BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 34741542)

  • 1. A defect in molybdenum cofactor binding causes an attenuated form of sulfite oxidase deficiency.
    Kaczmarek AT; Bender D; Gehling T; Kohl JB; Daimagüler HS; Santamaria-Araujo JA; Liebau MC; Koy A; Cirak S; Schwarz G
    J Inherit Metab Dis; 2022 Mar; 45(2):169-182. PubMed ID: 34741542
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Impaired mitochondrial maturation of sulfite oxidase in a patient with severe sulfite oxidase deficiency.
    Bender D; Kaczmarek AT; Santamaria-Araujo JA; Stueve B; Waltz S; Bartsch D; Kurian L; Cirak S; Schwarz G
    Hum Mol Genet; 2019 Sep; 28(17):2885-2899. PubMed ID: 31127934
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Oxygen and nitrite reduction by heme-deficient sulphite oxidase in a patient with mild sulphite oxidase deficiency.
    Bender D; Kaczmarek AT; Kuester S; Burlina AB; Schwarz G
    J Inherit Metab Dis; 2020 Jul; 43(4):748-757. PubMed ID: 31950508
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cofactor-dependent maturation of mammalian sulfite oxidase links two mitochondrial import pathways.
    Klein JM; Schwarz G
    J Cell Sci; 2012 Oct; 125(Pt 20):4876-85. PubMed ID: 22854042
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Obtaining the necessary molybdenum cofactor for sulfite oxidase activity in the nematode Caenorhabditis elegans surprisingly involves a dietary source.
    Oliphant KD; Fettig RR; Snoozy J; Mendel RR; Warnhoff K
    J Biol Chem; 2023 Jan; 299(1):102736. PubMed ID: 36423681
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.
    Sass JO; Gunduz A; Araujo Rodrigues Funayama C; Korkmaz B; Dantas Pinto KG; Tuysuz B; Yanasse Dos Santos L; Taskiran E; de Fátima Turcato M; Lam CW; Reiss J; Walter M; Yalcinkaya C; Camelo Junior JS
    Brain Dev; 2010 Aug; 32(7):544-9. PubMed ID: 19793632
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A mild case of molybdenum cofactor deficiency defines an alternative route of MOCS1 protein maturation.
    Mayr SJ; Sass JO; Vry J; Kirschner J; Mader I; Hövener JB; Reiss J; Santamaria-Araujo JA; Schwarz G; Grünert SC
    J Inherit Metab Dis; 2018 Mar; 41(2):187-196. PubMed ID: 29368224
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molybdenum Cofactor Deficiency in Humans.
    Johannes L; Fu CY; Schwarz G
    Molecules; 2022 Oct; 27(20):. PubMed ID: 36296488
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mechanistic complexities of sulfite oxidase: An enzyme with multiple domains, subunits, and cofactors.
    Enemark JH
    J Inorg Biochem; 2023 Oct; 247():112312. PubMed ID: 37441922
    [TBL] [Abstract][Full Text] [Related]  

  • 10. {Moco}
    Enemark JH
    J Inorg Biochem; 2022 Jun; 231():111801. PubMed ID: 35339771
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Oxygen reactivity of mammalian sulfite oxidase provides a concept for the treatment of sulfite oxidase deficiency.
    Belaidi AA; Röper J; Arjune S; Krizowski S; Trifunovic A; Schwarz G
    Biochem J; 2015 Jul; 469(2):211-21. PubMed ID: 26171830
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molybdenum cofactor transfer from bacteria to nematode mediates sulfite detoxification.
    Warnhoff K; Ruvkun G
    Nat Chem Biol; 2019 May; 15(5):480-488. PubMed ID: 30911177
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molybdenum cofactor and human disease.
    Schwarz G
    Curr Opin Chem Biol; 2016 Apr; 31():179-87. PubMed ID: 27055119
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients.
    Zaki MS; Selim L; El-Bassyouni HT; Issa MY; Mahmoud I; Ismail S; Girgis M; Sadek AA; Gleeson JG; Abdel Hamid MS
    Eur J Paediatr Neurol; 2016 Sep; 20(5):714-22. PubMed ID: 27289259
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a novel SUOX pathogenic variants as the cause of isolated sulfite oxidase deficiency in a Chinese pedigree.
    Du P; Hassan RN; Luo H; Xie J; Zhu Y; Hu Q; Yan J; Jiang W
    Mol Genet Genomic Med; 2021 Feb; 9(2):e1590. PubMed ID: 33405344
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole exome sequencing identified a homozygous novel mutation in SUOX gene causes extremely rare autosomal recessive isolated sulfite oxidase deficiency.
    Zhang R; Hao Y; Xu Y; Qin J; Wang Y; Kumar Dey S; Li C; Wang H; Banerjee S
    Clin Chim Acta; 2022 Jul; 532():115-122. PubMed ID: 35679912
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patients.
    Jakubiczka-Smorag J; Santamaria-Araujo JA; Metz I; Kumar A; Hakroush S; Brueck W; Schwarz G; Burfeind P; Reiss J; Smorag L
    Hum Genet; 2016 Jul; 135(7):813-26. PubMed ID: 27138983
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Elucidating the catalytic mechanism of sulfite oxidizing enzymes using structural, spectroscopic, and kinetic analyses.
    Johnson-Winters K; Tollin G; Enemark JH
    Biochemistry; 2010 Aug; 49(34):7242-54. PubMed ID: 20666399
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cell biology of molybdenum in plants.
    Mendel RR
    Plant Cell Rep; 2011 Oct; 30(10):1787-97. PubMed ID: 21660547
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Learning from the worm: the effectiveness of protein-bound Moco to treat Moco deficiency.
    Sewell AK; Han M
    Genes Dev; 2021 Feb; 35(3-4):177-179. PubMed ID: 33526584
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.