Extract from the Register of European Patents

EP Citations: EP4043562

Cited inSearch
Type:Patent literature
Publication No.:WO2018141958  [ID]
 (UNIV BONN RHEINISCHE FRIEDRICH WILHELMS [DE]) [ID] 1-16 * the abstract; page 9455 * * page 27 - page 28; examples 5,6; claim -; sequence 4 *;
Type:Non-patent literature
Publication information:[I]  - VON BÜLOW RIXA ET AL, "Defective Oligomerization of Arylsulfatase A as a Cause of Its Instability in Lysosomes and Metachromatic Leukodystrophy", JOURNAL OF BIOLOGICAL CHEMISTRY, US, (20020102), vol. 277, no. 11, doi:10.1074/jbc.M111993200, ISSN 0021-9258, pages 9455 - 9461, XP055820743 [I] 1-16 * page 9458, column l, paragraph 1 * * the abstract * * abstract; page 9457, paragraph last - column r; figure 3 *
DOI: http://dx.doi.org/10.1074/jbc.M111993200
Type:Non-patent literature
Publication information:[I]  - VAGEDES PETER ET AL, "Driving Forces of Protein Association: The Dimer-Octamer Equilibrium in Arylsulfatase A", BIOPHYSICAL JOURNAL, AMSTERDAM, NL, (20021201), vol. 83, no. 6, doi:10.1016/S0006-3495(02)75311-3, ISSN 0006-3495, pages 3066 - 3078, XP055820736 [I] 1-16 * abstract; page 3066 - page 3067 * * page 3069, column l, paragraph 4 - column r; figures 6,7 *
DOI: http://dx.doi.org/10.1016/S0006-3495(02)75311-3
Type:Non-patent literature
Publication information:[I]  - SIMONIS HEIDI ET AL, "Evolutionary redesign of the lysosomal enzyme arylsulfatase A increases efficacy of enzyme replacement therapy for metachromatic leukodystrophy", HUMAN MOLECULAR GENETICS, vol. 28, no. 11, doi:10.1093/hmg/ddz020, ISSN 0964-6906, (20190601), pages 1810 - 1821, URL: https://watermark.silverchair.com/ddz020.pdf?token=AQECAHi208BE49Ooan9kkhW_Ercy7Dm3ZL_9Cf3qfKAc485ysgAAAtQwggLQBgkqhkiG9w0BBwagggLBMIICvQIBADCCArYGCSqGSIb3DQEHATAeBglghkgBZQMEAS4wEQQMX7200E1paP41bFeQAgEQgIICh3mGLWSXi8dGKm-JKCAsgA1uC5gSwbz_ZZPVDlhrvam_Kwq0-DDt38HM0cimWxp8i0YdOzKops95bt9EVvhSXRcPeS7lS, (20210705), XP055821250 [I] 1-16 * page 1811 - page 1812 *
DOI: http://dx.doi.org/10.1093/hmg/ddz020
Type:Non-patent literature
Publication information:[I]  - LUKATEKA G ET AL, "Crystal Structure of Human Arylsulfatase A: The Aldehyde Function and the Metal Ion at the Active Site Suggest a Novel Mechanism of Sulfate Ester Hydrolysis", BIOCHEMISTRY,, vol. 37, doi:10.1021/BI9714924, ISSN 0006-2960, (19980101), pages 3654 - 3664, (19980228), XP008104159 [I] 1-16 * page 3662, column r, paragraph 3 - paragraph 5 *
DOI: http://dx.doi.org/10.1021/bi9714924
Type:Non-patent literature
Publication information:[AD]  - SEVIN C ET AL, "Enzyme, cell and gene-based therapies for metachromatic leukodystrophy", JOURNAL OF INHERITED METABOLIC DISEASE, KLUWER ACADEMIC PUBLISHERS, DO, (20070308), vol. 30, no. 2, doi:10.1007/S10545-007-0540-Z, ISSN 1573-2665, pages 175 - 183, XP019478094 [AD] 1-16 * the whole document *
DOI: http://dx.doi.org/10.1007/s10545-007-0540-z
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