Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H2S homeostasis-Reference-Cited by-同舟云学术

Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H2S homeostasis

Published:2022-12 Issue: Volume:58 Page:102517
ISSN:2213-2317
Container-title:Redox Biology
language:en
Short-container-title:Redox Biology

Author:

Kožich Viktor^ORCID,Schwahn Bernd C,Sokolová Jitka,Křížková Michaela,Ditroi Tamas,Krijt Jakub,Khalil Youssef,Křížek Tomáš,Vaculíková-Fantlová Tereza,Stibůrková Blanka,Mills Philippa,Clayton Peter,Barvíková Kristýna,Blessing Holger,Sykut-Cegielska Jolanta,Dionisi-Vici Carlo,Gasperini Serena,García-Cazorla Ángeles,Haack Tobias B,Honzík Tomáš,Ješina Pavel,Kuster Alice,Laugwitz Lucia,Martinelli Diego,Porta Francesco,Santer René,Schwarz Guenter,Nagy Peter

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,Clinical Biochemistry

Reference73 articles.

1. Controversies and conundrums in hydrogen sulfide biology;Olson;Nitric Oxide,2014

2. Physiological implications of hydrogen sulfide: a whiff exploration that blossomed;Wang;Physiol. Rev.,2012

3. Physiological roles of hydrogen sulfide in mammalian cells, tissues and organs;Cirino;Physiol. Rev.,2022

4. Gasotransmitters in cancer: from pathophysiology to experimental therapy;Szabo;Nat. Rev. Drug Discov.,2016

5. Hydrogen sulfide-based therapeutics: exploiting a unique but ubiquitous gasotransmitter;Wallace;Nat. Rev. Drug Discov.,2015

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