Pages that link to "Q37059497"

The following pages link to Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum (Q37059497):

Displaying 21 items.

• Inhibition of protein translation by the DISC1-Boymaw fusion gene from a Scottish family with major psychiatric disorders (Q30399814) (← links)
• Movement disorders and inborn errors of metabolism in adults: a diagnostic approach (Q31159730) (← links)
• A novel nine base deletion mutation in NADH-cytochrome b5 reductase gene in an Indian family with recessive congenital methemoglobinemia-type-II. (Q33800069) (← links)
• Membrane-bound CYB5R3 is a common effector of nutritional and oxidative stress response through FOXO3a and Nrf2. (Q34293370) (← links)
• Human cytochrome b5 reductase: structure, function, and potential applications (Q34309128) (← links)
• Molecular basis of two novel mutations found in type I methemoglobinemia. (Q34785789) (← links)
• A novel mutation in type II methemoglobinemia (Q34983185) (← links)
• Structure Guided Chemical Modifications of Propylthiouracil Reveal Novel Small Molecule Inhibitors of Cytochrome b5 Reductase 3 That Increase Nitric Oxide Bioavailability (Q35860552) (← links)
• Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy (Q35899112) (← links)
• Quantitative Systems Pharmacology Model of NO Metabolome and Methemoglobin Following Long-Term Infusion of Sodium Nitrite in Humans (Q37065414) (← links)
• Photoinitiated singlet and triplet electron transfer across a redesigned [myoglobin, cytochrome b5] interface (Q40506798) (← links)
• Neurometabolic disorder with microcephaly, dystonia, and central cyanosis masquerading as cerebral palsy. (Q41930834) (← links)
• Rare Case of Methemoglobinemia Complicating Pregnancy (Q42059530) (← links)
• The Role of Preoperative Evaluation for Congenital Methemoglobinemia (Q42740485) (← links)
• Cytochrome b5 Reductase 3 Modulates Soluble Guanylate Cyclase Redox State and cGMP Signaling (Q45060738) (← links)
• High expression of cytochrome b 5 reductase isoform 3/cytochrome b 5 system in the cerebellum and pyramidal neurons of adult rat brain. (Q46747223) (← links)
• Congenital methemoglobinemia type II in a 5-year-old boy. (Q48154829) (← links)
• Congenital Methemoglobinemia Type II-Clinical Improvement with Short-Term Methylene Blue Treatment. (Q50207187) (← links)
• Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India. (Q55057527) (← links)
• Cellular and Molecular Mechanisms of Recessive Hereditary Methaemoglobinaemia Type II (Q57478386) (← links)
• Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability (Q58716570) (← links)