Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Joshua B. Kohl"'
Autor:
Hülya-Sevcan Daimagüler, Max C. Liebau, Daniel Bender, Joshua B. Kohl, Guenter Schwarz, Anne Koy, Jose Angel Santamaria-Araujo, Titus Gehling, Alexander T. Kaczmarek, Sebahattin Cirak
Publikováno v:
Journal of inherited metabolic diseaseREFERENCES. 45(2)
Isolated sulfite oxidase deficiency (ISOD) is a rare recessive and infantile lethal metabolic disorder, which is caused by functional loss of sulfite oxidase (SO) due to mutations of the SUOX gene. SO is a mitochondrially localized molybdenum cofacto
Selective Persulfide Detection Reveals Evolutionarily Conserved Antiaging Effects of S-Sulfhydration
Autor:
Jasmina Zivanovic, Sonia Schott-Roux, James R. Mitchell, Bikash Adhikari, Biljana Bursac, Guenter Schwarz, Jan Lj. Miljkovic, Sarah J. Mitchell, Bindu D. Paul, Daniel Thomas-Lopez, Milos R. Filipovic, Ivana Ivanović-Burmazović, Moran Benhar, Joshua B. Kohl, Roberta Torregrossa, José-Eduardo Gomes, Solomon H. Snyder, Bruno Gonzalez-Zorn, Kate S. Carroll, Matthew Whiteman, Verica Milošević, Youngeun Jung, Marko Miler, Emilia Kouroussis, Dunja Petrovic
Publikováno v:
Cell Metab
Cell Metabolism
Cell Metabolism, Elsevier, 2019, 30, pp.1152-1170.e13. ⟨10.1016/j.cmet.2019.10.007⟩
Cell Metabolism
Cell Metabolism, Elsevier, 2019, 30, pp.1152-1170.e13. ⟨10.1016/j.cmet.2019.10.007⟩
Summary Life on Earth emerged in a hydrogen sulfide (H2S)-rich environment eons ago and with it protein persulfidation mediated by H2S evolved as a signaling mechanism. Protein persulfidation (S-sulfhydration) is a post-translational modification of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab5fa8c7df85425ffabdccc1dfc9a546
https://europepmc.org/articles/PMC7249486/
https://europepmc.org/articles/PMC7249486/
Publikováno v:
British Journal of Pharmacology. 176:554-570
Cysteine is one of the two key sulfur-containing amino acids with important functions in redox homeostasis, protein functionality and metabolism. Cysteine is taken up by mammals via their diet and can also be derived from methionine via the transsulf
Publikováno v:
Neurology: Genetics
ObjectiveTo define the phenotypic spectrum of isolated sulfite oxidase (ISOD) and molybdenum cofactor deficiency (MoCD), aiming to promote timely diagnosis and assist in future clinical trial design.MethodsWe analyzed clinical, radiographic, biochemi