A defect in molybdenum cofactor binding causes an attenuated form of sulfite oxidase deficiency.

Autor: Kaczmarek AT; Department of Chemistry, Institute of Biochemistry, University of Cologne, Cologne, Germany.; Centre for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany., Bender D; Department of Chemistry, Institute of Biochemistry, University of Cologne, Cologne, Germany.; Department of Pediatric Neurology, University Children's Hospital Zurich, University of Zurich, Zurich, Switzerland., Gehling T; Department of Chemistry, Institute of Biochemistry, University of Cologne, Cologne, Germany., Kohl JB; Department of Chemistry, Institute of Biochemistry, University of Cologne, Cologne, Germany., Daimagüler HS; Centre for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.; Department of Pediatrics, University Hospital Cologne and Faculty of Medicine, University of Cologne, Cologne, Germany., Santamaria-Araujo JA; Department of Chemistry, Institute of Biochemistry, University of Cologne, Cologne, Germany., Liebau MC; Centre for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.; Department of Pediatrics, University Hospital Cologne and Faculty of Medicine, University of Cologne, Cologne, Germany., Koy A; Department of Pediatrics, University Hospital Cologne and Faculty of Medicine, University of Cologne, Cologne, Germany., Cirak S; Centre for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.; Department of Pediatrics, University Hospital Cologne and Faculty of Medicine, University of Cologne, Cologne, Germany., Schwarz G; Department of Chemistry, Institute of Biochemistry, University of Cologne, Cologne, Germany.; Centre for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.

Publikováno v: Journal of inherited metabolic disease [J Inherit Metab Dis] 2022 Mar; Vol. 45 (2), pp. 169-182. Date of Electronic Publication: 2021 Nov 24.

Delineating the phenotypic spectrum of sulfite oxidase and molybdenum cofactor deficiency.

Autor: Misko AL; Departments of Neurology (A.L.M., Y.L., F.E.), Massachusetts General Hospital and Harvard Medical School, Boston; and the Department of Chemistry (J.B.K.), Institute of Biochemistry, University of Cologne, Germany., Liang Y; Departments of Neurology (A.L.M., Y.L., F.E.), Massachusetts General Hospital and Harvard Medical School, Boston; and the Department of Chemistry (J.B.K.), Institute of Biochemistry, University of Cologne, Germany., Kohl JB; Departments of Neurology (A.L.M., Y.L., F.E.), Massachusetts General Hospital and Harvard Medical School, Boston; and the Department of Chemistry (J.B.K.), Institute of Biochemistry, University of Cologne, Germany., Eichler F; Departments of Neurology (A.L.M., Y.L., F.E.), Massachusetts General Hospital and Harvard Medical School, Boston; and the Department of Chemistry (J.B.K.), Institute of Biochemistry, University of Cologne, Germany.

Publikováno v: Neurology. Genetics [Neurol Genet] 2020 Jul 14; Vol. 6 (4), pp. e486. Date of Electronic Publication: 2020 Jul 14 (Print Publication: 2020).

Selective Persulfide Detection Reveals Evolutionarily Conserved Antiaging Effects of S-Sulfhydration.

Autor: Zivanovic J; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Kouroussis E; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Kohl JB; Department of Biochemistry, Center for Molecular Medicine, Institute of Biochemistry, University of Cologne, Cologne, Germany., Adhikari B; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Bursac B; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Schott-Roux S; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Petrovic D; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Miljkovic JL; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Thomas-Lopez D; Departamento de Sanidad Animal, Facultad de Veterinaria and VISAVET, Universidad Complutense de Madrid, Madrid, Spain., Jung Y; Department of Chemistry, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA., Miler M; Department of Cytology, Institute for Biological Research 'Sinisa Stankovic', National Institute of Republic of Serbia, University of Belgrade, Belgrade, Serbia., Mitchell S; Department of Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA 02115, USA., Milosevic V; Department of Cytology, Institute for Biological Research 'Sinisa Stankovic', National Institute of Republic of Serbia, University of Belgrade, Belgrade, Serbia., Gomes JE; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France., Benhar M; Department of Biochemistry, Rappaport Institute for Research in the Medical Sciences, Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel., Gonzalez-Zorn B; Departamento de Sanidad Animal, Facultad de Veterinaria and VISAVET, Universidad Complutense de Madrid, Madrid, Spain., Ivanovic-Burmazovic I; Department of Chemistry and Pharmacy, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany., Torregrossa R; University of Exeter Medical School, St. Luke's Campus, Exeter, UK., Mitchell JR; Department of Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA 02115, USA., Whiteman M; University of Exeter Medical School, St. Luke's Campus, Exeter, UK., Schwarz G; Department of Biochemistry, Center for Molecular Medicine, Institute of Biochemistry, University of Cologne, Cologne, Germany., Snyder SH; The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA., Paul BD; The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA., Carroll KS; Department of Chemistry, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA., Filipovic MR; CNRS, Institut de Biochimie et Génétique Cellulaires UMR5095, Université de Bordeaux, Bordeaux, France; Université de Bordeaux, CNRS, IBGC UMR5095, Bordeaux, France. Electronic address: milos.filipovic@ibgc.cnrs.fr.

Publikováno v: Cell metabolism [Cell Metab] 2019 Dec 03; Vol. 30 (6), pp. 1152-1170.e13. Date of Electronic Publication: 2019 Nov 14.

Chromatin balances cell redox and energy homeostasis.

Autor: Suganuma, Tamaki¹ (AUTHOR) tas@stowers.org, Workman, Jerry L.¹ (AUTHOR)

Publikováno v: Epigenetics & Chromatin. 11/28/2023, Vol. 16 Issue 1, p1-13. 13p.

Miro2 sulfhydration by CBS/H2S promotes human trophoblast invasion and migration via regulating mitochondria dynamics.

Autor: Feng, Hao, Sun, Zongxin, Han, Baoshi, Xia, Huitang, Chen, Lumei, Tian, Chunlei, Yan, Suhua, Shi, Yugen, Yin, Jie, Song, Wengang, Gong, Peipei, Wang, Shuanglian, Li, Yan

Publikováno v: Cell Death & Disease; Oct2024, Vol. 15 Issue 10, p1-18, 18p