Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1.

scientific article published on 15 April 2013

Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.BBADIS.2013.04.010
P698PubMed publication ID23597595
P5875ResearchGate publication ID236226807

P50authorSonia FargueQ43091297
P2093author name stringGill Rumsby
Christopher J Danpure
P433issue10
P921main subjectpyridoxineQ423746
primary hyperoxaluriaQ7243137
P304page(s)1776-1783
P577publication date2013-04-15
P1433published inBiochimica et Biophysica ActaQ864239
P1476titleMultiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1.
P478volume1832

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cites work (P2860)
Q36997186Assessment of Urine Proteomics in Type 1 Primary Hyperoxaluria
Q30834734Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation type
Q40015456Effects of alanine:glyoxylate aminotransferase variants and pyridoxine sensitivity on oxalate metabolism in a cell-based cytotoxicity assay.
Q90280443Endpoints for Clinical Trials in Primary Hyperoxaluria
Q36188475Engineering a pyridoxal 5'-phosphate supply for cadaverine production by using Escherichia coli whole-cell biocatalysis
Q63441475Factors influencing clinical outcome in patients with primary hyperoxaluria type 1
Q47602222Folding Defects Leading to Primary Hyperoxaluria
Q36145370High throughput cell-based assay for identification of glycolate oxidase inhibitors as a potential treatment for Primary Hyperoxaluria Type 1
Q92439241Importance of Assessing Compliance with Conservative Treatment of Primary Hyperoxaluria Type 1: A Case Report of a Patient with I244T/c.969-3C>G Mutation
Q38200933Innovative strategies to treat protein misfolding in inborn errors of metabolism: pharmacological chaperones and proteostasis regulators.
Q34935451Kidney stones in primary hyperoxaluria: new lessons learnt
Q42182786Molecular recognition of PTS-1 cargo proteins by Pex5p: implications for protein mistargeting in primary hyperoxaluria.
Q34407663Pharmacologic rescue of an enzyme-trafficking defect in primary hyperoxaluria 1.
Q36104822Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria
Q36432868Predictors of Incident ESRD among Patients with Primary Hyperoxaluria Presenting Prior to Kidney Failure
Q38292247Primary hyperoxalurias: diagnosis and treatment
Q29147458Proline dehydrogenase 2 (PRODH2) is a hydroxyproline dehydrogenase (HYPDH) and molecular target for treating primary hyperoxaluria
Q30355120Protein homeostasis disorders of key enzymes of amino acids metabolism: mutation-induced protein kinetic destabilization and new therapeutic strategies.
Q50576688Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I.
Q90395008Recent advances in the identification and management of inherited hyperoxalurias
Q34379056S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation
Q53170036SNP Variants in RET and PAX2 and Their Possible Contribution to the Primary Hyperoxaluria Type 1 Phenotype.
Q35977167Sustained pyridoxine response in primary hyperoxaluria type 1 recipients of kidney alone transplant
Q58609046The Effect of Calcium and Vitamin B6 Supplementation on Oxalate Excretion in a Rodent Gastric Bypass Model of Enteric Hyperoxaluria
Q98463100The ILE56 mutation on different genetic backgrounds of alanine: Glyoxylate aminotransferase: Clinical features and biochemical characterization
Q27680557The Role of Protein Denaturation Energetics and Molecular Chaperones in the Aggregation and Mistargeting of Mutants Causing Primary Hyperoxaluria Type I
Q37267462Two novel AGXT mutations identified in primary hyperoxaluria type-1 and distinct morphological and structural difference in kidney stones
Q57818861Updated Genetic Testing of Primary Hyperoxaluria Type 1 in a Chinese Population: Results from a Single Center Study and a Systematic Review
Q37621553Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practice

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