| 1 | ARSG, USH4
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| A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans.
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| Khateb S, Kowalewski B, Bedoni N, Damme M, Pollack N, Saada A, Obolensky A, Ben-Yosef T, Gross M, Dierks T, Banin E, Rivolta C, Sharon D.
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| Genet Med 20(9):1004-1012. doi: 10.1038/gim.2017.227. Epub 2018 Jan 4.
2018
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| 2 | ARSG
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| Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia.
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| Nibbeling E, Schaake S, Tijssen MA, Weissbach A, Groen JL, Altenmüller E, Verbeek DS, Lohmann K.
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| J Neurol 262(5):1340-3. doi: 10.1007/s00415-015-7718-3. Epub 2015 Apr 1.
2015
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| 3 | ARSG
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| Ataxia is the major neuropathological finding in arylsulfatase G-deficient mice: similarities and dissimilarities to Sanfilippo disease (mucopolysaccharidosis type III).
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| Kowalewski B, Heimann P, Ortkras T, Lüllmann-Rauch R, Sawada T, Walkley SU, Dierks T, Damme M.
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| Hum Mol Genet 24(7):1856-68. doi: 10.1093/hmg/ddu603. Epub 2014 Dec 1.
2015
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| 4 | ANK2, ARSG, CDH13, DCLK1, GRM8, RIMBP2, SLC16A6
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| Expression and replication studies to identify new candidate genes involved in normal hearing function.
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| Girotto G, Vuckovic D, Buniello A, Lorente-Cánovas B, Lewis M, Gasparini P, Steel KP.
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| PLoS One 9(1):e85352. doi: 10.1371/journal.pone.0085352. eCollection 2014. Erratum in: PLoS One. 2014;9(3):e91446.
2014
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| 5 | ARSG
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| Molecular characterization of arylsulfatase G: expression, processing, glycosylation, transport, and activity.
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| Kowalewski B, Lübke T, Kollmann K, Braulke T, Reinheckel T, Dierks T, Damme M.
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| J Biol Chem 289(40):27992-8005. doi: 10.1074/jbc.M114.584144. Epub 2014 Aug 18.
2014
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| 6 | ARSG
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| Arylsulfatase G inactivation causes loss of heparan sulfate 3-O-sulfatase activity and mucopolysaccharidosis in mice.
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| Kowalewski B, Lamanna WC, Lawrence R, Damme M, Stroobants S, Padva M, Kalus I, Frese MA, Lübke T, Lüllmann-Rauch R, D'Hooge R, Esko JD, Dierks T.
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| Proc Natl Acad Sci U S A 109(26):10310-5. doi: 10.1073/pnas.1202071109. Epub 2012 Jun 11.
2012
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| 7 | ARSG
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| Arylsulfatase g, a novel lysosomal sulfatase.
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| Frese MA, Schulz S, Dierks T.
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| J Biol Chem 283(17):11388-95. Epub 2008 Feb 18. 2008
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| 8 | ARSA, ARSB, ARSC2, ARSD, ARSE, ARSF, ARSG, ARSH, ARSJ, ARSK, ARSI, SUMF1, GALNS, SULF1, SULF2, SGSH, GNS, IDS
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| Sulfatases and sulfatase modifying factors: an exclusive and promiscuous relationship.
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| Sardiello M, Annunziata I, Roma G, Ballabio A.
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| Hum Mol Genet 14(21):3203-17. Epub 2005 Sep 20. 2005
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| 9 | ARSG
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| Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG).
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| Ferrante P, Messali S, Meroni G, Ballabio A.
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| Eur J Hum Genet 10(12):813-8. 2002
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| 10 | AKAP2, AMOTL2, ANKRD6, ARSG, ASXL1, ATG4B, BAHD1, BIRC6, BTBD3, C6orf84, CAMK2A, CAMKK2, CARD8, CHSY1, CORO2A, CPEB3, DIP2C, DLGAP4, DNAJC16, DNAJC9, DZIP1, EFR3B, EXOC6B, FAIM2, FASTKD2, FNBP4, INPP5F, LRCH1, NLGN4Y, NLRP1, NRXN2, PADI2, PCNX, PDS5B, PLEKHA6, PSD3, R3HDM2, RPH3A, SBNO2, SEZ6L, STK38L, TBC1D30, THOC5, TLL2, USP20, ZBTB1, ZFP30
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| Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
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| Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A,Kotani H, Nomura N, Ohara O.
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| DNA Res 6(1):63-70. 1999
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