These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 33120425)

  • 1. Lysosomal sulfatases: a growing family.
    Lübke T; Damme M
    Biochem J; 2020 Oct; 477(20):3963-3983. PubMed ID: 33120425
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and disease.
    von Figura K; Schmidt B; Selmer T; Dierks T
    Bioessays; 1998 Jun; 20(6):505-10. PubMed ID: 9699462
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Arylsulfatase K, a novel lysosomal sulfatase.
    Wiegmann EM; Westendorf E; Kalus I; Pringle TH; Lübke T; Dierks T
    J Biol Chem; 2013 Oct; 288(42):30019-30028. PubMed ID: 23986440
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Arylsulfatase G, a novel lysosomal sulfatase.
    Frese MA; Schulz S; Dierks T
    J Biol Chem; 2008 Apr; 283(17):11388-95. PubMed ID: 18283100
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes.
    Landgrebe J; Dierks T; Schmidt B; von Figura K
    Gene; 2003 Oct; 316():47-56. PubMed ID: 14563551
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction.
    Peng J; Alam S; Radhakrishnan K; Mariappan M; Rudolph MG; May C; Dierks T; von Figura K; Schmidt B
    FEBS J; 2015 Sep; 282(17):3262-74. PubMed ID: 26077311
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
    Schlotawa L; Adang LA; Radhakrishnan K; Ahrens-Nicklas RC
    Int J Mol Sci; 2020 May; 21(10):. PubMed ID: 32414121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulum.
    Mariappan M; Gande SL; Radhakrishnan K; Schmidt B; Dierks T; von Figura K
    J Biol Chem; 2008 Apr; 283(17):11556-64. PubMed ID: 18305113
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Conversion of cysteine to formylglycine: a protein modification in the endoplasmic reticulum.
    Dierks T; Schmidt B; von Figura K
    Proc Natl Acad Sci U S A; 1997 Oct; 94(22):11963-8. PubMed ID: 9342345
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sulfatases and human disease.
    Diez-Roux G; Ballabio A
    Annu Rev Genomics Hum Genet; 2005; 6():355-79. PubMed ID: 16124866
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mammalian Sulfatases: Biochemistry, Disease Manifestation, and Therapy.
    Mashima R; Nakanishi M
    Int J Mol Sci; 2022 Jul; 23(15):. PubMed ID: 35897729
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme.
    Dierks T; Schmidt B; Borissenko LV; Peng J; Preusser A; Mariappan M; von Figura K
    Cell; 2003 May; 113(4):435-44. PubMed ID: 12757705
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme.
    Dierks T; Dickmanns A; Preusser-Kunze A; Schmidt B; Mariappan M; von Figura K; Ficner R; Rudolph MG
    Cell; 2005 May; 121(4):541-552. PubMed ID: 15907468
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Measurement of recombinant human arylsulfatase A and leukocyte sulfatase activities by analytical isotachophoresis.
    Pajarola S; Weißenberg C; Baysal F; Bruchelt G; Krägeloh-Mann I; Böhringer J
    J Chromatogr B Analyt Technol Biomed Life Sci; 2019 Aug; 1124():109-113. PubMed ID: 31195190
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Posttranslational modification of serine to formylglycine in bacterial sulfatases. Recognition of the modification motif by the iron-sulfur protein AtsB.
    Marquordt C; Fang Q; Will E; Peng J; von Figura K; Dierks T
    J Biol Chem; 2003 Jan; 278(4):2212-8. PubMed ID: 12419807
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SUMF1 enhances sulfatase activities in vivo in five sulfatase deficiencies.
    Fraldi A; Biffi A; Lombardi A; Visigalli I; Pepe S; Settembre C; Nusco E; Auricchio A; Naldini L; Ballabio A; Cosma MP
    Biochem J; 2007 Apr; 403(2):305-12. PubMed ID: 17206939
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency.
    Schmidt B; Selmer T; Ingendoh A; von Figura K
    Cell; 1995 Jul; 82(2):271-8. PubMed ID: 7628016
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human sulfatases: a structural perspective to catalysis.
    Ghosh D
    Cell Mol Life Sci; 2007 Aug; 64(15):2013-22. PubMed ID: 17558559
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Purification, Characterization, and Structural Studies of a Sulfatase from
    Schlachter CR; O'Malley A; Grimes LL; Tomashek JJ; Chruszcz M; Lee LA
    Molecules; 2021 Dec; 27(1):. PubMed ID: 35011319
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Structure of a human lysosomal sulfatase.
    Bond CS; Clements PR; Ashby SJ; Collyer CA; Harrop SJ; Hopwood JJ; Guss JM
    Structure; 1997 Feb; 5(2):277-89. PubMed ID: 9032078
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.