Regular ArticleIdentification by Shotgun Sequencing, Genomic Organization, and Functional Analysis of a Fourth Arylsulfatase Gene (ARSF) from the Xp22.3 Region☆
References (28)
- et al.
Basic local alignment search tool
J. Mol. Biol.
(1990) A streamlined random sequencing strategy for finding coding exons
Genomics
(1994)- et al.
A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
Cell
(1995) - et al.
Characterization of rat and human steroid sulfatases
Biochim. Biophys. Acta
(1989) General methods of sequence comparison
Bull. Math. Biol.
(1984)- et al.
Metabolism of3
J. Inherited Metab. Dis.
(1988) - et al.
Characterization of a murine gene expressed from the inactive X chromosome
Nature
(1991) - et al.
Biophysical Chemistry. Part I. The Conformation of Biological Macromolecules
(1980) - et al.
Long-range sequence analysis in Xq28: Thirteen known and six candidate genes in 219.4 kb of high GC DNA between theRCP/GCPG6PD
Hum. Mol. Genet.
(1996) Large-scale sequence analysis
Automated DNA Sequencing and Analysis Techniques
(1994)
Alu alert
Nature
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
Nature
Identification ofFMR2,FRAXE
Nature Genet.
Cited by (30)
Comparative and evolutionary studies of mammalian arylsulfatase and sterylsulfatase genes and proteins encoded on the X-chromosome
2017, Computational Biology and ChemistryCitation Excerpt :At least ninteen human sulfatase genes have been described, which encode enzymes with diverse metabolic roles in hydrolysing biological sulfate esters (Ratzka et al., 2010). These include a cluster of five arylsulfatase-like (ARS) genes located on the X-chromosome: sterylsulfatase (STS) (Yen et al., 1998); ARSD (Urbitsch et al., 2000); ARSE (Parenti et al., 1997); ARSF (Puca et al., 1997); and ARSH (Sardiello et al., 2005). Several X-linked diseases associated with variants for these genes have been described, including chronic lymphocytic leukemia for ARSD (Trojani et al., 2011), chrondrodysplasia punctata for ARSE (Franco et al., 1995), and X-linked ichthyosis for STS (Basler et al., 1992).
Cloning and characterization of two extracellular heparin-degrading endosulfatases in mice and humans
2002, Journal of Biological ChemistryBiochemical characterization' of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata
1998, American Journal of Human Genetics
- ☆
M. D. AdamsC. FieldsJ. C. Venter, Eds.
- 1
The first two authors contributed equally to the work.
- 2
To whom correspondence should be addressed at Telethon Institute of Genetics and Medicine (TIGEM), San Raffaele Biomedical Science Park, Via Olgettina 58, 20132 Milan, Italy. Telephone: +39-2-21560202. Fax: +39-2-21560220. E-mail: [email protected].