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Page 1
[Methemoglobinemia].
Batton R, Villard S, Popoff B. Batton R, et al. Rev Med Interne. 2024 Aug;45(8):479-487. doi: 10.1016/j.revmed.2024.05.001. Epub 2024 May 21. Rev Med Interne. 2024. PMID: 38777656 Free article. Review. French.
The pathophysiology of MetHb involves NADH, NADPH and glucose cycle enzymes such as cytochrome-b5-reductase. MetHb can be acquired or more rarely, congenital. Acquired causes include drug-induced effects such as topical anesthetics, or toxic effects such as n …
The pathophysiology of MetHb involves NADH, NADPH and glucose cycle enzymes such as cytochrome-b5-reductase. MetHb can …
Concise review: methemoglobinemia.
Mansouri A, Lurie AA. Mansouri A, et al. Am J Hematol. 1993 Jan;42(1):7-12. doi: 10.1002/ajh.2830420104. Am J Hematol. 1993. PMID: 8416301 Review.
Under physiological conditions, methemoglobin reduction is accomplished mainly by red cell NADH-cytochrome b5 reductase (NADH-methemoglobin reductase) so efficiently that there is insignificant amounts of methemoglobin in the circulating blood. However …
Under physiological conditions, methemoglobin reduction is accomplished mainly by red cell NADH-cytochrome b5 reductase
Cytochrome b5 reductases: Redox regulators of cell homeostasis.
Hall R, Yuan S, Wood K, Katona M, Straub AC. Hall R, et al. J Biol Chem. 2022 Dec;298(12):102654. doi: 10.1016/j.jbc.2022.102654. Epub 2022 Oct 29. J Biol Chem. 2022. PMID: 36441026 Free PMC article. Review.
The cytochrome-b(5) reductase (CYB5R) family of flavoproteins is known to regulate reduction-oxidation (redox) balance in cells. ...Among the CYB5R genetic variants, CYB5R3 is well-characterized and deficiency in expression and activity is assoc …
The cytochrome-b(5) reductase (CYB5R) family of flavoproteins is known to regulate reduction-oxidation (redox) b …
Methaemoglobinaemia.
Jaffé ER. Jaffé ER. Clin Haematol. 1981 Feb;10(1):99-122. Clin Haematol. 1981. PMID: 7011627 Review. No abstract available.
Human cytochrome b5 reductase: structure, function, and potential applications.
Elahian F, Sepehrizadeh Z, Moghimi B, Mirzaei SA. Elahian F, et al. Crit Rev Biotechnol. 2014 Jun;34(2):134-43. doi: 10.3109/07388551.2012.732031. Epub 2012 Nov 1. Crit Rev Biotechnol. 2014. PMID: 23113554 Review.
Cytochrome b5 reductase is a flavoprotein that is produced as two different isoforms that have different localizations. ...Cytochrome b5 reductase is involved in the transfer of reducing equivalents from the physiological electron donor,
Cytochrome b5 reductase is a flavoprotein that is produced as two different isoforms that have different localizations.
Methemoglobin pathophysiology.
Jaffé ER. Jaffé ER. Prog Clin Biol Res. 1981;51:133-51. Prog Clin Biol Res. 1981. PMID: 7022466 Review.
Special emphasis is directed to the major and minor metabolic pathways in human erythrocytes that are involved in the reduction of methemoglobin, and evidence is presented that the NADH-methemoglobin reductase system, involving a soluble cytochrome b5 and NAD …
Special emphasis is directed to the major and minor metabolic pathways in human erythrocytes that are involved in the reduction of methemogl …
Enzymopenic hereditary methemoglobinemia.
Jaffé ER. Jaffé ER. Haematologia (Budap). 1982 Dec;15(4):389-99. Haematologia (Budap). 1982. PMID: 6764628 Review.
The major mechanism for this reductive capacity resides in the soluble cytochrome b5/NADH cytochrome b5 reductase of the cytosol which presumably arise from the microsomal proteins of the endoplasmic reticulum through proteolytic cleavage of the …
The major mechanism for this reductive capacity resides in the soluble cytochrome b5/NADH cytochrome b5 reduc
Disorders of oxidised haemoglobin.
Percy MJ, McFerran NV, Lappin TR. Percy MJ, et al. Blood Rev. 2005 Mar;19(2):61-8. doi: 10.1016/j.blre.2004.02.001. Blood Rev. 2005. PMID: 15603910 Review.
It can develop by three distinct mechanisms: genetic mutation resulting in the presence of abnormal haemoglobin, a deficiency of methaemoglobin reductase enzyme and toxin-induced oxidation of haemoglobin. ...Normally, haemoglobin continually oxidises but significant …
It can develop by three distinct mechanisms: genetic mutation resulting in the presence of abnormal haemoglobin, a deficiency of meth …
Adrenal changes associated with adrenarche.
Nakamura Y, Gang HX, Suzuki T, Sasano H, Rainey WE. Nakamura Y, et al. Rev Endocr Metab Disord. 2009 Mar;10(1):19-26. doi: 10.1007/s11154-008-9092-2. Rev Endocr Metab Disord. 2009. PMID: 18821019 Free PMC article. Review.
As adrenarche proceeds, the expanding ZR expresses greater levels of cytochrome b5 (CYB5) and steroid sulfotransferase (SULT2A1) than the adjacent fasciculata. In contrast, the growing ZR is deficient in 3beta-hydroxysteroid dehydrogenase type 2 (HSD3B2). The …
As adrenarche proceeds, the expanding ZR expresses greater levels of cytochrome b5 (CYB5) and steroid sulfotransferase (SULT2A …
Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency.
Percy MJ, Lappin TR. Percy MJ, et al. Br J Haematol. 2008 May;141(3):298-308. doi: 10.1111/j.1365-2141.2008.07017.x. Epub 2008 Mar 3. Br J Haematol. 2008. PMID: 18318771 Free article. Review.
This disorder, now known as recessive congenital methaemoglobinaemia (RCM), is caused by NADH-cytochrome b5 reductase (cb(5)r) deficiency. Two distinct clinical forms, types I and II, have been recognized, both characterized by cyanosis from birth. In …
This disorder, now known as recessive congenital methaemoglobinaemia (RCM), is caused by NADH-cytochrome b5 reductase ( …
28 results