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Article title matches
- Category:Kanzaki disease (46 bytes)
1: List of pages with the keyword Kanzaki disease - Category:Kaneko-Kanzaki, Y (48 bytes)
1: List of pages with the keyword Kaneko-Kanzaki, Y - Category:Kanzaki, H (41 bytes)
1: List of pages with the keyword Kanzaki, H - Category:Kanzaki H (40 bytes)
1: List of pages with the keyword Kanzaki H - Category:Kanzaki, Y (41 bytes)
1: List of pages with the keyword Kanzaki, Y - Category:Kaneko-Kanzaki Y (47 bytes)
1: List of pages with the keyword Kaneko-Kanzaki Y
Page text matches
- 2zoc (2,644 bytes)
11: [https://www.uniprot.org/uniprot/ANXA4_HUMAN ANXA4_HUMAN] Calcium/phospholipid-binding protein which p...
31: [[Category: Kaneko-Kanzaki Y]] - 3h53 (5,740 bytes)
11: ... deficiency type II or Schindler disease type II. Kanzaki disease is an autosomal recessive disorder charac...
13: [https://www.uniprot.org/uniprot/NAGAB_HUMAN NAGAB_HUMAN] Removes terminal alpha-N-acetylgalactosamine...
26: ...lysosomal storage disorders Schindler disease and Kanzaki disease. To better understand the molecular defec...
28: ...osaminidase: The molecular basis of Schindler and Kanzaki diseases.,Clark NE, Garman SC J Mol Biol. 2009 Oc... - 3h54 (5,835 bytes)
11: ... deficiency type II or Schindler disease type II. Kanzaki disease is an autosomal recessive disorder charac...
13: [https://www.uniprot.org/uniprot/NAGAB_HUMAN NAGAB_HUMAN] Removes terminal alpha-N-acetylgalactosamine...
26: ...lysosomal storage disorders Schindler disease and Kanzaki disease. To better understand the molecular defec...
28: ...osaminidase: The molecular basis of Schindler and Kanzaki diseases.,Clark NE, Garman SC J Mol Biol. 2009 Oc... - 3h55 (5,826 bytes)
11: ... deficiency type II or Schindler disease type II. Kanzaki disease is an autosomal recessive disorder charac...
13: [https://www.uniprot.org/uniprot/NAGAB_HUMAN NAGAB_HUMAN] Removes terminal alpha-N-acetylgalactosamine...
26: ...lysosomal storage disorders Schindler disease and Kanzaki disease. To better understand the molecular defec...
28: ...osaminidase: The molecular basis of Schindler and Kanzaki diseases.,Clark NE, Garman SC J Mol Biol. 2009 Oc... - 3igu (5,850 bytes)
11: ... deficiency type II or Schindler disease type II. Kanzaki disease is an autosomal recessive disorder charac...
13: [https://www.uniprot.org/uniprot/NAGAB_HUMAN NAGAB_HUMAN] Removes terminal alpha-N-acetylgalactosamine...
26: ...lysosomal storage disorders Schindler disease and Kanzaki disease. To better understand the molecular defec...
28: ...osaminidase: The molecular basis of Schindler and Kanzaki diseases.,Clark NE, Garman SC J Mol Biol. 2009 Oc... - Category:Kanzaki disease (46 bytes)
1: List of pages with the keyword Kanzaki disease - 4do4 (5,205 bytes)
11: ... deficiency type II or Schindler disease type II. Kanzaki disease is an autosomal recessive disorder charac...
13: [https://www.uniprot.org/uniprot/NAGAB_HUMAN NAGAB_HUMAN] Removes terminal alpha-N-acetylgalactosamine...
16: ...sults open two avenues for treatment of Schindler/Kanzaki disease and elucidate the atomic basis for pharma... - 4do5 (5,078 bytes)
11: ... deficiency type II or Schindler disease type II. Kanzaki disease is an autosomal recessive disorder charac...
13: [https://www.uniprot.org/uniprot/NAGAB_HUMAN NAGAB_HUMAN] Removes terminal alpha-N-acetylgalactosamine...
16: ...sults open two avenues for treatment of Schindler/Kanzaki disease and elucidate the atomic basis for pharma... - 4do6 (5,162 bytes)
11: ... deficiency type II or Schindler disease type II. Kanzaki disease is an autosomal recessive disorder charac...
13: [https://www.uniprot.org/uniprot/NAGAB_HUMAN NAGAB_HUMAN] Removes terminal alpha-N-acetylgalactosamine...
16: ...sults open two avenues for treatment of Schindler/Kanzaki disease and elucidate the atomic basis for pharma... - 3wv2 (4,597 bytes)
11: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Defects in MMP13 are the cause of spondyloep...
13: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Degrades collagen type I. Does not act on ge...
18: ... Mototani H, Oki H, Yamamoto Y, Kuno H, Santou T, Kanzaki N, Terauchi J, Uchikawa O, Kori M Bioorg Med Chem... - 3wv3 (4,730 bytes)
11: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Defects in MMP13 are the cause of spondyloep...
13: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Degrades collagen type I. Does not act on ge...
18: ... Mototani H, Oki H, Yamamoto Y, Kuno H, Santou T, Kanzaki N, Terauchi J, Uchikawa O, Kori M Bioorg Med Chem... - Category:Kaneko-Kanzaki, Y (48 bytes)
1: List of pages with the keyword Kaneko-Kanzaki, Y - 5a6p (3,240 bytes)
15: ...Saitoh H, Franceschetti M, Stevenson C, Uemura A, Kanzaki H, Kamoun S, Terauchi R, Banfield MJ Elife. 2015 ...
29: [[Category: Kanzaki H]] - Category:Kanzaki, H (41 bytes)
1: List of pages with the keyword Kanzaki, H - 5a6w (3,605 bytes)
16: ...Saitoh H, Franceschetti M, Stevenson C, Uemura A, Kanzaki H, Kamoun S, Terauchi R, Banfield MJ Elife. 2015 ...
31: [[Category: Kanzaki H]] - 5b5o (4,967 bytes)
11: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Defects in MMP13 are the cause of spondyloep...
13: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Degrades collagen type I. Does not act on ge...
18: ... Mototani H, Oki H, Yamamoto Y, Kuno H, Santou T, Kanzaki N, Terauchi J, Uchikawa O, Kori M J Med Chem. 201... - 5b5p (4,913 bytes)
11: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Defects in MMP13 are the cause of spondyloep...
13: [https://www.uniprot.org/uniprot/MMP13_HUMAN MMP13_HUMAN] Degrades collagen type I. Does not act on ge...
18: ... Mototani H, Oki H, Yamamoto Y, Kuno H, Santou T, Kanzaki N, Terauchi J, Uchikawa O, Kori M J Med Chem. 201... - Category:Kanzaki H (40 bytes)
1: List of pages with the keyword Kanzaki H - Category:Kanzaki, Y (41 bytes)
1: List of pages with the keyword Kanzaki, Y - Category:Kaneko-Kanzaki Y (47 bytes)
1: List of pages with the keyword Kaneko-Kanzaki Y
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