Cargando…

Cellular and Molecular Mechanisms of Recessive Hereditary Methaemoglobinaemia Type II

Cytochrome b5 reductase 3 (CYB5R3) is a membrane-bound NADH-dependent redox enzyme anchored to the mitochondrial outer membrane, endoplasmic reticulum, and plasma membrane. Recessive hereditary methaemoglobinaemia (RHM) type II is caused by CYB5R3 deficiency and is an incurable disease characterized...

Descripción completa

Detalles Bibliográficos
Autores principales:	Siendones, Emilio, Ballesteros, Manuel, Navas, Plácido
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2018
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210646/ https://www.ncbi.nlm.nih.gov/pubmed/30309019 http://dx.doi.org/10.3390/jcm7100341

Ejemplares similares

Undiagnosed intraoperative methaemoglobinaemia
por: Verma, Swapnil, et al.
Publicado: (2018)

Methaemoglobinaemia: Recognition and realisation at bedside
por: Senthilkumaran, Subramanian, et al.
Publicado: (2018)

Dapsone: Methaemoglobinaemia: case report
Publicado: (2021)

Acute Management of Cocaine-Associated Methaemoglobinaemia
por: Weichert, Immo
Publicado: (2011)

CYB5R3: a key player in aerobic metabolism and aging?
por: de Cabo, Rafael, et al.
Publicado: (2009)

Poppers Use and High Methaemoglobinaemia: ‘Dangerous Liaisons’
por: Barrangou-Poueys-Darlas, Malcolm, et al.
Publicado: (2021)

Phenazopyridine-Induced Methaemoglobinaemia The Aftermath of Dysuria Treatment
por: Hamza, Amina, et al.
Publicado: (2022)

Acute methaemoglobinaemia due to ingestion of nitrobenzene (paint solvent)
por: Saxena, Hema, et al.
Publicado: (2010)

Methaemoglobinaemia and the radical curative efficacy of 8-aminoquinoline antimalarials
por: White, Nicholas J, et al.
Publicado: (2022)

Chloroquine: Off-label use, haemolysis and methaemoglobinaemia: case report
Publicado: (2020)

Methaemoglobinaemia Can Complicate Normothermic Machine Perfusion of Human Livers
por: Tingle, Samuel J., et al.
Publicado: (2021)

Cell Survival from Chemotherapy Depends on NF-κB Transcriptional Up-Regulation of Coenzyme Q Biosynthesis
por: Brea-Calvo, Gloria, et al.
Publicado: (2009)

Acute methaemoglobinaemia initially treated as organophosphate poisoning leading to atropine toxicity
por: Kakhandki, Srinivas, et al.
Publicado: (2012)

Global methaemoglobinaemia research output (1940–2013): a bibliometric analysis
por: Zyoud, Sa’ed H., et al.
Publicado: (2015)

Dapsone: Methaemoglobinaemia, intravascular haemolysis and acute on chronic anaemia: case report
Publicado: (2021)

Dexamethasone/remdesivir/tocilizumab: Methaemoglobinaemia and off-label use: case report
Publicado: (2021)

Methaemoglobinaemia associated with use of glyceryl trinitrate patches in an extremely preterm infant
por: Pereira, Sujith S., et al.
Publicado: (2022)

Monitoring methaemoglobinaemia in birds using 5 μL of whole blood
por: Marks, Clive A., et al.
Publicado: (2023)

Molecular and Cellular Basis of Autosomal Recessive Primary Microcephaly
por: Barbelanne, Marine, et al.
Publicado: (2014)

Fatal oxidative haemolysis and methaemoglobinaemia in a patient with alkaptonuria and acute kidney injury
por: Mullan, Adam, et al.
Publicado: (2015)

N-acetylcysteine: a novel approach to methaemoglobinaemia in normothermic liver machine perfusion
por: Clarke, George, et al.
Publicado: (2023)

Neurological and Neuroimaging Features of CYB5R3-Related Recessive Hereditary Methemoglobinemia Type II
por: Nicita, Francesco, et al.
Publicado: (2022)

Fatal acute haemolysis and methaemoglobinaemia in a man with renal failure and Alkaptonuria – Is nitisinone the solution?
por: Davison, A.S., et al.
Publicado: (2020)

Methaemoglobinaemia in a patient scheduled for double valve replacement surgery - A case study
por: Manjunath, Girish, et al.
Publicado: (2023)

Methaemalbumin: a diagnostic surrogate for methaemoglobinaemia and treatment with red cell exchange in a patient with thalassaemia
por: Prus-Czarnecka, Zofia, et al.
Publicado: (2023)

The Autosomal Recessive Inheritance of Hereditary Gingival Fibromatosis
por: Majumder, Poulami, et al.
Publicado: (2013)

Sudden onset methaemoglobinaemia in a previously well Ugandan child: a case report and literature review
por: Nabukeera-Barungi, Nicolette, et al.
Publicado: (2012)

Molecular Mechanisms of Renal Cellular Nephrotoxicity due to Radiocontrast Media
por: Michael, Ashour, et al.
Publicado: (2014)

Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis
por: Hannah, Dawn M., et al.
Publicado: (2017)

Case Series of Autosomal Recessive Hereditary Spastic Paraplegia in Adults
por: Chakor, Rahul T., et al.
Publicado: (2021)

Hereditary sensory and autonomic neuropathies: types II, III, and IV
por: Axelrod, Felicia B, et al.
Publicado: (2007)

Brain arteriovenous malformation in hereditary hemorrhagic telangiectasia: Recent advances in cellular and molecular mechanisms
por: Drapé, Elise, et al.
Publicado: (2022)

Variants in MME are associated with autosomal‐recessive distal hereditary motor neuropathy
por: Hong, Daojun, et al.
Publicado: (2019)

Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy
por: Gerber, Sylvie, et al.
Publicado: (2023)

Autosomal recessive osteopetrosis: mechanisms and treatments
por: Penna, Sara, et al.
Publicado: (2021)

Editorial: Coenzyme Q Redox State and Cellular Homeostasis
por: Sanz, Alberto, et al.
Publicado: (2018)

Endometriosis: Cellular and Molecular Mechanisms Leading to Fibrosis
por: Garcia Garcia, Jose Manuel, et al.
Publicado: (2022)

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia
por: Wei, Qiao, et al.
Publicado: (2019)

Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy
por: Stenton, Sarah L., et al.
Publicado: (2021)

Association of SORD mutation with autosomal recessive asymmetric distal hereditary motor neuropathy
por: Alluqmani, Majed, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_9lof78sbjnv6bo4voptp8u471d