Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation
about
Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme functionHuman liver type pyruvate kinase: complete amino acid sequence and the expression in mammalian cellsStructure of a rabbit muscle fructose-1,6-bisphosphate aldolase A dimer variantFructose-bisphosphate aldolase a is a potential metastasis-associated marker of lung squamous cell carcinoma and promotes lung cell tumorigenesis and migrationSNPs, protein structure, and disease.Roles of 3-nitrotyrosine- and 4-hydroxynonenal-modified brain proteins in the progression and pathogenesis of Alzheimer's disease.Accumulation of citrullinated proteins by up-regulated peptidylarginine deiminase 2 in brains of scrapie-infected mice: a possible role in pathogenesisProteomic identification of nitrated brain proteins in early Alzheimer's disease inferior parietal lobuleA thermolabile aldolase A mutant causes fever-induced recurrent rhabdomyolysis without hemolytic anemia.Hereditary fructose intolerance caused by a nonsense mutation of the aldolase B gene.Oxidative proteome alterations during skeletal muscle ageingSubunit interface mutants of rabbit muscle aldolase form active dimersAcute rhabdomyolysis and inflammation.Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.Zebrafish homologs of genes within 16p11.2, a genomic region associated with brain disorders, are active during brain development, and include two deletion dosage sensor genes.Thermodynamic analysis of the dissociation of the aldolase tetramer substituted at one or both of the subunit interfaces.Studies with type I aldolase to understand fructose intolerance and combat parasitic disease.
P2860
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P2860
Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation
description
1987 nî lūn-bûn
@nan
1987 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Human aldolase A deficiency as ...... due to a single base mutation
@ast
Human aldolase A deficiency as ...... due to a single base mutation
@en
Human aldolase A deficiency as ...... due to a single base mutation
@nl
type
label
Human aldolase A deficiency as ...... due to a single base mutation
@ast
Human aldolase A deficiency as ...... due to a single base mutation
@en
Human aldolase A deficiency as ...... due to a single base mutation
@nl
prefLabel
Human aldolase A deficiency as ...... due to a single base mutation
@ast
Human aldolase A deficiency as ...... due to a single base mutation
@en
Human aldolase A deficiency as ...... due to a single base mutation
@nl
P2093
P2860
P356
P1476
Human aldolase A deficiency as ...... due to a single base mutation
@en
P2093
P2860
P304
P356
10.1073/PNAS.84.23.8623
P407
P577
1987-12-01T00:00:00Z