-458. 1984
25ARSB
Assignment of the gene for human arylsulfatase B, ARSB, to chromosome region 5p11->5qter.
Fidzianska E, et al.
Cytogenet Cell Genet 38 : 150-151. 1984
26ARSB, GLA, HEXB
Regional localization of alpha-galactosidase (GLA) to Xpter->q22, hexosaminidase B (HEXB) to 5q13->qter, and arylsulfatase B (ARSB) to 5pter->q13.
Fox MF, et al.
Cytogenet Cell Genet 38 : 45-49. 1984
27ARSA, ARSB
Lysosomal arylsulfatase deficiencies in humans: chromosome assignments for arylsulfatase A and B.
De Luca C, et al.
Proc Natl Acad Sci U S A 76 : 1957-1961. 1979
28ARSB
Assignment of a gene for arylsulfatase B to human chromosome 5 using human-mouse somatic cell hybrids.
Hellkuhl B, et al.
Cytogenet Cell Genet 22 : 203-206. 1978
29ARSB, MPS6
Une nouvelle dysostose avec Žlimination urinaire de chondro•tine-sulfate B.
Maroteaux P, et al.
Presse Med 71 : 1849-1852. 1963